geneid | 2572 |
---|---|
ensemblid | ENSG00000136750.13 |
hgncid | 4093 |
symbol | GAD2 |
name | glutamate decarboxylase 2 |
refseq_nuc | NM_001134366.2 |
refseq_prot | NP_001127838.1 |
ensembl_nuc | ENST00000376261.8 |
ensembl_prot | ENSP00000365437.3 |
mane_status | MANE Select |
chr | chr10 |
start | 26216774 |
end | 26304558 |
strand | + |
ver | v1.2 |
region | chr10:26216774-26304558 |
region5000 | chr10:26211774-26309558 |
regionname0 | GAD2_chr10_26216774_26304558 |
regionname5000 | GAD2_chr10_26211774_26309558 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 585 | 286 | 82 | 57 | 110 | 9 | 26 | 80 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0002 | 0/0 | 585 | 5 | 0 | 3 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0003 | 0/0 | 585 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0004 | 0/0 | 585 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1758 | 255 | 70 | 50 | 100 | 9 | 25 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
c0002 | 0/1 | 1758 | 17 | 0 | 5 | 10 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
c0003 | 0/0 | 1758 | 11 | 10 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
c0004 | 0/0 | 1758 | 5 | 0 | 3 | 0 | 2 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
c0005 | 0/0 | 1758 | 2 | 0 | 2 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
c0006 | 0/0 | 1758 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
c0007 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
c0008 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
c0009 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3632 | 83 | 15 | 16 | 43 | 2 | 7 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0002 | 1/0 | 3634 | 72 | 11 | 19 | 25 | 4 | 12 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0003 | 0/0 | 3634 | 42 | 0 | 7 | 26 | 5 | 4 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0004 | 0/0 | 3853 | 16 | 0 | 5 | 10 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0005 | 0/0 | 3637 | 14 | 13 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0006 | 0/0 | 3634 | 11 | 0 | 7 | 3 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0007 | 0/0 | 3675 | 8 | 7 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0008 | 0/0 | 3671 | 7 | 6 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0009 | 0/0 | 3638 | 6 | 5 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0010 | 0/0 | 3638 | 4 | 4 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0011 | 0/0 | 3638 | 4 | 3 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0012 | 0/0 | 3634 | 3 | 3 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0013 | 0/0 | 3638 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0014 | 0/0 | 3681 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0015 | 0/0 | 3632 | 2 | 1 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0016 | 0/0 | 3638 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0017 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0018 | 0/0 | 3634 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0019 | 0/0 | 3638 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0020 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0021 | 0/0 | 3634 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0022 | 0/0 | 3634 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0023 | 0/0 | 3638 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0024 | 0/0 | 3632 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0025 | 0/0 | 3646 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0026 | 0/0 | 3634 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0027 | 0/0 | 3568 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0028 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0029 | 0/0 | 3800 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0030 | 0/1 | 3853 | 1 | 0 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0031 | 0/0 | 3634 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
t0032 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1758 | 255 | 70 | 50 | 100 | 9 | 25 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0002 | 0/1 | 1758 | 17 | 0 | 5 | 10 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0003 | 0/0 | 1758 | 11 | 10 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0007 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0008 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0009 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0002c0004 | 0/0 | 1758 | 5 | 0 | 3 | 0 | 2 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0003c0005 | 0/0 | 1758 | 2 | 0 | 2 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0004c0006 | 0/0 | 1758 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5389 | 83 | 15 | 16 | 43 | 2 | 7 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0002 | 1/0 | 5391 | 67 | 10 | 17 | 25 | 2 | 12 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0003 | 0/0 | 5391 | 38 | 0 | 3 | 26 | 5 | 4 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0005 | 0/0 | 5394 | 10 | 9 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0006 | 0/0 | 5391 | 11 | 0 | 7 | 3 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0007 | 0/0 | 5432 | 8 | 7 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0008 | 0/0 | 5428 | 7 | 6 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0009 | 0/0 | 5395 | 5 | 4 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0011 | 0/0 | 5395 | 4 | 3 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0012 | 0/0 | 5391 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0013 | 0/0 | 5395 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0014 | 0/0 | 5438 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0015 | 0/0 | 5389 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0016 | 0/0 | 5395 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0017 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0018 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0019 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0020 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0021 | 0/0 | 5391 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0022 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0023 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0024 | 0/0 | 5389 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0025 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0026 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0027 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0028 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0001t0031 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0002t0004 | 0/0 | 5610 | 16 | 0 | 5 | 10 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0002t0030 | 0/1 | 5610 | 1 | 0 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0003t0002 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0003t0005 | 0/0 | 5394 | 4 | 4 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0003t0009 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0003t0010 | 0/0 | 5395 | 4 | 4 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0003t0015 | 0/0 | 5389 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0007t0012 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0008t0003 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0001c0009t0032 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0002c0004t0002 | 0/0 | 5391 | 2 | 0 | 0 | 0 | 2 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0002c0004t0003 | 0/0 | 5391 | 3 | 0 | 3 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0003c0005t0002 | 0/0 | 5391 | 2 | 0 | 2 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
a0004c0006t0029 | 0/0 | 5557 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | copy fasta | chr10 | 26211774 | 26309558 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0006g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0007g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0007g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0008g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0008g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0008g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0009g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0009g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0011g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0011g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0013g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0013g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0014g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0016g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0016g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0017g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0018g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0019g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0020g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0021g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0022g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0023g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0024g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0025g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0026g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0027g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0028g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0001t0031g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0002t0030g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0003t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0003t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0003t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0003t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0003t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0003t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0003t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0003t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0003t0010g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0003t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0003t0015g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0007t0012g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0008t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0001c0009t0032g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0002c0004t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0002c0004t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0002c0004t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0002c0004t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0002c0004t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0003c0005t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0003c0005t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
a0004c0006t0029g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0169 | EUR | GBR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0170 | EUR | FIN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0210 | EUR | FIN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | FIN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00323 | hp2 | a0004 | c0006 | t0029 | g0117 | EUR | FIN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00438 | hp2 | a0001 | c0001 | t0025 | g0199 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00544 | hp2 | a0001 | c0002 | t0004 | g0239 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00639 | hp2 | a0001 | c0002 | t0004 | g0118 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00642 | hp1 | a0001 | c0001 | t0011 | g0109 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00642 | hp2 | a0001 | c0001 | t0007 | g0104 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00735 | hp1 | a0001 | c0001 | t0009 | g0009 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01070 | hp1 | a0002 | c0004 | t0003 | g0197 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01071 | hp2 | a0002 | c0004 | t0003 | g0198 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0153 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01168 | hp1 | a0001 | c0002 | t0004 | g0115 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0036 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01169 | hp2 | a0001 | c0002 | t0004 | g0116 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01192 | hp1 | a0001 | c0001 | t0008 | g0065 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0243 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01243 | hp2 | a0001 | c0003 | t0015 | g0267 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01255 | hp2 | a0001 | c0002 | t0004 | g0120 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01256 | hp1 | a0002 | c0004 | t0003 | g0214 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01358 | hp1 | a0001 | c0001 | t0018 | g0222 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01516 | hp1 | a0002 | c0004 | t0002 | g0193 | EUR | IBS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0233 | EUR | IBS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0221 | EUR | IBS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01517 | hp2 | a0002 | c0004 | t0002 | g0194 | EUR | IBS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01884 | hp1 | a0001 | c0009 | t0032 | g0265 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01884 | hp2 | a0001 | c0001 | t0012 | g0106 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01934 | hp1 | a0001 | c0001 | t0006 | g0158 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01952 | hp2 | a0003 | c0005 | t0002 | g0227 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01978 | hp1 | a0001 | c0001 | t0006 | g0172 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01981 | hp1 | a0003 | c0005 | t0002 | g0226 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02004 | hp1 | a0001 | c0002 | t0004 | g0119 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02004 | hp2 | a0001 | c0001 | t0006 | g0171 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02080 | hp1 | a0001 | c0002 | t0004 | g0240 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02083 | hp1 | a0001 | c0002 | t0004 | g0007 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02145 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02148 | hp2 | a0001 | c0008 | t0003 | g0002 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02155 | hp1 | a0001 | c0002 | t0004 | g0007 | EAS | CDX | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CDX | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02165 | hp2 | a0001 | c0002 | t0004 | g0237 | EAS | CDX | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02257 | hp1 | a0001 | c0003 | t0002 | g0266 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0064 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02258 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02273 | hp2 | a0001 | c0001 | t0006 | g0035 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0108 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02293 | hp2 | a0001 | c0001 | t0031 | g0147 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0203 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0062 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02451 | hp2 | a0001 | c0001 | t0014 | g0105 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02572 | hp1 | a0001 | c0003 | t0010 | g0248 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0262 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02615 | hp2 | a0001 | c0003 | t0010 | g0246 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02622 | hp1 | a0001 | c0001 | t0011 | g0112 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0257 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02630 | hp1 | a0001 | c0003 | t0009 | g0249 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0256 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02647 | hp1 | a0001 | c0003 | t0005 | g0113 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02735 | hp2 | a0001 | c0001 | t0021 | g0195 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02809 | hp1 | a0001 | c0001 | t0016 | g0279 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02818 | hp1 | a0001 | c0001 | t0011 | g0110 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02818 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02886 | hp1 | a0001 | c0001 | t0011 | g0111 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02886 | hp2 | a0001 | c0003 | t0010 | g0247 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0255 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02896 | hp2 | a0001 | c0001 | t0008 | g0271 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0273 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02922 | hp2 | a0001 | c0003 | t0005 | g0264 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0270 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0258 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0252 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03139 | hp2 | a0001 | c0001 | t0008 | g0272 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03195 | hp1 | a0001 | c0001 | t0019 | g0107 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03195 | hp2 | a0001 | c0003 | t0005 | g0250 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03209 | hp2 | a0001 | c0001 | t0013 | g0268 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03225 | hp1 | a0001 | c0001 | t0023 | g0251 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03225 | hp2 | a0001 | c0003 | t0010 | g0245 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03486 | hp1 | a0001 | c0007 | t0012 | g0259 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03486 | hp2 | a0001 | c0001 | t0028 | g0280 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03516 | hp1 | a0001 | c0001 | t0017 | g0012 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0254 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03540 | hp1 | a0001 | c0001 | t0024 | g0075 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03831 | hp1 | a0001 | c0002 | t0004 | g0241 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03927 | hp1 | a0001 | c0001 | t0006 | g0204 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0201 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | STU | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | STU | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18522 | hp1 | a0001 | c0001 | t0016 | g0274 | AFR | YRI | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0215 | AFR | YRI | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | CHB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | CHB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0079 | EAS | CHB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0100 | AFR | YRI | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18960 | hp1 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18960 | hp2 | a0001 | c0002 | t0004 | g0031 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18965 | hp1 | a0001 | c0002 | t0004 | g0008 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18988 | hp1 | a0001 | c0002 | t0004 | g0236 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18995 | hp2 | a0001 | c0001 | t0022 | g0220 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18999 | hp1 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19030 | hp2 | a0001 | c0003 | t0005 | g0242 | AFR | LWK | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | LWK | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0253 | AFR | LWK | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19074 | hp1 | a0001 | c0002 | t0004 | g0235 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19085 | hp2 | a0001 | c0001 | t0026 | g0098 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19087 | hp1 | a0001 | c0002 | t0004 | g0008 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA20129 | hp1 | a0001 | c0001 | t0015 | g0101 | AFR | ASW | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ASW | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | TSI | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | GIH | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | GIH | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0263 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03471 | hp1 | a0001 | c0001 | t0014 | g0059 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG03471 | hp2 | a0001 | c0001 | t0013 | g0269 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | USA | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
HG06807 | hp2 | a0001 | c0001 | t0020 | g0283 | AFR | USA | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | USA | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
NA20300 | hp2 | a0001 | c0001 | t0027 | g0202 | AFR | USA | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0030 | g0114 | REF | REF | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0151 | REF | REF | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:26224539
|
G | A | 1 | a0004 | 1 | HG00323.hp2 | missense_variant&splice_region_variant | MODERATE | c.612G>A | p.Met204Ile | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/16 | 648/5391 | 612/1758 | 204/585 | chr10 | 26224539 | ||
chr10:26224610
|
T | C | 1 | a0003 | 2 | HG01952.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.683T>C | p.Ile228Thr | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/16 | 719/5391 | 683/1758 | 228/585 | chr10 | 26224610 | ||
chr10:26224622
|
G | A | 1 | a0002 | 5 | HG01070.hp1 HG01071.hp2 HG01256.hp1 others(2): Show |
missense_variant | MODERATE | c.695G>A | p.Gly232Glu | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/16 | 731/5391 | 695/1758 | 232/585 | chr10 | 26224622 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:26216842
|
C | T | 2 | a0001c0003a0001c0009 | 12 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(9): Show |
synonymous_variant | LOW | c.33C>T | p.Phe11Phe | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/16 | 69/5391 | 33/1758 | 11/585 | chr10 | 26216842 | ||
chr10:26217930
|
C | T | 1 | a0001c0008 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.225C>T | p.Cys75Cys | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/16 | 261/5391 | 225/1758 | 75/585 | chr10 | 26217930 | ||
chr10:26270642
|
G | C | 2 | a0001c0002a0004c0006 | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
splice_region_variant&synonymous_variant | LOW | c.978G>C | p.Gly326Gly | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/16 | 1014/5391 | 978/1758 | 326/585 | chr10 | 26270642 | ||
chr10:26273650
|
G | A | 1 | a0001c0009 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1107G>A | p.Gly369Gly | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/16 | 1143/5391 | 1107/1758 | 369/585 | chr10 | 26273650 | ||
chr10:26281024
|
G | A | 1 | a0001c0007 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1173G>A | p.Thr391Thr | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/16 | 1209/5391 | 1173/1758 | 391/585 | chr10 | 26281024 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:26301147
|
C | T | 1 | a0001c0009t0032 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 186 | chr10 | 26301147 | |||||
chr10:26301152
|
C | G | 1 | a0001c0001t0031 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 191 | chr10 | 26301152 | |||||
chr10:26301387
|
A | T | 3 | a0001c0002t0004a0001c0002t0030a0004c0006t0029 | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*426A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 426 | chr10 | 26301387 | |||||
chr10:26301517
|
T | C | 1 | a0001c0001t0017 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*556T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 556 | chr10 | 26301517 | |||||
chr10:26301566
|
AT | A | 3 | a0001c0002t0004a0001c0002t0030a0004c0006t0029 | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*614delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 614 | INFO_REALIGN_3_PRIME | chr10 | 26301566 | ||||
chr10:26301670
|
A | G | 1 | a0001c0001t0028 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*709A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 709 | chr10 | 26301670 | |||||
chr10:26301711
|
A | C | 1 | a0001c0001t0008 | 7 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*750A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 750 | chr10 | 26301711 | |||||
chr10:26301720
|
A | G | 1 | a0001c0001t0008 | 7 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*759A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 759 | chr10 | 26301720 | |||||
chr10:26301735
|
G | A | 1 | a0001c0001t0018 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 774 | chr10 | 26301735 | |||||
chr10:26301795
|
A | G | 1 | a0001c0002t0030 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*834A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 834 | chr10 | 26301795 | |||||
chr10:26301852
|
AGATTAAA others(59): Show |
A | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*893_*958delATTAAA others(60): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 893 | INFO_REALIGN_3_PRIME | chr10 | 26301852 | ||||
chr10:26301920
|
C | T | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*959C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 959 | chr10 | 26301920 | |||||
chr10:26302005
|
C | G | 7 | a0001c0001t0003a0001c0001t0006a0001c0001t0025others(4): Show | 56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1044C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1044 | chr10 | 26302005 | |||||
chr10:26302081
|
A | G | 7 | a0001c0001t0001a0001c0001t0009a0001c0001t0015others(4): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1120A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1120 | chr10 | 26302081 | |||||
chr10:26302228
|
A | G | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1267A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1267 | chr10 | 26302228 | |||||
chr10:26302229
|
C | A | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1268C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1268 | chr10 | 26302229 | |||||
chr10:26302232
|
A | C | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1271 | chr10 | 26302232 | |||||
chr10:26302257
|
G | C | 1 | a0001c0001t0024 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1296G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1296 | chr10 | 26302257 | |||||
chr10:26302341
|
C | T | 3 | a0001c0002t0004a0001c0002t0030a0004c0006t0029 | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1380C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1380 | chr10 | 26302341 | |||||
chr10:26302352
|
G | A | 2 | a0001c0001t0013a0001c0003t0010 | 6 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1391G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1391 | chr10 | 26302352 | |||||
chr10:26302459
|
C | T | 1 | a0001c0001t0023 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1498C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1498 | chr10 | 26302459 | |||||
chr10:26302465
|
T | C | 1 | a0001c0001t0013 | 2 | HG03209.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1504T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1504 | chr10 | 26302465 | |||||
chr10:26302650
|
G | A | 16 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(13): Show | 120 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1689G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1689 | chr10 | 26302650 | |||||
chr10:26302652
|
C | T | 1 | a0001c0001t0026 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1691C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1691 | chr10 | 26302652 | |||||
chr10:26302942
|
C | T | 1 | a0001c0001t0022 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1981C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1981 | chr10 | 26302942 | |||||
chr10:26302994
|
A | T | 2 | a0001c0001t0009a0001c0003t0009 | 6 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2033A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2033 | chr10 | 26302994 | |||||
chr10:26303059
|
G | T | 12 | a0001c0001t0001a0001c0001t0009a0001c0001t0014others(9): Show | 100 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2098G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2098 | chr10 | 26303059 | |||||
chr10:26303146
|
T | C | 1 | a0001c0001t0014 | 2 | HG02451.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2185T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2185 | chr10 | 26303146 | |||||
chr10:26303261
|
G | A | 7 | a0001c0001t0005a0001c0001t0013a0001c0001t0017others(4): Show | 23 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2300G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2300 | chr10 | 26303261 | |||||
chr10:26303269
|
AC | A | 6 | a0001c0001t0005a0001c0001t0017a0001c0001t0020others(3): Show | 18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2312delC | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2312 | INFO_REALIGN_3_PRIME | chr10 | 26303269 | ||||
chr10:26303293
|
T | C | 1 | a0001c0001t0014 | 2 | HG02451.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2332T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2332 | chr10 | 26303293 | |||||
chr10:26303432
|
G | C | 2 | a0001c0001t0015a0001c0003t0015 | 2 | HG01243.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2471G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2471 | chr10 | 26303432 | |||||
chr10:26303444
|
A | AAGGGAGG others(5): Show |
1 | a0001c0001t0025 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2497_*2508dupGGGA others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2509 | INFO_REALIGN_3_PRIME | chr10 | 26303444 | ||||
chr10:26303448
|
G | GAGGGAGG others(38): Show |
1 | a0001c0001t0014 | 2 | HG02451.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2498_*2499insAAGG others(41): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2499 | INFO_REALIGN_3_PRIME | chr10 | 26303448 | ||||
chr10:26303448
|
G | GAGGGAGG others(148): Show |
1 | a0004c0006t0029 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2498_*2499insAAGG others(151): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2499 | INFO_REALIGN_3_PRIME | chr10 | 26303448 | ||||
chr10:26303448
|
G | GAGGGAGG others(201): Show |
2 | a0001c0002t0004a0001c0002t0030 | 17 | HG00544.hp2 HG00639.hp2 HG01168.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2498_*2499insAAGG others(204): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2499 | INFO_REALIGN_3_PRIME | chr10 | 26303448 | ||||
chr10:26303456
|
G | GAGGA | 15 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(12): Show | 121 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2498_*2499insAAGG | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2499 | INFO_REALIGN_3_PRIME | chr10 | 26303456 | ||||
chr10:26303456
|
G | GAGGAAGG others(34): Show |
1 | a0001c0001t0007 | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2498_*2499insAAGG others(37): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2499 | INFO_REALIGN_3_PRIME | chr10 | 26303456 | ||||
chr10:26303460
|
G | A | 4 | a0001c0001t0008a0001c0001t0017a0001c0001t0020others(1): Show | 10 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2499G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2499 | chr10 | 26303460 | |||||
chr10:26303462
|
G | A | 15 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(12): Show | 121 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2501G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2501 | chr10 | 26303462 | |||||
chr10:26303466
|
G | A | 4 | a0001c0001t0008a0001c0001t0017a0001c0001t0020others(1): Show | 10 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2505G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2505 | chr10 | 26303466 | |||||
chr10:26303468
|
G | A | 4 | a0001c0001t0014a0001c0002t0004a0001c0002t0030others(1): Show | 20 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2507G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2507 | chr10 | 26303468 | |||||
chr10:26303470
|
A | G | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(17): Show | 139 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*2509A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2509 | chr10 | 26303470 | |||||
chr10:26303476
|
G | A | 14 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(11): Show | 124 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2515G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2515 | chr10 | 26303476 | |||||
chr10:26303480
|
G | A | 19 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(16): Show | 132 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*2519G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2519 | chr10 | 26303480 | |||||
chr10:26303480
|
G | GAGGAAGG others(1): Show |
4 | a0001c0001t0014a0001c0002t0004a0001c0002t0030others(1): Show | 20 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2521_*2528dupGGAA others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2529 | INFO_REALIGN_3_PRIME | chr10 | 26303480 | ||||
chr10:26303480
|
G | GAGGAAGG others(30): Show |
1 | a0001c0001t0008 | 7 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2528_*2529insGGAA others(33): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2529 | INFO_REALIGN_3_PRIME | chr10 | 26303480 | ||||
chr10:26303483
|
G | A | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2522G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2522 | chr10 | 26303483 | |||||
chr10:26303491
|
T | G | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2530T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2530 | chr10 | 26303491 | |||||
chr10:26303493
|
A | AAGGG | 3 | a0001c0002t0004a0001c0002t0030a0004c0006t0029 | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2548_*2551dupGAGG | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2552 | INFO_REALIGN_3_PRIME | chr10 | 26303493 | ||||
chr10:26303499
|
G | C | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2538G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2538 | chr10 | 26303499 | |||||
chr10:26303511
|
G | A | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2550G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2550 | chr10 | 26303511 | |||||
chr10:26303513
|
A | G | 2 | a0001c0001t0006a0001c0001t0027 | 12 | HG01109.hp2 HG01168.hp2 HG01934.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2552A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2552 | chr10 | 26303513 | |||||
chr10:26303514
|
A | G | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2553A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2553 | chr10 | 26303514 | |||||
chr10:26303541
|
C | T | 1 | a0001c0001t0021 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2580C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2580 | chr10 | 26303541 | |||||
chr10:26303656
|
T | C | 5 | a0001c0001t0009a0001c0001t0016a0001c0001t0019others(2): Show | 10 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2695T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2695 | chr10 | 26303656 | |||||
chr10:26303689
|
G | A | 2 | a0001c0001t0012a0001c0007t0012 | 3 | HG01884.hp2 HG02451.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2728G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2728 | chr10 | 26303689 | |||||
chr10:26303931
|
G | A | 1 | a0001c0001t0011 | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2970G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2970 | chr10 | 26303931 | |||||
chr10:26303980
|
TTCTCTC | T | 6 | a0001c0001t0001a0001c0001t0014a0001c0001t0015others(3): Show | 89 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*3031_*3036delCTCT others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 3031 | INFO_REALIGN_3_PRIME | chr10 | 26303980 | ||||
chr10:26304014
|
C | G | 2 | a0001c0001t0020a0001c0001t0028 | 2 | HG03486.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3053C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 3053 | chr10 | 26304014 | |||||
chr10:26304154
|
T | C | 1 | a0001c0001t0021 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3193T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 3193 | chr10 | 26304154 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:26216893
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(94): Show | 101 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
splice_region_variant&intron_variant | LOW | c.76+8G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | chr10 | 26216893 | ||||||
chr10:26216930
|
G | A | 1 | a0001c0001t0007g0104 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.76+45G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | chr10 | 26216930 | ||||||
chr10:26217001
|
G | C | 3 | a0001c0001t0009g0003a0001c0001t0009g0009a0001c0001t0009g0010 | 4 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.76+116G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | chr10 | 26217001 | ||||||
chr10:26217230
|
G | GA | 10 | a0001c0001t0001g0011a0001c0001t0005g0108a0001c0001t0011g0109others(7): Show | 10 | HG00642.hp1 HG01884.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.76+355dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr10 | 26217230 | |||||
chr10:26217253
|
G | T | 1 | a0001c0001t0020g0283 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.77-357G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | chr10 | 26217253 | ||||||
chr10:26217392
|
C | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0028g0280 | 3 | HG01106.hp1 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.77-218C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | chr10 | 26217392 | ||||||
chr10:26217455
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.77-155C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | chr10 | 26217455 | ||||||
chr10:26217823
|
G | T | 6 | a0001c0001t0005g0108a0001c0001t0011g0109a0001c0001t0011g0110others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.137-19G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 2/15 | chr10 | 26217823 | ||||||
chr10:26218060
|
C | A | 1 | a0001c0003t0005g0113 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286+69C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218060 | ||||||
chr10:26218070
|
G | A | 7 | a0001c0002t0004g0115a0001c0002t0004g0116a0001c0002t0004g0118others(4): Show | 7 | HG00323.hp2 HG00639.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+79G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218070 | ||||||
chr10:26218070
|
G | T | 1 | a0001c0001t0001g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.286+79G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218070 | ||||||
chr10:26218079
|
C | G | 2 | a0001c0001t0015g0101a0001c0001t0017g0012 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.286+88C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218079 | ||||||
chr10:26218080
|
G | A | 1 | a0001c0001t0006g0121 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.286+89G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218080 | ||||||
chr10:26218101
|
A | G | 70 | a0001c0001t0001g0238a0001c0001t0001g0281a0001c0001t0001g0282others(67): Show | 72 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.286+110A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218101 | ||||||
chr10:26218227
|
C | G | 1 | a0001c0001t0002g0234 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.286+236C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218227 | ||||||
chr10:26218233
|
C | T | 1 | a0001c0001t0002g0234 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.286+242C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218233 | ||||||
chr10:26218259
|
C | T | 47 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(44): Show | 47 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.286+268C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218259 | ||||||
chr10:26218295
|
G | T | 6 | a0001c0001t0005g0108a0001c0001t0011g0109a0001c0001t0011g0110others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+304G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218295 | ||||||
chr10:26218535
|
G | GCT | 14 | a0001c0001t0001g0014a0001c0001t0001g0057a0001c0001t0001g0058others(11): Show | 15 | HG00735.hp1 HG01099.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.287-492_287-491dup others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218535 | |||||
chr10:26218535
|
G | GCTCT | 16 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0007g0104others(13): Show | 16 | HG00642.hp2 HG01346.hp1 HG02300.hp2 others(13): Show |
intron_variant | MODIFIER | c.287-494_287-491dup others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218535 | |||||
chr10:26218535
|
G | GCTCTCT | 3 | a0001c0001t0001g0053a0001c0001t0012g0106a0001c0001t0013g0268 | 3 | HG01884.hp2 HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.287-496_287-491dup others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218535 | |||||
chr10:26218535
|
G | GCTCTCTC others(1): Show |
9 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(6): Show | 9 | HG02559.hp1 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-498_287-491dup others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218535 | |||||
chr10:26218544
|
C | G | 1 | a0001c0001t0003g0233 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.287-499C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218544 | ||||||
chr10:26218551
|
T | A | 3 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0009g0100 | 3 | HG03831.hp2 HG04199.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.287-492T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218551 | ||||||
chr10:26218551
|
T | TCA | 4 | a0001c0001t0002g0004a0001c0001t0002g0148a0001c0001t0002g0149others(1): Show | 5 | HG01257.hp2 HG01258.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-456_287-455dup others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCACA | 3 | a0001c0001t0001g0146a0001c0001t0002g0145a0001c0001t0031g0147 | 3 | HG01169.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.287-458_287-455dup others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCACACA | 10 | a0001c0001t0001g0137a0001c0001t0002g0135a0001c0001t0002g0136others(7): Show | 10 | HG00735.hp2 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-460_287-455dup others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCACACAC others(3): Show |
3 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0002t0004g0235 | 3 | NA18980.hp1 NA18997.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.287-464_287-455dup others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCACACAC others(5): Show |
5 | a0001c0001t0002g0132a0001c0001t0003g0129a0001c0001t0003g0130others(2): Show | 5 | HG06807.hp1 NA18964.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-466_287-455dup others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCACACAC others(9): Show |
3 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127 | 3 | HG02083.hp2 HG02129.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.287-470_287-455dup others(16): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCACACAC others(11): Show |
1 | a0001c0001t0002g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.287-472_287-455dup others(18): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCACA | 3 | a0001c0001t0003g0223a0001c0001t0005g0244a0001c0001t0018g0222 | 3 | HG01346.hp2 HG01358.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.287-491_287-490ins others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCACAC others(1): Show |
8 | a0001c0001t0002g0216a0001c0001t0002g0217a0001c0001t0002g0218others(5): Show | 8 | HG01243.hp1 HG01517.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCACAC others(3): Show |
15 | a0001c0001t0001g0213a0001c0001t0002g0211a0001c0001t0002g0212others(12): Show | 15 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCACAC others(5): Show |
40 | a0001c0001t0002g0006a0001c0001t0002g0177a0001c0001t0002g0178others(37): Show | 43 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCACAC others(7): Show |
19 | a0001c0001t0001g0238a0001c0001t0002g0164a0001c0001t0002g0165others(16): Show | 21 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(14): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCACAC others(9): Show |
8 | a0001c0001t0002g0157a0001c0001t0002g0159a0001c0001t0002g0160others(5): Show | 8 | HG00738.hp2 HG01934.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(16): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCACAC others(11): Show |
2 | a0001c0001t0002g0155a0001c0001t0003g0156 | 2 | HG00741.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.287-491_287-490ins others(18): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCACAC others(13): Show |
2 | a0001c0001t0002g0154a0001c0001t0006g0153 | 2 | HG01109.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.287-491_287-490ins others(20): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCCACA others(10): Show |
1 | a0001c0001t0003g0225 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.287-491_287-490ins others(17): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCTCAC others(3): Show |
9 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(6): Show | 9 | HG01106.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCTCAC others(5): Show |
8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0003g0230others(5): Show | 8 | HG01952.hp2 HG01981.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCTCTC others(3): Show |
1 | a0001c0001t0023g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.287-491_287-490ins others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCTCTC others(5): Show |
1 | a0001c0001t0003g0232 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.287-491_287-490ins others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCTCTC others(3): Show |
4 | a0001c0001t0011g0109a0001c0003t0002g0266a0001c0003t0015g0267others(1): Show | 4 | HG00642.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCTCTC others(5): Show |
1 | a0001c0003t0005g0264 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.287-491_287-490ins others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCTCTC others(7): Show |
2 | a0001c0001t0005g0262a0001c0001t0005g0263 | 2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.287-491_287-490ins others(14): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
T | TCTCTCTC others(11): Show |
2 | a0001c0001t0005g0260a0001c0001t0005g0261 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-491_287-490ins others(18): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218551
|
TCA | T | 18 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG00597.hp2 HG01070.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.287-456_287-455del others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | |||||
chr10:26218553
|
A | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(94): Show | 100 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.287-490A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218553 | ||||||
chr10:26218555
|
A | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(92): Show | 98 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.287-488A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218555 | ||||||
chr10:26218557
|
A | T | 56 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(53): Show | 56 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.287-486A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218557 | ||||||
chr10:26218559
|
A | T | 2 | a0001c0001t0001g0099a0001c0001t0026g0098 | 2 | NA19085.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.287-484A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218559 | ||||||
chr10:26218666
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(91): Show | 98 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.287-377A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218666 | ||||||
chr10:26218721
|
A | C | 1 | a0001c0001t0002g0210 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.287-322A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218721 | ||||||
chr10:26218722
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.287-321C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218722 | ||||||
chr10:26218732
|
C | T | 1 | a0001c0001t0019g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.287-311C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218732 | ||||||
chr10:26218844
|
A | G | 47 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(44): Show | 47 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.287-199A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218844 | ||||||
chr10:26218918
|
C | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(163): Show | 172 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.287-125C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218918 | ||||||
chr10:26219034
|
A | G | 1 | a0001c0001t0003g0208 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.287-9A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26219034 | ||||||
chr10:26219336
|
T | C | 1 | a0001c0001t0019g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.520+60T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219336 | ||||||
chr10:26219400
|
C | T | 1 | a0001c0003t0010g0247 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.520+124C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219400 | ||||||
chr10:26219522
|
G | A | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.520+246G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219522 | ||||||
chr10:26219537
|
A | G | 1 | a0001c0001t0003g0097 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.520+261A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219537 | ||||||
chr10:26219721
|
C | T | 1 | a0001c0001t0012g0106 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.520+445C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219721 | ||||||
chr10:26219769
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.520+493A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219769 | ||||||
chr10:26219779
|
C | T | 1 | a0001c0001t0006g0036 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.520+503C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219779 | ||||||
chr10:26219931
|
G | T | 2 | a0001c0001t0002g0209a0001c0001t0005g0215 | 2 | HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.520+655G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219931 | ||||||
chr10:26220029
|
A | G | 47 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(44): Show | 47 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.520+753A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220029 | ||||||
chr10:26220062
|
C | T | 1 | a0001c0001t0023g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.520+786C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220062 | ||||||
chr10:26220081
|
A | G | 1 | a0001c0001t0003g0223 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.520+805A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220081 | ||||||
chr10:26220115
|
C | G | 1 | a0001c0003t0005g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.520+839C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220115 | ||||||
chr10:26220123
|
C | A | 1 | a0001c0001t0002g0211 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.520+847C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220123 | ||||||
chr10:26220182
|
G | A | 16 | a0001c0001t0001g0238a0001c0002t0004g0007a0001c0002t0004g0008others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.520+906G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220182 | ||||||
chr10:26220185
|
A | C | 16 | a0001c0001t0001g0238a0001c0002t0004g0007a0001c0002t0004g0008others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.520+909A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220185 | ||||||
chr10:26220342
|
TTTTGCTG others(5): Show |
T | 1 | a0001c0001t0003g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.520+1069_520+1080d others(14): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr10 | 26220342 | |||||
chr10:26220367
|
C | T | 1 | a0001c0001t0003g0207 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.520+1091C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220367 | ||||||
chr10:26220650
|
G | A | 47 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(44): Show | 47 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.520+1374G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220650 | ||||||
chr10:26220656
|
G | A | 1 | a0001c0001t0016g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.520+1380G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220656 | ||||||
chr10:26220690
|
C | A | 1 | a0001c0001t0019g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.520+1414C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220690 | ||||||
chr10:26220690
|
C | T | 1 | a0001c0001t0002g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.520+1414C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220690 | ||||||
chr10:26220886
|
G | A | 16 | a0001c0001t0001g0238a0001c0002t0004g0007a0001c0002t0004g0008others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.520+1610G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220886 | ||||||
chr10:26220917
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.520+1641C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220917 | ||||||
chr10:26220935
|
A | G | 70 | a0001c0001t0001g0238a0001c0001t0001g0281a0001c0001t0001g0282others(67): Show | 72 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.520+1659A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220935 | ||||||
chr10:26221123
|
C | T | 2 | a0001c0003t0005g0242a0001c0003t0005g0250 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.520+1847C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26221123 | ||||||
chr10:26221396
|
T | G | 3 | a0001c0002t0004g0115a0001c0002t0004g0116a0001c0002t0030g0114 | 3 | HG01168.hp1 HG01169.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.520+2120T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26221396 | ||||||
chr10:26221547
|
A | G | 47 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(44): Show | 47 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.520+2271A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26221547 | ||||||
chr10:26221790
|
T | C | 70 | a0001c0001t0001g0238a0001c0001t0001g0281a0001c0001t0001g0282others(67): Show | 72 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.521-2097T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26221790 | ||||||
chr10:26221928
|
G | A | 1 | a0001c0001t0003g0133 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.521-1959G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26221928 | ||||||
chr10:26221987
|
T | C | 48 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(45): Show | 48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.521-1900T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26221987 | ||||||
chr10:26222157
|
G | A | 2 | a0001c0001t0005g0108a0001c0001t0023g0251 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.521-1730G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222157 | ||||||
chr10:26222160
|
G | A | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.521-1727G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222160 | ||||||
chr10:26222303
|
C | T | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.521-1584C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222303 | ||||||
chr10:26222390
|
C | T | 48 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(45): Show | 48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.521-1497C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222390 | ||||||
chr10:26222452
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0028g0280 | 3 | HG01106.hp1 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.521-1435G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222452 | ||||||
chr10:26222550
|
A | G | 1 | a0001c0001t0023g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.521-1337A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222550 | ||||||
chr10:26222822
|
T | C | 1 | a0001c0001t0019g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.521-1065T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222822 | ||||||
chr10:26222853
|
A | G | 48 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(45): Show | 48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.521-1034A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222853 | ||||||
chr10:26222931
|
ATCT | A | 3 | a0001c0001t0002g0038a0001c0001t0003g0037a0001c0001t0026g0098 | 3 | NA18942.hp1 NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.521-952_521-950del others(3): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr10 | 26222931 | |||||
chr10:26223115
|
A | G | 46 | a0001c0001t0002g0173a0001c0001t0002g0188a0001c0001t0002g0191others(43): Show | 48 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.521-772A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26223115 | ||||||
chr10:26223153
|
T | C | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0028g0280 | 3 | HG01106.hp1 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.521-734T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26223153 | ||||||
chr10:26223435
|
G | A | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.521-452G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26223435 | ||||||
chr10:26223446
|
C | T | 15 | a0001c0001t0001g0213a0001c0001t0002g0006a0001c0001t0002g0167others(12): Show | 16 | HG00280.hp2 HG00639.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.521-441C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26223446 | ||||||
chr10:26223677
|
C | T | 1 | a0001c0001t0003g0175 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.521-210C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26223677 | ||||||
chr10:26223686
|
GGT | G | 54 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(51): Show | 54 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.521-186_521-185del others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr10 | 26223686 | |||||
chr10:26223709
|
A | ATG | 7 | a0001c0001t0001g0137a0001c0001t0002g0135a0001c0001t0002g0136others(4): Show | 7 | HG01516.hp2 HG01981.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.521-160_521-159dup others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr10 | 26223709 | |||||
chr10:26223709
|
ATGTG | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.521-162_521-159del others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr10 | 26223709 | |||||
chr10:26223745
|
G | A | 1 | a0001c0001t0019g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.521-142G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26223745 | ||||||
chr10:26224018
|
A | G | 2 | a0001c0002t0004g0236a0001c0002t0004g0239 | 2 | HG00544.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.611+41A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 5/15 | chr10 | 26224018 | ||||||
chr10:26224187
|
CAA | C | 16 | a0001c0001t0001g0238a0001c0002t0004g0007a0001c0002t0004g0008others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.611+213_611+214del others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr10 | 26224187 | |||||
chr10:26224227
|
A | G | 1 | a0001c0001t0003g0206 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.611+250A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 5/15 | chr10 | 26224227 | ||||||
chr10:26224253
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.611+276A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 5/15 | chr10 | 26224253 | ||||||
chr10:26224331
|
A | G | 6 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.612-208A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 5/15 | chr10 | 26224331 | ||||||
chr10:26224378
|
T | C | 16 | a0001c0001t0001g0238a0001c0002t0004g0007a0001c0002t0004g0008others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.612-161T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 5/15 | chr10 | 26224378 | ||||||
chr10:26224661
|
A | G | 1 | a0001c0002t0004g0241 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.724+10A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26224661 | ||||||
chr10:26224927
|
G | A | 13 | a0001c0001t0014g0105a0001c0003t0002g0266a0001c0003t0005g0113others(10): Show | 13 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.724+276G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26224927 | ||||||
chr10:26224990
|
T | A | 1 | a0001c0001t0020g0283 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.724+339T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26224990 | ||||||
chr10:26225065
|
A | ATATC | 13 | a0001c0001t0014g0105a0001c0003t0002g0266a0001c0003t0005g0113others(10): Show | 13 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.724+417_724+420dup others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr10 | 26225065 | |||||
chr10:26225114
|
C | A | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.724+463C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225114 | ||||||
chr10:26225118
|
A | T | 2 | a0001c0001t0002g0160a0001c0001t0003g0233 | 2 | HG00738.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.724+467A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225118 | ||||||
chr10:26225283
|
A | C | 70 | a0001c0001t0001g0238a0001c0001t0001g0281a0001c0001t0001g0282others(67): Show | 72 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.724+632A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225283 | ||||||
chr10:26225294
|
C | A | 8 | a0001c0001t0005g0108a0001c0001t0005g0243a0001c0001t0005g0244others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.724+643C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225294 | ||||||
chr10:26225400
|
G | C | 1 | a0001c0001t0006g0039 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.724+749G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225400 | ||||||
chr10:26225520
|
T | G | 8 | a0001c0001t0001g0238a0001c0002t0004g0007a0001c0002t0004g0008others(5): Show | 10 | HG00544.hp2 HG02080.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.724+869T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225520 | ||||||
chr10:26225670
|
C | T | 1 | a0001c0001t0003g0231 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.724+1019C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225670 | ||||||
chr10:26225676
|
T | C | 1 | a0001c0001t0002g0216 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.724+1025T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225676 | ||||||
chr10:26225679
|
C | A | 2 | a0001c0001t0005g0108a0001c0001t0023g0251 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.724+1028C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225679 | ||||||
chr10:26225902
|
G | A | 48 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(45): Show | 48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.724+1251G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225902 | ||||||
chr10:26225991
|
T | A | 1 | a0001c0001t0002g0145 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.724+1340T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225991 | ||||||
chr10:26226079
|
A | AT | 39 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(36): Show | 39 | HG01106.hp1 HG01243.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.724+1437dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr10 | 26226079 | |||||
chr10:26226148
|
C | T | 32 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(29): Show | 32 | HG01106.hp1 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.724+1497C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226148 | ||||||
chr10:26226181
|
C | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0054a0001c0001t0001g0055others(3): Show | 6 | HG01099.hp2 HG01109.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.724+1530C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226181 | ||||||
chr10:26226277
|
T | G | 70 | a0001c0001t0001g0238a0001c0001t0001g0281a0001c0001t0001g0282others(67): Show | 72 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.724+1626T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226277 | ||||||
chr10:26226323
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.724+1672C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226323 | ||||||
chr10:26226327
|
C | T | 54 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(51): Show | 54 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.724+1676C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226327 | ||||||
chr10:26226586
|
C | T | 48 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(45): Show | 48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.724+1935C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226586 | ||||||
chr10:26226727
|
A | C | 1 | a0001c0002t0004g0241 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.724+2076A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226727 | ||||||
chr10:26226737
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 93 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.724+2086G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226737 | ||||||
chr10:26226745
|
G | C | 48 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(45): Show | 48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.724+2094G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226745 | ||||||
chr10:26226993
|
T | C | 6 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(3): Show | 6 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.724+2342T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226993 | ||||||
chr10:26227159
|
A | G | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-2503A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227159 | ||||||
chr10:26227311
|
A | G | 48 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(45): Show | 48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.725-2351A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227311 | ||||||
chr10:26227588
|
C | T | 70 | a0001c0001t0001g0238a0001c0001t0001g0281a0001c0001t0001g0282others(67): Show | 72 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.725-2074C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227588 | ||||||
chr10:26227649
|
A | G | 1 | a0001c0001t0015g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.725-2013A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227649 | ||||||
chr10:26227710
|
C | G | 48 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(45): Show | 48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.725-1952C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227710 | ||||||
chr10:26227866
|
T | G | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.725-1796T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227866 | ||||||
chr10:26227881
|
A | G | 48 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(45): Show | 48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.725-1781A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227881 | ||||||
chr10:26227909
|
G | A | 2 | a0001c0001t0005g0108a0001c0001t0023g0251 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.725-1753G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227909 | ||||||
chr10:26228048
|
C | T | 16 | a0001c0001t0001g0238a0001c0002t0004g0007a0001c0002t0004g0008others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.725-1614C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228048 | ||||||
chr10:26228124
|
G | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-1538G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228124 | ||||||
chr10:26228256
|
A | G | 48 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(45): Show | 48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.725-1406A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228256 | ||||||
chr10:26228370
|
C | G | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.725-1292C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228370 | ||||||
chr10:26228534
|
C | T | 1 | a0001c0001t0015g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.725-1128C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228534 | ||||||
chr10:26228541
|
C | G | 1 | a0001c0001t0001g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.725-1121C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228541 | ||||||
chr10:26228553
|
C | T | 7 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.725-1109C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228553 | ||||||
chr10:26228554
|
G | A | 2 | a0001c0001t0005g0108a0001c0001t0023g0251 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.725-1108G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228554 | ||||||
chr10:26228607
|
G | T | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.725-1055G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228607 | ||||||
chr10:26228680
|
G | A | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.725-982G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228680 | ||||||
chr10:26228852
|
C | T | 4 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0008g0272others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-810C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228852 | ||||||
chr10:26229005
|
T | C | 22 | a0001c0001t0001g0238a0001c0001t0009g0100a0001c0001t0011g0109others(19): Show | 24 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.725-657T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229005 | ||||||
chr10:26229172
|
C | T | 6 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(3): Show | 6 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.725-490C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229172 | ||||||
chr10:26229196
|
GA | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(115): Show | 124 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.725-452delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr10 | 26229196 | |||||
chr10:26229219
|
G | A | 30 | a0001c0001t0001g0238a0001c0001t0007g0104a0001c0001t0007g0252others(27): Show | 32 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.725-443G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229219 | ||||||
chr10:26229236
|
C | T | 2 | a0001c0001t0013g0268a0001c0001t0013g0269 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.725-426C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229236 | ||||||
chr10:26229284
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.725-378G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229284 | ||||||
chr10:26229284
|
G | GA | 29 | a0001c0001t0001g0238a0001c0001t0007g0104a0001c0001t0007g0252others(26): Show | 31 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.725-367dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr10 | 26229284 | |||||
chr10:26229318
|
C | T | 1 | a0001c0001t0005g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.725-344C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229318 | ||||||
chr10:26229469
|
A | G | 30 | a0001c0001t0001g0238a0001c0001t0007g0104a0001c0001t0007g0252others(27): Show | 32 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.725-193A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229469 | ||||||
chr10:26229489
|
C | A | 30 | a0001c0001t0001g0238a0001c0001t0007g0104a0001c0001t0007g0252others(27): Show | 32 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.725-173C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229489 | ||||||
chr10:26229489
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(226): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.725-173C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229489 | ||||||
chr10:26229550
|
T | G | 30 | a0001c0001t0001g0238a0001c0001t0007g0104a0001c0001t0007g0252others(27): Show | 32 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.725-112T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229550 | ||||||
chr10:26229876
|
T | C | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+99T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26229876 | ||||||
chr10:26229939
|
T | A | 4 | a0001c0001t0003g0129a0001c0001t0003g0133a0001c0001t0003g0134others(1): Show | 4 | NA18977.hp1 NA18980.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+162T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26229939 | ||||||
chr10:26230048
|
C | CACAA | 29 | a0001c0001t0001g0238a0001c0001t0007g0104a0001c0001t0007g0252others(26): Show | 31 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.840+273_840+274ins others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26230048 | |||||
chr10:26230066
|
G | A | 2 | a0001c0001t0012g0106a0001c0007t0012g0259 | 2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.840+289G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230066 | ||||||
chr10:26230107
|
G | T | 1 | a0001c0001t0002g0168 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.840+330G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230107 | ||||||
chr10:26230129
|
C | T | 3 | a0001c0001t0005g0108a0001c0001t0005g0261a0001c0001t0023g0251 | 3 | HG02280.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.840+352C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230129 | ||||||
chr10:26230131
|
A | G | 71 | a0001c0001t0001g0238a0001c0001t0001g0281a0001c0001t0001g0282others(68): Show | 73 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.840+354A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230131 | ||||||
chr10:26230310
|
T | C | 12 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(9): Show | 12 | HG00642.hp1 HG00642.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.840+533T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230310 | ||||||
chr10:26230425
|
T | TTTTG | 6 | a0001c0001t0002g0132a0001c0001t0002g0141a0001c0001t0002g0142others(3): Show | 6 | HG00741.hp1 HG01106.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+669_840+672dup others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26230425 | |||||
chr10:26230425
|
T | TTTTGTTT others(5): Show |
1 | a0001c0001t0005g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.840+661_840+672dup others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26230425 | |||||
chr10:26230425
|
TTTTGTTT others(1): Show |
T | 16 | a0001c0001t0001g0238a0001c0002t0004g0007a0001c0002t0004g0008others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.840+665_840+672del others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26230425 | |||||
chr10:26230670
|
G | A | 29 | a0001c0001t0001g0238a0001c0001t0007g0104a0001c0001t0007g0252others(26): Show | 31 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.840+893G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230670 | ||||||
chr10:26230815
|
C | T | 1 | a0001c0001t0006g0035 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.840+1038C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230815 | ||||||
chr10:26230964
|
A | C | 29 | a0001c0001t0001g0238a0001c0001t0007g0104a0001c0001t0007g0252others(26): Show | 31 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.840+1187A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230964 | ||||||
chr10:26230995
|
C | A | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+1218C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230995 | ||||||
chr10:26231023
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(160): Show | 169 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.840+1246A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231023 | ||||||
chr10:26231044
|
C | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+1267C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231044 | ||||||
chr10:26231223
|
G | C | 2 | a0001c0001t0019g0107a0001c0001t0020g0283 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.840+1446G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231223 | ||||||
chr10:26231303
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.840+1526C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231303 | ||||||
chr10:26231475
|
C | T | 1 | a0001c0001t0003g0205 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.840+1698C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231475 | ||||||
chr10:26231558
|
G | A | 4 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0138others(1): Show | 4 | HG01981.hp2 HG03017.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.840+1781G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231558 | ||||||
chr10:26231578
|
A | G | 29 | a0001c0001t0001g0238a0001c0001t0007g0104a0001c0001t0007g0252others(26): Show | 31 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.840+1801A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231578 | ||||||
chr10:26231584
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(86): Show | 92 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.840+1807C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231584 | ||||||
chr10:26231588
|
C | G | 8 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+1811C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231588 | ||||||
chr10:26231621
|
T | A | 1 | a0001c0001t0003g0040 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.840+1844T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231621 | ||||||
chr10:26232007
|
A | T | 1 | a0001c0001t0002g0145 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.840+2230A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232007 | ||||||
chr10:26232012
|
C | T | 16 | a0001c0001t0001g0238a0001c0002t0004g0007a0001c0002t0004g0008others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.840+2235C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232012 | ||||||
chr10:26232027
|
G | A | 2 | a0001c0001t0005g0108a0001c0001t0023g0251 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.840+2250G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232027 | ||||||
chr10:26232170
|
T | C | 1 | a0001c0001t0003g0189 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.840+2393T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232170 | ||||||
chr10:26232223
|
T | C | 1 | a0001c0001t0005g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.840+2446T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232223 | ||||||
chr10:26232245
|
G | A | 29 | a0001c0001t0001g0238a0001c0001t0007g0104a0001c0001t0007g0252others(26): Show | 31 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.840+2468G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232245 | ||||||
chr10:26232405
|
T | C | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | NA18979.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.840+2628T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232405 | ||||||
chr10:26232447
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.840+2670C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232447 | ||||||
chr10:26232468
|
AC | A | 3 | a0001c0001t0011g0109a0001c0001t0011g0112a0001c0002t0004g0239 | 3 | HG00544.hp2 HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.840+2692delC | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232468 | ||||||
chr10:26232468
|
ACT | A | 17 | a0001c0001t0001g0238a0001c0001t0009g0100a0001c0001t0011g0110others(14): Show | 19 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.840+2692_840+2693d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232468 | ||||||
chr10:26232469
|
C | CT | 19 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 22 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.840+2715dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26232469 | |||||
chr10:26232469
|
C | T | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+2692C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232469 | ||||||
chr10:26232469
|
CT | C | 26 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0070others(23): Show | 26 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.840+2715delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26232469 | |||||
chr10:26232469
|
CTT | C | 15 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0015g0101others(12): Show | 15 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.840+2714_840+2715d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26232469 | |||||
chr10:26232646
|
G | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+2869G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232646 | ||||||
chr10:26232649
|
C | T | 1 | a0001c0001t0006g0204 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.840+2872C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232649 | ||||||
chr10:26232840
|
G | A | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+3063G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232840 | ||||||
chr10:26232954
|
T | G | 1 | a0001c0001t0005g0262 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.840+3177T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232954 | ||||||
chr10:26233031
|
CT | C | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+3255delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233031 | ||||||
chr10:26233361
|
T | C | 2 | a0001c0003t0005g0242a0001c0003t0005g0250 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.840+3584T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233361 | ||||||
chr10:26233428
|
C | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+3651C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233428 | ||||||
chr10:26233456
|
T | C | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.840+3679T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233456 | ||||||
chr10:26233487
|
C | T | 6 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(3): Show | 6 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+3710C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233487 | ||||||
chr10:26233526
|
C | T | 8 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+3749C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233526 | ||||||
chr10:26233567
|
G | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+3790G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233567 | ||||||
chr10:26233835
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.840+4058G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233835 | ||||||
chr10:26233872
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.840+4095G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233872 | ||||||
chr10:26233888
|
G | A | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+4111G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233888 | ||||||
chr10:26234046
|
G | A | 8 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+4269G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234046 | ||||||
chr10:26234052
|
G | A | 1 | a0001c0001t0005g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.840+4275G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234052 | ||||||
chr10:26234243
|
G | A | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.840+4466G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234243 | ||||||
chr10:26234278
|
C | T | 8 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+4501C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234278 | ||||||
chr10:26234335
|
A | G | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+4558A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234335 | ||||||
chr10:26234338
|
C | CA | 107 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(104): Show | 112 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.840+4577dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26234338 | |||||
chr10:26234338
|
C | CAA | 7 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(4): Show | 7 | HG02922.hp1 HG03139.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.840+4576_840+4577d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26234338 | |||||
chr10:26234338
|
CA | C | 47 | a0001c0001t0001g0213a0001c0001t0002g0006a0001c0001t0002g0124others(44): Show | 48 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.840+4577delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26234338 | |||||
chr10:26234338
|
CAA | C | 8 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0003g0176others(5): Show | 8 | HG02559.hp1 HG02735.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+4576_840+4577d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26234338 | |||||
chr10:26234442
|
A | G | 49 | a0001c0001t0001g0238a0001c0001t0001g0281a0001c0001t0001g0282others(46): Show | 51 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.840+4665A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234442 | ||||||
chr10:26234594
|
G | A | 21 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(18): Show | 21 | HG00642.hp1 HG00642.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.840+4817G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234594 | ||||||
chr10:26234642
|
A | T | 8 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126others(5): Show | 8 | HG02040.hp1 HG02083.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+4865A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234642 | ||||||
chr10:26234736
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.840+4959A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234736 | ||||||
chr10:26234772
|
C | G | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+4995C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234772 | ||||||
chr10:26234880
|
CT | C | 9 | a0001c0001t0001g0014a0001c0001t0002g0275a0001c0001t0002g0276others(6): Show | 9 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.840+5113delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26234880 | |||||
chr10:26235089
|
G | C | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | NA18979.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.840+5312G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235089 | ||||||
chr10:26235128
|
C | T | 1 | a0001c0001t0015g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.840+5351C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235128 | ||||||
chr10:26235153
|
C | T | 6 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(3): Show | 6 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+5376C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235153 | ||||||
chr10:26235175
|
C | T | 16 | a0001c0001t0001g0238a0001c0002t0004g0007a0001c0002t0004g0008others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.840+5398C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235175 | ||||||
chr10:26235188
|
T | C | 65 | a0001c0001t0001g0238a0001c0001t0001g0281a0001c0001t0001g0282others(62): Show | 67 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.840+5411T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235188 | ||||||
chr10:26235231
|
C | A | 4 | a0001c0001t0005g0108a0001c0001t0005g0261a0001c0001t0019g0107others(1): Show | 4 | HG02280.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+5454C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235231 | ||||||
chr10:26235423
|
T | G | 12 | a0001c0001t0014g0105a0001c0003t0002g0266a0001c0003t0005g0113others(9): Show | 12 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.840+5646T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235423 | ||||||
chr10:26235438
|
C | G | 1 | a0001c0001t0020g0283 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.840+5661C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235438 | ||||||
chr10:26235445
|
G | A | 83 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 83 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.840+5668G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235445 | ||||||
chr10:26235457
|
G | A | 71 | a0001c0001t0001g0238a0001c0001t0001g0281a0001c0001t0001g0282others(68): Show | 73 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.840+5680G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235457 | ||||||
chr10:26235551
|
T | C | 3 | a0002c0004t0002g0193a0002c0004t0002g0194a0002c0004t0003g0214 | 3 | HG01256.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.840+5774T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235551 | ||||||
chr10:26235608
|
A | C | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+5831A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235608 | ||||||
chr10:26235684
|
G | A | 17 | a0001c0001t0009g0100a0001c0001t0011g0109a0001c0001t0011g0110others(14): Show | 17 | HG00642.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.840+5907G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235684 | ||||||
chr10:26235877
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG01099.hp2 HG01109.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.840+6100C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235877 | ||||||
chr10:26235911
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840+6134T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235911 | ||||||
chr10:26235971
|
G | A | 8 | a0001c0001t0009g0003a0001c0001t0009g0009a0001c0001t0009g0100others(5): Show | 9 | HG00642.hp1 HG00735.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.840+6194G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235971 | ||||||
chr10:26235982
|
G | A | 43 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0275others(40): Show | 44 | HG00642.hp1 HG00735.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.840+6205G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235982 | ||||||
chr10:26236001
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(163): Show | 172 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.840+6224A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236001 | ||||||
chr10:26236057
|
C | T | 27 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(24): Show | 27 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.840+6280C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236057 | ||||||
chr10:26236064
|
G | A | 25 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(22): Show | 25 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.840+6287G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236064 | ||||||
chr10:26236091
|
A | G | 13 | a0001c0001t0001g0078a0001c0001t0001g0281a0001c0001t0001g0282others(10): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.840+6314A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236091 | ||||||
chr10:26236092
|
T | G | 13 | a0001c0001t0005g0215a0001c0001t0011g0109a0001c0001t0011g0110others(10): Show | 13 | HG00642.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.840+6315T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236092 | ||||||
chr10:26236187
|
C | T | 1 | a0001c0001t0002g0004 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.840+6410C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236187 | ||||||
chr10:26236235
|
C | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG03139.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.840+6458C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236235 | ||||||
chr10:26236301
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.840+6524T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236301 | ||||||
chr10:26236302
|
C | CT | 110 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(107): Show | 114 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.840+6540dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26236302 | |||||
chr10:26236302
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.840+6525C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236302 | ||||||
chr10:26236307
|
T | A | 1 | a0001c0001t0001g0014 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.840+6530T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236307 | ||||||
chr10:26236347
|
C | T | 1 | a0001c0001t0026g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.840+6570C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236347 | ||||||
chr10:26236354
|
G | A | 6 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+6577G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236354 | ||||||
chr10:26236383
|
C | T | 1 | a0001c0001t0002g0004 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.840+6606C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236383 | ||||||
chr10:26236394
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG00140.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.840+6617G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236394 | ||||||
chr10:26236436
|
A | G | 10 | a0001c0001t0001g0081a0001c0001t0007g0104a0001c0001t0007g0252others(7): Show | 10 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.840+6659A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236436 | ||||||
chr10:26236445
|
C | T | 5 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(2): Show | 5 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.840+6668C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236445 | ||||||
chr10:26236471
|
C | T | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.840+6694C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236471 | ||||||
chr10:26236490
|
G | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+6713G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236490 | ||||||
chr10:26236590
|
C | T | 2 | a0001c0001t0015g0101a0001c0003t0015g0267 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.840+6813C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236590 | ||||||
chr10:26236754
|
C | G | 1 | a0001c0001t0005g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.840+6977C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236754 | ||||||
chr10:26236815
|
T | C | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG01243.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.840+7038T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236815 | ||||||
chr10:26236851
|
A | G | 3 | a0001c0001t0012g0062a0001c0001t0012g0106a0001c0007t0012g0259 | 3 | HG01884.hp2 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.840+7074A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236851 | ||||||
chr10:26236991
|
G | A | 12 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(9): Show | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.840+7214G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236991 | ||||||
chr10:26237009
|
C | G | 64 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(61): Show | 66 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.840+7232C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237009 | ||||||
chr10:26237067
|
C | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(278): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.840+7290C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237067 | ||||||
chr10:26237089
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.840+7312G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237089 | ||||||
chr10:26237215
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840+7438G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237215 | ||||||
chr10:26237268
|
A | T | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.840+7491A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237268 | ||||||
chr10:26237401
|
T | C | 6 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0008g0272others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.840+7624T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237401 | ||||||
chr10:26237410
|
C | T | 13 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(10): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.840+7633C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237410 | ||||||
chr10:26237412
|
C | T | 1 | a0001c0001t0005g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.840+7635C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237412 | ||||||
chr10:26237423
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(6): Show | 9 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.840+7646G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237423 | ||||||
chr10:26237449
|
G | A | 1 | a0001c0001t0028g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.840+7672G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237449 | ||||||
chr10:26237524
|
A | G | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.840+7747A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237524 | ||||||
chr10:26237601
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | NA19060.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.840+7824C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237601 | ||||||
chr10:26237729
|
C | T | 17 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(14): Show | 17 | HG00642.hp1 HG01106.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.840+7952C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237729 | ||||||
chr10:26237773
|
T | C | 64 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(61): Show | 66 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.840+7996T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237773 | ||||||
chr10:26237774
|
G | A | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.840+7997G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237774 | ||||||
chr10:26237892
|
A | G | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-8029A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237892 | ||||||
chr10:26237913
|
AGGAGAAT others(12): Show |
A | 1 | a0001c0001t0001g0043 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.841-8004_841-7986d others(21): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26237913 | |||||
chr10:26237932
|
G | A | 5 | a0001c0001t0008g0013a0001c0001t0009g0003a0001c0001t0009g0009others(2): Show | 6 | HG00735.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-7989G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237932 | ||||||
chr10:26237998
|
TCACACAG others(1): Show |
T | 3 | a0001c0001t0005g0215a0001c0002t0004g0118a0001c0003t0015g0267 | 3 | HG00639.hp2 HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.841-7916_841-7909d others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26237998 | |||||
chr10:26237998
|
TCACACAG others(3): Show |
T | 3 | a0001c0001t0011g0109a0001c0001t0011g0111a0001c0001t0011g0112 | 3 | HG00642.hp1 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.841-7916_841-7907d others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26237998 | |||||
chr10:26237998
|
TCACACAG others(5): Show |
T | 3 | a0001c0001t0008g0271a0001c0001t0008g0273a0001c0001t0014g0105 | 3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.841-7916_841-7905d others(14): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26237998 | |||||
chr10:26237998
|
TCACACAG others(7): Show |
T | 7 | a0001c0001t0008g0270a0001c0001t0008g0272a0001c0001t0011g0110others(4): Show | 7 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.841-7916_841-7903d others(16): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26237998 | |||||
chr10:26237999
|
CACACAG | C | 16 | a0001c0001t0007g0253a0001c0001t0013g0269a0001c0002t0004g0007others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.841-7916_841-7911d others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26237999 | |||||
chr10:26238001
|
CACAG | C | 12 | a0001c0001t0001g0281a0001c0001t0005g0108a0001c0001t0005g0243others(9): Show | 12 | HG01106.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.841-7916_841-7913d others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238001 | |||||
chr10:26238003
|
CAG | C | 16 | a0001c0001t0001g0282a0001c0001t0005g0261a0001c0001t0007g0104others(13): Show | 16 | HG00642.hp2 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.841-7916_841-7915d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238003 | |||||
chr10:26238005
|
G | C | 4 | a0001c0003t0005g0113a0001c0003t0005g0250a0001c0003t0010g0247others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.841-7916G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238005 | ||||||
chr10:26238005
|
G | GAC | 22 | a0001c0001t0002g0006a0001c0001t0002g0125a0001c0001t0002g0138others(19): Show | 23 | HG00280.hp2 HG00639.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.841-7874_841-7873d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238005 | |||||
chr10:26238005
|
G | GACAC | 4 | a0001c0001t0002g0154a0001c0001t0002g0163a0001c0001t0002g0211others(1): Show | 4 | HG01993.hp1 HG02145.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.841-7876_841-7873d others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238005 | |||||
chr10:26238005
|
GAC | G | 52 | a0001c0001t0001g0030a0001c0001t0001g0047a0001c0001t0001g0083others(49): Show | 55 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.841-7874_841-7873d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238005 | |||||
chr10:26238005
|
GACAC | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(65): Show | 71 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.841-7876_841-7873d others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238005 | |||||
chr10:26238005
|
GACACAC | G | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0042others(11): Show | 14 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.841-7878_841-7873d others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238005 | |||||
chr10:26238118
|
C | T | 17 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(14): Show | 17 | HG00642.hp1 HG01106.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.841-7803C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238118 | ||||||
chr10:26238129
|
T | C | 4 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0008g0272others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.841-7792T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238129 | ||||||
chr10:26238144
|
A | G | 64 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(61): Show | 66 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.841-7777A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238144 | ||||||
chr10:26238254
|
G | C | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.841-7667G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238254 | ||||||
chr10:26238352
|
T | G | 1 | a0001c0002t0004g0237 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.841-7569T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238352 | ||||||
chr10:26238461
|
G | A | 36 | a0001c0001t0005g0215a0001c0001t0005g0243a0001c0001t0005g0244others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.841-7460G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238461 | ||||||
chr10:26238632
|
G | A | 1 | a0001c0001t0005g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.841-7289G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238632 | ||||||
chr10:26238661
|
G | A | 45 | a0001c0001t0002g0006a0001c0001t0002g0124a0001c0001t0002g0125others(42): Show | 46 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.841-7260G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238661 | ||||||
chr10:26238791
|
TC | T | 8 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0008g0272others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-7129delC | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238791 | ||||||
chr10:26238797
|
G | A | 17 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(14): Show | 17 | HG00642.hp1 HG01106.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.841-7124G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238797 | ||||||
chr10:26238831
|
G | A | 17 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(14): Show | 17 | HG00642.hp1 HG01106.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.841-7090G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238831 | ||||||
chr10:26238902
|
G | A | 1 | a0001c0001t0011g0112 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.841-7019G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238902 | ||||||
chr10:26238909
|
G | A | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.841-7012G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238909 | ||||||
chr10:26238921
|
A | G | 35 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(32): Show | 35 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.841-7000A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238921 | ||||||
chr10:26238979
|
TG | T | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-6940delG | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238979 | |||||
chr10:26239004
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.841-6917G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239004 | ||||||
chr10:26239135
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02132.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.841-6786G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239135 | ||||||
chr10:26239374
|
G | A | 12 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(9): Show | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-6547G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239374 | ||||||
chr10:26239420
|
T | C | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-6501T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239420 | ||||||
chr10:26239444
|
C | T | 11 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(8): Show | 11 | HG00642.hp2 HG01243.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.841-6477C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239444 | ||||||
chr10:26239555
|
T | G | 1 | a0001c0001t0019g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.841-6366T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239555 | ||||||
chr10:26239626
|
G | C | 11 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(8): Show | 11 | HG00642.hp2 HG01243.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.841-6295G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239626 | ||||||
chr10:26239651
|
T | A | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-6270T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239651 | ||||||
chr10:26239906
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(159): Show | 168 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.841-6015A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239906 | ||||||
chr10:26240194
|
A | G | 12 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(9): Show | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-5727A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240194 | ||||||
chr10:26240250
|
T | C | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.841-5671T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240250 | ||||||
chr10:26240269
|
C | T | 1 | a0001c0001t0016g0279 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.841-5652C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240269 | ||||||
chr10:26240347
|
C | T | 12 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(9): Show | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-5574C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240347 | ||||||
chr10:26240392
|
C | T | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-5529C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240392 | ||||||
chr10:26240427
|
A | G | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.841-5494A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240427 | ||||||
chr10:26240432
|
G | A | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.841-5489G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240432 | ||||||
chr10:26240454
|
A | G | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0003t0010g0245others(3): Show | 6 | HG01106.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-5467A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240454 | ||||||
chr10:26240474
|
G | T | 1 | a0001c0001t0005g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.841-5447G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240474 | ||||||
chr10:26240503
|
G | T | 8 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0008g0272others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-5418G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240503 | ||||||
chr10:26240586
|
G | A | 1 | a0001c0001t0019g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.841-5335G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240586 | ||||||
chr10:26240687
|
A | G | 51 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(48): Show | 53 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.841-5234A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240687 | ||||||
chr10:26240731
|
C | CA | 27 | a0001c0001t0001g0069a0001c0001t0002g0135a0001c0001t0002g0192others(24): Show | 28 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.841-5175dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26240731 | |||||
chr10:26240731
|
C | CAA | 54 | a0001c0001t0002g0180a0001c0001t0002g0191a0001c0001t0003g0002others(51): Show | 56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.841-5176_841-5175d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26240731 | |||||
chr10:26240733
|
A | C | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-5188A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240733 | ||||||
chr10:26240735
|
A | C | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-5186A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240735 | ||||||
chr10:26240737
|
A | C | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-5184A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240737 | ||||||
chr10:26240739
|
A | C | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.841-5182A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240739 | ||||||
chr10:26240851
|
G | A | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-5070G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240851 | ||||||
chr10:26240967
|
G | A | 6 | a0001c0001t0005g0261a0001c0003t0005g0113a0001c0003t0005g0242others(3): Show | 6 | HG01884.hp1 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-4954G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240967 | ||||||
chr10:26240984
|
G | A | 1 | a0001c0001t0028g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.841-4937G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240984 | ||||||
chr10:26241006
|
C | G | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.841-4915C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241006 | ||||||
chr10:26241030
|
A | G | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-4891A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241030 | ||||||
chr10:26241066
|
T | A | 27 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(24): Show | 27 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.841-4855T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241066 | ||||||
chr10:26241086
|
T | C | 2 | a0001c0001t0013g0268a0001c0001t0013g0269 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.841-4835T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241086 | ||||||
chr10:26241179
|
G | A | 1 | a0001c0001t0003g0040 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.841-4742G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241179 | ||||||
chr10:26241287
|
G | C | 1 | a0001c0001t0001g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.841-4634G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241287 | ||||||
chr10:26241330
|
C | A | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.841-4591C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241330 | ||||||
chr10:26241428
|
A | G | 64 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(61): Show | 66 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.841-4493A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241428 | ||||||
chr10:26241476
|
T | C | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-4445T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241476 | ||||||
chr10:26241550
|
C | CT | 22 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(19): Show | 22 | HG00642.hp1 HG01106.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.841-4357dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26241550 | |||||
chr10:26241550
|
C | CTT | 44 | a0001c0001t0005g0215a0001c0001t0005g0243a0001c0001t0005g0244others(41): Show | 46 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.841-4358_841-4357d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26241550 | |||||
chr10:26241554
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.841-4367T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241554 | ||||||
chr10:26241638
|
T | C | 21 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(18): Show | 23 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.841-4283T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241638 | ||||||
chr10:26241652
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.841-4269T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241652 | ||||||
chr10:26241673
|
A | G | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-4248A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241673 | ||||||
chr10:26241738
|
A | G | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.841-4183A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241738 | ||||||
chr10:26241837
|
C | T | 18 | a0001c0001t0005g0261a0001c0001t0007g0104a0001c0001t0007g0252others(15): Show | 18 | HG00642.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.841-4084C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241837 | ||||||
chr10:26241838
|
G | A | 1 | a0001c0002t0004g0119 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.841-4083G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241838 | ||||||
chr10:26241912
|
A | C | 1 | a0001c0001t0003g0156 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.841-4009A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241912 | ||||||
chr10:26241969
|
A | ATTTG | 8 | a0001c0001t0005g0215a0001c0001t0005g0261a0001c0001t0014g0105others(5): Show | 8 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-3928_841-3925d others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26241969 | |||||
chr10:26241969
|
A | ATTTGTTT others(1): Show |
11 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(8): Show | 11 | HG00642.hp2 HG01243.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.841-3932_841-3925d others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26241969 | |||||
chr10:26242134
|
C | T | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.841-3787C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242134 | ||||||
chr10:26242135
|
G | A | 2 | a0001c0001t0003g0205a0001c0001t0003g0223 | 2 | HG01346.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.841-3786G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242135 | ||||||
chr10:26242179
|
A | G | 12 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(9): Show | 12 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-3742A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242179 | ||||||
chr10:26242202
|
G | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.841-3719G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242202 | ||||||
chr10:26242277
|
C | T | 1 | a0001c0001t0017g0012 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.841-3644C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242277 | ||||||
chr10:26242282
|
G | A | 1 | a0001c0002t0030g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.841-3639G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242282 | ||||||
chr10:26242301
|
A | G | 2 | a0001c0001t0009g0100a0001c0001t0014g0105 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.841-3620A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242301 | ||||||
chr10:26242321
|
C | A | 1 | a0001c0001t0002g0150 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.841-3600C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242321 | ||||||
chr10:26242335
|
T | C | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.841-3586T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242335 | ||||||
chr10:26242435
|
A | G | 12 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(9): Show | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-3486A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242435 | ||||||
chr10:26242468
|
G | A | 1 | a0001c0001t0002g0004 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.841-3453G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242468 | ||||||
chr10:26242586
|
G | A | 2 | a0001c0001t0009g0100a0001c0001t0014g0105 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.841-3335G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242586 | ||||||
chr10:26242631
|
C | T | 12 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(9): Show | 12 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-3290C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242631 | ||||||
chr10:26242741
|
C | T | 14 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(11): Show | 14 | HG00642.hp1 HG00642.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.841-3180C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242741 | ||||||
chr10:26242754
|
C | A | 1 | a0001c0001t0002g0004 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.841-3167C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242754 | ||||||
chr10:26242930
|
G | T | 16 | a0001c0001t0005g0215a0001c0001t0005g0261a0001c0001t0007g0104others(13): Show | 16 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.841-2991G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242930 | ||||||
chr10:26243027
|
C | A | 1 | a0001c0001t0003g0205 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.841-2894C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243027 | ||||||
chr10:26243040
|
A | AAAG | 53 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(50): Show | 55 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.841-2879_841-2878i others(5): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26243040 | |||||
chr10:26243041
|
A | C | 1 | a0001c0001t0008g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.841-2880A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243041 | ||||||
chr10:26243042
|
A | AGAAC | 12 | a0001c0001t0007g0104a0001c0001t0007g0253a0001c0001t0007g0254others(9): Show | 13 | HG00642.hp2 HG00735.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.841-2879_841-2878i others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243042 | ||||||
chr10:26243042
|
A | C | 11 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0050others(8): Show | 11 | HG02040.hp1 HG02083.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.841-2879A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243042 | ||||||
chr10:26243043
|
C | T | 1 | a0001c0001t0005g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.841-2878C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243043 | ||||||
chr10:26243044
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.841-2877C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243044 | ||||||
chr10:26243383
|
G | T | 12 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(9): Show | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-2538G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243383 | ||||||
chr10:26243564
|
G | A | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.841-2357G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243564 | ||||||
chr10:26243721
|
C | T | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-2200C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243721 | ||||||
chr10:26243832
|
C | A | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-2089C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243832 | ||||||
chr10:26243883
|
A | G | 1 | a0001c0009t0032g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.841-2038A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243883 | ||||||
chr10:26243898
|
T | C | 12 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(9): Show | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-2023T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243898 | ||||||
chr10:26244000
|
T | C | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-1921T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244000 | ||||||
chr10:26244015
|
T | C | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-1906T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244015 | ||||||
chr10:26244169
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.841-1752C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244169 | ||||||
chr10:26244320
|
T | G | 3 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0003g0176 | 3 | HG00639.hp1 HG01192.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.841-1601T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244320 | ||||||
chr10:26244437
|
T | G | 19 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(16): Show | 19 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.841-1484T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244437 | ||||||
chr10:26244479
|
A | G | 1 | a0001c0001t0022g0220 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.841-1442A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244479 | ||||||
chr10:26244536
|
A | T | 1 | a0001c0001t0002g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.841-1385A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244536 | ||||||
chr10:26244554
|
A | G | 19 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(16): Show | 19 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.841-1367A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244554 | ||||||
chr10:26244808
|
A | T | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-1113A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244808 | ||||||
chr10:26244825
|
A | G | 8 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0008g0272others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-1096A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244825 | ||||||
chr10:26244836
|
A | G | 62 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(59): Show | 65 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.841-1085A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244836 | ||||||
chr10:26244878
|
A | G | 62 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(59): Show | 65 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.841-1043A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244878 | ||||||
chr10:26244917
|
T | C | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-1004T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244917 | ||||||
chr10:26244942
|
A | G | 12 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(9): Show | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-979A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244942 | ||||||
chr10:26244997
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.841-924C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244997 | ||||||
chr10:26245053
|
T | C | 1 | a0001c0001t0028g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.841-868T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245053 | ||||||
chr10:26245131
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.841-790C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245131 | ||||||
chr10:26245146
|
T | C | 12 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(9): Show | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-775T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245146 | ||||||
chr10:26245153
|
C | CAA | 12 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0215others(9): Show | 12 | HG01106.hp1 HG01243.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-753_841-752dup others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245153 | |||||
chr10:26245153
|
CA | C | 14 | a0001c0001t0001g0052a0001c0001t0001g0086a0001c0001t0002g0219others(11): Show | 14 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.841-752delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245153 | |||||
chr10:26245153
|
CAAAAA | C | 6 | a0001c0001t0005g0108a0001c0001t0012g0062a0001c0001t0012g0106others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-756_841-752del others(5): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245153 | |||||
chr10:26245163
|
AAAAAAAG | A | 8 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(5): Show | 8 | HG01346.hp2 HG02293.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-743_841-737del others(7): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245163 | |||||
chr10:26245193
|
G | A | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.841-728G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245193 | ||||||
chr10:26245230
|
G | T | 5 | a0001c0001t0001g0137a0001c0001t0009g0003a0001c0001t0009g0009others(2): Show | 6 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-691G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245230 | ||||||
chr10:26245231
|
G | GC | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-690_841-689ins others(1): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245231 | ||||||
chr10:26245354
|
C | T | 1 | a0001c0001t0008g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.841-567C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245354 | ||||||
chr10:26245355
|
G | A | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-566G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245355 | ||||||
chr10:26245383
|
T | TA | 6 | a0001c0001t0002g0157a0001c0001t0005g0243a0001c0001t0005g0244others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-528dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245383 | |||||
chr10:26245383
|
TA | T | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-528delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245383 | |||||
chr10:26245390
|
A | AT | 4 | a0001c0001t0009g0003a0001c0001t0009g0009a0001c0001t0009g0010others(1): Show | 5 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.841-531_841-530ins others(1): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245390 | ||||||
chr10:26245390
|
A | T | 19 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(16): Show | 19 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.841-531A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245390 | ||||||
chr10:26245404
|
C | T | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-517C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245404 | ||||||
chr10:26245418
|
TTTAAG | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.841-499_841-495del others(5): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245418 | |||||
chr10:26245442
|
A | AT | 63 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0281others(60): Show | 66 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.841-467dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245442 | |||||
chr10:26245442
|
A | ATT | 73 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(70): Show | 76 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.841-468_841-467dup others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245442 | |||||
chr10:26245442
|
A | ATTT | 9 | a0001c0001t0001g0046a0001c0001t0001g0061a0001c0001t0001g0068others(6): Show | 9 | HG02055.hp2 HG02922.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.841-469_841-467dup others(3): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245442 | |||||
chr10:26245524
|
G | A | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-397G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245524 | ||||||
chr10:26245604
|
A | AT | 14 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0027others(11): Show | 14 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.841-306dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245604 | |||||
chr10:26245680
|
G | T | 1 | a0001c0001t0018g0222 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.841-241G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245680 | ||||||
chr10:26245720
|
G | A | 1 | a0003c0005t0002g0227 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.841-201G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245720 | ||||||
chr10:26245725
|
A | C | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.841-196A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245725 | ||||||
chr10:26245827
|
GAAAGGAA others(1): Show |
G | 4 | a0001c0001t0009g0003a0001c0001t0009g0009a0001c0001t0009g0010others(1): Show | 5 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.841-84_841-77delAA others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245827 | |||||
chr10:26245880
|
G | T | 53 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(50): Show | 55 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.841-41G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245880 | ||||||
chr10:26245882
|
A | G | 1 | a0001c0001t0009g0010 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.841-39A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245882 | ||||||
chr10:26245907
|
TA | T | 11 | a0001c0001t0003g0225a0001c0001t0007g0104a0001c0001t0007g0252others(8): Show | 11 | HG00642.hp2 HG02451.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.841-13delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245907 | ||||||
chr10:26246008
|
C | T | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.920+8C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246008 | ||||||
chr10:26246021
|
C | A | 2 | a0001c0002t0004g0236a0001c0002t0004g0239 | 2 | HG00544.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.920+21C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246021 | ||||||
chr10:26246094
|
C | T | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.920+94C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246094 | ||||||
chr10:26246251
|
C | T | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+251C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246251 | ||||||
chr10:26246348
|
T | C | 9 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(6): Show | 9 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.920+348T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246348 | ||||||
chr10:26246409
|
A | C | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+409A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246409 | ||||||
chr10:26246433
|
A | G | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+433A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246433 | ||||||
chr10:26246614
|
A | G | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+614A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246614 | ||||||
chr10:26246783
|
C | T | 9 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(6): Show | 9 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.920+783C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246783 | ||||||
chr10:26246812
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.920+812C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246812 | ||||||
chr10:26246825
|
A | G | 18 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(15): Show | 18 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.920+825A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246825 | ||||||
chr10:26246909
|
C | T | 53 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(50): Show | 55 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.920+909C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246909 | ||||||
chr10:26246924
|
G | A | 2 | a0001c0001t0015g0101a0001c0003t0015g0267 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.920+924G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246924 | ||||||
chr10:26247154
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.920+1154T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247154 | ||||||
chr10:26247215
|
A | C | 1 | a0001c0001t0005g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.920+1215A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247215 | ||||||
chr10:26247286
|
G | A | 2 | a0001c0001t0003g0161a0001c0001t0003g0162 | 2 | NA19009.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.920+1286G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247286 | ||||||
chr10:26247379
|
C | CATCTT | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+1379_920+1380i others(7): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247379 | ||||||
chr10:26247568
|
A | G | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+1568A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247568 | ||||||
chr10:26247595
|
C | A | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+1595C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247595 | ||||||
chr10:26247614
|
G | A | 2 | a0002c0004t0003g0197a0002c0004t0003g0198 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.920+1614G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247614 | ||||||
chr10:26247622
|
G | T | 18 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(15): Show | 18 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.920+1622G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247622 | ||||||
chr10:26247731
|
A | G | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.920+1731A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247731 | ||||||
chr10:26247768
|
C | A | 5 | a0001c0001t0005g0261a0001c0003t0005g0113a0001c0003t0005g0242others(2): Show | 5 | HG02647.hp1 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+1768C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247768 | ||||||
chr10:26247790
|
G | A | 6 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(3): Show | 6 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.920+1790G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247790 | ||||||
chr10:26247895
|
C | CA | 61 | a0001c0001t0001g0043a0001c0001t0002g0178a0001c0001t0002g0185others(58): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.920+1912dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26247895 | |||||
chr10:26247895
|
CA | C | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.920+1912delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26247895 | |||||
chr10:26247919
|
G | GA | 134 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0038others(131): Show | 140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.920+1931dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26247919 | |||||
chr10:26247919
|
GA | G | 11 | a0001c0001t0001g0071a0001c0001t0001g0281a0001c0001t0001g0282others(8): Show | 11 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.920+1931delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26247919 | |||||
chr10:26247970
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.920+1970G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247970 | ||||||
chr10:26248069
|
C | G | 19 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(16): Show | 20 | HG00642.hp2 HG00735.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.920+2069C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248069 | ||||||
chr10:26248112
|
G | A | 12 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(9): Show | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.920+2112G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248112 | ||||||
chr10:26248155
|
G | T | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+2155G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248155 | ||||||
chr10:26248241
|
A | G | 62 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(59): Show | 65 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.920+2241A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248241 | ||||||
chr10:26248481
|
G | C | 1 | a0001c0001t0002g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.920+2481G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248481 | ||||||
chr10:26248701
|
A | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(81): Show | 87 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.920+2701A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248701 | ||||||
chr10:26248810
|
G | GA | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.920+2819dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26248810 | |||||
chr10:26248880
|
C | T | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+2880C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248880 | ||||||
chr10:26248934
|
C | T | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+2934C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248934 | ||||||
chr10:26249008
|
A | AT | 9 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(6): Show | 9 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.920+3010dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26249008 | |||||
chr10:26249008
|
AT | A | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.920+3010delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26249008 | |||||
chr10:26249073
|
C | T | 1 | a0001c0001t0005g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920+3073C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249073 | ||||||
chr10:26249099
|
G | A | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.920+3099G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249099 | ||||||
chr10:26249127
|
G | A | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(25): Show | 28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.920+3127G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249127 | ||||||
chr10:26249180
|
A | C | 1 | a0001c0001t0007g0257 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.920+3180A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249180 | ||||||
chr10:26249214
|
A | G | 1 | a0001c0001t0005g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920+3214A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249214 | ||||||
chr10:26249219
|
G | A | 1 | a0001c0001t0005g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920+3219G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249219 | ||||||
chr10:26249308
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.920+3308C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249308 | ||||||
chr10:26249411
|
A | C | 1 | a0001c0001t0005g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920+3411A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249411 | ||||||
chr10:26249523
|
C | T | 6 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(3): Show | 6 | HG00642.hp1 HG01243.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.920+3523C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249523 | ||||||
chr10:26249651
|
G | A | 1 | a0001c0001t0009g0010 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.920+3651G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249651 | ||||||
chr10:26249690
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(90): Show | 96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.920+3690G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249690 | ||||||
chr10:26249723
|
G | A | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.920+3723G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249723 | ||||||
chr10:26249730
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.920+3730G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249730 | ||||||
chr10:26249732
|
C | G | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.920+3732C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249732 | ||||||
chr10:26249747
|
A | G | 9 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0008g0272others(6): Show | 9 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.920+3747A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249747 | ||||||
chr10:26249868
|
T | C | 2 | a0001c0003t0005g0242a0001c0003t0005g0250 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.920+3868T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249868 | ||||||
chr10:26249917
|
A | C | 13 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(10): Show | 13 | HG00642.hp1 HG01106.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.920+3917A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249917 | ||||||
chr10:26249962
|
G | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.920+3962G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249962 | ||||||
chr10:26250017
|
T | G | 2 | a0001c0001t0015g0101a0001c0003t0015g0267 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.920+4017T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250017 | ||||||
chr10:26250081
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.920+4081G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250081 | ||||||
chr10:26250144
|
G | C | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | NA18948.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.920+4144G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250144 | ||||||
chr10:26250519
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.920+4519C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250519 | ||||||
chr10:26250520
|
G | A | 17 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(14): Show | 17 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.920+4520G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250520 | ||||||
chr10:26250566
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(105): Show | 112 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.920+4566A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250566 | ||||||
chr10:26250708
|
A | G | 4 | a0001c0001t0009g0003a0001c0001t0009g0009a0001c0001t0009g0010others(1): Show | 5 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+4708A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250708 | ||||||
chr10:26250754
|
A | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(104): Show | 110 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.920+4754A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250754 | ||||||
chr10:26250780
|
A | G | 9 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(6): Show | 9 | HG01106.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.920+4780A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250780 | ||||||
chr10:26250867
|
G | T | 2 | a0001c0001t0013g0268a0001c0001t0013g0269 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.920+4867G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250867 | ||||||
chr10:26250875
|
T | C | 1 | a0001c0001t0003g0189 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.920+4875T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250875 | ||||||
chr10:26250877
|
C | CT | 96 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(93): Show | 100 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.920+4897dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26250877 | |||||
chr10:26250877
|
C | CTT | 10 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0049others(7): Show | 10 | HG01255.hp1 HG01256.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+4896_920+4897d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26250877 | |||||
chr10:26250877
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.920+4877C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250877 | ||||||
chr10:26250877
|
CT | C | 10 | a0001c0001t0005g0108a0001c0001t0005g0243a0001c0001t0005g0244others(7): Show | 10 | HG01070.hp1 HG01168.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.920+4897delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26250877 | |||||
chr10:26250918
|
C | T | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+4918C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250918 | ||||||
chr10:26250930
|
A | C | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.920+4930A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250930 | ||||||
chr10:26251040
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(111): Show | 119 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.920+5040C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251040 | ||||||
chr10:26251044
|
A | AT | 17 | a0001c0001t0002g0135a0001c0002t0004g0007a0001c0002t0004g0008others(14): Show | 19 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.920+5054dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26251044 | |||||
chr10:26251055
|
G | T | 2 | a0001c0001t0001g0074a0001c0001t0005g0215 | 2 | NA18522.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.920+5055G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251055 | ||||||
chr10:26251056
|
C | CT | 6 | a0001c0001t0002g0178a0001c0001t0003g0133a0001c0001t0003g0162others(3): Show | 6 | HG02027.hp1 HG03471.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.920+5072dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26251056 | |||||
chr10:26251056
|
C | G | 2 | a0001c0001t0001g0074a0001c0001t0005g0215 | 2 | NA18522.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.920+5056C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251056 | ||||||
chr10:26251056
|
CT | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(98): Show | 105 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.920+5072delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26251056 | |||||
chr10:26251057
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0005g0215 | 2 | NA18522.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.920+5057T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251057 | ||||||
chr10:26251242
|
C | A | 6 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0008g0272others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.920+5242C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251242 | ||||||
chr10:26251266
|
A | G | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+5266A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251266 | ||||||
chr10:26251351
|
G | A | 2 | a0001c0001t0015g0101a0001c0003t0015g0267 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.920+5351G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251351 | ||||||
chr10:26251451
|
G | A | 9 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(6): Show | 9 | HG01106.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.920+5451G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251451 | ||||||
chr10:26251510
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.920+5510A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251510 | ||||||
chr10:26251585
|
G | A | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.920+5585G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251585 | ||||||
chr10:26251600
|
C | T | 1 | a0001c0001t0008g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.920+5600C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251600 | ||||||
chr10:26251683
|
T | G | 30 | a0001c0001t0008g0013a0001c0001t0008g0270a0001c0001t0008g0271others(27): Show | 33 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.920+5683T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251683 | ||||||
chr10:26251761
|
G | A | 3 | a0001c0001t0012g0062a0001c0001t0012g0106a0001c0007t0012g0259 | 3 | HG01884.hp2 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.920+5761G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251761 | ||||||
chr10:26251800
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(137): Show | 146 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.920+5800T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251800 | ||||||
chr10:26251842
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(146): Show | 155 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.920+5842G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251842 | ||||||
chr10:26251920
|
G | A | 1 | a0001c0001t0003g0208 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.920+5920G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251920 | ||||||
chr10:26252347
|
C | CTT | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+6353_920+6354d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26252347 | |||||
chr10:26252355
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(142): Show | 150 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.920+6355C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26252355 | ||||||
chr10:26252492
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.920+6492G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26252492 | ||||||
chr10:26252501
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.920+6501C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26252501 | ||||||
chr10:26252762
|
G | A | 1 | a0001c0001t0009g0009 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.920+6762G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26252762 | ||||||
chr10:26252883
|
C | G | 9 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(6): Show | 9 | HG01106.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.920+6883C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26252883 | ||||||
chr10:26252896
|
G | A | 1 | a0001c0001t0013g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920+6896G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26252896 | ||||||
chr10:26253076
|
G | A | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+7076G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253076 | ||||||
chr10:26253113
|
T | C | 1 | a0001c0001t0017g0012 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.920+7113T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253113 | ||||||
chr10:26253238
|
T | G | 10 | a0001c0001t0008g0013a0001c0001t0008g0270a0001c0001t0008g0271others(7): Show | 10 | HG02145.hp1 HG02451.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+7238T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253238 | ||||||
chr10:26253316
|
C | T | 1 | a0001c0001t0005g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920+7316C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253316 | ||||||
chr10:26253342
|
G | A | 2 | a0001c0001t0020g0283a0001c0001t0028g0280 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.920+7342G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253342 | ||||||
chr10:26253343
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.920+7343T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253343 | ||||||
chr10:26253369
|
A | G | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+7369A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253369 | ||||||
chr10:26253456
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.920+7456G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253456 | ||||||
chr10:26253489
|
C | A | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+7489C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253489 | ||||||
chr10:26254041
|
A | T | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.920+8041A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254041 | ||||||
chr10:26254060
|
C | T | 1 | a0001c0003t0005g0264 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.920+8060C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254060 | ||||||
chr10:26254190
|
G | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(142): Show | 150 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.920+8190G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254190 | ||||||
chr10:26254198
|
G | A | 9 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0005g0108others(6): Show | 9 | HG01106.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.920+8198G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254198 | ||||||
chr10:26254210
|
T | C | 1 | a0001c0001t0005g0262 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.920+8210T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254210 | ||||||
chr10:26254439
|
A | T | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.920+8439A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254439 | ||||||
chr10:26254453
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0068 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920+8453G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254453 | ||||||
chr10:26254455
|
T | C | 4 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0008g0272others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.920+8455T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254455 | ||||||
chr10:26254463
|
C | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.920+8463C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254463 | ||||||
chr10:26254515
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(116): Show | 124 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.920+8515C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254515 | ||||||
chr10:26254685
|
G | A | 1 | a0001c0001t0008g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.920+8685G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254685 | ||||||
chr10:26254805
|
C | G | 1 | a0001c0001t0008g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.920+8805C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254805 | ||||||
chr10:26254884
|
G | A | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.920+8884G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254884 | ||||||
chr10:26254929
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(146): Show | 155 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.920+8929G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254929 | ||||||
chr10:26255064
|
G | C | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.920+9064G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255064 | ||||||
chr10:26255274
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.920+9274G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255274 | ||||||
chr10:26255397
|
G | A | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+9397G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255397 | ||||||
chr10:26255424
|
C | G | 1 | a0001c0001t0002g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.920+9424C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255424 | ||||||
chr10:26255550
|
T | TTTCGCTA others(8): Show |
1 | a0001c0001t0001g0011 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.920+9551_920+9565d others(17): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26255550 | |||||
chr10:26255600
|
G | GGAAA | 154 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(151): Show | 160 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.920+9604_920+9607d others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26255600 | |||||
chr10:26255608
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0005g0215 | 3 | HG01099.hp2 HG01346.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.920+9608G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255608 | ||||||
chr10:26255646
|
AGGGGAG | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(133): Show | 141 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.920+9652_920+9657d others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26255646 | |||||
chr10:26255670
|
G | T | 3 | a0001c0001t0005g0215a0001c0001t0015g0101a0001c0003t0015g0267 | 3 | HG01243.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.920+9670G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255670 | ||||||
chr10:26255702
|
AAAGG | A | 3 | a0001c0001t0005g0215a0001c0001t0015g0101a0001c0003t0015g0267 | 3 | HG01243.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.920+9717_920+9720d others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26255702 | |||||
chr10:26255741
|
A | T | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+9741A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255741 | ||||||
chr10:26255766
|
C | T | 3 | a0001c0001t0012g0062a0001c0001t0012g0106a0001c0007t0012g0259 | 3 | HG01884.hp2 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.920+9766C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255766 | ||||||
chr10:26255858
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(133): Show | 141 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.920+9858G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255858 | ||||||
chr10:26255914
|
A | T | 1 | a0001c0001t0005g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920+9914A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255914 | ||||||
chr10:26255915
|
T | C | 15 | a0001c0001t0006g0153a0001c0001t0008g0270a0001c0001t0008g0271others(12): Show | 15 | HG00642.hp1 HG01109.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.920+9915T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255915 | ||||||
chr10:26255933
|
G | T | 1 | a0001c0001t0001g0011 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.920+9933G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255933 | ||||||
chr10:26255939
|
A | G | 3 | a0001c0001t0012g0062a0001c0001t0012g0106a0001c0007t0012g0259 | 3 | HG01884.hp2 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.920+9939A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255939 | ||||||
chr10:26256248
|
T | TTA | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+10261_920+1026 others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26256248 | |||||
chr10:26256257
|
T | G | 17 | a0001c0001t0001g0089a0001c0001t0007g0104a0001c0001t0007g0252others(14): Show | 17 | HG00642.hp2 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.920+10257T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256257 | ||||||
chr10:26256259
|
T | G | 109 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(106): Show | 112 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.920+10259T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256259 | ||||||
chr10:26256261
|
T | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(165): Show | 175 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.920+10261T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256261 | ||||||
chr10:26256435
|
C | T | 2 | a0001c0001t0016g0274a0001c0001t0016g0279 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.920+10435C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256435 | ||||||
chr10:26256474
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(137): Show | 145 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.920+10474C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256474 | ||||||
chr10:26256573
|
A | G | 1 | a0001c0001t0005g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920+10573A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256573 | ||||||
chr10:26256750
|
T | C | 11 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(8): Show | 11 | HG00642.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.920+10750T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256750 | ||||||
chr10:26256760
|
G | T | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.920+10760G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256760 | ||||||
chr10:26256771
|
G | A | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+10771G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256771 | ||||||
chr10:26256862
|
C | A | 4 | a0001c0001t0009g0003a0001c0001t0009g0009a0001c0001t0009g0010others(1): Show | 5 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+10862C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256862 | ||||||
chr10:26256864
|
C | T | 1 | a0001c0001t0005g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920+10864C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256864 | ||||||
chr10:26257095
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.920+11095C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257095 | ||||||
chr10:26257115
|
T | G | 1 | a0001c0001t0001g0028 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.920+11115T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257115 | ||||||
chr10:26257260
|
C | T | 3 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0258 | 3 | HG00642.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.920+11260C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257260 | ||||||
chr10:26257295
|
T | C | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.920+11295T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257295 | ||||||
chr10:26257301
|
C | T | 1 | a0001c0001t0028g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.920+11301C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257301 | ||||||
chr10:26257303
|
G | T | 1 | a0001c0001t0003g0144 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.920+11303G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257303 | ||||||
chr10:26257308
|
C | A | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+11308C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257308 | ||||||
chr10:26257342
|
C | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(135): Show | 144 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.920+11342C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257342 | ||||||
chr10:26257433
|
T | C | 1 | a0001c0002t0004g0241 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.920+11433T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257433 | ||||||
chr10:26257507
|
A | G | 4 | a0001c0003t0010g0245a0001c0003t0010g0246a0001c0003t0010g0247others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+11507A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257507 | ||||||
chr10:26257580
|
C | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | NA18999.hp2 NA19060.hp2 NA19076.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-11539C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257580 | ||||||
chr10:26257634
|
AC | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(131): Show | 139 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.921-11483delC | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26257634 | |||||
chr10:26257832
|
G | A | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-11287G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257832 | ||||||
chr10:26257833
|
C | T | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-11286C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257833 | ||||||
chr10:26257908
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.921-11211C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257908 | ||||||
chr10:26258100
|
T | TA | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-11018dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26258100 | |||||
chr10:26258213
|
T | C | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-10906T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258213 | ||||||
chr10:26258257
|
C | A | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.921-10862C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258257 | ||||||
chr10:26258578
|
C | T | 1 | a0001c0001t0017g0012 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.921-10541C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258578 | ||||||
chr10:26258605
|
G | T | 3 | a0001c0001t0002g0135a0001c0001t0002g0138a0001c0001t0002g0173 | 3 | HG03017.hp1 HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.921-10514G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258605 | ||||||
chr10:26258684
|
T | C | 2 | a0001c0001t0016g0274a0001c0001t0016g0279 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.921-10435T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258684 | ||||||
chr10:26258742
|
C | T | 1 | a0001c0001t0005g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.921-10377C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258742 | ||||||
chr10:26258787
|
G | A | 1 | a0001c0001t0020g0283 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.921-10332G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258787 | ||||||
chr10:26258812
|
AT | A | 13 | a0001c0001t0001g0011a0001c0001t0002g0166a0001c0001t0005g0108others(10): Show | 14 | HG00735.hp1 HG02165.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.921-10292delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26258812 | |||||
chr10:26258812
|
ATT | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 138 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.921-10293_921-1029 others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26258812 | |||||
chr10:26259023
|
G | T | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.921-10096G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259023 | ||||||
chr10:26259024
|
G | A | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-10095G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259024 | ||||||
chr10:26259106
|
C | A | 1 | a0001c0001t0005g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.921-10013C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259106 | ||||||
chr10:26259147
|
C | T | 7 | a0001c0001t0005g0108a0001c0001t0013g0268a0001c0001t0013g0269others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.921-9972C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259147 | ||||||
chr10:26259276
|
C | T | 6 | a0001c0001t0005g0128a0001c0001t0005g0261a0001c0003t0005g0113others(3): Show | 6 | HG02647.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.921-9843C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259276 | ||||||
chr10:26259517
|
T | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(85): Show | 91 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.921-9602T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259517 | ||||||
chr10:26259539
|
C | G | 1 | a0001c0001t0002g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.921-9580C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259539 | ||||||
chr10:26259546
|
T | C | 4 | a0001c0001t0009g0003a0001c0001t0009g0009a0001c0001t0009g0010others(1): Show | 5 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.921-9573T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259546 | ||||||
chr10:26259696
|
T | A | 4 | a0001c0003t0010g0245a0001c0003t0010g0246a0001c0003t0010g0247others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-9423T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259696 | ||||||
chr10:26259869
|
A | G | 1 | a0001c0001t0002g0004 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.921-9250A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259869 | ||||||
chr10:26260000
|
T | A | 7 | a0001c0001t0005g0108a0001c0001t0013g0268a0001c0001t0013g0269others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.921-9119T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260000 | ||||||
chr10:26260387
|
G | A | 6 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0008g0272others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.921-8732G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260387 | ||||||
chr10:26260394
|
C | T | 9 | a0001c0001t0006g0079a0001c0001t0006g0121a0001c0001t0006g0153others(6): Show | 9 | HG01109.hp2 HG01934.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.921-8725C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260394 | ||||||
chr10:26260466
|
T | G | 1 | a0001c0001t0020g0283 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.921-8653T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260466 | ||||||
chr10:26260496
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.921-8623C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260496 | ||||||
chr10:26260497
|
G | A | 6 | a0001c0001t0002g0004a0001c0001t0002g0135a0001c0001t0002g0136others(3): Show | 7 | HG01257.hp2 HG01258.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.921-8622G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260497 | ||||||
chr10:26260498
|
C | T | 1 | a0001c0001t0002g0004 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.921-8621C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260498 | ||||||
chr10:26260518
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.921-8601C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260518 | ||||||
chr10:26260550
|
C | T | 1 | a0001c0001t0015g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.921-8569C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260550 | ||||||
chr10:26260647
|
T | G | 1 | a0001c0001t0008g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.921-8472T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260647 | ||||||
chr10:26260685
|
G | A | 7 | a0001c0001t0005g0108a0001c0001t0013g0268a0001c0001t0013g0269others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.921-8434G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260685 | ||||||
chr10:26260774
|
C | G | 1 | a0001c0001t0008g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.921-8345C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260774 | ||||||
chr10:26260824
|
T | C | 1 | a0001c0001t0003g0231 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.921-8295T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260824 | ||||||
chr10:26260936
|
G | C | 1 | a0001c0001t0006g0079 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.921-8183G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260936 | ||||||
chr10:26261075
|
G | C | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-8044G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261075 | ||||||
chr10:26261151
|
C | A | 1 | a0001c0001t0012g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.921-7968C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261151 | ||||||
chr10:26261214
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.921-7905T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261214 | ||||||
chr10:26261433
|
C | T | 1 | a0001c0001t0005g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.921-7686C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261433 | ||||||
chr10:26261529
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.921-7590C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261529 | ||||||
chr10:26261548
|
T | G | 7 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0073others(4): Show | 7 | HG02922.hp1 HG03139.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.921-7571T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261548 | ||||||
chr10:26261629
|
A | G | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.921-7490A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261629 | ||||||
chr10:26261831
|
A | G | 1 | a0001c0001t0002g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.921-7288A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261831 | ||||||
chr10:26262031
|
T | C | 1 | a0001c0001t0014g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.921-7088T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262031 | ||||||
chr10:26262145
|
TA | T | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.921-6973delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262145 | ||||||
chr10:26262269
|
G | GT | 109 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(106): Show | 113 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.921-6837dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26262269 | |||||
chr10:26262308
|
A | G | 3 | a0001c0001t0002g0006a0001c0001t0002g0167a0001c0001t0002g0185 | 4 | HG02080.hp2 NA18970.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-6811A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262308 | ||||||
chr10:26262353
|
C | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-6766C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262353 | ||||||
chr10:26262501
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.921-6618T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262501 | ||||||
chr10:26262850
|
CT | C | 46 | a0001c0001t0001g0014a0001c0001t0005g0108a0001c0001t0005g0243others(43): Show | 48 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.921-6257delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26262850 | |||||
chr10:26262858
|
T | A | 6 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0008g0272others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.921-6261T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262858 | ||||||
chr10:26262860
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.921-6259T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262860 | ||||||
chr10:26262870
|
A | G | 1 | a0001c0001t0017g0012 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.921-6249A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262870 | ||||||
chr10:26262894
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.921-6225C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262894 | ||||||
chr10:26263074
|
A | G | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.921-6045A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263074 | ||||||
chr10:26263137
|
T | C | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-5982T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263137 | ||||||
chr10:26263185
|
C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(83): Show | 89 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.921-5934C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263185 | ||||||
chr10:26263337
|
C | A | 1 | a0001c0001t0002g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.921-5782C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263337 | ||||||
chr10:26263374
|
C | T | 23 | a0001c0001t0005g0108a0001c0001t0007g0104a0001c0001t0007g0252others(20): Show | 23 | HG00642.hp2 HG01884.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.921-5745C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263374 | ||||||
chr10:26263478
|
G | A | 2 | a0001c0001t0003g0207a0001c0001t0017g0012 | 2 | HG03516.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.921-5641G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263478 | ||||||
chr10:26263565
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.921-5554C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263565 | ||||||
chr10:26263648
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(144): Show | 153 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.921-5471C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263648 | ||||||
chr10:26263736
|
G | A | 8 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0073others(5): Show | 8 | HG02559.hp2 HG02922.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.921-5383G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263736 | ||||||
chr10:26263794
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(138): Show | 147 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.921-5325G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263794 | ||||||
chr10:26263890
|
G | T | 1 | a0001c0001t0002g0143 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.921-5229G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263890 | ||||||
chr10:26263942
|
C | T | 1 | a0001c0001t0003g0161 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.921-5177C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263942 | ||||||
chr10:26264056
|
A | G | 2 | a0001c0001t0014g0059a0001c0001t0014g0105 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.921-5063A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264056 | ||||||
chr10:26264160
|
A | G | 1 | a0001c0003t0005g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.921-4959A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264160 | ||||||
chr10:26264161
|
C | G | 4 | a0001c0003t0010g0245a0001c0003t0010g0246a0001c0003t0010g0247others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-4958C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264161 | ||||||
chr10:26264312
|
C | CT | 9 | a0001c0001t0001g0282a0001c0001t0005g0260a0001c0001t0009g0003others(6): Show | 10 | HG00735.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.921-4789dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26264312 | |||||
chr10:26264312
|
C | CTT | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.921-4790_921-4789d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26264312 | |||||
chr10:26264312
|
CT | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(79): Show | 85 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.921-4789delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26264312 | |||||
chr10:26264336
|
A | G | 6 | a0001c0001t0013g0268a0001c0001t0013g0269a0001c0003t0010g0245others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.921-4783A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264336 | ||||||
chr10:26264344
|
G | A | 26 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.921-4775G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264344 | ||||||
chr10:26264465
|
C | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.921-4654C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264465 | ||||||
chr10:26264467
|
C | G | 1 | a0001c0001t0002g0150 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.921-4652C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264467 | ||||||
chr10:26264474
|
G | GATTTTTT others(2): Show |
16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.921-4637_921-4629d others(11): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26264474 | |||||
chr10:26264500
|
C | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-4619C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264500 | ||||||
chr10:26264606
|
C | T | 2 | a0001c0001t0014g0059a0001c0001t0014g0105 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.921-4513C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264606 | ||||||
chr10:26264631
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(91): Show | 97 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.921-4488A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264631 | ||||||
chr10:26264646
|
T | G | 2 | a0001c0001t0014g0059a0001c0001t0014g0105 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.921-4473T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264646 | ||||||
chr10:26264786
|
A | G | 3 | a0001c0001t0012g0062a0001c0001t0012g0106a0001c0007t0012g0259 | 3 | HG01884.hp2 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.921-4333A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264786 | ||||||
chr10:26264817
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.921-4302C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264817 | ||||||
chr10:26264849
|
G | T | 1 | a0001c0001t0008g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.921-4270G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264849 | ||||||
chr10:26265038
|
T | C | 1 | a0001c0001t0002g0149 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.921-4081T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265038 | ||||||
chr10:26265040
|
G | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-4079G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265040 | ||||||
chr10:26265146
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.921-3973C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265146 | ||||||
chr10:26265202
|
C | T | 26 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.921-3917C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265202 | ||||||
chr10:26265203
|
G | A | 2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.921-3916G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265203 | ||||||
chr10:26265205
|
C | CT | 6 | a0001c0001t0002g0142a0001c0001t0002g0181a0001c0001t0005g0243others(3): Show | 6 | HG01106.hp2 HG01243.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.921-3896dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26265205 | |||||
chr10:26265205
|
CT | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(123): Show | 131 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.921-3896delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26265205 | |||||
chr10:26265205
|
CTT | C | 14 | a0001c0001t0001g0045a0001c0001t0001g0091a0001c0001t0005g0128others(11): Show | 15 | HG00735.hp1 HG02258.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.921-3897_921-3896d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26265205 | |||||
chr10:26265326
|
C | T | 4 | a0001c0003t0010g0245a0001c0003t0010g0246a0001c0003t0010g0247others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-3793C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265326 | ||||||
chr10:26265378
|
C | T | 26 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(23): Show | 27 | HG00642.hp2 HG00735.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.921-3741C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265378 | ||||||
chr10:26265439
|
G | A | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.921-3680G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265439 | ||||||
chr10:26265450
|
G | A | 2 | a0001c0001t0005g0108a0001c0001t0005g0215 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.921-3669G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265450 | ||||||
chr10:26265493
|
G | A | 1 | a0001c0001t0017g0012 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.921-3626G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265493 | ||||||
chr10:26265512
|
C | T | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.921-3607C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265512 | ||||||
chr10:26265699
|
T | C | 1 | a0001c0001t0008g0064 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.921-3420T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265699 | ||||||
chr10:26265736
|
A | G | 14 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(11): Show | 14 | HG00642.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.921-3383A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265736 | ||||||
chr10:26265926
|
C | T | 4 | a0001c0001t0008g0270a0001c0001t0008g0271a0001c0001t0008g0272others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-3193C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265926 | ||||||
chr10:26266333
|
C | A | 1 | a0001c0001t0001g0080 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.921-2786C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26266333 | ||||||
chr10:26266442
|
G | A | 1 | a0003c0005t0002g0227 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.921-2677G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26266442 | ||||||
chr10:26266792
|
A | C | 6 | a0001c0001t0005g0128a0001c0001t0005g0261a0001c0003t0005g0113others(3): Show | 6 | HG02647.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.921-2327A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26266792 | ||||||
chr10:26266815
|
T | G | 1 | a0001c0001t0002g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.921-2304T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26266815 | ||||||
chr10:26267188
|
G | C | 2 | a0001c0001t0015g0101a0001c0003t0015g0267 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.921-1931G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267188 | ||||||
chr10:26267270
|
C | A | 2 | a0001c0001t0015g0101a0001c0003t0015g0267 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.921-1849C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267270 | ||||||
chr10:26267489
|
C | T | 1 | a0001c0001t0013g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.921-1630C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267489 | ||||||
chr10:26267612
|
G | A | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.921-1507G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267612 | ||||||
chr10:26267631
|
G | A | 29 | a0001c0001t0002g0038a0001c0001t0002g0124a0001c0001t0002g0125others(26): Show | 29 | HG00544.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.921-1488G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267631 | ||||||
chr10:26267758
|
C | T | 2 | a0001c0001t0007g0254a0001c0001t0007g0256 | 2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.921-1361C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267758 | ||||||
chr10:26267948
|
G | A | 1 | a0001c0001t0003g0152 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.921-1171G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267948 | ||||||
chr10:26268038
|
A | G | 56 | a0001c0001t0001g0077a0001c0001t0001g0085a0001c0001t0007g0104others(53): Show | 59 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.921-1081A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268038 | ||||||
chr10:26268384
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(129): Show | 138 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.921-735T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268384 | ||||||
chr10:26268417
|
A | G | 1 | a0001c0001t0002g0275 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.921-702A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268417 | ||||||
chr10:26268467
|
C | CA | 42 | a0001c0001t0001g0072a0001c0001t0001g0093a0001c0001t0002g0125others(39): Show | 43 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.921-634dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26268467 | |||||
chr10:26268467
|
C | CAA | 72 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(69): Show | 75 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.921-635_921-634dup others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26268467 | |||||
chr10:26268467
|
C | CAAA | 14 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0044others(11): Show | 14 | HG01106.hp1 HG01109.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.921-636_921-634dup others(3): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26268467 | |||||
chr10:26268467
|
CA | C | 6 | a0001c0001t0003g0208a0001c0001t0006g0079a0001c0001t0012g0062others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.921-634delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26268467 | |||||
chr10:26268549
|
T | G | 1 | a0001c0001t0005g0244 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.921-570T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268549 | ||||||
chr10:26268681
|
A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(144): Show | 153 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.921-438A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268681 | ||||||
chr10:26268796
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(128): Show | 135 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.921-323A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268796 | ||||||
chr10:26268841
|
C | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(81): Show | 87 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.921-278C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268841 | ||||||
chr10:26269418
|
G | A | 1 | a0001c0001t0008g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.975+245G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26269418 | ||||||
chr10:26269440
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.975+267G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26269440 | ||||||
chr10:26269556
|
G | A | 1 | a0001c0001t0016g0279 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.975+383G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26269556 | ||||||
chr10:26269806
|
T | G | 2 | a0001c0001t0005g0108a0001c0001t0005g0215 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.975+633T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26269806 | ||||||
chr10:26270049
|
C | A | 2 | a0001c0001t0014g0059a0001c0001t0014g0105 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.976-591C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270049 | ||||||
chr10:26270106
|
G | A | 4 | a0001c0003t0010g0245a0001c0003t0010g0246a0001c0003t0010g0247others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.976-534G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270106 | ||||||
chr10:26270338
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.976-302G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270338 | ||||||
chr10:26270474
|
A | T | 1 | a0001c0001t0005g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.976-166A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270474 | ||||||
chr10:26270475
|
G | C | 7 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.976-165G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270475 | ||||||
chr10:26270510
|
G | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0009a0001c0001t0009g0010others(2): Show | 6 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-130G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270510 | ||||||
chr10:26270622
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.976-18G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270622 | ||||||
chr10:26270631
|
T | C | 1 | a0001c0001t0016g0279 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.976-9T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270631 | ||||||
chr10:26270798
|
C | T | 2 | a0001c0001t0001g0281a0001c0001t0001g0282 | 2 | HG01106.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1092+42C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26270798 | ||||||
chr10:26270934
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1092+178G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26270934 | ||||||
chr10:26270941
|
A | G | 1 | a0001c0001t0002g0168 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1092+185A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26270941 | ||||||
chr10:26271001
|
A | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(78): Show | 84 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1092+245A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271001 | ||||||
chr10:26271020
|
A | G | 4 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0002g0188others(1): Show | 4 | HG00735.hp2 HG01934.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092+264A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271020 | ||||||
chr10:26271028
|
G | C | 5 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+272G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271028 | ||||||
chr10:26271087
|
G | T | 1 | a0001c0001t0005g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1092+331G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271087 | ||||||
chr10:26271101
|
A | G | 3 | a0001c0001t0016g0274a0001c0001t0016g0279a0001c0009t0032g0265 | 3 | HG01884.hp1 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1092+345A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271101 | ||||||
chr10:26271104
|
A | G | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1092+348A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271104 | ||||||
chr10:26271173
|
G | A | 39 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0005g0260others(36): Show | 40 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1092+417G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271173 | ||||||
chr10:26271228
|
T | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0009a0001c0001t0009g0010others(2): Show | 6 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092+472T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271228 | ||||||
chr10:26271283
|
G | A | 1 | a0001c0001t0016g0279 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1092+527G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271283 | ||||||
chr10:26271376
|
GA | G | 6 | a0001c0001t0005g0260a0001c0001t0011g0109a0001c0001t0011g0110others(3): Show | 6 | HG00642.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1092+628delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr10 | 26271376 | |||||
chr10:26271453
|
G | T | 1 | a0001c0009t0032g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1092+697G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271453 | ||||||
chr10:26271711
|
G | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(116): Show | 123 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1092+955G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271711 | ||||||
chr10:26271846
|
G | A | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+1090G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271846 | ||||||
chr10:26271909
|
G | A | 2 | a0001c0001t0002g0006a0001c0001t0002g0185 | 3 | NA18970.hp2 NA18981.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1092+1153G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271909 | ||||||
chr10:26271987
|
T | C | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+1231T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271987 | ||||||
chr10:26272145
|
G | C | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+1389G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272145 | ||||||
chr10:26272173
|
G | C | 1 | a0001c0001t0002g0125 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1092+1417G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272173 | ||||||
chr10:26272292
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(152): Show | 161 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1093-1344T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272292 | ||||||
chr10:26272310
|
G | T | 8 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(5): Show | 8 | HG02280.hp1 HG02647.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1093-1326G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272310 | ||||||
chr10:26272333
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(123): Show | 130 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.1093-1303C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272333 | ||||||
chr10:26272554
|
C | CAG | 153 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(150): Show | 159 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1093-1081_1093-108 others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr10 | 26272554 | |||||
chr10:26272698
|
T | C | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0234 | 3 | HG00544.hp1 NA18941.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1093-938T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272698 | ||||||
chr10:26272747
|
C | A | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-889C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272747 | ||||||
chr10:26272755
|
T | C | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1093-881T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272755 | ||||||
chr10:26272790
|
G | A | 1 | a0001c0001t0003g0232 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1093-846G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272790 | ||||||
chr10:26272920
|
T | C | 47 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(44): Show | 49 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1093-716T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272920 | ||||||
chr10:26272949
|
C | T | 34 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(31): Show | 36 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1093-687C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272949 | ||||||
chr10:26272950
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(152): Show | 161 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1093-686A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272950 | ||||||
chr10:26273092
|
TAAG | T | 8 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(5): Show | 8 | HG02280.hp1 HG02647.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1093-542_1093-540d others(5): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr10 | 26273092 | |||||
chr10:26273249
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1093-387C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273249 | ||||||
chr10:26273401
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(280): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1093-235A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273401 | ||||||
chr10:26273422
|
C | T | 1 | a0001c0001t0028g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1093-214C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273422 | ||||||
chr10:26273485
|
G | A | 2 | a0001c0003t0005g0242a0001c0003t0005g0250 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1093-151G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273485 | ||||||
chr10:26273576
|
A | G | 2 | a0001c0001t0013g0268a0001c0001t0013g0269 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1093-60A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273576 | ||||||
chr10:26273601
|
A | G | 4 | a0001c0003t0010g0245a0001c0003t0010g0246a0001c0003t0010g0247others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093-35A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273601 | ||||||
chr10:26273622
|
T | C | 1 | a0001c0001t0007g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1093-14T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273622 | ||||||
chr10:26273968
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(142): Show | 151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1157+268G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26273968 | ||||||
chr10:26274024
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1157+324C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274024 | ||||||
chr10:26274041
|
A | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(152): Show | 161 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1157+341A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274041 | ||||||
chr10:26274105
|
T | A | 1 | a0001c0001t0006g0121 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1157+405T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274105 | ||||||
chr10:26274168
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1157+468G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274168 | ||||||
chr10:26274245
|
T | C | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+545T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274245 | ||||||
chr10:26274509
|
C | T | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+809C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274509 | ||||||
chr10:26274667
|
G | A | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+967G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274667 | ||||||
chr10:26274701
|
C | A | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+1001C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274701 | ||||||
chr10:26274716
|
G | A | 3 | a0001c0001t0003g0208a0001c0001t0003g0230a0001c0001t0025g0199 | 3 | HG00438.hp2 NA18962.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1157+1016G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274716 | ||||||
chr10:26274758
|
G | A | 1 | a0001c0001t0002g0229 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1157+1058G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274758 | ||||||
chr10:26274772
|
G | T | 1 | a0001c0001t0005g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1157+1072G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274772 | ||||||
chr10:26274844
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1157+1144C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274844 | ||||||
chr10:26275226
|
G | A | 34 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(31): Show | 36 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1157+1526G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275226 | ||||||
chr10:26275439
|
G | A | 8 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(5): Show | 8 | HG02280.hp1 HG02647.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+1739G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275439 | ||||||
chr10:26275480
|
C | A | 1 | a0001c0001t0003g0206 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1157+1780C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275480 | ||||||
chr10:26275504
|
T | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(92): Show | 99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1157+1804T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275504 | ||||||
chr10:26275598
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(152): Show | 161 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1157+1898T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275598 | ||||||
chr10:26275650
|
G | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1157+1950G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275650 | ||||||
chr10:26275907
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1157+2207G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275907 | ||||||
chr10:26275922
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(103): Show | 110 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1157+2222A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275922 | ||||||
chr10:26275927
|
G | A | 25 | a0001c0001t0003g0156a0001c0001t0005g0108a0001c0001t0005g0128others(22): Show | 27 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1157+2227G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275927 | ||||||
chr10:26275993
|
G | T | 9 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(6): Show | 9 | HG00642.hp2 HG02145.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1157+2293G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275993 | ||||||
chr10:26276227
|
C | T | 1 | a0001c0001t0007g0257 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1157+2527C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276227 | ||||||
chr10:26276309
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(103): Show | 110 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1157+2609G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276309 | ||||||
chr10:26276345
|
G | A | 1 | a0001c0003t0015g0267 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1157+2645G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276345 | ||||||
chr10:26276391
|
T | C | 1 | a0001c0001t0020g0283 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1157+2691T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276391 | ||||||
chr10:26276457
|
C | CT | 116 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(113): Show | 120 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.1157+2758dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr10 | 26276457 | |||||
chr10:26276506
|
T | C | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+2806T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276506 | ||||||
chr10:26276631
|
G | A | 11 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(8): Show | 11 | HG00642.hp2 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1157+2931G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276631 | ||||||
chr10:26276705
|
G | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(152): Show | 161 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1157+3005G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276705 | ||||||
chr10:26276744
|
G | A | 58 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0001t0002g0209others(55): Show | 60 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1157+3044G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276744 | ||||||
chr10:26276893
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(80): Show | 86 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1157+3193A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276893 | ||||||
chr10:26277010
|
T | C | 2 | a0001c0001t0008g0271a0001c0001t0008g0273 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1157+3310T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277010 | ||||||
chr10:26277030
|
G | A | 1 | a0001c0001t0024g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1157+3330G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277030 | ||||||
chr10:26277163
|
G | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0051 | 2 | NA18612.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1157+3463G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277163 | ||||||
chr10:26277306
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(115): Show | 122 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.1157+3606T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277306 | ||||||
chr10:26277363
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(92): Show | 99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1158-3646C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277363 | ||||||
chr10:26277417
|
C | G | 1 | a0001c0009t0032g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1158-3592C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277417 | ||||||
chr10:26277418
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0081 | 3 | HG02109.hp2 HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1158-3591G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277418 | ||||||
chr10:26277479
|
G | A | 1 | a0001c0001t0005g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1158-3530G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277479 | ||||||
chr10:26277498
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(153): Show | 162 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.1158-3511A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277498 | ||||||
chr10:26277527
|
C | T | 29 | a0001c0001t0002g0038a0001c0001t0002g0124a0001c0001t0002g0125others(26): Show | 29 | HG00544.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1158-3482C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277527 | ||||||
chr10:26277606
|
G | T | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-3403G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277606 | ||||||
chr10:26277616
|
G | C | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-3393G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277616 | ||||||
chr10:26277678
|
G | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(94): Show | 101 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1158-3331G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277678 | ||||||
chr10:26277704
|
T | C | 2 | a0001c0001t0015g0101a0001c0003t0015g0267 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1158-3305T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277704 | ||||||
chr10:26277789
|
A | G | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158-3220A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277789 | ||||||
chr10:26277860
|
G | A | 9 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(6): Show | 9 | HG02280.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1158-3149G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277860 | ||||||
chr10:26277920
|
A | G | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158-3089A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277920 | ||||||
chr10:26277989
|
GT | G | 19 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(16): Show | 19 | HG00642.hp2 HG02145.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.1158-3008delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr10 | 26277989 | |||||
chr10:26278252
|
C | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(124): Show | 133 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.1158-2757C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278252 | ||||||
chr10:26278291
|
A | G | 2 | a0001c0001t0019g0107a0001c0001t0023g0251 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1158-2718A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278291 | ||||||
chr10:26278411
|
C | T | 5 | a0001c0001t0008g0013a0001c0001t0008g0270a0001c0001t0008g0271others(2): Show | 5 | HG02145.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-2598C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278411 | ||||||
chr10:26278414
|
C | T | 1 | a0001c0009t0032g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1158-2595C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278414 | ||||||
chr10:26278473
|
T | A | 1 | a0001c0001t0003g0133 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1158-2536T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278473 | ||||||
chr10:26278523
|
G | A | 9 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(6): Show | 9 | HG02280.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1158-2486G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278523 | ||||||
chr10:26278716
|
T | C | 1 | a0001c0001t0002g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1158-2293T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278716 | ||||||
chr10:26278759
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(94): Show | 101 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1158-2250T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278759 | ||||||
chr10:26278897
|
G | A | 1 | a0001c0009t0032g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1158-2112G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278897 | ||||||
chr10:26278931
|
C | A | 13 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(10): Show | 13 | HG00642.hp2 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1158-2078C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278931 | ||||||
chr10:26278932
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(130): Show | 139 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1158-2077A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278932 | ||||||
chr10:26278978
|
G | A | 6 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0067others(3): Show | 6 | HG01192.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158-2031G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278978 | ||||||
chr10:26278986
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(150): Show | 159 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1158-2023A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278986 | ||||||
chr10:26279330
|
G | T | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1158-1679G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279330 | ||||||
chr10:26279353
|
C | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158-1656C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279353 | ||||||
chr10:26279433
|
C | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(150): Show | 159 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1158-1576C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279433 | ||||||
chr10:26279604
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1158-1405C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279604 | ||||||
chr10:26279605
|
G | A | 1 | a0001c0001t0006g0204 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1158-1404G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279605 | ||||||
chr10:26279776
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(96): Show | 103 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1158-1233A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279776 | ||||||
chr10:26279810
|
T | C | 6 | a0001c0001t0013g0268a0001c0001t0013g0269a0001c0003t0010g0245others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158-1199T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279810 | ||||||
chr10:26279935
|
T | C | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-1074T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279935 | ||||||
chr10:26280049
|
A | G | 1 | a0001c0001t0002g0228 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1158-960A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26280049 | ||||||
chr10:26280427
|
C | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | NA19060.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1158-582C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26280427 | ||||||
chr10:26280587
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1158-422G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26280587 | ||||||
chr10:26280675
|
A | G | 1 | a0001c0001t0012g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1158-334A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26280675 | ||||||
chr10:26280698
|
T | C | 2 | a0001c0001t0005g0108a0001c0001t0005g0215 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1158-311T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26280698 | ||||||
chr10:26280826
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(150): Show | 159 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1158-183A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26280826 | ||||||
chr10:26281267
|
G | A | 2 | a0001c0001t0013g0268a0001c0001t0013g0269 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1236+180G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281267 | ||||||
chr10:26281394
|
C | A | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1236+307C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281394 | ||||||
chr10:26281504
|
C | T | 1 | a0001c0001t0002g0168 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1236+417C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281504 | ||||||
chr10:26281505
|
A | C | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236+418A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281505 | ||||||
chr10:26281577
|
G | T | 1 | a0001c0001t0003g0175 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1236+490G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281577 | ||||||
chr10:26281749
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1236+662G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281749 | ||||||
chr10:26281754
|
C | T | 1 | a0001c0001t0003g0131 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1236+667C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281754 | ||||||
chr10:26281778
|
C | T | 1 | a0001c0001t0002g0038 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1236+691C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281778 | ||||||
chr10:26281792
|
G | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1236+705G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281792 | ||||||
chr10:26281996
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1236+909G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281996 | ||||||
chr10:26282044
|
G | A | 6 | a0001c0001t0013g0268a0001c0001t0013g0269a0001c0003t0010g0245others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1236+957G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26282044 | ||||||
chr10:26282080
|
A | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(150): Show | 159 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1236+993A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26282080 | ||||||
chr10:26282135
|
GT | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(133): Show | 142 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1236+1052delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr10 | 26282135 | |||||
chr10:26282513
|
T | C | 2 | a0001c0001t0019g0107a0001c0001t0023g0251 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1236+1426T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26282513 | ||||||
chr10:26282593
|
A | G | 30 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(27): Show | 30 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1236+1506A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26282593 | ||||||
chr10:26282981
|
C | T | 2 | a0001c0001t0014g0059a0001c0001t0014g0105 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1236+1894C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26282981 | ||||||
chr10:26282997
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0095 | 2 | HG00438.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1236+1910G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26282997 | ||||||
chr10:26283023
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1236+1936A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283023 | ||||||
chr10:26283077
|
G | T | 1 | a0001c0001t0003g0232 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1236+1990G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283077 | ||||||
chr10:26283144
|
C | A | 4 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0002g0188others(1): Show | 4 | HG00735.hp2 HG01934.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236+2057C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283144 | ||||||
chr10:26283237
|
A | G | 2 | a0001c0001t0016g0274a0001c0001t0016g0279 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1236+2150A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283237 | ||||||
chr10:26283253
|
G | A | 1 | a0001c0001t0003g0129 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1236+2166G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283253 | ||||||
chr10:26283851
|
G | C | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1237-2494G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283851 | ||||||
chr10:26283913
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(133): Show | 142 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1237-2432A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283913 | ||||||
chr10:26284109
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1237-2236C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284109 | ||||||
chr10:26284147
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(62): Show | 68 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1237-2198G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284147 | ||||||
chr10:26284478
|
A | G | 6 | a0001c0002t0004g0115a0001c0002t0004g0116a0001c0002t0004g0118others(3): Show | 6 | HG00323.hp2 HG00639.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1237-1867A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284478 | ||||||
chr10:26284544
|
A | G | 2 | a0001c0001t0013g0268a0001c0001t0013g0269 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1237-1801A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284544 | ||||||
chr10:26284564
|
C | CT | 83 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(80): Show | 87 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1237-1758dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr10 | 26284564 | |||||
chr10:26284564
|
C | CTT | 39 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0069others(36): Show | 41 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1237-1759_1237-175 others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr10 | 26284564 | |||||
chr10:26284564
|
C | CTTT | 8 | a0001c0001t0008g0013a0001c0001t0011g0109a0001c0001t0011g0110others(5): Show | 8 | HG00642.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1237-1760_1237-175 others(7): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr10 | 26284564 | |||||
chr10:26284564
|
CTTTTTTT others(3): Show |
C | 20 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(17): Show | 20 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1237-1767_1237-175 others(14): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr10 | 26284564 | |||||
chr10:26284628
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1237-1717G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284628 | ||||||
chr10:26284700
|
T | G | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | NA18948.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1237-1645T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284700 | ||||||
chr10:26284763
|
G | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-1582G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284763 | ||||||
chr10:26284808
|
A | T | 14 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1237-1537A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284808 | ||||||
chr10:26284820
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(80): Show | 86 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1237-1525C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284820 | ||||||
chr10:26284862
|
C | G | 2 | a0001c0001t0005g0108a0001c0001t0005g0215 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1237-1483C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284862 | ||||||
chr10:26284865
|
G | A | 3 | a0001c0001t0017g0012a0001c0001t0020g0283a0001c0001t0028g0280 | 3 | HG03486.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1237-1480G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284865 | ||||||
chr10:26285001
|
T | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(85): Show | 92 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1237-1344T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285001 | ||||||
chr10:26285020
|
T | C | 2 | a0001c0001t0003g0208a0001c0001t0003g0230 | 2 | NA18962.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1237-1325T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285020 | ||||||
chr10:26285253
|
C | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-1092C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285253 | ||||||
chr10:26285330
|
G | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(130): Show | 139 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1237-1015G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285330 | ||||||
chr10:26285365
|
T | C | 1 | a0001c0001t0020g0283 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1237-980T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285365 | ||||||
chr10:26285366
|
G | T | 1 | a0001c0003t0005g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1237-979G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285366 | ||||||
chr10:26285605
|
T | G | 2 | a0001c0001t0016g0274a0001c0001t0016g0279 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1237-740T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285605 | ||||||
chr10:26285651
|
C | G | 1 | a0001c0001t0003g0152 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1237-694C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285651 | ||||||
chr10:26285673
|
C | T | 1 | a0001c0003t0009g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1237-672C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285673 | ||||||
chr10:26285768
|
GT | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(128): Show | 137 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1237-563delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr10 | 26285768 | |||||
chr10:26285818
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1237-527C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285818 | ||||||
chr10:26285964
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(133): Show | 142 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1237-381T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285964 | ||||||
chr10:26286119
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1237-226C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26286119 | ||||||
chr10:26286292
|
A | G | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1237-53A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26286292 | ||||||
chr10:26286719
|
T | C | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1386+225T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26286719 | ||||||
chr10:26286861
|
G | A | 2 | a0001c0001t0019g0107a0001c0001t0023g0251 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1386+367G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26286861 | ||||||
chr10:26286935
|
T | C | 1 | a0001c0001t0009g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1386+441T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26286935 | ||||||
chr10:26286967
|
CT | C | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1386+474delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26286967 | ||||||
chr10:26287012
|
A | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(278): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1386+518A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287012 | ||||||
chr10:26287097
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(92): Show | 99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1386+603A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287097 | ||||||
chr10:26287164
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1386+670G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287164 | ||||||
chr10:26287321
|
A | G | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1386+827A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287321 | ||||||
chr10:26287333
|
G | A | 10 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(7): Show | 10 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1386+839G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287333 | ||||||
chr10:26287339
|
G | C | 4 | a0001c0001t0003g0174a0001c0001t0003g0196a0001c0001t0003g0206others(1): Show | 4 | HG00558.hp1 HG02523.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+845G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287339 | ||||||
chr10:26287576
|
G | A | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1386+1082G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287576 | ||||||
chr10:26287696
|
T | C | 7 | a0001c0001t0008g0013a0001c0001t0008g0064a0001c0001t0008g0065others(4): Show | 7 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386+1202T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287696 | ||||||
chr10:26287704
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0027 | 2 | NA18962.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1386+1210A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287704 | ||||||
chr10:26287853
|
A | C | 37 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(34): Show | 37 | HG00642.hp1 HG01192.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1386+1359A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287853 | ||||||
chr10:26287905
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1386+1411G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287905 | ||||||
chr10:26288097
|
C | A | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1386+1603C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288097 | ||||||
chr10:26288280
|
C | T | 1 | a0001c0009t0032g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1386+1786C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288280 | ||||||
chr10:26288355
|
T | A | 1 | a0001c0001t0002g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1386+1861T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288355 | ||||||
chr10:26288387
|
T | C | 2 | a0001c0001t0005g0108a0001c0001t0005g0215 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1386+1893T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288387 | ||||||
chr10:26288532
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1386+2038C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288532 | ||||||
chr10:26288563
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1386+2069C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288563 | ||||||
chr10:26288656
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1386+2162C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288656 | ||||||
chr10:26288706
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1386+2212C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288706 | ||||||
chr10:26288742
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(64): Show | 70 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1386+2248G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288742 | ||||||
chr10:26288881
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1386+2387T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288881 | ||||||
chr10:26289015
|
G | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(150): Show | 159 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1386+2521G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289015 | ||||||
chr10:26289036
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1386+2542C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289036 | ||||||
chr10:26289064
|
C | T | 1 | a0001c0003t0002g0266 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1386+2570C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289064 | ||||||
chr10:26289078
|
G | GT | 14 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1386+2593dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr10 | 26289078 | |||||
chr10:26289101
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1386+2607A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289101 | ||||||
chr10:26289186
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1386+2692C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289186 | ||||||
chr10:26289223
|
C | T | 2 | a0001c0001t0002g0123a0001c0001t0018g0222 | 2 | HG01358.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1386+2729C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289223 | ||||||
chr10:26289408
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(92): Show | 99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1386+2914C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289408 | ||||||
chr10:26289534
|
A | G | 37 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(34): Show | 37 | HG00642.hp1 HG01192.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1387-2931A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289534 | ||||||
chr10:26289541
|
A | T | 5 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1387-2924A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289541 | ||||||
chr10:26289710
|
A | G | 1 | a0001c0001t0028g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1387-2755A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289710 | ||||||
chr10:26289727
|
C | T | 1 | a0001c0001t0002g0219 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1387-2738C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289727 | ||||||
chr10:26289793
|
C | CT | 25 | a0001c0001t0002g0167a0001c0001t0002g0234a0001c0001t0005g0108others(22): Show | 25 | HG00642.hp1 HG00642.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.1387-2655dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr10 | 26289793 | |||||
chr10:26289793
|
CT | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(88): Show | 95 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1387-2655delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr10 | 26289793 | |||||
chr10:26289793
|
CTTT | C | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1387-2657_1387-265 others(7): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr10 | 26289793 | |||||
chr10:26290038
|
T | C | 1 | a0001c0001t0018g0222 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1387-2427T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26290038 | ||||||
chr10:26290401
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1387-2064A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26290401 | ||||||
chr10:26290534
|
C | T | 1 | a0001c0009t0032g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1387-1931C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26290534 | ||||||
chr10:26290601
|
G | T | 1 | a0001c0002t0004g0241 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1387-1864G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26290601 | ||||||
chr10:26290742
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1387-1723C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26290742 | ||||||
chr10:26290864
|
A | G | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1387-1601A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26290864 | ||||||
chr10:26291047
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1387-1418T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291047 | ||||||
chr10:26291107
|
T | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(150): Show | 159 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1387-1358T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291107 | ||||||
chr10:26291430
|
A | AAGAAGTG others(8): Show |
20 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(17): Show | 20 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1387-1033_1387-101 others(19): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr10 | 26291430 | |||||
chr10:26291455
|
G | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(80): Show | 86 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1387-1010G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291455 | ||||||
chr10:26291644
|
T | C | 3 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0144 | 3 | NA18980.hp1 NA18982.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1387-821T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291644 | ||||||
chr10:26291655
|
G | A | 1 | a0001c0001t0005g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1387-810G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291655 | ||||||
chr10:26291813
|
T | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 8 | NA18941.hp1 NA18948.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1387-652T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291813 | ||||||
chr10:26291997
|
A | G | 30 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(27): Show | 30 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1387-468A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291997 | ||||||
chr10:26292164
|
T | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(116): Show | 123 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1387-301T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26292164 | ||||||
chr10:26292392
|
G | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(117): Show | 124 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1387-73G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26292392 | ||||||
chr10:26292634
|
A | G | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494+62A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 14/15 | chr10 | 26292634 | ||||||
chr10:26293049
|
T | G | 2 | a0001c0001t0008g0271a0001c0001t0008g0273 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1584+58T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293049 | ||||||
chr10:26293172
|
CT | C | 12 | a0001c0001t0002g0180a0001c0001t0005g0128a0001c0001t0005g0261others(9): Show | 12 | HG01070.hp1 HG01256.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1584+204delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26293172 | |||||
chr10:26293193
|
T | C | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0016g0274 | 3 | HG01106.hp1 HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1584+202T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293193 | ||||||
chr10:26293193
|
T | TTC | 11 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0029others(8): Show | 11 | HG01070.hp2 HG01255.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1584+203_1584+204i others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26293193 | |||||
chr10:26293193
|
T | TTTC | 74 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(71): Show | 78 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1584+204_1584+205i others(5): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26293193 | |||||
chr10:26293201
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1584+210G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293201 | ||||||
chr10:26293456
|
G | A | 2 | a0001c0001t0002g0160a0002c0004t0002g0193 | 2 | HG00738.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1584+465G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293456 | ||||||
chr10:26293648
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0027 | 2 | NA18962.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1584+657A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293648 | ||||||
chr10:26293668
|
G | T | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1584+677G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293668 | ||||||
chr10:26293912
|
G | A | 3 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277 | 3 | HG02809.hp2 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1584+921G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293912 | ||||||
chr10:26294090
|
T | C | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1584+1099T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294090 | ||||||
chr10:26294102
|
G | A | 4 | a0001c0003t0010g0245a0001c0003t0010g0246a0001c0003t0010g0247others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1584+1111G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294102 | ||||||
chr10:26294396
|
A | G | 5 | a0001c0001t0014g0059a0001c0001t0014g0105a0001c0001t0017g0012others(2): Show | 5 | HG02451.hp2 HG03471.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1584+1405A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294396 | ||||||
chr10:26294449
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(92): Show | 99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1584+1458T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294449 | ||||||
chr10:26294459
|
G | T | 6 | a0001c0001t0013g0268a0001c0001t0013g0269a0001c0003t0010g0245others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1584+1468G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294459 | ||||||
chr10:26294747
|
G | C | 24 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(21): Show | 24 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1584+1756G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294747 | ||||||
chr10:26294779
|
A | T | 1 | a0001c0001t0002g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1584+1788A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294779 | ||||||
chr10:26294802
|
C | T | 2 | a0001c0001t0014g0059a0001c0001t0014g0105 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1584+1811C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294802 | ||||||
chr10:26294959
|
T | G | 4 | a0001c0003t0010g0245a0001c0003t0010g0246a0001c0003t0010g0247others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1584+1968T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294959 | ||||||
chr10:26295041
|
TG | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1584+2053delG | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295041 | |||||
chr10:26295052
|
A | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG00140.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1584+2061A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295052 | ||||||
chr10:26295073
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1584+2082G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295073 | ||||||
chr10:26295082
|
C | CA | 151 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(148): Show | 157 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1584+2091_1584+209 others(5): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295082 | ||||||
chr10:26295092
|
T | C | 1 | a0001c0001t0002g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1584+2101T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295092 | ||||||
chr10:26295124
|
G | T | 2 | a0001c0001t0012g0106a0001c0007t0012g0259 | 2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1584+2133G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295124 | ||||||
chr10:26295185
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1584+2194G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295185 | ||||||
chr10:26295434
|
T | A | 15 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(12): Show | 15 | HG00642.hp2 HG01192.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1584+2443T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295434 | ||||||
chr10:26295503
|
C | T | 5 | a0001c0001t0005g0128a0001c0001t0005g0261a0001c0003t0005g0113others(2): Show | 5 | HG02647.hp1 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1584+2512C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295503 | ||||||
chr10:26295505
|
C | T | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1584+2514C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295505 | ||||||
chr10:26295508
|
G | GCA | 31 | a0001c0001t0002g0124a0001c0001t0002g0138a0001c0001t0002g0139others(28): Show | 31 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1584+2556_1584+255 others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
G | GCACA | 16 | a0001c0001t0002g0127a0001c0001t0003g0189a0001c0001t0003g0230others(13): Show | 16 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1584+2554_1584+255 others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
G | GCACACA | 9 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0087others(6): Show | 9 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1584+2552_1584+255 others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
G | GCACACAC others(1): Show |
7 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0061others(4): Show | 7 | HG01243.hp2 HG02027.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.1584+2550_1584+255 others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
G | GCACACAC others(3): Show |
7 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0052others(4): Show | 7 | HG03669.hp1 NA18522.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1584+2548_1584+255 others(14): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
G | GCACACAC others(5): Show |
26 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0041others(23): Show | 26 | HG00597.hp2 HG00735.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1584+2546_1584+255 others(16): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
G | GCACACAC others(7): Show |
21 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0030others(18): Show | 21 | HG00558.hp2 HG01109.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1584+2544_1584+255 others(18): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
G | GCACACAC others(9): Show |
26 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0019others(23): Show | 30 | HG00140.hp1 HG01099.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1584+2542_1584+255 others(20): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
G | GCACACAC others(11): Show |
4 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0005g0262others(1): Show | 4 | HG01993.hp2 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1584+2540_1584+255 others(22): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
G | GCACACAC others(13): Show |
5 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0084others(2): Show | 5 | HG01256.hp2 HG01258.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1584+2538_1584+255 others(24): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
G | GCACACAC others(15): Show |
9 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0042others(6): Show | 9 | HG00438.hp1 HG00642.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1584+2536_1584+255 others(26): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
G | GCACACAC others(17): Show |
2 | a0001c0001t0001g0017a0001c0001t0011g0112 | 2 | HG01069.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1584+2534_1584+255 others(28): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
GCA | G | 19 | a0001c0001t0002g0006a0001c0001t0002g0167a0001c0001t0002g0183others(16): Show | 20 | HG00280.hp2 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1584+2556_1584+255 others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295508
|
GCACA | G | 4 | a0001c0001t0002g0168a0001c0001t0003g0205a0001c0003t0005g0242others(1): Show | 4 | HG02293.hp1 HG03195.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1584+2554_1584+255 others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | |||||
chr10:26295946
|
G | A | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1584+2955G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295946 | ||||||
chr10:26296060
|
G | A | 2 | a0001c0001t0014g0059a0001c0001t0014g0105 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1584+3069G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296060 | ||||||
chr10:26296087
|
C | T | 1 | a0001c0001t0003g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1584+3096C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296087 | ||||||
chr10:26296104
|
C | G | 5 | a0001c0001t0014g0059a0001c0001t0014g0105a0001c0001t0017g0012others(2): Show | 5 | HG02451.hp2 HG03471.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1584+3113C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296104 | ||||||
chr10:26296159
|
G | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0009a0001c0001t0009g0010others(2): Show | 6 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1584+3168G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296159 | ||||||
chr10:26296211
|
C | T | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1584+3220C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296211 | ||||||
chr10:26296248
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1584+3257T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296248 | ||||||
chr10:26296425
|
GTTA | G | 25 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(22): Show | 25 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1584+3438_1584+344 others(7): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26296425 | |||||
chr10:26296432
|
A | G | 1 | a0001c0001t0003g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1584+3441A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296432 | ||||||
chr10:26296576
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1584+3585A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296576 | ||||||
chr10:26296589
|
G | A | 25 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(22): Show | 25 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1584+3598G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296589 | ||||||
chr10:26296673
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(92): Show | 99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1584+3682A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296673 | ||||||
chr10:26296882
|
A | C | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1584+3891A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296882 | ||||||
chr10:26296920
|
AT | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(92): Show | 99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1585-3856delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26296920 | |||||
chr10:26297174
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(92): Show | 99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1585-3614A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26297174 | ||||||
chr10:26297176
|
C | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1585-3612C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26297176 | ||||||
chr10:26297281
|
C | A | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1585-3507C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26297281 | ||||||
chr10:26297872
|
T | A | 2 | a0001c0001t0014g0059a0001c0001t0014g0105 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1585-2916T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26297872 | ||||||
chr10:26297997
|
A | G | 1 | a0001c0001t0016g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1585-2791A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26297997 | ||||||
chr10:26298221
|
C | T | 1 | a0001c0001t0017g0012 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1585-2567C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298221 | ||||||
chr10:26298225
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1585-2563G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298225 | ||||||
chr10:26298239
|
T | C | 1 | a0001c0002t0004g0240 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1585-2549T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298239 | ||||||
chr10:26298315
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1585-2473C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298315 | ||||||
chr10:26298440
|
C | T | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1585-2348C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298440 | ||||||
chr10:26298457
|
G | A | 1 | a0001c0001t0011g0112 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1585-2331G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298457 | ||||||
chr10:26298612
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(92): Show | 99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1585-2176A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298612 | ||||||
chr10:26298794
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1585-1994G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298794 | ||||||
chr10:26298805
|
A | G | 1 | a0001c0001t0002g0149 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1585-1983A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298805 | ||||||
chr10:26298817
|
C | T | 3 | a0001c0001t0002g0157a0001c0001t0002g0178a0001c0001t0002g0179 | 3 | HG03710.hp1 HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1585-1971C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298817 | ||||||
chr10:26298992
|
G | A | 2 | a0001c0003t0005g0242a0001c0003t0005g0250 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1585-1796G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298992 | ||||||
chr10:26299361
|
T | G | 1 | a0001c0002t0004g0241 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1585-1427T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26299361 | ||||||
chr10:26299434
|
A | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(117): Show | 124 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1585-1354A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26299434 | ||||||
chr10:26299664
|
A | G | 16 | a0001c0002t0004g0007a0001c0002t0004g0008a0001c0002t0004g0031others(13): Show | 18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1585-1124A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26299664 | ||||||
chr10:26299926
|
T | C | 2 | a0001c0001t0013g0268a0001c0001t0013g0269 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1585-862T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26299926 | ||||||
chr10:26299962
|
A | G | 1 | a0001c0001t0002g0228 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1585-826A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26299962 | ||||||
chr10:26300203
|
G | A | 18 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(15): Show | 18 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1585-585G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300203 | ||||||
chr10:26300318
|
A | G | 1 | a0001c0001t0002g0173 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1585-470A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300318 | ||||||
chr10:26300456
|
T | C | 30 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(27): Show | 30 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1585-332T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300456 | ||||||
chr10:26300464
|
A | C | 4 | a0001c0003t0010g0245a0001c0003t0010g0246a0001c0003t0010g0247others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1585-324A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300464 | ||||||
chr10:26300498
|
A | G | 30 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(27): Show | 30 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1585-290A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300498 | ||||||
chr10:26300508
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0067 | 2 | HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1585-280T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300508 | ||||||
chr10:26300528
|
A | C | 1 | a0001c0003t0010g0247 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1585-260A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300528 | ||||||
chr10:26300528
|
A | G | 1 | a0001c0002t0030g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1585-260A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300528 | ||||||
chr10:26300618
|
C | T | 8 | a0001c0001t0007g0104a0001c0001t0007g0252a0001c0001t0007g0253others(5): Show | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1585-170C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300618 | ||||||
chr10:26300675
|
A | G | 24 | a0001c0001t0005g0108a0001c0001t0005g0128a0001c0001t0005g0215others(21): Show | 24 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1585-113A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300675 | ||||||
chr10:26300696
|
T | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(87): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1585-92T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300696 | ||||||
chr10:26300709
|
C | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0009a0001c0001t0009g0010others(2): Show | 6 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1585-79C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300709 | ||||||
chr10:26300742
|
A | G | 1 | a0001c0003t0005g0113 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1585-46A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300742 |