geneid | 80318 |
---|---|
ensemblid | ENSG00000165113.13 |
hgncid | 17496 |
symbol | GKAP1 |
name | G kinase anchoring protein 1 |
refseq_nuc | NM_025211.4 |
refseq_prot | NP_079487.2 |
ensembl_nuc | ENST00000376371.7 |
ensembl_prot | ENSP00000365550.2 |
mane_status | MANE Select |
chr | chr9 |
start | 83739425 |
end | 83817769 |
strand | - |
ver | v1.2 |
region | chr9:83739425-83817769 |
region5000 | chr9:83734425-83822769 |
regionname0 | GKAP1_chr9_83739425_83817769 |
regionname5000 | GKAP1_chr9_83734425_83822769 |
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 | 366 | 336 | 80 | 50 | 146 | 16 | 42 | 116 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
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 | 1/1 | 1101 | 335 | 80 | 50 | 145 | 16 | 42 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
c0002 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
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 | 701 | 146 | 38 | 23 | 56 | 8 | 21 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
t0002 | 0/1 | 701 | 118 | 23 | 15 | 63 | 5 | 11 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
t0003 | 0/0 | 701 | 56 | 10 | 11 | 23 | 3 | 9 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
t0004 | 0/0 | 701 | 6 | 6 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
t0005 | 0/0 | 701 | 3 | 3 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
t0006 | 0/0 | 701 | 3 | 0 | 0 | 3 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
t0007 | 0/0 | 701 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
t0008 | 1/0 | 701 | 1 | 0 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
t0009 | 0/0 | 701 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
t0010 | 0/0 | 701 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
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 | 1/1 | 1101 | 335 | 80 | 50 | 145 | 16 | 42 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
a0001c0002 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1801 | 145 | 38 | 23 | 55 | 8 | 21 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
a0001c0001t0002 | 0/1 | 1801 | 118 | 23 | 15 | 63 | 5 | 11 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
a0001c0001t0003 | 0/0 | 1801 | 56 | 10 | 11 | 23 | 3 | 9 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
a0001c0001t0004 | 0/0 | 1801 | 6 | 6 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
a0001c0001t0005 | 0/0 | 1801 | 3 | 3 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
a0001c0001t0006 | 0/0 | 1801 | 3 | 0 | 0 | 3 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
a0001c0001t0007 | 0/0 | 1801 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
a0001c0001t0008 | 1/0 | 1801 | 1 | 0 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
a0001c0001t0009 | 0/0 | 1801 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
a0001c0001t0010 | 0/0 | 1801 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
a0001c0002t0001 | 0/0 | 1801 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | copy fasta | chr9 | 83734425 | 83822769 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0008g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0009g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0001t0010g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0262 | EUR | GBR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0294 | EUR | GBR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0216 | EUR | FIN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | CHS | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | CHS | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | CHS | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01081 | hp2 | a0001 | c0001 | t0009 | g0318 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | CLM | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | CLM | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | CLM | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | CLM | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | CLM | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | CLM | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0177 | EUR | IBS | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0319 | EUR | IBS | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0176 | EUR | IBS | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PEL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0315 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | CDX | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | CDX | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PEL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | PEL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | MSL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0314 | AFR | MSL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0306 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0161 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | MSL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | MSL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0304 | AFR | MSL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | GWD | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | MSL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | STU | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0205 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | BEB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | BEB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | BEB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | BEB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG04115 | hp1 | a0001 | c0001 | t0010 | g0320 | SAS | STU | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | STU | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0287 | SAS | BEB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | STU | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | STU | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | STU | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | YRI | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | YRI | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | CHB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | YRI | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | YRI | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18965 | hp2 | a0001 | c0001 | t0007 | g0206 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18970 | hp2 | a0001 | c0001 | t0006 | g0097 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | LWK | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | LWK | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19082 | hp2 | a0001 | c0001 | t0006 | g0098 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | ASW | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ASW | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | TSI | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0235 | EUR | TSI | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0163 | EUR | TSI | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | GIH | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | GIH | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | MSL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | USA | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | USA | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | USA | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | USA | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0264 | REF | REF | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0008 | g0233 | REF | REF | GKAP1_chr9_83734425_83822769 | GKAP1 | chr9 | 83734425 | 83822769 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:83768863
|
T | C | 1 | a0001c0002 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.693A>G | p.Thr231Thr | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/13 | 1121/1801 | 693/1101 | 231/366 | chr9 | 83768863 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:83739596
|
G | C | 5 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(2): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*101C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 13/13 | 101 | chr9 | 83739596 | |||||
chr9:83806518
|
C | T | 1 | a0001c0001t0006 | 3 | NA18970.hp2 NA18979.hp1 NA19082.hp2 |
5_prime_UTR_variant | MODIFIER | c.-1G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/13 | 1 | chr9 | 83806518 | |||||
chr9:83817074
|
G | C | 1 | a0001c0001t0009 | 1 | HG01081.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-122C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/13 | chr9 | 83817074 | ||||||
chr9:83817664
|
G | T | 4 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(1): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
5_prime_UTR_variant | MODIFIER | c.-323C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 1/13 | 11147 | chr9 | 83817664 | |||||
chr9:83817674
|
C | T | 1 | a0001c0001t0007 | 1 | NA18965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-333G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 1/13 | 11157 | chr9 | 83817674 | |||||
chr9:83817680
|
A | G | 7 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(4): Show | 215 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(212): Show |
5_prime_UTR_variant | MODIFIER | c.-339T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 1/13 | 11163 | chr9 | 83817680 | |||||
chr9:83817735
|
C | A | 1 | a0001c0001t0010 | 1 | HG04115.hp1 | 5_prime_UTR_variant | MODIFIER | c.-394G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 1/13 | 11218 | chr9 | 83817735 | |||||
chr9:83817745
|
C | T | 1 | a0001c0001t0005 | 3 | HG02559.hp2 HG03130.hp1 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-404G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 1/13 | 11228 | chr9 | 83817745 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:83739795
|
G | A | 1 | a0001c0001t0006g0098 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1054-51C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83739795 | ||||||
chr9:83739808
|
T | A | 1 | a0001c0001t0003g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1054-64A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83739808 | ||||||
chr9:83739895
|
T | C | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1054-151A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83739895 | ||||||
chr9:83740118
|
T | G | 49 | a0001c0001t0002g0255a0001c0001t0003g0011a0001c0001t0003g0148others(46): Show | 50 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1054-374A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83740118 | ||||||
chr9:83740202
|
A | C | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1054-458T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83740202 | ||||||
chr9:83740363
|
TTAACA | T | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1054-624_1054-620d others(7): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83740363 | ||||||
chr9:83740434
|
G | C | 49 | a0001c0001t0002g0255a0001c0001t0003g0011a0001c0001t0003g0148others(46): Show | 50 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1054-690C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83740434 | ||||||
chr9:83740766
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1054-1022C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83740766 | ||||||
chr9:83740942
|
A | C | 1 | a0001c0001t0001g0058 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1053+1010T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83740942 | ||||||
chr9:83741027
|
A | G | 2 | a0001c0001t0004g0200a0001c0001t0004g0202 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1053+925T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741027 | ||||||
chr9:83741355
|
ATC | A | 5 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0005g0015others(2): Show | 5 | HG01255.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+595_1053+596d others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741355 | ||||||
chr9:83741358
|
T | TCACACAC others(3): Show |
1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1053+593_1053+594i others(12): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741358 | ||||||
chr9:83741358
|
TCTCA | T | 50 | a0001c0001t0002g0255a0001c0001t0002g0263a0001c0001t0003g0011others(47): Show | 51 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1053+590_1053+593d others(6): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741358 | ||||||
chr9:83741358
|
TCTCACA | T | 6 | a0001c0001t0002g0257a0001c0001t0003g0152a0001c0001t0003g0153others(3): Show | 6 | HG02132.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053+588_1053+593d others(8): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741358 | ||||||
chr9:83741358
|
TCTCACAC others(1): Show |
T | 113 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1053+586_1053+593d others(10): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741358 | ||||||
chr9:83741360
|
T | A | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1053+592A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741360 | ||||||
chr9:83741360
|
T | TCA | 31 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(28): Show | 34 | HG00609.hp1 HG00735.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.1053+590_1053+591d others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741360 | ||||||
chr9:83741360
|
T | TCACA | 21 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0023others(18): Show | 23 | HG00621.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1053+588_1053+591d others(6): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741360 | ||||||
chr9:83741360
|
T | TCACACA | 3 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073 | 4 | HG02155.hp2 NA18986.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+586_1053+591d others(8): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741360 | ||||||
chr9:83741362
|
A | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0095others(1): Show | 4 | HG01167.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+590T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741362 | ||||||
chr9:83741393
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1053+559T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741393 | ||||||
chr9:83741505
|
A | G | 1 | a0001c0001t0002g0291 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1053+447T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741505 | ||||||
chr9:83741563
|
T | C | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1053+389A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741563 | ||||||
chr9:83741611
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1053+341G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741611 | ||||||
chr9:83741705
|
T | C | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1053+247A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741705 | ||||||
chr9:83741803
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1053+149A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741803 | ||||||
chr9:83741834
|
C | T | 1 | a0001c0001t0002g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1053+118G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 12/12 | chr9 | 83741834 | ||||||
chr9:83742064
|
T | G | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.976-35A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 11/12 | chr9 | 83742064 | ||||||
chr9:83742266
|
GT | G | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.976-238delA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 11/12 | chr9 | 83742266 | ||||||
chr9:83742428
|
C | T | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+102G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 11/12 | chr9 | 83742428 | ||||||
chr9:83743185
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.905-585A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83743185 | ||||||
chr9:83743231
|
G | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0045 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.905-631C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83743231 | ||||||
chr9:83743342
|
C | A | 1 | a0001c0001t0002g0274 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.905-742G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83743342 | ||||||
chr9:83743389
|
G | T | 2 | a0001c0001t0004g0200a0001c0001t0004g0202 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.905-789C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83743389 | ||||||
chr9:83743424
|
G | T | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.905-824C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83743424 | ||||||
chr9:83743589
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.905-989C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83743589 | ||||||
chr9:83743681
|
T | C | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-1081A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83743681 | ||||||
chr9:83744057
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.905-1457A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83744057 | ||||||
chr9:83744143
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.905-1543G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83744143 | ||||||
chr9:83744173
|
C | T | 1 | a0001c0001t0004g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.905-1573G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83744173 | ||||||
chr9:83744413
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.905-1813G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83744413 | ||||||
chr9:83744421
|
T | C | 1 | a0001c0001t0002g0215 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.905-1821A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83744421 | ||||||
chr9:83744663
|
T | C | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-2063A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83744663 | ||||||
chr9:83744669
|
G | A | 1 | a0001c0001t0003g0197 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.905-2069C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83744669 | ||||||
chr9:83744669
|
G | C | 2 | a0001c0001t0003g0165a0001c0001t0003g0178 | 2 | NA18987.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.905-2069C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83744669 | ||||||
chr9:83744737
|
G | T | 1 | a0001c0001t0010g0320 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.905-2137C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83744737 | ||||||
chr9:83744839
|
C | T | 9 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(6): Show | 9 | HG01255.hp1 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-2239G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83744839 | ||||||
chr9:83745150
|
C | T | 1 | a0001c0001t0004g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.905-2550G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83745150 | ||||||
chr9:83745175
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0084 | 2 | HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.905-2575G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83745175 | ||||||
chr9:83745194
|
A | G | 9 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(6): Show | 9 | HG02055.hp2 HG02818.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-2594T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83745194 | ||||||
chr9:83745210
|
T | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0060others(10): Show | 15 | HG00609.hp1 NA18612.hp1 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.905-2610A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83745210 | ||||||
chr9:83745232
|
T | C | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.905-2632A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83745232 | ||||||
chr9:83745301
|
G | A | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.905-2701C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83745301 | ||||||
chr9:83745504
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.904+2805C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83745504 | ||||||
chr9:83745650
|
T | G | 1 | a0001c0001t0001g0058 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.904+2659A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83745650 | ||||||
chr9:83745834
|
A | T | 9 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0003g0168others(6): Show | 9 | HG01257.hp2 HG01258.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.904+2475T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83745834 | ||||||
chr9:83746473
|
C | T | 1 | a0001c0001t0002g0254 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.904+1836G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83746473 | ||||||
chr9:83746474
|
G | A | 42 | a0001c0001t0002g0255a0001c0001t0003g0011a0001c0001t0003g0148others(39): Show | 43 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.904+1835C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83746474 | ||||||
chr9:83746530
|
G | A | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0115others(33): Show | 38 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.904+1779C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83746530 | ||||||
chr9:83746663
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.904+1646G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83746663 | ||||||
chr9:83746724
|
T | A | 1 | a0001c0001t0002g0260 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.904+1585A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83746724 | ||||||
chr9:83746724
|
T | TA | 172 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(169): Show | 177 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.904+1584dupT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83746724 | ||||||
chr9:83746729
|
A | AAAATTGT others(17): Show |
1 | a0001c0001t0002g0253 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.904+1579_904+1580i others(26): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83746729 | ||||||
chr9:83746875
|
T | C | 5 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0005g0015others(2): Show | 5 | HG01255.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.904+1434A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83746875 | ||||||
chr9:83746908
|
G | C | 1 | a0001c0001t0003g0154 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.904+1401C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83746908 | ||||||
chr9:83747364
|
G | T | 1 | a0001c0001t0001g0114 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.904+945C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83747364 | ||||||
chr9:83747461
|
A | C | 1 | a0001c0001t0001g0006 | 2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.904+848T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83747461 | ||||||
chr9:83747502
|
T | G | 1 | a0001c0001t0001g0054 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.904+807A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83747502 | ||||||
chr9:83747640
|
A | AT | 24 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0027others(21): Show | 24 | HG01192.hp1 HG01255.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.904+668dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83747640 | ||||||
chr9:83747936
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.904+373T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83747936 | ||||||
chr9:83748060
|
T | A | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+249A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83748060 | ||||||
chr9:83748103
|
C | A | 1 | a0001c0001t0002g0292 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.904+206G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 10/12 | chr9 | 83748103 | ||||||
chr9:83748462
|
G | C | 1 | a0001c0001t0001g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.841-90C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83748462 | ||||||
chr9:83748529
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.841-157T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83748529 | ||||||
chr9:83748746
|
T | C | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.841-374A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83748746 | ||||||
chr9:83748754
|
T | C | 49 | a0001c0001t0002g0255a0001c0001t0003g0011a0001c0001t0003g0148others(46): Show | 50 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.841-382A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83748754 | ||||||
chr9:83748859
|
A | T | 1 | a0001c0001t0001g0054 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.841-487T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83748859 | ||||||
chr9:83748923
|
A | G | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.841-551T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83748923 | ||||||
chr9:83748994
|
T | A | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.841-622A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83748994 | ||||||
chr9:83749226
|
C | CT | 45 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0037others(42): Show | 48 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(45): Show |
intron_variant | MODIFIER | c.841-855dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83749226 | ||||||
chr9:83749226
|
CT | C | 13 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(10): Show | 13 | HG01099.hp1 HG01167.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.841-855delA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83749226 | ||||||
chr9:83749474
|
G | A | 3 | a0001c0001t0002g0264a0001c0001t0002g0294a0001c0001t0002g0295 | 3 | HG00140.hp1 HG00738.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.841-1102C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83749474 | ||||||
chr9:83749520
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.841-1148C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83749520 | ||||||
chr9:83749769
|
TTGA | T | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.841-1400_841-1398d others(5): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83749769 | ||||||
chr9:83749797
|
G | A | 2 | a0001c0001t0003g0193a0001c0001t0003g0194 | 2 | HG01255.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.841-1425C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83749797 | ||||||
chr9:83749820
|
A | G | 1 | a0001c0001t0004g0202 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.841-1448T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83749820 | ||||||
chr9:83749856
|
A | G | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.841-1484T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83749856 | ||||||
chr9:83749925
|
G | A | 1 | a0001c0001t0002g0282 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.841-1553C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83749925 | ||||||
chr9:83750158
|
CA | C | 107 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0207others(104): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.841-1787delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83750158 | ||||||
chr9:83750306
|
TGACA | T | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-1938_841-1935d others(6): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83750306 | ||||||
chr9:83750367
|
A | G | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.841-1995T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83750367 | ||||||
chr9:83750378
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.841-2006A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83750378 | ||||||
chr9:83750462
|
T | C | 1 | a0001c0001t0002g0274 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.841-2090A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83750462 | ||||||
chr9:83750672
|
G | C | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-2300C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83750672 | ||||||
chr9:83750746
|
A | C | 6 | a0001c0001t0002g0235a0001c0001t0002g0237a0001c0001t0002g0238others(3): Show | 6 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-2374T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83750746 | ||||||
chr9:83750897
|
A | ACGATCT | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+2355_840+2360d others(8): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83750897 | ||||||
chr9:83751068
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.840+2190G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83751068 | ||||||
chr9:83751190
|
G | T | 2 | a0001c0001t0002g0249a0001c0001t0007g0206 | 2 | NA18945.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.840+2068C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83751190 | ||||||
chr9:83751575
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.840+1683T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83751575 | ||||||
chr9:83751777
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.840+1481A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83751777 | ||||||
chr9:83751823
|
A | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0067 | 2 | NA18983.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.840+1435T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83751823 | ||||||
chr9:83751876
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.840+1382C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83751876 | ||||||
chr9:83751910
|
G | T | 1 | a0001c0001t0003g0154 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.840+1348C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83751910 | ||||||
chr9:83751984
|
G | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0113 | 3 | HG01192.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.840+1274C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83751984 | ||||||
chr9:83752002
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.840+1256G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752002 | ||||||
chr9:83752006
|
T | C | 1 | a0001c0001t0002g0296 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.840+1252A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752006 | ||||||
chr9:83752014
|
C | T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.840+1244G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752014 | ||||||
chr9:83752103
|
C | T | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+1155G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752103 | ||||||
chr9:83752156
|
C | T | 2 | a0001c0001t0002g0255a0001c0001t0003g0158 | 2 | NA18983.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.840+1102G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752156 | ||||||
chr9:83752247
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.840+1011G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752247 | ||||||
chr9:83752307
|
T | C | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.840+951A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752307 | ||||||
chr9:83752324
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.840+934C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752324 | ||||||
chr9:83752403
|
G | A | 2 | a0001c0001t0004g0200a0001c0001t0004g0202 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.840+855C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752403 | ||||||
chr9:83752482
|
C | T | 49 | a0001c0001t0002g0255a0001c0001t0003g0011a0001c0001t0003g0148others(46): Show | 50 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.840+776G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752482 | ||||||
chr9:83752628
|
C | T | 1 | a0001c0001t0004g0202 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.840+630G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752628 | ||||||
chr9:83752672
|
C | A | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.840+586G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752672 | ||||||
chr9:83752697
|
GGTTAT | G | 7 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0003g0184others(4): Show | 7 | HG03041.hp1 HG03710.hp1 NA19060.hp1 others(4): Show |
intron_variant | MODIFIER | c.840+556_840+560del others(5): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752697 | ||||||
chr9:83752724
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.840+534G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752724 | ||||||
chr9:83752780
|
A | T | 1 | a0001c0001t0001g0087 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.840+478T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752780 | ||||||
chr9:83752792
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.840+466G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752792 | ||||||
chr9:83752808
|
T | A | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0115others(33): Show | 38 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.840+450A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752808 | ||||||
chr9:83752928
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.840+330C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752928 | ||||||
chr9:83752978
|
G | A | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.840+280C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752978 | ||||||
chr9:83752980
|
T | C | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+278A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83752980 | ||||||
chr9:83753001
|
A | G | 39 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0037others(36): Show | 41 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(38): Show |
intron_variant | MODIFIER | c.840+257T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83753001 | ||||||
chr9:83753004
|
G | A | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.840+254C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83753004 | ||||||
chr9:83753060
|
A | AAAC | 42 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(39): Show | 44 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(41): Show |
intron_variant | MODIFIER | c.840+195_840+197dup others(3): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83753060 | ||||||
chr9:83753079
|
A | AT | 172 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(169): Show | 177 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.840+178_840+179ins others(1): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83753079 | ||||||
chr9:83753081
|
C | A | 173 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(170): Show | 178 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.840+177G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83753081 | ||||||
chr9:83753081
|
C | CATAA | 57 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(54): Show | 64 | HG00609.hp1 HG00621.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.840+173_840+176dup others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83753081 | ||||||
chr9:83753190
|
A | G | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.840+68T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83753190 | ||||||
chr9:83753207
|
C | T | 3 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219 | 3 | HG02818.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.840+51G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 9/12 | chr9 | 83753207 | ||||||
chr9:83753400
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.739-41G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83753400 | ||||||
chr9:83753495
|
T | A | 1 | a0001c0001t0005g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.739-136A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83753495 | ||||||
chr9:83753559
|
G | C | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.739-200C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83753559 | ||||||
chr9:83753649
|
G | C | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.739-290C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83753649 | ||||||
chr9:83753690
|
C | A | 1 | a0001c0001t0002g0290 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.739-331G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83753690 | ||||||
chr9:83753745
|
G | A | 223 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0018others(220): Show | 231 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.739-386C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83753745 | ||||||
chr9:83753965
|
G | A | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.739-606C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83753965 | ||||||
chr9:83754024
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.739-665C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83754024 | ||||||
chr9:83754441
|
A | G | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.739-1082T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83754441 | ||||||
chr9:83754674
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.739-1315C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83754674 | ||||||
chr9:83754949
|
G | T | 39 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0037others(36): Show | 41 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(38): Show |
intron_variant | MODIFIER | c.739-1590C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83754949 | ||||||
chr9:83755124
|
G | A | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.739-1765C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83755124 | ||||||
chr9:83755144
|
G | T | 5 | a0001c0001t0002g0014a0001c0001t0002g0306a0001c0001t0002g0307others(2): Show | 6 | HG02109.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.739-1785C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83755144 | ||||||
chr9:83755268
|
T | C | 2 | a0001c0001t0004g0200a0001c0001t0004g0202 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.739-1909A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83755268 | ||||||
chr9:83755418
|
T | A | 178 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(175): Show | 184 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.739-2059A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83755418 | ||||||
chr9:83755587
|
T | G | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.739-2228A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83755587 | ||||||
chr9:83755739
|
CA | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.739-2381delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83755739 | ||||||
chr9:83755799
|
C | CT | 19 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0034others(16): Show | 19 | HG00609.hp2 HG01106.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.739-2441dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83755799 | ||||||
chr9:83755799
|
CT | C | 16 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0037others(13): Show | 16 | HG01243.hp1 HG01255.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.739-2441delA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83755799 | ||||||
chr9:83755810
|
T | G | 1 | a0001c0001t0002g0261 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.739-2451A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83755810 | ||||||
chr9:83755842
|
T | C | 49 | a0001c0001t0002g0255a0001c0001t0003g0011a0001c0001t0003g0148others(46): Show | 50 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.739-2483A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83755842 | ||||||
chr9:83755859
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.739-2500G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83755859 | ||||||
chr9:83756066
|
A | C | 115 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(112): Show | 119 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.739-2707T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83756066 | ||||||
chr9:83756084
|
C | T | 1 | a0001c0001t0002g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.739-2725G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83756084 | ||||||
chr9:83756124
|
A | T | 1 | a0001c0001t0002g0287 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.739-2765T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83756124 | ||||||
chr9:83756142
|
G | T | 1 | a0001c0001t0001g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.739-2783C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83756142 | ||||||
chr9:83756328
|
G | A | 1 | a0001c0001t0002g0296 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.739-2969C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83756328 | ||||||
chr9:83756428
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.739-3069C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83756428 | ||||||
chr9:83756470
|
CA | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 261 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.739-3112delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83756470 | ||||||
chr9:83756470
|
CAA | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0093others(13): Show | 18 | HG01106.hp1 HG01192.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.739-3113_739-3112d others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83756470 | ||||||
chr9:83756482
|
A | G | 1 | a0001c0001t0003g0149 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.739-3123T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83756482 | ||||||
chr9:83756527
|
CTCA | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.739-3171_739-3169d others(5): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83756527 | ||||||
chr9:83756847
|
C | T | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.739-3488G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83756847 | ||||||
chr9:83757200
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 54 | HG00609.hp1 HG00621.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.739-3841C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83757200 | ||||||
chr9:83757267
|
G | A | 1 | a0001c0001t0002g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.739-3908C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83757267 | ||||||
chr9:83757375
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.739-4016A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83757375 | ||||||
chr9:83757378
|
T | C | 12 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.739-4019A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83757378 | ||||||
chr9:83757395
|
C | T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.739-4036G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83757395 | ||||||
chr9:83757823
|
A | G | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.739-4464T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83757823 | ||||||
chr9:83757902
|
A | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0059a0001c0001t0001g0061 | 3 | HG02630.hp1 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.739-4543T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83757902 | ||||||
chr9:83757908
|
C | T | 5 | a0001c0001t0002g0014a0001c0001t0002g0306a0001c0001t0002g0307others(2): Show | 6 | HG02109.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.739-4549G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83757908 | ||||||
chr9:83758162
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.739-4803G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758162 | ||||||
chr9:83758206
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.739-4847G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758206 | ||||||
chr9:83758240
|
T | A | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.739-4881A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758240 | ||||||
chr9:83758254
|
A | G | 1 | a0001c0001t0003g0156 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.739-4895T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758254 | ||||||
chr9:83758345
|
A | T | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.739-4986T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758345 | ||||||
chr9:83758373
|
C | T | 28 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0230others(25): Show | 31 | HG00621.hp2 HG02071.hp2 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.739-5014G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758373 | ||||||
chr9:83758381
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.739-5022A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758381 | ||||||
chr9:83758390
|
T | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0077 | 2 | HG01928.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.739-5031A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758390 | ||||||
chr9:83758400
|
C | G | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.739-5041G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758400 | ||||||
chr9:83758591
|
C | T | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0115others(33): Show | 38 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.739-5232G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758591 | ||||||
chr9:83758662
|
T | C | 1 | a0001c0001t0002g0304 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.739-5303A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758662 | ||||||
chr9:83758893
|
T | C | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.739-5534A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758893 | ||||||
chr9:83758971
|
T | C | 1 | a0001c0001t0002g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.739-5612A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758971 | ||||||
chr9:83758989
|
A | T | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.739-5630T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83758989 | ||||||
chr9:83759032
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.739-5673C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83759032 | ||||||
chr9:83759050
|
C | T | 9 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(6): Show | 9 | HG01255.hp1 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.739-5691G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83759050 | ||||||
chr9:83759406
|
G | A | 3 | a0001c0001t0006g0097a0001c0001t0006g0098a0001c0001t0006g0099 | 3 | NA18970.hp2 NA18979.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.739-6047C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83759406 | ||||||
chr9:83759455
|
A | T | 1 | a0001c0001t0003g0166 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.739-6096T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83759455 | ||||||
chr9:83759790
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.739-6431A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83759790 | ||||||
chr9:83759807
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(2): Show | 5 | HG02055.hp1 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.739-6448G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83759807 | ||||||
chr9:83759808
|
G | A | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-6449C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83759808 | ||||||
chr9:83759809
|
G | GT | 5 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0005g0015others(2): Show | 5 | HG01255.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.739-6451dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83759809 | ||||||
chr9:83759892
|
C | T | 2 | a0001c0001t0002g0309a0001c0001t0004g0012 | 3 | HG02280.hp1 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.739-6533G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83759892 | ||||||
chr9:83759902
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.739-6543G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83759902 | ||||||
chr9:83760139
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.739-6780A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83760139 | ||||||
chr9:83760362
|
T | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.739-7003A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83760362 | ||||||
chr9:83760394
|
A | T | 1 | a0001c0001t0003g0186 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.739-7035T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83760394 | ||||||
chr9:83760547
|
T | C | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.739-7188A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83760547 | ||||||
chr9:83760548
|
G | C | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.739-7189C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83760548 | ||||||
chr9:83760591
|
C | T | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.739-7232G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83760591 | ||||||
chr9:83761231
|
A | T | 1 | a0001c0001t0002g0277 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.738+7587T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83761231 | ||||||
chr9:83761391
|
G | A | 1 | a0001c0001t0002g0277 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.738+7427C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83761391 | ||||||
chr9:83761410
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.738+7408A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83761410 | ||||||
chr9:83761729
|
A | C | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.738+7089T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83761729 | ||||||
chr9:83762084
|
G | C | 1 | a0001c0001t0004g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.738+6734C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83762084 | ||||||
chr9:83762543
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.738+6275T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83762543 | ||||||
chr9:83762687
|
G | A | 1 | a0001c0001t0004g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.738+6131C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83762687 | ||||||
chr9:83762704
|
C | T | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.738+6114G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83762704 | ||||||
chr9:83762723
|
C | A | 274 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(271): Show | 289 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.738+6095G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83762723 | ||||||
chr9:83762746
|
A | G | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.738+6072T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83762746 | ||||||
chr9:83763138
|
T | C | 1 | a0001c0001t0002g0304 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.738+5680A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83763138 | ||||||
chr9:83763291
|
G | A | 1 | a0001c0001t0002g0255 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.738+5527C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83763291 | ||||||
chr9:83763612
|
T | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.738+5206A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83763612 | ||||||
chr9:83763726
|
C | T | 3 | a0001c0001t0006g0097a0001c0001t0006g0098a0001c0001t0006g0099 | 3 | NA18970.hp2 NA18979.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.738+5092G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83763726 | ||||||
chr9:83763795
|
A | G | 5 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0005g0015others(2): Show | 5 | HG01255.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.738+5023T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83763795 | ||||||
chr9:83763852
|
T | C | 49 | a0001c0001t0002g0216a0001c0001t0003g0011a0001c0001t0003g0148others(46): Show | 50 | HG00323.hp1 HG00609.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.738+4966A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83763852 | ||||||
chr9:83763876
|
G | C | 1 | a0001c0001t0002g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.738+4942C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83763876 | ||||||
chr9:83764054
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.738+4764C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83764054 | ||||||
chr9:83764168
|
G | A | 2 | a0001c0001t0002g0208a0001c0001t0002g0227 | 2 | NA18953.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.738+4650C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83764168 | ||||||
chr9:83764249
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.738+4569C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83764249 | ||||||
chr9:83764322
|
G | A | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.738+4496C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83764322 | ||||||
chr9:83764670
|
A | T | 1 | a0001c0001t0001g0004 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.738+4148T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83764670 | ||||||
chr9:83764824
|
C | G | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.738+3994G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83764824 | ||||||
chr9:83764961
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.738+3857G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83764961 | ||||||
chr9:83765139
|
C | T | 48 | a0001c0001t0003g0011a0001c0001t0003g0148a0001c0001t0003g0149others(45): Show | 49 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.738+3679G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83765139 | ||||||
chr9:83765152
|
G | A | 2 | a0001c0001t0005g0016a0001c0001t0005g0017 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.738+3666C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83765152 | ||||||
chr9:83765321
|
C | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0052others(7): Show | 12 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.738+3497G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83765321 | ||||||
chr9:83765336
|
G | T | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.738+3482C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83765336 | ||||||
chr9:83765400
|
G | A | 9 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(6): Show | 9 | HG01255.hp1 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.738+3418C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83765400 | ||||||
chr9:83765510
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.738+3308C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83765510 | ||||||
chr9:83765720
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.738+3098G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83765720 | ||||||
chr9:83765860
|
A | G | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.738+2958T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83765860 | ||||||
chr9:83765937
|
G | A | 1 | a0001c0001t0003g0186 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.738+2881C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83765937 | ||||||
chr9:83765980
|
C | T | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.738+2838G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83765980 | ||||||
chr9:83766403
|
CA | C | 223 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0018others(220): Show | 231 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.738+2414delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83766403 | ||||||
chr9:83766427
|
A | G | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.738+2391T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83766427 | ||||||
chr9:83766667
|
A | G | 285 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(282): Show | 300 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.738+2151T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83766667 | ||||||
chr9:83766723
|
G | C | 97 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0207others(94): Show | 100 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.738+2095C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83766723 | ||||||
chr9:83766793
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.738+2025T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83766793 | ||||||
chr9:83766836
|
G | A | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.738+1982C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83766836 | ||||||
chr9:83766870
|
TAA | T | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.738+1946_738+1947d others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83766870 | ||||||
chr9:83766899
|
G | A | 118 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0002others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.738+1919C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83766899 | ||||||
chr9:83767127
|
C | A | 1 | a0001c0001t0005g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.738+1691G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83767127 | ||||||
chr9:83767255
|
A | G | 11 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(8): Show | 11 | HG01192.hp1 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.738+1563T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83767255 | ||||||
chr9:83767347
|
A | G | 5 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0005g0015others(2): Show | 5 | HG01255.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.738+1471T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83767347 | ||||||
chr9:83767363
|
A | AT | 8 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.738+1454dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83767363 | ||||||
chr9:83767483
|
C | T | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.738+1335G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83767483 | ||||||
chr9:83767503
|
C | A | 164 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(161): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.738+1315G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83767503 | ||||||
chr9:83767512
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.738+1306G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83767512 | ||||||
chr9:83767587
|
C | T | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.738+1231G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83767587 | ||||||
chr9:83767813
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA20805.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.738+1005G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83767813 | ||||||
chr9:83768078
|
A | C | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.738+740T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83768078 | ||||||
chr9:83768186
|
A | G | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.738+632T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83768186 | ||||||
chr9:83768289
|
T | C | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.738+529A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83768289 | ||||||
chr9:83768359
|
C | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0121others(2): Show | 5 | HG02523.hp1 NA18951.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.738+459G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83768359 | ||||||
chr9:83768429
|
T | C | 1 | a0001c0001t0003g0161 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.738+389A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83768429 | ||||||
chr9:83768500
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.738+318A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83768500 | ||||||
chr9:83768513
|
C | G | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.738+305G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83768513 | ||||||
chr9:83768570
|
G | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0084 | 2 | HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.738+248C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83768570 | ||||||
chr9:83768662
|
T | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.738+156A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 8/12 | chr9 | 83768662 | ||||||
chr9:83769037
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.586-67G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83769037 | ||||||
chr9:83769387
|
C | T | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-417G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83769387 | ||||||
chr9:83769427
|
A | C | 3 | a0001c0001t0002g0211a0001c0001t0002g0303a0001c0001t0002g0310 | 3 | HG01081.hp1 HG02004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.586-457T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83769427 | ||||||
chr9:83769783
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.586-813G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83769783 | ||||||
chr9:83769784
|
G | A | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.586-814C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83769784 | ||||||
chr9:83769813
|
T | C | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.586-843A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83769813 | ||||||
chr9:83769955
|
G | A | 2 | a0001c0001t0002g0268a0001c0001t0002g0269 | 2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.586-985C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83769955 | ||||||
chr9:83769976
|
T | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.586-1006A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83769976 | ||||||
chr9:83770032
|
T | C | 1 | a0001c0001t0003g0192 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.586-1062A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770032 | ||||||
chr9:83770035
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.586-1065G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770035 | ||||||
chr9:83770246
|
A | C | 116 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(113): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.586-1276T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770246 | ||||||
chr9:83770453
|
T | C | 1 | a0001c0001t0003g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.586-1483A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770453 | ||||||
chr9:83770579
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0050 | 2 | HG00639.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.586-1609G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770579 | ||||||
chr9:83770589
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.586-1619G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770589 | ||||||
chr9:83770598
|
C | T | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-1628G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770598 | ||||||
chr9:83770684
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.586-1714G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770684 | ||||||
chr9:83770736
|
T | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 5 | HG02074.hp1 NA18969.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-1766A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770736 | ||||||
chr9:83770859
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0002g0295 | 2 | HG00609.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.586-1889C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770859 | ||||||
chr9:83770868
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.586-1898G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770868 | ||||||
chr9:83770869
|
G | A | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.586-1899C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770869 | ||||||
chr9:83770908
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.586-1938C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770908 | ||||||
chr9:83770992
|
T | A | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.586-2022A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83770992 | ||||||
chr9:83771237
|
G | GTTGT | 64 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0002g0014others(61): Show | 67 | HG00609.hp2 HG01070.hp1 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.586-2271_586-2268d others(6): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83771237 | ||||||
chr9:83771237
|
G | GTTGTTTG others(1): Show |
8 | a0001c0001t0003g0159a0001c0001t0003g0163a0001c0001t0003g0174others(5): Show | 8 | HG00735.hp1 HG01099.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.586-2275_586-2268d others(10): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83771237 | ||||||
chr9:83771237
|
G | GTTGTTTG others(5): Show |
1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.586-2279_586-2268d others(14): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83771237 | ||||||
chr9:83771237
|
GTTGT | G | 111 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(108): Show | 114 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.586-2271_586-2268d others(6): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83771237 | ||||||
chr9:83771310
|
T | G | 1 | a0001c0001t0001g0128 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.586-2340A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83771310 | ||||||
chr9:83771527
|
T | C | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-2557A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83771527 | ||||||
chr9:83771548
|
T | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.586-2578A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83771548 | ||||||
chr9:83771561
|
T | C | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.586-2591A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83771561 | ||||||
chr9:83771764
|
A | G | 4 | a0001c0001t0002g0014a0001c0001t0002g0307a0001c0001t0002g0308others(1): Show | 5 | HG02109.hp1 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.586-2794T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83771764 | ||||||
chr9:83771884
|
T | A | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.586-2914A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83771884 | ||||||
chr9:83771903
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA18952.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.586-2933A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83771903 | ||||||
chr9:83771982
|
GC | G | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.586-3013delG | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83771982 | ||||||
chr9:83772015
|
T | C | 1 | a0001c0001t0005g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.586-3045A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83772015 | ||||||
chr9:83772114
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.586-3144A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83772114 | ||||||
chr9:83772147
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.586-3177T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83772147 | ||||||
chr9:83772321
|
A | T | 1 | a0001c0001t0003g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.586-3351T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83772321 | ||||||
chr9:83772373
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.586-3403T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83772373 | ||||||
chr9:83772594
|
C | A | 1 | a0001c0001t0010g0320 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.586-3624G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83772594 | ||||||
chr9:83772636
|
A | G | 1 | a0001c0001t0002g0293 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.586-3666T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83772636 | ||||||
chr9:83772662
|
G | T | 1 | a0001c0001t0001g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.586-3692C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83772662 | ||||||
chr9:83772796
|
G | A | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-3826C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83772796 | ||||||
chr9:83772938
|
G | A | 2 | a0001c0001t0004g0200a0001c0001t0004g0202 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.586-3968C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83772938 | ||||||
chr9:83773195
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.586-4225C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83773195 | ||||||
chr9:83773228
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.586-4258C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83773228 | ||||||
chr9:83773538
|
A | C | 1 | a0001c0001t0002g0285 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.586-4568T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83773538 | ||||||
chr9:83773639
|
G | A | 5 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0005g0015others(2): Show | 5 | HG01255.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-4669C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83773639 | ||||||
chr9:83773647
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.586-4677T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83773647 | ||||||
chr9:83773960
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.586-4990G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83773960 | ||||||
chr9:83774016
|
C | T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.586-5046G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774016 | ||||||
chr9:83774062
|
G | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0113 | 3 | HG01192.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.586-5092C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774062 | ||||||
chr9:83774148
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.586-5178C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774148 | ||||||
chr9:83774177
|
T | C | 5 | a0001c0001t0002g0014a0001c0001t0002g0306a0001c0001t0002g0307others(2): Show | 6 | HG02109.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-5207A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774177 | ||||||
chr9:83774339
|
C | T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.586-5369G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774339 | ||||||
chr9:83774613
|
T | C | 1 | a0001c0001t0002g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586-5643A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774613 | ||||||
chr9:83774655
|
G | A | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.586-5685C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774655 | ||||||
chr9:83774665
|
G | A | 1 | a0001c0001t0005g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.586-5695C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774665 | ||||||
chr9:83774694
|
G | GA | 96 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(93): Show | 100 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.585+5687dupT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774694 | ||||||
chr9:83774698
|
C | A | 78 | a0001c0001t0001g0058a0001c0001t0002g0209a0001c0001t0002g0217others(75): Show | 79 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.585+5684G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774698 | ||||||
chr9:83774699
|
C | A | 1 | a0001c0001t0003g0168 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.585+5683G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774699 | ||||||
chr9:83774701
|
C | CTT | 35 | a0001c0001t0002g0209a0001c0001t0002g0217a0001c0001t0002g0221others(32): Show | 35 | HG00597.hp1 HG00642.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.585+5680_585+5681i others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774701 | ||||||
chr9:83774701
|
C | T | 96 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(93): Show | 100 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.585+5681G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774701 | ||||||
chr9:83774702
|
C | CT | 21 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(18): Show | 21 | HG00642.hp1 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.585+5679dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774702 | ||||||
chr9:83774702
|
C | T | 177 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(174): Show | 182 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.585+5680G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774702 | ||||||
chr9:83774702
|
CT | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0101others(3): Show | 7 | HG01516.hp2 HG03130.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.585+5679delA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774702 | ||||||
chr9:83774707
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.585+5675A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774707 | ||||||
chr9:83774812
|
C | T | 1 | a0001c0001t0002g0249 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.585+5570G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774812 | ||||||
chr9:83774876
|
G | T | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.585+5506C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83774876 | ||||||
chr9:83775011
|
C | CT | 197 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0117others(194): Show | 204 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.585+5370dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775011 | ||||||
chr9:83775053
|
T | C | 1 | a0001c0001t0002g0303 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.585+5329A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775053 | ||||||
chr9:83775083
|
A | G | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.585+5299T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775083 | ||||||
chr9:83775234
|
T | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.585+5148A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775234 | ||||||
chr9:83775286
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.585+5096G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775286 | ||||||
chr9:83775569
|
A | T | 114 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0207others(111): Show | 117 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.585+4813T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775569 | ||||||
chr9:83775579
|
A | C | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.585+4803T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775579 | ||||||
chr9:83775747
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.585+4635G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775747 | ||||||
chr9:83775758
|
C | T | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.585+4624G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775758 | ||||||
chr9:83775790
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0045 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.585+4592C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775790 | ||||||
chr9:83775874
|
C | CA | 24 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0077others(21): Show | 25 | HG00597.hp2 HG00621.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.585+4507dupT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775874 | ||||||
chr9:83775874
|
CA | C | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0018others(84): Show | 90 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.585+4507delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775874 | ||||||
chr9:83775874
|
CAA | C | 13 | a0001c0001t0001g0115a0001c0001t0001g0121a0001c0001t0001g0130others(10): Show | 13 | HG00323.hp2 HG01975.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+4506_585+4507d others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775874 | ||||||
chr9:83775982
|
A | G | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+4400T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83775982 | ||||||
chr9:83776120
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.585+4262G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83776120 | ||||||
chr9:83776273
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.585+4109G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83776273 | ||||||
chr9:83776407
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.585+3975A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83776407 | ||||||
chr9:83776475
|
T | C | 15 | a0001c0001t0002g0208a0001c0001t0002g0210a0001c0001t0002g0213others(12): Show | 15 | HG00597.hp1 HG02027.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+3907A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83776475 | ||||||
chr9:83776666
|
G | A | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+3716C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83776666 | ||||||
chr9:83776783
|
C | A | 2 | a0001c0001t0002g0268a0001c0001t0002g0269 | 2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.585+3599G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83776783 | ||||||
chr9:83776926
|
AT | A | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.585+3455delA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83776926 | ||||||
chr9:83776997
|
G | A | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+3385C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83776997 | ||||||
chr9:83777017
|
T | C | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.585+3365A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83777017 | ||||||
chr9:83777044
|
A | C | 1 | a0001c0001t0002g0287 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.585+3338T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83777044 | ||||||
chr9:83777381
|
T | C | 2 | a0001c0001t0003g0174a0001c0001t0003g0198 | 2 | HG00735.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.585+3001A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83777381 | ||||||
chr9:83777628
|
T | C | 1 | a0001c0001t0002g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.585+2754A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83777628 | ||||||
chr9:83777796
|
T | A | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.585+2586A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83777796 | ||||||
chr9:83778511
|
T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0036others(1): Show | 4 | HG02451.hp1 HG03471.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+1871A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83778511 | ||||||
chr9:83778698
|
T | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0121a0001c0001t0001g0139 | 3 | NA18951.hp1 NA18974.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.585+1684A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83778698 | ||||||
chr9:83778727
|
T | C | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.585+1655A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83778727 | ||||||
chr9:83778731
|
A | T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.585+1651T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83778731 | ||||||
chr9:83778788
|
TTAGACTG others(52): Show |
T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.585+1535_585+1593d others(61): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83778788 | ||||||
chr9:83778884
|
A | AATT | 178 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(175): Show | 184 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.585+1497_585+1498i others(5): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83778884 | ||||||
chr9:83778887
|
A | T | 1 | a0001c0001t0002g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.585+1495T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83778887 | ||||||
chr9:83778889
|
G | T | 1 | a0001c0001t0002g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.585+1493C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83778889 | ||||||
chr9:83778890
|
G | A | 1 | a0001c0001t0002g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.585+1492C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83778890 | ||||||
chr9:83778942
|
T | A | 1 | a0001c0001t0002g0232 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.585+1440A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83778942 | ||||||
chr9:83778952
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.585+1430T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83778952 | ||||||
chr9:83778998
|
A | T | 1 | a0001c0001t0001g0127 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.585+1384T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83778998 | ||||||
chr9:83779351
|
T | C | 164 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(161): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.585+1031A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779351 | ||||||
chr9:83779426
|
CAT | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 58 | HG00609.hp1 HG00621.hp1 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.585+954_585+955del others(2): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779426 | ||||||
chr9:83779442
|
T | TAC | 3 | a0001c0001t0003g0152a0001c0001t0003g0154a0001c0001t0003g0155 | 3 | HG02622.hp2 HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.585+939_585+940ins others(2): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779442 | ||||||
chr9:83779442
|
T | TACACACA others(3): Show |
2 | a0001c0001t0002g0230a0001c0001t0002g0298 | 2 | NA18971.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.585+939_585+940ins others(10): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779442 | ||||||
chr9:83779444
|
T | C | 5 | a0001c0001t0002g0230a0001c0001t0002g0298a0001c0001t0003g0152others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+938A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779444 | ||||||
chr9:83779444
|
T | TACACACA others(3): Show |
28 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(25): Show | 32 | HG00099.hp1 HG00621.hp2 HG02071.hp2 others(29): Show |
intron_variant | MODIFIER | c.585+937_585+938ins others(10): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779444 | ||||||
chr9:83779444
|
T | TACACACA others(5): Show |
11 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0223others(8): Show | 11 | HG02080.hp1 HG02165.hp1 HG04184.hp2 others(8): Show |
intron_variant | MODIFIER | c.585+937_585+938ins others(12): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779444 | ||||||
chr9:83779444
|
T | TACACACA others(7): Show |
4 | a0001c0001t0003g0166a0001c0001t0003g0188a0001c0001t0003g0191others(1): Show | 4 | HG02293.hp2 HG03490.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+937_585+938ins others(14): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779444 | ||||||
chr9:83779444
|
T | TACACACA others(9): Show |
1 | a0001c0001t0003g0192 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.585+937_585+938ins others(16): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779444 | ||||||
chr9:83779446
|
T | C | 55 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(52): Show | 59 | HG00099.hp1 HG00621.hp2 HG02071.hp2 others(56): Show |
intron_variant | MODIFIER | c.585+936A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779446 | ||||||
chr9:83779446
|
T | TACACACA others(1): Show |
8 | a0001c0001t0002g0234a0001c0001t0002g0245a0001c0001t0002g0251others(5): Show | 9 | HG00140.hp1 HG01081.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.585+935_585+936ins others(8): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779446 | ||||||
chr9:83779446
|
T | TACACACA others(3): Show |
3 | a0001c0001t0002g0216a0001c0001t0002g0240a0001c0001t0002g0319 | 3 | HG00323.hp1 HG01516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.585+935_585+936ins others(10): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779446 | ||||||
chr9:83779446
|
T | TACACACA others(5): Show |
53 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(50): Show | 53 | HG00597.hp1 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.585+935_585+936ins others(12): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779446 | ||||||
chr9:83779446
|
T | TACACACA others(7): Show |
4 | a0001c0001t0002g0263a0001c0001t0002g0271a0001c0001t0002g0286others(1): Show | 4 | HG02083.hp2 HG02135.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+935_585+936ins others(14): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779446 | ||||||
chr9:83779446
|
T | TACACACA others(9): Show |
9 | a0001c0001t0002g0303a0001c0001t0003g0150a0001c0001t0003g0161others(6): Show | 9 | HG00735.hp1 HG01081.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.585+935_585+936ins others(16): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779446 | ||||||
chr9:83779448
|
T | C | 159 | a0001c0001t0001g0077a0001c0001t0002g0002a0001c0001t0002g0013others(156): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.585+934A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779448 | ||||||
chr9:83779448
|
T | TACAC | 3 | a0001c0001t0003g0160a0001c0001t0003g0193a0001c0001t0003g0194 | 3 | HG01255.hp1 HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.585+930_585+933dup others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779448 | ||||||
chr9:83779448
|
T | TACACACA others(7): Show |
3 | a0001c0001t0002g0281a0001c0001t0002g0283a0001c0001t0002g0310 | 3 | HG03654.hp2 NA19083.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.585+920_585+933dup others(14): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779448 | ||||||
chr9:83779448
|
T | TATACACA others(7): Show |
1 | a0001c0001t0002g0304 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.585+933_585+934ins others(14): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779448 | ||||||
chr9:83779448
|
T | TATACACA others(13): Show |
2 | a0001c0001t0003g0183a0001c0001t0003g0205 | 2 | HG03710.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.585+933_585+934ins others(20): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779448 | ||||||
chr9:83779448
|
T | TATATACA others(3): Show |
2 | a0001c0001t0005g0016a0001c0001t0005g0017 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.585+933_585+934ins others(10): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779448 | ||||||
chr9:83779465
|
G | A | 35 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0002g0305others(32): Show | 36 | HG00609.hp2 HG00642.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.585+917C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779465 | ||||||
chr9:83779466
|
C | CACACACA others(21): Show |
2 | a0001c0001t0003g0162a0001c0001t0003g0185 | 2 | HG01975.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.585+915_585+916ins others(28): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779466 | ||||||
chr9:83779466
|
C | CACACACA others(19): Show |
8 | a0001c0001t0003g0156a0001c0001t0003g0169a0001c0001t0003g0174others(5): Show | 8 | HG02683.hp1 HG03041.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.585+915_585+916ins others(26): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779466 | ||||||
chr9:83779466
|
C | CACACACA others(17): Show |
20 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0003g0011others(17): Show | 21 | HG00642.hp2 HG01071.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.585+915_585+916ins others(24): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779466 | ||||||
chr9:83779470
|
T | C | 5 | a0001c0001t0002g0305a0001c0001t0003g0171a0001c0001t0004g0199others(2): Show | 5 | HG00609.hp2 HG02257.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+912A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779470 | ||||||
chr9:83779471
|
A | G | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.585+911T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779471 | ||||||
chr9:83779472
|
T | C | 35 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0002g0305others(32): Show | 36 | HG00609.hp2 HG00642.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.585+910A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779472 | ||||||
chr9:83779472
|
T | TACATAC | 144 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(141): Show | 149 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.585+909_585+910ins others(6): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779472 | ||||||
chr9:83779476
|
T | C | 1 | a0001c0001t0003g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.585+906A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779476 | ||||||
chr9:83779478
|
T | C | 1 | a0001c0001t0003g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.585+904A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779478 | ||||||
chr9:83779482
|
T | C | 1 | a0001c0001t0003g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.585+900A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779482 | ||||||
chr9:83779483
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.585+899T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779483 | ||||||
chr9:83779484
|
C | CACATATA others(35): Show |
1 | a0001c0001t0002g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.585+897_585+898ins others(42): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779484 | ||||||
chr9:83779486
|
T | C | 2 | a0001c0001t0003g0171a0001c0001t0004g0199 | 2 | HG00609.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.585+896A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779486 | ||||||
chr9:83779492
|
CACATAT | C | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.585+884_585+889del others(6): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779492 | ||||||
chr9:83779497
|
A | G | 1 | a0001c0001t0002g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.585+885T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779497 | ||||||
chr9:83779500
|
C | T | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.585+882G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779500 | ||||||
chr9:83779503
|
A | ATATATGT others(17): Show |
3 | a0001c0001t0001g0116a0001c0001t0001g0124a0001c0001t0001g0147 | 3 | HG01515.hp1 HG03704.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.585+855_585+878dup others(24): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779503 | ||||||
chr9:83779503
|
ATATATGT others(17): Show |
A | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.585+855_585+878del others(24): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779503 | ||||||
chr9:83779507
|
ATGTG | A | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.585+871_585+874del others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779507 | ||||||
chr9:83779510
|
T | C | 1 | a0001c0001t0003g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.585+872A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779510 | ||||||
chr9:83779511
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.585+871C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779511 | ||||||
chr9:83779514
|
T | C | 4 | a0001c0001t0003g0171a0001c0001t0004g0199a0001c0001t0004g0200others(1): Show | 4 | HG00609.hp2 HG02257.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+868A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779514 | ||||||
chr9:83779516
|
T | C | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.585+866A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779516 | ||||||
chr9:83779524
|
CGT | C | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.585+856_585+857del others(2): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779524 | ||||||
chr9:83779524
|
CGTGTATA others(35): Show |
C | 1 | a0001c0001t0003g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.585+816_585+857del others(42): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779524 | ||||||
chr9:83779525
|
G | A | 173 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(170): Show | 178 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.585+857C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779525 | ||||||
chr9:83779527
|
G | A | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.585+855C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779527 | ||||||
chr9:83779527
|
GTATATGT others(19): Show |
G | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.585+829_585+854del others(26): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779527 | ||||||
chr9:83779528
|
T | TATGTGTA others(15): Show |
1 | a0001c0001t0002g0319 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.585+853_585+854ins others(22): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779528 | ||||||
chr9:83779529
|
A | ATATGTGT others(15): Show |
1 | a0001c0001t0001g0146 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.585+831_585+852dup others(22): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779529 | ||||||
chr9:83779536
|
T | TATATATA others(7): Show |
1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.585+845_585+846ins others(14): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779536 | ||||||
chr9:83779548
|
C | G | 5 | a0001c0001t0003g0167a0001c0001t0003g0168a0001c0001t0003g0189others(2): Show | 5 | HG01257.hp2 HG01258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+834G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779548 | ||||||
chr9:83779549
|
G | A | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.585+833C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779549 | ||||||
chr9:83779551
|
GTA | G | 169 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(166): Show | 174 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.585+829_585+830del others(2): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779551 | ||||||
chr9:83779553
|
A | ATGTGTAT others(13): Show |
3 | a0001c0001t0002g0247a0001c0001t0002g0248a0001c0001t0002g0290 | 3 | HG02071.hp2 NA18959.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.585+828_585+829ins others(20): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779553 | ||||||
chr9:83779555
|
A | G | 1 | a0001c0001t0003g0188 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.585+827T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779555 | ||||||
chr9:83779559
|
G | A | 1 | a0001c0001t0003g0188 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.585+823C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779559 | ||||||
chr9:83779582
|
T | C | 1 | a0001c0001t0002g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.585+800A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779582 | ||||||
chr9:83779586
|
C | CAT | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(193): Show | 207 | HG00323.hp2 HG00597.hp2 HG00609.hp1 others(204): Show |
intron_variant | MODIFIER | c.585+795_585+796ins others(2): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779586 | ||||||
chr9:83779586
|
C | CATGTATA others(33): Show |
1 | a0001c0001t0001g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.585+795_585+796ins others(40): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779586 | ||||||
chr9:83779586
|
C | CATGTATA others(31): Show |
2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.585+795_585+796ins others(38): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779586 | ||||||
chr9:83779586
|
C | CATGTATA others(67): Show |
1 | a0001c0001t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.585+795_585+796ins others(74): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779586 | ||||||
chr9:83779586
|
C | T | 1 | a0001c0001t0002g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.585+796G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779586 | ||||||
chr9:83779606
|
C | T | 1 | a0001c0001t0003g0156 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.585+776G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779606 | ||||||
chr9:83779610
|
T | C | 2 | a0001c0001t0003g0156a0001c0001t0004g0201 | 2 | HG02818.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.585+772A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779610 | ||||||
chr9:83779610
|
T | TAC | 40 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(37): Show | 45 | HG00609.hp1 HG01106.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.585+771_585+772ins others(2): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779610 | ||||||
chr9:83779610
|
T | TACAC | 4 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0111others(1): Show | 4 | HG00621.hp1 NA18940.hp2 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+771_585+772ins others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779610 | ||||||
chr9:83779612
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 54 | HG00609.hp1 HG00621.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.585+770A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779612 | ||||||
chr9:83779612
|
T | TAC | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG01192.hp1 HG01515.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+768_585+769dup others(2): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779612 | ||||||
chr9:83779612
|
T | TACACACA others(29): Show |
1 | a0001c0001t0001g0022 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.585+769_585+770ins others(36): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779612 | ||||||
chr9:83779612
|
TAC | T | 170 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0031others(167): Show | 175 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.585+768_585+769del others(2): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779612 | ||||||
chr9:83779612
|
TACAC | T | 12 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(9): Show | 12 | HG01106.hp1 HG01255.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.585+766_585+769del others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779612 | ||||||
chr9:83779614
|
C | T | 3 | a0001c0001t0003g0156a0001c0001t0004g0012a0001c0001t0004g0201 | 4 | HG02280.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+768G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779614 | ||||||
chr9:83779616
|
C | T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.585+766G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779616 | ||||||
chr9:83779638
|
CACAT | C | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.585+740_585+743del others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779638 | ||||||
chr9:83779640
|
CAT | C | 2 | a0001c0001t0004g0012a0001c0001t0004g0201 | 3 | HG02280.hp1 HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.585+740_585+741del others(2): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779640 | ||||||
chr9:83779644
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.585+738G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779644 | ||||||
chr9:83779833
|
T | C | 3 | a0001c0001t0002g0264a0001c0001t0002g0294a0001c0001t0002g0295 | 3 | HG00140.hp1 HG00738.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.585+549A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83779833 | ||||||
chr9:83780100
|
T | C | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+282A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83780100 | ||||||
chr9:83780148
|
T | C | 2 | a0001c0001t0003g0193a0001c0001t0003g0194 | 2 | HG01255.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.585+234A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83780148 | ||||||
chr9:83780240
|
A | T | 1 | a0001c0001t0001g0116 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.585+142T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 7/12 | chr9 | 83780240 | ||||||
chr9:83780412
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | splice_region_variant&intron_variant | LOW | c.563-8A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780412 | ||||||
chr9:83780465
|
T | TA | 125 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(122): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.563-62dupT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780465 | ||||||
chr9:83780465
|
T | TAA | 9 | a0001c0001t0001g0018a0001c0001t0001g0048a0001c0001t0002g0221others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.563-63_563-62dupTT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780465 | ||||||
chr9:83780465
|
TA | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(50): Show | 59 | HG00609.hp1 HG00621.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.563-62delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780465 | ||||||
chr9:83780481
|
A | C | 2 | a0001c0001t0001g0108a0001c0002t0001g0109 | 2 | HG00621.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.563-77T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780481 | ||||||
chr9:83780483
|
C | T | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.563-79G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780483 | ||||||
chr9:83780558
|
G | A | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.563-154C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780558 | ||||||
chr9:83780653
|
A | T | 1 | a0001c0001t0002g0304 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.563-249T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780653 | ||||||
chr9:83780756
|
G | A | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.563-352C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780756 | ||||||
chr9:83780785
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0050 | 2 | HG00639.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.563-381T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780785 | ||||||
chr9:83780820
|
G | A | 48 | a0001c0001t0003g0011a0001c0001t0003g0148a0001c0001t0003g0149others(45): Show | 49 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.563-416C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780820 | ||||||
chr9:83780903
|
T | C | 48 | a0001c0001t0003g0011a0001c0001t0003g0148a0001c0001t0003g0149others(45): Show | 49 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.563-499A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780903 | ||||||
chr9:83780934
|
A | C | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.563-530T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780934 | ||||||
chr9:83780964
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0064 | 2 | NA18953.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.563-560G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780964 | ||||||
chr9:83780998
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.563-594C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83780998 | ||||||
chr9:83781000
|
T | C | 317 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(314): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.563-596A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83781000 | ||||||
chr9:83781138
|
G | A | 48 | a0001c0001t0003g0011a0001c0001t0003g0148a0001c0001t0003g0149others(45): Show | 49 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.563-734C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83781138 | ||||||
chr9:83781302
|
G | A | 3 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302 | 3 | NA18962.hp2 NA18981.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.563-898C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83781302 | ||||||
chr9:83781336
|
C | T | 3 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017 | 3 | HG02559.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.563-932G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83781336 | ||||||
chr9:83781341
|
C | T | 1 | a0001c0001t0002g0278 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.563-937G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83781341 | ||||||
chr9:83781383
|
G | A | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.563-979C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83781383 | ||||||
chr9:83781636
|
C | T | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.563-1232G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83781636 | ||||||
chr9:83781846
|
C | CT | 7 | a0001c0001t0001g0005a0001c0001t0002g0229a0001c0001t0002g0266others(4): Show | 9 | HG01167.hp1 HG01169.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.563-1443dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83781846 | ||||||
chr9:83781846
|
C | CTT | 166 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(163): Show | 171 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.563-1444_563-1443d others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83781846 | ||||||
chr9:83781892
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.563-1488C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83781892 | ||||||
chr9:83781946
|
T | C | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.563-1542A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83781946 | ||||||
chr9:83782084
|
C | T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.563-1680G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782084 | ||||||
chr9:83782095
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.563-1691C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782095 | ||||||
chr9:83782121
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0043a0001c0001t0001g0059others(1): Show | 4 | HG02258.hp2 HG02630.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-1717G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782121 | ||||||
chr9:83782223
|
T | C | 1 | a0001c0001t0001g0008 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.563-1819A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782223 | ||||||
chr9:83782284
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.563-1880T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782284 | ||||||
chr9:83782355
|
A | AT | 6 | a0001c0001t0001g0107a0001c0001t0002g0224a0001c0001t0002g0272others(3): Show | 6 | HG01255.hp2 HG02132.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.563-1952dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782355 | ||||||
chr9:83782362
|
T | A | 1 | a0001c0001t0002g0311 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.563-1958A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782362 | ||||||
chr9:83782400
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.563-1996G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782400 | ||||||
chr9:83782494
|
G | C | 5 | a0001c0001t0002g0014a0001c0001t0002g0306a0001c0001t0002g0307others(2): Show | 6 | HG02109.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.563-2090C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782494 | ||||||
chr9:83782583
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.562+2132G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782583 | ||||||
chr9:83782638
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.562+2077C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782638 | ||||||
chr9:83782660
|
C | CT | 42 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0036others(39): Show | 45 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.562+2054dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782660 | ||||||
chr9:83782660
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.562+2042_562+2054d others(15): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782660 | ||||||
chr9:83782732
|
C | T | 97 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0207others(94): Show | 100 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.562+1983G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782732 | ||||||
chr9:83782767
|
A | G | 165 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(162): Show | 170 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.562+1948T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782767 | ||||||
chr9:83782857
|
C | A | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.562+1858G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782857 | ||||||
chr9:83782872
|
T | A | 5 | a0001c0001t0002g0014a0001c0001t0002g0306a0001c0001t0002g0307others(2): Show | 6 | HG02109.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.562+1843A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782872 | ||||||
chr9:83782889
|
G | C | 2 | a0001c0001t0002g0294a0001c0001t0002g0295 | 2 | HG00140.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.562+1826C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782889 | ||||||
chr9:83782897
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.562+1818C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782897 | ||||||
chr9:83782938
|
AG | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0052others(7): Show | 12 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.562+1776delC | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83782938 | ||||||
chr9:83783106
|
T | G | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.562+1609A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783106 | ||||||
chr9:83783116
|
G | A | 1 | a0001c0001t0009g0318 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.562+1599C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783116 | ||||||
chr9:83783201
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.562+1514T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783201 | ||||||
chr9:83783256
|
T | C | 2 | a0001c0001t0002g0230a0001c0001t0002g0305 | 2 | HG02922.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.562+1459A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783256 | ||||||
chr9:83783396
|
C | T | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.562+1319G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783396 | ||||||
chr9:83783461
|
T | G | 9 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(6): Show | 9 | HG01255.hp1 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.562+1254A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783461 | ||||||
chr9:83783551
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.562+1164C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783551 | ||||||
chr9:83783690
|
C | T | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.562+1025G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783690 | ||||||
chr9:83783711
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(2): Show | 5 | HG02055.hp1 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.562+1004T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783711 | ||||||
chr9:83783719
|
A | G | 2 | a0001c0001t0002g0221a0001c0001t0002g0228 | 2 | NA18987.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.562+996T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783719 | ||||||
chr9:83783767
|
A | T | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.562+948T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783767 | ||||||
chr9:83783781
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.562+934T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783781 | ||||||
chr9:83783937
|
C | T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.562+778G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783937 | ||||||
chr9:83783986
|
C | T | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.562+729G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83783986 | ||||||
chr9:83784092
|
C | T | 2 | a0001c0001t0003g0193a0001c0001t0003g0194 | 2 | HG01255.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.562+623G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83784092 | ||||||
chr9:83784102
|
TA | T | 116 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(113): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.562+612delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83784102 | ||||||
chr9:83784160
|
G | A | 1 | a0001c0001t0003g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.562+555C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83784160 | ||||||
chr9:83784170
|
G | C | 1 | a0001c0001t0002g0317 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.562+545C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83784170 | ||||||
chr9:83784198
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0043a0001c0001t0001g0059others(1): Show | 4 | HG02258.hp2 HG02630.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.562+517G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83784198 | ||||||
chr9:83784199
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(2): Show | 5 | HG02055.hp1 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.562+516C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83784199 | ||||||
chr9:83784269
|
A | C | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.562+446T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83784269 | ||||||
chr9:83784420
|
C | A | 12 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.562+295G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83784420 | ||||||
chr9:83784678
|
T | C | 3 | a0001c0001t0002g0013a0001c0001t0002g0272a0001c0001t0002g0274 | 4 | NA18612.hp2 NA18984.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.562+37A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83784678 | ||||||
chr9:83784700
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.562+15A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83784700 | ||||||
chr9:83784708
|
A | G | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.562+7T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 6/12 | chr9 | 83784708 | ||||||
chr9:83784856
|
C | G | 1 | a0001c0001t0002g0288 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.439-18G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83784856 | ||||||
chr9:83784900
|
C | T | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.439-62G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83784900 | ||||||
chr9:83784942
|
G | A | 1 | a0001c0001t0002g0299 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.439-104C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83784942 | ||||||
chr9:83785001
|
A | G | 3 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017 | 3 | HG02559.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.439-163T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83785001 | ||||||
chr9:83785016
|
T | A | 2 | a0001c0001t0002g0210a0001c0001t0002g0273 | 2 | NA18982.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.439-178A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83785016 | ||||||
chr9:83785053
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.439-215A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83785053 | ||||||
chr9:83785179
|
G | A | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.439-341C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83785179 | ||||||
chr9:83785236
|
T | A | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.439-398A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83785236 | ||||||
chr9:83785314
|
G | A | 5 | a0001c0001t0002g0014a0001c0001t0002g0306a0001c0001t0002g0307others(2): Show | 6 | HG02109.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.439-476C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83785314 | ||||||
chr9:83785369
|
C | T | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.439-531G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83785369 | ||||||
chr9:83785385
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.439-547G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83785385 | ||||||
chr9:83785614
|
G | C | 1 | a0001c0001t0002g0274 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.439-776C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83785614 | ||||||
chr9:83785838
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.439-1000T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83785838 | ||||||
chr9:83785925
|
C | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 54 | HG00609.hp1 HG00621.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.439-1087G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83785925 | ||||||
chr9:83786072
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.439-1234A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786072 | ||||||
chr9:83786091
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.439-1253T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786091 | ||||||
chr9:83786184
|
C | T | 110 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0207others(107): Show | 113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.439-1346G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786184 | ||||||
chr9:83786327
|
C | G | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.439-1489G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786327 | ||||||
chr9:83786423
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.439-1585G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786423 | ||||||
chr9:83786448
|
G | A | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0115others(33): Show | 38 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.439-1610C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786448 | ||||||
chr9:83786476
|
G | C | 1 | a0001c0001t0002g0288 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.439-1638C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786476 | ||||||
chr9:83786489
|
C | T | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.439-1651G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786489 | ||||||
chr9:83786541
|
CA | C | 175 | a0001c0001t0001g0062a0001c0001t0002g0002a0001c0001t0002g0013others(172): Show | 180 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.439-1704delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786541 | ||||||
chr9:83786586
|
G | T | 1 | a0001c0001t0003g0174 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.439-1748C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786586 | ||||||
chr9:83786696
|
C | A | 274 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(271): Show | 289 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.439-1858G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786696 | ||||||
chr9:83786715
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.439-1877A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786715 | ||||||
chr9:83786746
|
A | C | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.438+1855T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786746 | ||||||
chr9:83786759
|
G | A | 4 | a0001c0001t0003g0163a0001c0001t0003g0174a0001c0001t0003g0175others(1): Show | 4 | HG00735.hp1 HG01099.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+1842C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786759 | ||||||
chr9:83786759
|
G | T | 1 | a0001c0001t0002g0304 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.438+1842C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786759 | ||||||
chr9:83786838
|
C | T | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.438+1763G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83786838 | ||||||
chr9:83787095
|
A | G | 1 | a0001c0001t0002g0301 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.438+1506T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83787095 | ||||||
chr9:83787099
|
T | C | 110 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0207others(107): Show | 113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.438+1502A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83787099 | ||||||
chr9:83787253
|
A | G | 2 | a0001c0001t0003g0165a0001c0001t0003g0178 | 2 | NA18987.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.438+1348T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83787253 | ||||||
chr9:83787403
|
A | AT | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+1197dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83787403 | ||||||
chr9:83787405
|
T | TA | 175 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(172): Show | 181 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.438+1195dupT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83787405 | ||||||
chr9:83787416
|
T | A | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.438+1185A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83787416 | ||||||
chr9:83787694
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.438+907A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83787694 | ||||||
chr9:83787701
|
G | A | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.438+900C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83787701 | ||||||
chr9:83787729
|
G | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(31): Show | 38 | HG00609.hp1 HG00621.hp1 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.438+872C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83787729 | ||||||
chr9:83787790
|
G | A | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+811C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83787790 | ||||||
chr9:83787846
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0002g0241 | 2 | HG02074.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.438+755C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83787846 | ||||||
chr9:83787951
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.438+650A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83787951 | ||||||
chr9:83788213
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.438+388C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83788213 | ||||||
chr9:83788221
|
T | G | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.438+380A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83788221 | ||||||
chr9:83788466
|
G | A | 48 | a0001c0001t0003g0011a0001c0001t0003g0148a0001c0001t0003g0149others(45): Show | 49 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.438+135C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 5/12 | chr9 | 83788466 | ||||||
chr9:83789106
|
A | T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.361-428T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83789106 | ||||||
chr9:83789124
|
A | G | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-446T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83789124 | ||||||
chr9:83789401
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.361-723A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83789401 | ||||||
chr9:83789474
|
C | T | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0115others(33): Show | 38 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.361-796G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83789474 | ||||||
chr9:83789533
|
T | C | 2 | a0001c0001t0003g0193a0001c0001t0003g0194 | 2 | HG01255.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.361-855A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83789533 | ||||||
chr9:83789669
|
C | T | 110 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0207others(107): Show | 113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.361-991G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83789669 | ||||||
chr9:83789774
|
T | TG | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.361-1097dupC | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83789774 | ||||||
chr9:83790029
|
G | A | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.361-1351C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790029 | ||||||
chr9:83790108
|
C | T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.361-1430G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790108 | ||||||
chr9:83790179
|
T | C | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.361-1501A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790179 | ||||||
chr9:83790361
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | NA18985.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.361-1683A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790361 | ||||||
chr9:83790520
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.361-1842G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790520 | ||||||
chr9:83790545
|
G | A | 2 | a0001c0001t0003g0176a0001c0001t0003g0177 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.361-1867C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790545 | ||||||
chr9:83790558
|
G | A | 1 | a0001c0001t0002g0316 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.361-1880C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790558 | ||||||
chr9:83790577
|
G | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0141others(1): Show | 4 | HG01516.hp2 HG01517.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-1899C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790577 | ||||||
chr9:83790648
|
AC | A | 109 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0207others(106): Show | 112 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.361-1971delG | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790648 | ||||||
chr9:83790649
|
C | A | 1 | a0001c0001t0002g0275 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.361-1971G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790649 | ||||||
chr9:83790741
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.361-2063C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790741 | ||||||
chr9:83790958
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.361-2280A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790958 | ||||||
chr9:83790979
|
A | G | 9 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(6): Show | 9 | HG01255.hp1 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.361-2301T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83790979 | ||||||
chr9:83791129
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.361-2451C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83791129 | ||||||
chr9:83791269
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA18952.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.361-2591C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83791269 | ||||||
chr9:83791311
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0002g0241 | 2 | HG02074.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.361-2633C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83791311 | ||||||
chr9:83791381
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0061 | 2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.361-2703G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83791381 | ||||||
chr9:83791386
|
G | A | 2 | a0001c0001t0002g0237a0001c0001t0002g0238 | 2 | HG00642.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.361-2708C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83791386 | ||||||
chr9:83791389
|
C | T | 1 | a0001c0001t0003g0194 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.361-2711G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83791389 | ||||||
chr9:83791402
|
CA | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.361-2725delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83791402 | ||||||
chr9:83791564
|
T | TA | 5 | a0001c0001t0002g0014a0001c0001t0002g0306a0001c0001t0002g0307others(2): Show | 6 | HG02109.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-2887dupT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83791564 | ||||||
chr9:83791802
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.361-3124C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83791802 | ||||||
chr9:83792119
|
C | T | 1 | a0001c0001t0002g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.361-3441G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83792119 | ||||||
chr9:83792120
|
T | C | 1 | a0001c0001t0002g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.361-3442A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83792120 | ||||||
chr9:83792126
|
T | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(31): Show | 38 | HG00609.hp1 HG00621.hp1 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.361-3448A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83792126 | ||||||
chr9:83792649
|
A | G | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.361-3971T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83792649 | ||||||
chr9:83792855
|
T | C | 1 | a0001c0001t0002g0304 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.361-4177A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83792855 | ||||||
chr9:83793055
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.361-4377G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83793055 | ||||||
chr9:83793324
|
A | C | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.361-4646T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83793324 | ||||||
chr9:83793375
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.361-4697T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83793375 | ||||||
chr9:83793580
|
G | A | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-4902C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83793580 | ||||||
chr9:83793708
|
A | G | 1 | a0001c0001t0002g0241 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.361-5030T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83793708 | ||||||
chr9:83793717
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.361-5039G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83793717 | ||||||
chr9:83793921
|
C | T | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-5243G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83793921 | ||||||
chr9:83794116
|
A | G | 1 | a0001c0001t0002g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.360+5069T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83794116 | ||||||
chr9:83794386
|
T | A | 1 | a0001c0001t0001g0006 | 2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.360+4799A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83794386 | ||||||
chr9:83794600
|
C | T | 1 | a0001c0001t0002g0316 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.360+4585G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83794600 | ||||||
chr9:83794671
|
C | T | 48 | a0001c0001t0003g0011a0001c0001t0003g0148a0001c0001t0003g0149others(45): Show | 49 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.360+4514G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83794671 | ||||||
chr9:83794803
|
C | A | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.360+4382G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83794803 | ||||||
chr9:83794831
|
G | A | 1 | a0001c0001t0009g0318 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.360+4354C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83794831 | ||||||
chr9:83794936
|
A | T | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.360+4249T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83794936 | ||||||
chr9:83794949
|
A | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG02622.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+4236T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83794949 | ||||||
chr9:83794998
|
T | C | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+4187A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83794998 | ||||||
chr9:83795105
|
G | A | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.360+4080C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795105 | ||||||
chr9:83795107
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.360+4078C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795107 | ||||||
chr9:83795134
|
C | T | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+4051G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795134 | ||||||
chr9:83795152
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.360+4033T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795152 | ||||||
chr9:83795156
|
C | CA | 37 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0041others(34): Show | 37 | HG00735.hp1 HG01192.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.360+4028dupT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795156 | ||||||
chr9:83795156
|
CA | C | 112 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(109): Show | 117 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.360+4028delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795156 | ||||||
chr9:83795183
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0050 | 2 | HG00639.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.360+4002T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795183 | ||||||
chr9:83795588
|
C | CT | 37 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0049others(34): Show | 39 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(36): Show |
intron_variant | MODIFIER | c.360+3596dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795588 | ||||||
chr9:83795588
|
C | CTT | 21 | a0001c0001t0001g0103a0001c0001t0001g0129a0001c0001t0002g0220others(18): Show | 21 | HG01255.hp1 HG01928.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.360+3595_360+3596d others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795588 | ||||||
chr9:83795588
|
C | CTTT | 136 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(133): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.360+3594_360+3596d others(5): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795588 | ||||||
chr9:83795588
|
C | CTTTT | 21 | a0001c0001t0001g0118a0001c0001t0002g0209a0001c0001t0002g0215others(18): Show | 21 | HG00642.hp2 HG01071.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.360+3593_360+3596d others(6): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795588 | ||||||
chr9:83795644
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.360+3541A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795644 | ||||||
chr9:83795649
|
T | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG02258.hp1 HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.360+3536A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795649 | ||||||
chr9:83795967
|
A | G | 179 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(176): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.360+3218T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83795967 | ||||||
chr9:83796054
|
G | A | 1 | a0001c0001t0003g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.360+3131C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83796054 | ||||||
chr9:83796230
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.360+2955G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83796230 | ||||||
chr9:83796445
|
C | T | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.360+2740G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83796445 | ||||||
chr9:83796524
|
G | C | 1 | a0001c0001t0002g0209 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.360+2661C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83796524 | ||||||
chr9:83796678
|
G | C | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.360+2507C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83796678 | ||||||
chr9:83796744
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.360+2441C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83796744 | ||||||
chr9:83796788
|
C | T | 4 | a0001c0001t0002g0220a0001c0001t0002g0224a0001c0001t0002g0225others(1): Show | 4 | HG01928.hp1 HG01943.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+2397G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83796788 | ||||||
chr9:83796888
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.360+2297C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83796888 | ||||||
chr9:83796925
|
A | G | 174 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(171): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.360+2260T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83796925 | ||||||
chr9:83797037
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.360+2148G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83797037 | ||||||
chr9:83797109
|
A | G | 1 | a0001c0001t0002g0288 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.360+2076T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83797109 | ||||||
chr9:83797146
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0143 | 2 | NA19001.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.360+2039A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83797146 | ||||||
chr9:83797253
|
G | A | 173 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(170): Show | 178 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.360+1932C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83797253 | ||||||
chr9:83797475
|
G | GCCCTTAT others(55): Show |
1 | a0001c0001t0002g0221 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.360+1648_360+1709d others(64): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83797475 | ||||||
chr9:83797679
|
TCCTTTTC others(7): Show |
T | 12 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0038others(9): Show | 13 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+1492_360+1505d others(16): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83797679 | ||||||
chr9:83798504
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.360+681G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83798504 | ||||||
chr9:83798547
|
C | T | 1 | a0001c0001t0003g0163 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.360+638G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83798547 | ||||||
chr9:83798560
|
A | G | 1 | a0001c0001t0002g0228 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.360+625T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83798560 | ||||||
chr9:83798689
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.360+496A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83798689 | ||||||
chr9:83798763
|
G | A | 1 | a0001c0001t0002g0223 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.360+422C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83798763 | ||||||
chr9:83799065
|
T | C | 1 | a0001c0001t0002g0282 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.360+120A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 4/12 | chr9 | 83799065 | ||||||
chr9:83799698
|
A | T | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.217-370T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83799698 | ||||||
chr9:83799717
|
G | A | 116 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(113): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.217-389C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83799717 | ||||||
chr9:83799765
|
G | C | 7 | a0001c0001t0002g0208a0001c0001t0002g0220a0001c0001t0002g0224others(4): Show | 7 | HG01928.hp1 HG01943.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.217-437C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83799765 | ||||||
chr9:83799950
|
G | A | 1 | a0001c0001t0003g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.217-622C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83799950 | ||||||
chr9:83800331
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.217-1003C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83800331 | ||||||
chr9:83800331
|
G | GT | 9 | a0001c0001t0002g0287a0001c0001t0002g0310a0001c0001t0002g0311others(6): Show | 9 | HG02615.hp2 HG02717.hp1 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-1004dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83800331 | ||||||
chr9:83800342
|
G | GT | 10 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0056others(7): Show | 10 | HG01106.hp2 HG02055.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.217-1015dupA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83800342 | ||||||
chr9:83800342
|
G | T | 165 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(162): Show | 170 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.217-1014C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83800342 | ||||||
chr9:83800343
|
T | G | 161 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0014others(158): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.217-1015A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83800343 | ||||||
chr9:83800344
|
T | G | 1 | a0001c0001t0002g0228 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.217-1016A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83800344 | ||||||
chr9:83800495
|
AGAT | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0095 | 3 | HG01167.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.217-1170_217-1168d others(5): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83800495 | ||||||
chr9:83800557
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.217-1229G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83800557 | ||||||
chr9:83800648
|
T | TTAC | 5 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(2): Show | 5 | HG01169.hp1 HG01243.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-1323_217-1321d others(5): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83800648 | ||||||
chr9:83800695
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.217-1367A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83800695 | ||||||
chr9:83800787
|
T | C | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.217-1459A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83800787 | ||||||
chr9:83800897
|
G | C | 1 | a0001c0001t0001g0022 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217-1569C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83800897 | ||||||
chr9:83801133
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.217-1805C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83801133 | ||||||
chr9:83801395
|
T | TG | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 149 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.217-2068dupC | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83801395 | ||||||
chr9:83801397
|
T | G | 15 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(12): Show | 16 | HG01255.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.217-2069A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83801397 | ||||||
chr9:83801873
|
A | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.217-2545T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83801873 | ||||||
chr9:83801916
|
A | T | 1 | a0001c0001t0003g0185 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.217-2588T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83801916 | ||||||
chr9:83801965
|
A | G | 1 | a0001c0001t0003g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.217-2637T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83801965 | ||||||
chr9:83802026
|
G | C | 1 | a0001c0001t0002g0285 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.217-2698C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83802026 | ||||||
chr9:83802040
|
C | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0117others(13): Show | 17 | HG02074.hp1 HG02080.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.217-2712G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83802040 | ||||||
chr9:83802085
|
C | T | 4 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG02080.hp2 NA18984.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.217-2757G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83802085 | ||||||
chr9:83802296
|
T | C | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0115others(33): Show | 38 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.217-2968A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83802296 | ||||||
chr9:83802355
|
T | C | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.217-3027A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83802355 | ||||||
chr9:83802384
|
CAGA | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.217-3059_217-3057d others(5): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83802384 | ||||||
chr9:83802483
|
GA | G | 10 | a0001c0001t0001g0107a0001c0001t0001g0124a0001c0001t0001g0125others(7): Show | 10 | HG00323.hp2 HG01975.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.217-3156delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83802483 | ||||||
chr9:83802536
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 156 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.217-3208T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83802536 | ||||||
chr9:83802636
|
C | A | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.217-3308G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83802636 | ||||||
chr9:83802650
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.217-3322C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83802650 | ||||||
chr9:83802831
|
T | TA | 7 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 7 | HG01169.hp1 HG01243.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.216+3470dupT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83802831 | ||||||
chr9:83803220
|
T | G | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+3082A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803220 | ||||||
chr9:83803224
|
T | TCCCTCTC | 49 | a0001c0001t0003g0011a0001c0001t0003g0148a0001c0001t0003g0149others(46): Show | 50 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.216+3071_216+3077d others(9): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803224 | ||||||
chr9:83803233
|
C | A | 1 | a0001c0001t0003g0185 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.216+3069G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803233 | ||||||
chr9:83803271
|
C | G | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+3031G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803271 | ||||||
chr9:83803292
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.216+3010A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803292 | ||||||
chr9:83803305
|
C | T | 1 | a0001c0001t0002g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.216+2997G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803305 | ||||||
chr9:83803306
|
G | A | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.216+2996C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803306 | ||||||
chr9:83803317
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.216+2985C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803317 | ||||||
chr9:83803390
|
T | G | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+2912A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803390 | ||||||
chr9:83803399
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 214 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.216+2903A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803399 | ||||||
chr9:83803444
|
G | A | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.216+2858C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803444 | ||||||
chr9:83803492
|
T | C | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+2810A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803492 | ||||||
chr9:83803507
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 104 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.216+2795C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803507 | ||||||
chr9:83803534
|
C | T | 3 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219 | 3 | HG02818.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.216+2768G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803534 | ||||||
chr9:83803665
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.216+2637G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803665 | ||||||
chr9:83803705
|
T | C | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.216+2597A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803705 | ||||||
chr9:83803709
|
A | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 156 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.216+2593T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803709 | ||||||
chr9:83803726
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.216+2576C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803726 | ||||||
chr9:83803786
|
G | C | 1 | a0001c0001t0003g0185 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.216+2516C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803786 | ||||||
chr9:83803821
|
C | A | 2 | a0001c0001t0004g0200a0001c0001t0004g0202 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.216+2481G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803821 | ||||||
chr9:83803890
|
C | T | 2 | a0001c0001t0004g0200a0001c0001t0004g0202 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.216+2412G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803890 | ||||||
chr9:83803910
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.216+2392C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803910 | ||||||
chr9:83803920
|
T | C | 1 | a0001c0001t0002g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.216+2382A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803920 | ||||||
chr9:83803928
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.216+2374C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803928 | ||||||
chr9:83803938
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.216+2364C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83803938 | ||||||
chr9:83804011
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.216+2291C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804011 | ||||||
chr9:83804055
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.216+2247C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804055 | ||||||
chr9:83804067
|
G | A | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.216+2235C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804067 | ||||||
chr9:83804079
|
A | T | 3 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017 | 3 | HG02559.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.216+2223T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804079 | ||||||
chr9:83804085
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.216+2217C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804085 | ||||||
chr9:83804094
|
C | T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.216+2208G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804094 | ||||||
chr9:83804096
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.216+2206C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804096 | ||||||
chr9:83804097
|
C | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 156 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.216+2205G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804097 | ||||||
chr9:83804102
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.216+2200C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804102 | ||||||
chr9:83804132
|
GC | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(47): Show | 57 | HG00609.hp1 HG00621.hp1 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.216+2169delG | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804132 | ||||||
chr9:83804203
|
T | C | 3 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0003g0184 | 3 | NA19060.hp1 NA19072.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.216+2099A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804203 | ||||||
chr9:83804220
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG02970.hp2 HG02976.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+2082C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804220 | ||||||
chr9:83804233
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG02258.hp1 HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.216+2069G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804233 | ||||||
chr9:83804242
|
G | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 156 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.216+2060C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804242 | ||||||
chr9:83804260
|
C | T | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.216+2042G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804260 | ||||||
chr9:83804286
|
T | C | 1 | a0001c0001t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.216+2016A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804286 | ||||||
chr9:83804297
|
T | TG | 10 | a0001c0001t0001g0023a0001c0001t0001g0113a0001c0001t0001g0123others(7): Show | 10 | HG00597.hp2 HG01192.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.216+2004dupC | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804297 | ||||||
chr9:83804310
|
A | ACCCCGCC others(42): Show |
1 | a0001c0001t0002g0220 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.216+1943_216+1991d others(51): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804310 | ||||||
chr9:83804315
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.216+1987C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804315 | ||||||
chr9:83804327
|
G | A | 1 | a0001c0001t0005g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.216+1975C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804327 | ||||||
chr9:83804332
|
A | G | 1 | a0001c0001t0002g0292 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.216+1970T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804332 | ||||||
chr9:83804359
|
C | A | 1 | a0001c0001t0002g0292 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.216+1943G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804359 | ||||||
chr9:83804367
|
CG | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 104 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.216+1934delC | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804367 | ||||||
chr9:83804401
|
G | C | 1 | a0001c0001t0002g0293 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.216+1901C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804401 | ||||||
chr9:83804403
|
G | A | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.216+1899C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804403 | ||||||
chr9:83804408
|
C | T | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.216+1894G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804408 | ||||||
chr9:83804440
|
G | A | 3 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302 | 3 | NA18962.hp2 NA18981.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.216+1862C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804440 | ||||||
chr9:83804502
|
CCGCCCCG others(42): Show |
C | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.216+1751_216+1799d others(51): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804502 | ||||||
chr9:83804512
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0139a0001c0001t0001g0145 | 3 | NA18974.hp1 NA18985.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.216+1790G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804512 | ||||||
chr9:83804513
|
G | A | 2 | a0001c0001t0002g0294a0001c0001t0002g0295 | 2 | HG00140.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.216+1789C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804513 | ||||||
chr9:83804524
|
G | C | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.216+1778C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804524 | ||||||
chr9:83804524
|
GGGGGGGT others(41): Show |
G | 5 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0139others(2): Show | 5 | HG02738.hp2 HG04184.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+1730_216+1777d others(50): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804524 | ||||||
chr9:83804535
|
CCCCCCGC others(41): Show |
C | 1 | a0001c0001t0001g0145 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.216+1719_216+1766d others(50): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804535 | ||||||
chr9:83804540
|
C | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | NA19043.hp1 NA20805.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.216+1762G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804540 | ||||||
chr9:83804541
|
G | A | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | HG00639.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.216+1761C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804541 | ||||||
chr9:83804543
|
C | CCGGCCAG others(444): Show |
2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA20805.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.216+1758_216+1759i others(453): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804543 | ||||||
chr9:83804545
|
A | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | NA19043.hp1 NA20805.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.216+1757T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804545 | ||||||
chr9:83804551
|
A | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | NA19043.hp1 NA20805.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.216+1751T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804551 | ||||||
chr9:83804558
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1744C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804558 | ||||||
chr9:83804561
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0121others(13): Show | 17 | HG00597.hp2 HG02074.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.216+1741G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804561 | ||||||
chr9:83804562
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1740C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804562 | ||||||
chr9:83804588
|
C | T | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+1714G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804588 | ||||||
chr9:83804589
|
G | C | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1713C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804589 | ||||||
chr9:83804593
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1709G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804593 | ||||||
chr9:83804611
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1691T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804611 | ||||||
chr9:83804629
|
G | T | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1673C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804629 | ||||||
chr9:83804630
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1672A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804630 | ||||||
chr9:83804634
|
C | T | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.216+1668G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804634 | ||||||
chr9:83804643
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0002g0298 | 2 | NA18971.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.216+1659A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804643 | ||||||
chr9:83804657
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 149 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.216+1645C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804657 | ||||||
chr9:83804659
|
C | A | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1643G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804659 | ||||||
chr9:83804680
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1622G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804680 | ||||||
chr9:83804693
|
C | G | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1609G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804693 | ||||||
chr9:83804696
|
C | CCAGCCAC others(71): Show |
1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1605_216+1606i others(80): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804696 | ||||||
chr9:83804707
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1595C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804707 | ||||||
chr9:83804709
|
A | C | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1593T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804709 | ||||||
chr9:83804739
|
G | C | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1563C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804739 | ||||||
chr9:83804748
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+1554T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804748 | ||||||
chr9:83804748
|
ACCCCGTC others(119): Show |
A | 2 | a0001c0001t0004g0012a0001c0001t0006g0099 | 3 | HG02280.hp1 HG02723.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.216+1428_216+1553d others(2): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804748 | ||||||
chr9:83804752
|
C | T | 3 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017 | 3 | HG02559.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.216+1550G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804752 | ||||||
chr9:83804811
|
T | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 149 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.216+1491A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804811 | ||||||
chr9:83804831
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 148 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.216+1471C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804831 | ||||||
chr9:83804845
|
T | TG | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.216+1456dupC | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804845 | ||||||
chr9:83804897
|
G | A | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.216+1405C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804897 | ||||||
chr9:83804911
|
G | A | 1 | a0001c0001t0003g0186 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.216+1391C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83804911 | ||||||
chr9:83805027
|
G | A | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.216+1275C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805027 | ||||||
chr9:83805027
|
G | C | 5 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0005g0015others(2): Show | 5 | HG01255.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+1275C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805027 | ||||||
chr9:83805127
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.216+1175A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805127 | ||||||
chr9:83805134
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.216+1168A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805134 | ||||||
chr9:83805158
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.216+1144C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805158 | ||||||
chr9:83805158
|
G | T | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.216+1144C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805158 | ||||||
chr9:83805229
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.216+1073C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805229 | ||||||
chr9:83805246
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.216+1056C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805246 | ||||||
chr9:83805283
|
A | G | 15 | a0001c0001t0001g0029a0001c0001t0001g0050a0001c0001t0001g0057others(12): Show | 15 | HG00639.hp1 HG01255.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.216+1019T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805283 | ||||||
chr9:83805329
|
C | G | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0115others(33): Show | 38 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.216+973G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805329 | ||||||
chr9:83805338
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.216+964C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805338 | ||||||
chr9:83805372
|
T | C | 3 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0299 | 3 | NA19001.hp2 NA19085.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.216+930A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805372 | ||||||
chr9:83805439
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.216+863G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805439 | ||||||
chr9:83805470
|
A | T | 1 | a0001c0001t0001g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.216+832T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805470 | ||||||
chr9:83805471
|
AT | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(127): Show | 139 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.216+830delA | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805471 | ||||||
chr9:83805472
|
T | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0036others(1): Show | 5 | HG02451.hp1 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.216+830A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805472 | ||||||
chr9:83805472
|
TA | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(2): Show | 5 | HG02055.hp1 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.216+829delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805472 | ||||||
chr9:83805592
|
G | A | 1 | a0001c0001t0003g0194 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.216+710C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805592 | ||||||
chr9:83805642
|
G | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.216+660C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805642 | ||||||
chr9:83805960
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 222 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.216+342G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83805960 | ||||||
chr9:83806091
|
T | G | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.216+211A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83806091 | ||||||
chr9:83806108
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0056 | 3 | HG01106.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.216+194G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83806108 | ||||||
chr9:83806286
|
C | A | 1 | a0001c0001t0003g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.216+16G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83806286 | ||||||
chr9:83806293
|
T | C | 1 | a0001c0001t0002g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.216+9A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 3/12 | chr9 | 83806293 | ||||||
chr9:83806734
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0052others(7): Show | 12 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-174G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83806734 | ||||||
chr9:83806832
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.-43-272T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83806832 | ||||||
chr9:83806852
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-43-292A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83806852 | ||||||
chr9:83807163
|
G | A | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-43-603C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83807163 | ||||||
chr9:83807241
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01167.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-43-681A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83807241 | ||||||
chr9:83807599
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-43-1039T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83807599 | ||||||
chr9:83807698
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-43-1138T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83807698 | ||||||
chr9:83807755
|
A | G | 1 | a0001c0001t0002g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43-1195T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83807755 | ||||||
chr9:83807825
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-43-1265A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83807825 | ||||||
chr9:83807919
|
T | C | 3 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302 | 3 | NA18962.hp2 NA18981.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-43-1359A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83807919 | ||||||
chr9:83808017
|
T | C | 1 | a0001c0001t0002g0303 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-43-1457A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83808017 | ||||||
chr9:83808049
|
T | C | 4 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-1489A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83808049 | ||||||
chr9:83808076
|
G | C | 1 | a0001c0001t0003g0188 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-43-1516C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83808076 | ||||||
chr9:83808614
|
T | C | 1 | a0001c0001t0004g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-43-2054A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83808614 | ||||||
chr9:83808637
|
G | C | 1 | a0001c0001t0001g0122 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-43-2077C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83808637 | ||||||
chr9:83808833
|
G | A | 2 | a0001c0001t0004g0200a0001c0001t0004g0202 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-43-2273C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83808833 | ||||||
chr9:83808918
|
T | C | 5 | a0001c0001t0001g0096a0001c0001t0003g0152a0001c0001t0003g0153others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-2358A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83808918 | ||||||
chr9:83808987
|
T | A | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-43-2427A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83808987 | ||||||
chr9:83809155
|
T | C | 1 | a0001c0001t0002g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43-2595A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83809155 | ||||||
chr9:83809211
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.-43-2651A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83809211 | ||||||
chr9:83809283
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.-43-2723G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83809283 | ||||||
chr9:83809359
|
C | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0039others(5): Show | 9 | HG00099.hp2 HG00642.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43-2799G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83809359 | ||||||
chr9:83809385
|
C | T | 1 | a0001c0001t0002g0230 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-43-2825G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83809385 | ||||||
chr9:83809408
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-43-2848G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83809408 | ||||||
chr9:83809489
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-43-2929A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83809489 | ||||||
chr9:83809549
|
C | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.-43-2989G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83809549 | ||||||
chr9:83809651
|
C | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 156 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-43-3091G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83809651 | ||||||
chr9:83809777
|
T | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(1): Show | 4 | HG02622.hp1 HG02723.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-3217A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83809777 | ||||||
chr9:83809799
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 156 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-43-3239A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83809799 | ||||||
chr9:83809859
|
T | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 156 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-43-3299A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83809859 | ||||||
chr9:83810280
|
T | C | 1 | a0001c0001t0002g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-43-3720A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83810280 | ||||||
chr9:83810493
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 155 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.-43-3933T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83810493 | ||||||
chr9:83810655
|
C | T | 3 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017 | 3 | HG02559.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-43-4095G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83810655 | ||||||
chr9:83810715
|
G | A | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-4155C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83810715 | ||||||
chr9:83810783
|
T | C | 1 | a0001c0001t0003g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-43-4223A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83810783 | ||||||
chr9:83810995
|
A | C | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-43-4435T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83810995 | ||||||
chr9:83811150
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | NA18985.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-43-4590C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83811150 | ||||||
chr9:83811359
|
A | G | 13 | a0001c0001t0002g0208a0001c0001t0002g0212a0001c0001t0002g0220others(10): Show | 13 | HG01928.hp1 HG01943.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43-4799T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83811359 | ||||||
chr9:83811463
|
T | C | 1 | a0001c0001t0004g0202 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-43-4903A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83811463 | ||||||
chr9:83811705
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 222 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.-43-5145A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83811705 | ||||||
chr9:83812178
|
T | C | 8 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0110others(5): Show | 8 | HG00621.hp1 HG02027.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+4818A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812178 | ||||||
chr9:83812184
|
T | TATATATA others(5): Show |
2 | a0001c0001t0001g0008a0001c0001t0001g0113 | 3 | HG01192.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-44+4800_-44+4811d others(14): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812184 | ||||||
chr9:83812218
|
TAC | T | 3 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219 | 3 | HG02818.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-44+4776_-44+4777d others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812218 | ||||||
chr9:83812228
|
CATGTATA others(15): Show |
C | 1 | a0001c0001t0002g0215 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-44+4746_-44+4767d others(24): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812228 | ||||||
chr9:83812230
|
T | C | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-44+4766A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812230 | ||||||
chr9:83812245
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-44+4751C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812245 | ||||||
chr9:83812298
|
T | C | 1 | a0001c0001t0002g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-44+4698A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812298 | ||||||
chr9:83812302
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.-44+4694G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812302 | ||||||
chr9:83812314
|
T | C | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-44+4682A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812314 | ||||||
chr9:83812318
|
T | A | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-44+4678A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812318 | ||||||
chr9:83812330
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-44+4666G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812330 | ||||||
chr9:83812341
|
A | C | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-44+4655T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812341 | ||||||
chr9:83812361
|
T | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 154 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.-44+4635A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812361 | ||||||
chr9:83812385
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 156 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-44+4611T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812385 | ||||||
chr9:83812396
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-44+4600G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812396 | ||||||
chr9:83812465
|
G | A | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0202 | 3 | HG02257.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-44+4531C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812465 | ||||||
chr9:83812552
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-44+4444G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812552 | ||||||
chr9:83812589
|
C | T | 6 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0032others(3): Show | 6 | HG02622.hp1 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+4407G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812589 | ||||||
chr9:83812658
|
TA | T | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0037others(37): Show | 42 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(39): Show |
intron_variant | MODIFIER | c.-44+4337delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812658 | ||||||
chr9:83812778
|
G | C | 3 | a0001c0001t0006g0097a0001c0001t0006g0098a0001c0001t0006g0099 | 3 | NA18970.hp2 NA18979.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-44+4218C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812778 | ||||||
chr9:83812813
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0002g0215 | 2 | NA18963.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-44+4183G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812813 | ||||||
chr9:83812877
|
A | G | 1 | a0001c0001t0001g0004 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-44+4119T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812877 | ||||||
chr9:83812889
|
C | T | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | NA19001.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-44+4107G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812889 | ||||||
chr9:83812908
|
C | G | 1 | a0001c0001t0002g0306 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-44+4088G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812908 | ||||||
chr9:83812914
|
A | G | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-44+4082T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812914 | ||||||
chr9:83812991
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-44+4005A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83812991 | ||||||
chr9:83813008
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3988T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813008 | ||||||
chr9:83813009
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3987A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813009 | ||||||
chr9:83813011
|
G | C | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3985C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813011 | ||||||
chr9:83813013
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3983C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813013 | ||||||
chr9:83813014
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3982T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813014 | ||||||
chr9:83813015
|
G | C | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3981C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813015 | ||||||
chr9:83813016
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3980T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813016 | ||||||
chr9:83813018
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3978A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813018 | ||||||
chr9:83813018
|
T | C | 35 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0115others(32): Show | 37 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.-44+3978A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813018 | ||||||
chr9:83813019
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3977T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813019 | ||||||
chr9:83813020
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3976C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813020 | ||||||
chr9:83813022
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3974T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813022 | ||||||
chr9:83813023
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3973T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813023 | ||||||
chr9:83813024
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3972T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813024 | ||||||
chr9:83813231
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0111 | 2 | NA18940.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-44+3765A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813231 | ||||||
chr9:83813331
|
G | T | 1 | a0001c0001t0003g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-44+3665C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813331 | ||||||
chr9:83813420
|
T | A | 1 | a0001c0001t0002g0210 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-44+3576A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813420 | ||||||
chr9:83813582
|
G | C | 5 | a0001c0001t0004g0012a0001c0001t0004g0199a0001c0001t0004g0200others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+3414C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813582 | ||||||
chr9:83813732
|
CATAA | C | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 4 | NA18950.hp1 NA19001.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+3260_-44+3263d others(6): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813732 | ||||||
chr9:83813733
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-44+3263T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813733 | ||||||
chr9:83813982
|
C | T | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-44+3014G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813982 | ||||||
chr9:83813986
|
G | A | 4 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 4 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+3010C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813986 | ||||||
chr9:83813994
|
G | A | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0003g0152others(8): Show | 11 | HG01255.hp1 HG01516.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44+3002C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83813994 | ||||||
chr9:83814008
|
T | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0113a0001c0001t0001g0147others(1): Show | 4 | HG01192.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+2988A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83814008 | ||||||
chr9:83814078
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-44+2918A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83814078 | ||||||
chr9:83814091
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+2905G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83814091 | ||||||
chr9:83814132
|
A | G | 2 | a0001c0001t0004g0200a0001c0001t0004g0202 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-44+2864T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83814132 | ||||||
chr9:83814390
|
T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 104 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.-44+2606A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83814390 | ||||||
chr9:83814612
|
G | A | 3 | a0001c0001t0003g0189a0001c0001t0003g0190a0001c0001t0003g0191 | 3 | HG03098.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-44+2384C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83814612 | ||||||
chr9:83814793
|
A | C | 1 | a0001c0001t0003g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-44+2203T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83814793 | ||||||
chr9:83814932
|
G | A | 2 | a0001c0001t0003g0192a0001c0001t0003g0203 | 2 | NA18962.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-44+2064C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83814932 | ||||||
chr9:83814944
|
C | T | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0115others(33): Show | 38 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.-44+2052G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83814944 | ||||||
chr9:83815242
|
A | G | 1 | a0001c0001t0003g0158 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-44+1754T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815242 | ||||||
chr9:83815269
|
G | T | 1 | a0001c0001t0002g0212 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-44+1727C>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815269 | ||||||
chr9:83815385
|
T | A | 1 | a0001c0001t0001g0102 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+1611A>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815385 | ||||||
chr9:83815472
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 156 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-44+1524A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815472 | ||||||
chr9:83815533
|
A | C | 1 | a0001c0001t0002g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-44+1463T>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815533 | ||||||
chr9:83815533
|
A | G | 1 | a0001c0001t0004g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-44+1463T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815533 | ||||||
chr9:83815573
|
A | AAC | 15 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0038others(12): Show | 16 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-44+1421_-44+1422d others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815573 | ||||||
chr9:83815573
|
A | AACAC | 6 | a0001c0001t0001g0037a0001c0001t0003g0156a0001c0001t0004g0199others(3): Show | 6 | HG02257.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+1419_-44+1422d others(6): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815573 | ||||||
chr9:83815573
|
A | AACACAC | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 6 | HG02280.hp1 HG02723.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+1417_-44+1422d others(8): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815573 | ||||||
chr9:83815575
|
C | A | 9 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0154others(6): Show | 9 | HG01255.hp1 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44+1421G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815575 | ||||||
chr9:83815636
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+1360T>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815636 | ||||||
chr9:83815700
|
A | G | 1 | a0001c0001t0002g0211 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-44+1296T>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815700 | ||||||
chr9:83815833
|
T | C | 1 | a0001c0001t0003g0195 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-44+1163A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815833 | ||||||
chr9:83815872
|
T | C | 1 | a0001c0001t0003g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-44+1124A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815872 | ||||||
chr9:83815958
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 222 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.-44+1038A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83815958 | ||||||
chr9:83816011
|
C | T | 11 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(8): Show | 11 | HG01192.hp1 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-44+985G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816011 | ||||||
chr9:83816014
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-44+982G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816014 | ||||||
chr9:83816031
|
C | CA | 19 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(16): Show | 19 | HG00639.hp1 HG00735.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.-44+964dupT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816031 | ||||||
chr9:83816031
|
C | CAA | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-44+963_-44+964dup others(2): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816031 | ||||||
chr9:83816031
|
C | CAAA | 18 | a0001c0001t0001g0019a0001c0001t0001g0101a0001c0001t0001g0102others(15): Show | 19 | HG00621.hp1 HG02132.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-44+962_-44+964dup others(3): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816031 | ||||||
chr9:83816031
|
C | CAAAA | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02027.hp2 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+961_-44+964dup others(4): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816031 | ||||||
chr9:83816031
|
CA | C | 10 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210others(7): Show | 10 | HG01255.hp2 HG02083.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44+964delT | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816031 | ||||||
chr9:83816130
|
T | G | 1 | a0001c0001t0002g0316 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-44+866A>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816130 | ||||||
chr9:83816170
|
C | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0113 | 3 | HG01192.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-44+826G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816170 | ||||||
chr9:83816285
|
T | C | 1 | a0001c0001t0003g0203 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-44+711A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816285 | ||||||
chr9:83816363
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-44+633G>A | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816363 | ||||||
chr9:83816670
|
T | C | 1 | a0001c0001t0002g0317 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-44+326A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816670 | ||||||
chr9:83816738
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.-44+258A>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816738 | ||||||
chr9:83816843
|
G | A | 1 | a0001c0001t0003g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-44+153C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816843 | ||||||
chr9:83816852
|
C | G | 1 | a0001c0001t0003g0148 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-44+144G>C | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 2/12 | chr9 | 83816852 | ||||||
chr9:83817221
|
G | A | 1 | a0001c0001t0004g0012 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-175-94C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 1/12 | chr9 | 83817221 | ||||||
chr9:83817262
|
G | C | 1 | a0001c0001t0002g0319 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-175-135C>G | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 1/12 | chr9 | 83817262 | ||||||
chr9:83817337
|
C | A | 1 | a0001c0001t0001g0114 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-176+180G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 1/12 | chr9 | 83817337 | ||||||
chr9:83817342
|
C | CGCGGCCC others(10): Show |
1 | a0001c0001t0001g0114 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-176+174_-176+175i others(19): Show |
GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 1/12 | chr9 | 83817342 | ||||||
chr9:83817376
|
G | A | 1 | a0001c0001t0003g0205 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-176+141C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 1/12 | chr9 | 83817376 | ||||||
chr9:83817478
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG00323.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-176+39C>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 1/12 | chr9 | 83817478 | ||||||
chr9:83817489
|
C | A | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0115others(33): Show | 38 | HG00323.hp2 HG00597.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.-176+28G>T | GKAP1 | ENSG00000165113.13 | transcript | ENST00000376371.7 | protein_coding | 1/12 | chr9 | 83817489 |