geneid | 343578 |
---|---|
ensemblid | ENSG00000124143.11 |
hgncid | 16226 |
symbol | ARHGAP40 |
name | Rho GTPase activating protein 40 |
refseq_nuc | NM_001164431.3 |
refseq_prot | NP_001157903.2 |
ensembl_nuc | ENST00000373345.9 |
ensembl_prot | ENSP00000362442.5 |
mane_status | MANE Select |
chr | chr20 |
start | 38601809 |
end | 38650653 |
strand | + |
ver | v1.2 |
region | chr20:38601809-38650653 |
region5000 | chr20:38596809-38655653 |
regionname0 | ARHGAP40_chr20_38601809_38650653 |
regionname5000 | ARHGAP40_chr20_38596809_38655653 |
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 | 675 | 278 | 48 | 61 | 125 | 12 | 30 | 88 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0002 | 0/0 | 675 | 16 | 6 | 3 | 0 | 2 | 5 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0003 | 0/0 | 675 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0004 | 0/0 | 675 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0005 | 0/0 | 675 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0006 | 0/0 | 675 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0007 | 0/0 | 675 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0008 | 0/0 | 675 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0009 | 0/0 | 675 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0010 | 0/0 | 675 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0011 | 0/0 | 675 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0012 | 0/0 | 675 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0013 | 0/0 | 675 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0014 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0015 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0016 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0017 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0018 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0019 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0020 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0021 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0022 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0023 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0024 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
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 | 2028 | 196 | 21 | 38 | 99 | 10 | 26 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0002 | 0/0 | 2028 | 59 | 6 | 21 | 26 | 2 | 4 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0003 | 0/0 | 2028 | 15 | 5 | 3 | 0 | 2 | 5 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0004 | 0/0 | 2028 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0005 | 0/0 | 2028 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0006 | 0/0 | 2028 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0007 | 0/0 | 2028 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0008 | 0/0 | 2028 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0009 | 0/0 | 2028 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0010 | 0/0 | 2028 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0011 | 0/0 | 2028 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0012 | 0/0 | 2028 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0013 | 0/0 | 2028 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0014 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0015 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0016 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0017 | 0/0 | 2028 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0018 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0019 | 0/0 | 2028 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0020 | 0/0 | 2028 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0021 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0022 | 0/0 | 2028 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0023 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0024 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0025 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0026 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0027 | 0/0 | 2028 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0028 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0029 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0030 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0031 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0032 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0033 | 0/0 | 2028 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0034 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0035 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0036 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0037 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0038 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0039 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
c0040 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
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 | 940 | 87 | 10 | 12 | 50 | 5 | 10 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0002 | 0/0 | 940 | 68 | 31 | 11 | 18 | 3 | 5 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0003 | 0/1 | 940 | 67 | 4 | 18 | 34 | 2 | 8 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0004 | 0/0 | 940 | 34 | 18 | 2 | 6 | 2 | 6 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0005 | 0/0 | 940 | 31 | 8 | 11 | 6 | 2 | 4 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0006 | 1/0 | 940 | 24 | 5 | 5 | 12 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0007 | 0/0 | 940 | 17 | 8 | 6 | 0 | 0 | 3 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0008 | 0/0 | 938 | 6 | 5 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0009 | 0/0 | 940 | 4 | 0 | 2 | 1 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0010 | 0/0 | 940 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0011 | 0/0 | 938 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0012 | 0/0 | 940 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0013 | 0/0 | 940 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0014 | 0/0 | 940 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0015 | 0/0 | 940 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
t0016 | 0/0 | 940 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0003 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
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 | 2028 | 196 | 21 | 38 | 99 | 10 | 26 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0002 | 0/0 | 2028 | 59 | 6 | 21 | 26 | 2 | 4 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0004 | 0/0 | 2028 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0007 | 0/0 | 2028 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0008 | 0/0 | 2028 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0020 | 0/0 | 2028 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0021 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0029 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0030 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0038 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0002c0003 | 0/0 | 2028 | 15 | 5 | 3 | 0 | 2 | 5 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0002c0024 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0003c0005 | 0/0 | 2028 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0003c0036 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0004c0011 | 0/0 | 2028 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0004c0014 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0005c0006 | 0/0 | 2028 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0006c0009 | 0/0 | 2028 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0006c0026 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0007c0010 | 0/0 | 2028 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0007c0040 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0008c0013 | 0/0 | 2028 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0008c0017 | 0/0 | 2028 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0009c0019 | 0/0 | 2028 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0009c0035 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0010c0012 | 0/0 | 2028 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0011c0016 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0012c0018 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0013c0015 | 0/0 | 2028 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0014c0022 | 0/0 | 2028 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0015c0025 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0016c0028 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0017c0034 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0018c0031 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0019c0039 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0020c0033 | 0/0 | 2028 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0021c0032 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0022c0023 | 0/0 | 2028 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0023c0027 | 0/0 | 2028 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0024c0037 | 0/0 | 2028 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2967 | 68 | 5 | 11 | 38 | 5 | 9 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0001t0002 | 0/0 | 2967 | 39 | 11 | 6 | 14 | 3 | 5 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0001t0003 | 0/1 | 2967 | 62 | 3 | 15 | 33 | 2 | 8 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0001t0004 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0001t0005 | 0/0 | 2967 | 5 | 0 | 0 | 2 | 0 | 3 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0001t0006 | 1/0 | 2967 | 19 | 1 | 4 | 12 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0001t0009 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0001t0014 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0002t0001 | 0/0 | 2967 | 11 | 0 | 0 | 10 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0002t0002 | 0/0 | 2967 | 6 | 0 | 3 | 3 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0002t0003 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0002t0004 | 0/0 | 2967 | 10 | 2 | 1 | 6 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0002t0005 | 0/0 | 2967 | 18 | 0 | 11 | 4 | 2 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0002t0007 | 0/0 | 2967 | 8 | 2 | 5 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0002t0008 | 0/0 | 2965 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0002t0009 | 0/0 | 2967 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0002t0010 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0002t0015 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0004t0002 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0004t0004 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0004t0007 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0004t0016 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0007t0001 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0007t0002 | 0/0 | 2967 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0008t0004 | 0/0 | 2967 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0008t0006 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0008t0007 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0020t0003 | 0/0 | 2967 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0021t0002 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0029t0003 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0030t0001 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0001c0038t0002 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0002c0003t0003 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0002c0003t0004 | 0/0 | 2967 | 10 | 2 | 1 | 0 | 2 | 5 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0002c0003t0005 | 0/0 | 2967 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0002c0003t0006 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0002c0024t0002 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0003c0005t0001 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0003c0005t0002 | 0/0 | 2967 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0003c0036t0002 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0004c0011t0004 | 0/0 | 2967 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0004c0011t0007 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0004c0014t0005 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0005c0006t0002 | 0/0 | 2967 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0006c0009t0006 | 0/0 | 2967 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0006c0009t0013 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0006c0026t0002 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0007c0010t0010 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0007c0010t0012 | 0/0 | 2967 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0007c0040t0004 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0008c0013t0008 | 0/0 | 2965 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0008c0017t0008 | 0/0 | 2965 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0009c0019t0002 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0009c0019t0007 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0009c0035t0011 | 0/0 | 2965 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0010c0012t0007 | 0/0 | 2967 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0010c0012t0009 | 0/0 | 2967 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0011c0016t0004 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0012c0018t0004 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0013c0015t0005 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0014c0022t0007 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0015c0025t0004 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0016c0028t0001 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0017c0034t0007 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0018c0031t0002 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0019c0039t0013 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0020c0033t0002 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0021c0032t0005 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0022c0023t0011 | 0/0 | 2965 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0023c0027t0001 | 0/0 | 2967 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
a0024c0037t0001 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | copy fasta | chr20 | 38596809 | 38655653 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0006g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0009g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0001t0014g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0007g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0007g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0007g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0007g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0009g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0009g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0010g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0002t0015g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0004t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0004t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0004t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0004t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0004t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0004t0016g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0007t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0007t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0007t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0007t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0007t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0008t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0008t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0008t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0008t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0020t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0020t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0021t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0021t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0029t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0030t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0001c0038t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0003t0006g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0002c0024t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0003c0005t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0003c0005t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0003c0005t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0003c0005t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0003c0005t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0003c0036t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0004c0011t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0004c0011t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0004c0011t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0004c0011t0007g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0004c0014t0005g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0005c0006t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0005c0006t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0005c0006t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0005c0006t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0006c0009t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0006c0009t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0006c0009t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0006c0009t0013g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0006c0026t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0007c0010t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0007c0010t0010g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0007c0010t0012g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0007c0010t0012g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0007c0040t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0008c0013t0008g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0008c0013t0008g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0008c0017t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0008c0017t0008g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0009c0019t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0009c0019t0007g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0009c0035t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0010c0012t0007g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0010c0012t0007g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0010c0012t0009g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0011c0016t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0011c0016t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0012c0018t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0012c0018t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0013c0015t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0013c0015t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0014c0022t0007g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0015c0025t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0016c0028t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0017c0034t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0018c0031t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0019c0039t0013g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0020c0033t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0021c0032t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0022c0023t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0023c0027t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
a0024c0037t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0195 | EUR | FIN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00558 | hp1 | a0001 | c0002 | t0003 | g0276 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0030 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00639 | hp2 | a0001 | c0002 | t0005 | g0222 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00642 | hp2 | a0002 | c0003 | t0004 | g0304 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | CHS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0092 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00741 | hp1 | a0001 | c0002 | t0005 | g0128 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01069 | hp1 | a0001 | c0002 | t0005 | g0203 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01069 | hp2 | a0001 | c0002 | t0007 | g0007 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01070 | hp1 | a0001 | c0002 | t0005 | g0121 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01071 | hp1 | a0001 | c0002 | t0005 | g0207 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01071 | hp2 | a0001 | c0002 | t0005 | g0206 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0063 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01106 | hp2 | a0001 | c0002 | t0005 | g0215 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01109 | hp1 | a0007 | c0010 | t0012 | g0129 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0083 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01168 | hp1 | a0001 | c0002 | t0007 | g0007 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01168 | hp2 | a0001 | c0002 | t0005 | g0155 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0091 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01169 | hp2 | a0001 | c0002 | t0007 | g0044 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01192 | hp1 | a0001 | c0001 | t0014 | g0261 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0308 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01243 | hp2 | a0014 | c0022 | t0007 | g0101 | AMR | PUR | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01256 | hp1 | a0001 | c0002 | t0005 | g0273 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01256 | hp2 | a0020 | c0033 | t0002 | g0056 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01261 | hp1 | a0008 | c0017 | t0008 | g0105 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01346 | hp1 | a0001 | c0002 | t0005 | g0197 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01346 | hp2 | a0001 | c0002 | t0005 | g0184 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01361 | hp2 | a0009 | c0019 | t0002 | g0032 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01433 | hp2 | a0002 | c0003 | t0003 | g0168 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0109 | EUR | IBS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0260 | EUR | IBS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01516 | hp1 | a0001 | c0002 | t0005 | g0157 | EUR | IBS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01516 | hp2 | a0002 | c0003 | t0004 | g0010 | EUR | IBS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01517 | hp1 | a0002 | c0003 | t0004 | g0010 | EUR | IBS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0110 | EUR | IBS | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01884 | hp1 | a0008 | c0013 | t0008 | g0028 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01884 | hp2 | a0015 | c0025 | t0004 | g0054 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01891 | hp1 | a0009 | c0019 | t0007 | g0311 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01891 | hp2 | a0008 | c0013 | t0008 | g0303 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01934 | hp1 | a0001 | c0002 | t0004 | g0090 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01952 | hp1 | a0001 | c0001 | t0009 | g0115 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01952 | hp2 | a0023 | c0027 | t0001 | g0004 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0039 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0034 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01993 | hp1 | a0002 | c0003 | t0006 | g0043 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02004 | hp1 | a0001 | c0002 | t0007 | g0011 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02004 | hp2 | a0001 | c0020 | t0003 | g0204 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02015 | hp2 | a0001 | c0001 | t0006 | g0296 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02027 | hp2 | a0001 | c0001 | t0006 | g0062 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02055 | hp1 | a0002 | c0003 | t0004 | g0080 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02056 | hp2 | a0024 | c0037 | t0001 | g0185 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02071 | hp1 | a0001 | c0002 | t0004 | g0306 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02071 | hp2 | a0001 | c0001 | t0006 | g0212 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0089 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02132 | hp1 | a0001 | c0001 | t0006 | g0161 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02145 | hp1 | a0017 | c0034 | t0007 | g0100 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0267 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | CDX | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CDX | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02165 | hp1 | a0001 | c0001 | t0006 | g0213 | EAS | CDX | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02165 | hp2 | a0001 | c0002 | t0015 | g0274 | EAS | CDX | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02257 | hp1 | a0011 | c0016 | t0004 | g0085 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02258 | hp1 | a0001 | c0002 | t0004 | g0073 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02258 | hp2 | a0001 | c0002 | t0007 | g0081 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02273 | hp1 | a0001 | c0020 | t0003 | g0277 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02293 | hp2 | a0001 | c0002 | t0007 | g0011 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02300 | hp2 | a0001 | c0002 | t0009 | g0149 | AMR | PEL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02451 | hp1 | a0002 | c0003 | t0005 | g0179 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02451 | hp2 | a0001 | c0007 | t0001 | g0189 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02572 | hp1 | a0001 | c0008 | t0004 | g0309 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02572 | hp2 | a0003 | c0005 | t0001 | g0138 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02602 | hp1 | a0002 | c0003 | t0004 | g0295 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02622 | hp1 | a0022 | c0023 | t0011 | g0117 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02622 | hp2 | a0001 | c0007 | t0002 | g0280 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02630 | hp1 | a0004 | c0011 | t0004 | g0312 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02630 | hp2 | a0006 | c0026 | t0002 | g0086 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02647 | hp1 | a0001 | c0004 | t0007 | g0287 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02647 | hp2 | a0012 | c0018 | t0004 | g0078 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0314 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02698 | hp1 | a0010 | c0012 | t0007 | g0098 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02717 | hp2 | a0001 | c0007 | t0002 | g0037 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02723 | hp1 | a0001 | c0007 | t0001 | g0243 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02723 | hp2 | a0001 | c0008 | t0006 | g0286 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02809 | hp1 | a0003 | c0036 | t0002 | g0077 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02809 | hp2 | a0004 | c0011 | t0004 | g0313 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02818 | hp1 | a0004 | c0014 | t0005 | g0024 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02886 | hp1 | a0001 | c0004 | t0007 | g0113 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02886 | hp2 | a0005 | c0006 | t0002 | g0029 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02895 | hp1 | a0006 | c0009 | t0006 | g0070 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02895 | hp2 | a0005 | c0006 | t0002 | g0029 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02896 | hp1 | a0005 | c0006 | t0002 | g0106 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02896 | hp2 | a0007 | c0010 | t0012 | g0223 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02897 | hp1 | a0005 | c0006 | t0002 | g0108 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02897 | hp2 | a0006 | c0009 | t0006 | g0069 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02922 | hp1 | a0003 | c0005 | t0002 | g0008 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02965 | hp2 | a0006 | c0009 | t0006 | g0068 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02970 | hp1 | a0001 | c0004 | t0004 | g0045 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02970 | hp2 | a0001 | c0030 | t0001 | g0228 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02976 | hp1 | a0001 | c0002 | t0010 | g0082 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02976 | hp2 | a0001 | c0021 | t0002 | g0285 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03041 | hp1 | a0013 | c0015 | t0005 | g0163 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03041 | hp2 | a0001 | c0008 | t0004 | g0026 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03098 | hp1 | a0001 | c0021 | t0002 | g0282 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03098 | hp2 | a0011 | c0016 | t0004 | g0040 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03130 | hp1 | a0003 | c0005 | t0002 | g0008 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03130 | hp2 | a0009 | c0035 | t0011 | g0124 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03139 | hp2 | a0002 | c0024 | t0002 | g0051 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03195 | hp1 | a0002 | c0003 | t0005 | g0133 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03209 | hp2 | a0007 | c0010 | t0010 | g0307 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03225 | hp1 | a0001 | c0007 | t0002 | g0093 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0035 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03239 | hp2 | a0002 | c0003 | t0004 | g0297 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03453 | hp1 | a0012 | c0018 | t0004 | g0088 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03453 | hp2 | a0001 | c0008 | t0007 | g0281 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03486 | hp1 | a0004 | c0014 | t0005 | g0024 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03486 | hp2 | a0001 | c0008 | t0004 | g0026 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03491 | hp1 | a0002 | c0003 | t0004 | g0036 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03516 | hp1 | a0001 | c0002 | t0004 | g0071 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03516 | hp2 | a0003 | c0005 | t0002 | g0047 | AFR | ESN | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03540 | hp1 | a0001 | c0038 | t0002 | g0310 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03540 | hp2 | a0019 | c0039 | t0013 | g0284 | AFR | GWD | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03579 | hp1 | a0004 | c0011 | t0007 | g0292 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03579 | hp2 | a0007 | c0010 | t0010 | g0224 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03654 | hp1 | a0010 | c0012 | t0007 | g0060 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03669 | hp1 | a0010 | c0012 | t0009 | g0239 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03688 | hp1 | a0002 | c0003 | t0004 | g0027 | SAS | STU | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03831 | hp1 | a0001 | c0002 | t0007 | g0067 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03831 | hp2 | a0001 | c0002 | t0005 | g0268 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03834 | hp1 | a0001 | c0002 | t0004 | g0095 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0255 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03927 | hp1 | a0001 | c0001 | t0006 | g0252 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0218 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0187 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG04184 | hp2 | a0002 | c0003 | t0004 | g0027 | SAS | BEB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18522 | hp1 | a0002 | c0003 | t0005 | g0120 | AFR | YRI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | YRI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | CHB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0021 | EAS | CHB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18906 | hp1 | a0005 | c0006 | t0002 | g0087 | AFR | YRI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18906 | hp2 | a0001 | c0004 | t0002 | g0075 | AFR | YRI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18941 | hp1 | a0001 | c0001 | t0006 | g0299 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18969 | hp2 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18973 | hp1 | a0001 | c0002 | t0004 | g0057 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18975 | hp2 | a0001 | c0001 | t0006 | g0162 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18977 | hp1 | a0018 | c0031 | t0002 | g0290 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18977 | hp2 | a0001 | c0002 | t0005 | g0194 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18981 | hp2 | a0001 | c0001 | t0006 | g0305 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18995 | hp2 | a0001 | c0002 | t0009 | g0135 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18999 | hp1 | a0001 | c0002 | t0005 | g0164 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18999 | hp2 | a0001 | c0001 | t0006 | g0289 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19012 | hp2 | a0001 | c0002 | t0004 | g0055 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19030 | hp1 | a0006 | c0009 | t0013 | g0042 | AFR | LWK | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19030 | hp2 | a0021 | c0032 | t0005 | g0230 | AFR | LWK | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19043 | hp1 | a0008 | c0017 | t0008 | g0046 | AFR | LWK | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | LWK | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19057 | hp1 | a0001 | c0002 | t0004 | g0033 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19058 | hp1 | a0001 | c0002 | t0005 | g0216 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19063 | hp2 | a0001 | c0002 | t0004 | g0058 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19065 | hp1 | a0001 | c0001 | t0006 | g0302 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19074 | hp1 | a0016 | c0028 | t0001 | g0116 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19086 | hp1 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19087 | hp2 | a0001 | c0002 | t0005 | g0217 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19091 | hp1 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | YRI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | ASW | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20129 | hp2 | a0013 | c0015 | t0005 | g0248 | AFR | ASW | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0294 | EUR | TSI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | TSI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20805 | hp2 | a0001 | c0002 | t0005 | g0202 | EUR | TSI | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | GIH | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20905 | hp2 | a0001 | c0001 | t0005 | g0236 | SAS | GIH | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02109 | hp1 | a0001 | c0029 | t0003 | g0137 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02109 | hp2 | a0003 | c0005 | t0001 | g0196 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02486 | hp1 | a0001 | c0004 | t0016 | g0231 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02486 | hp2 | a0001 | c0002 | t0007 | g0052 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02559 | hp1 | a0004 | c0011 | t0004 | g0114 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG02559 | hp2 | a0001 | c0002 | t0008 | g0074 | AFR | ACB | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03471 | hp1 | a0001 | c0004 | t0002 | g0048 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG03471 | hp2 | a0007 | c0040 | t0004 | g0283 | AFR | MSL | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG06807 | hp1 | a0002 | c0003 | t0004 | g0031 | AFR | USA | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | USA | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | USA | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA20300 | hp2 | a0008 | c0013 | t0008 | g0028 | AFR | USA | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
NA21309 | hp2 | a0003 | c0005 | t0002 | g0076 | AFR | LWK | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0214 | REF | REF | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0288 | REF | REF | ARHGAP40_chr20_38596809_38655653 | ARHGAP40 | chr20 | 38596809 | 38655653 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:38601952
|
C | T | 1 | a0024 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.10C>T | p.Pro4Ser | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 144/2967 | 10/2028 | 4/675 | chr20 | 38601952 | ||
chr20:38602019
|
G | A | 1 | a0014 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.77G>A | p.Arg26Gln | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 211/2967 | 77/2028 | 26/675 | chr20 | 38602019 | ||
chr20:38623364
|
G | A | 1 | a0005 | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
missense_variant | MODERATE | c.143G>A | p.Gly48Asp | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/15 | 277/2967 | 143/2028 | 48/675 | chr20 | 38623364 | ||
chr20:38623375
|
G | A | 2 | a0002a0013 | 18 | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(15): Show |
missense_variant | MODERATE | c.154G>A | p.Gly52Ser | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/15 | 288/2967 | 154/2028 | 52/675 | chr20 | 38623375 | ||
chr20:38623379
|
G | A | 3 | a0006a0011a0015 | 8 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
missense_variant | MODERATE | c.158G>A | p.Arg53Gln | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/15 | 292/2967 | 158/2028 | 53/675 | chr20 | 38623379 | ||
chr20:38623540
|
G | A | 1 | a0010 | 3 | HG02698.hp1 HG03654.hp1 HG03669.hp1 |
missense_variant | MODERATE | c.319G>A | p.Glu107Lys | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/15 | 453/2967 | 319/2028 | 107/675 | chr20 | 38623540 | ||
chr20:38627126
|
C | T | 2 | a0003a0009 | 10 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
missense_variant | MODERATE | c.469C>T | p.Arg157Trp | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/15 | 603/2967 | 469/2028 | 157/675 | chr20 | 38627126 | ||
chr20:38628933
|
T | A | 1 | a0023 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.565T>A | p.Ser189Thr | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/15 | 699/2967 | 565/2028 | 189/675 | chr20 | 38628933 | ||
chr20:38629553
|
A | G | 2 | a0004a0022 | 7 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
missense_variant | MODERATE | c.686A>G | p.Asn229Ser | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/15 | 820/2967 | 686/2028 | 229/675 | chr20 | 38629553 | ||
chr20:38629619
|
G | A | 1 | a0016 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.752G>A | p.Gly251Asp | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/15 | 886/2967 | 752/2028 | 251/675 | chr20 | 38629619 | ||
chr20:38634765
|
C | T | 3 | a0004a0021a0022 | 8 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
missense_variant | MODERATE | c.929C>T | p.Ala310Val | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/15 | 1063/2967 | 929/2028 | 310/675 | chr20 | 38634765 | ||
chr20:38639281
|
G | A | 1 | a0020 | 1 | HG01256.hp2 | missense_variant | MODERATE | c.1174G>A | p.Glu392Lys | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/15 | 1308/2967 | 1174/2028 | 392/675 | chr20 | 38639281 | ||
chr20:38639303
|
C | G | 1 | a0012 | 2 | HG02647.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.1196C>G | p.Ser399Cys | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/15 | 1330/2967 | 1196/2028 | 399/675 | chr20 | 38639303 | ||
chr20:38639336
|
C | T | 1 | a0013 | 2 | HG03041.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.1229C>T | p.Pro410Leu | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/15 | 1363/2967 | 1229/2028 | 410/675 | chr20 | 38639336 | ||
chr20:38643737
|
C | T | 2 | a0008a0022 | 6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
missense_variant | MODERATE | c.1396C>T | p.Arg466Trp | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/15 | 1530/2967 | 1396/2028 | 466/675 | chr20 | 38643737 | ||
chr20:38643747
|
A | T | 2 | a0007a0011 | 7 | HG01109.hp1 HG02257.hp1 HG02896.hp2 others(4): Show |
missense_variant | MODERATE | c.1406A>T | p.His469Leu | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/15 | 1540/2967 | 1406/2028 | 469/675 | chr20 | 38643747 | ||
chr20:38643813
|
G | A | 1 | a0017 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1472G>A | p.Arg491Gln | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/15 | 1606/2967 | 1472/2028 | 491/675 | chr20 | 38643813 | ||
chr20:38643825
|
T | C | 1 | a0015 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1484T>C | p.Leu495Pro | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/15 | 1618/2967 | 1484/2028 | 495/675 | chr20 | 38643825 | ||
chr20:38643887
|
C | A | 2 | a0007a0011 | 7 | HG01109.hp1 HG02257.hp1 HG02896.hp2 others(4): Show |
missense_variant | MODERATE | c.1546C>A | p.His516Asn | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/15 | 1680/2967 | 1546/2028 | 516/675 | chr20 | 38643887 | ||
chr20:38646065
|
G | T | 1 | a0019 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1588G>T | p.Ala530Ser | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/15 | 1722/2967 | 1588/2028 | 530/675 | chr20 | 38646065 | ||
chr20:38646101
|
C | G | 1 | a0003 | 7 | HG02109.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
missense_variant | MODERATE | c.1624C>G | p.Arg542Gly | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/15 | 1758/2967 | 1624/2028 | 542/675 | chr20 | 38646101 | ||
chr20:38646146
|
A | C | 1 | a0018 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.1669A>C | p.Met557Leu | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/15 | 1803/2967 | 1669/2028 | 557/675 | chr20 | 38646146 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:38601948
|
C | T | 5 | a0001c0008a0001c0021a0001c0038others(2): Show | 10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
synonymous_variant | LOW | c.6C>T | p.Ala2Ala | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 140/2967 | 6/2028 | 2/675 | chr20 | 38601948 | ||
chr20:38601957
|
C | T | 5 | a0001c0008a0001c0021a0001c0038others(2): Show | 10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
synonymous_variant | LOW | c.15C>T | p.Ala5Ala | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 149/2967 | 15/2028 | 5/675 | chr20 | 38601957 | ||
chr20:38601969
|
C | T | 1 | a0001c0020 | 2 | HG02004.hp2 HG02273.hp1 |
synonymous_variant | LOW | c.27C>T | p.Ala9Ala | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 161/2967 | 27/2028 | 9/675 | chr20 | 38601969 | ||
chr20:38601990
|
C | T | 5 | a0001c0008a0001c0021a0001c0038others(2): Show | 10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
synonymous_variant | LOW | c.48C>T | p.Ala16Ala | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 182/2967 | 48/2028 | 16/675 | chr20 | 38601990 | ||
chr20:38623362
|
T | G | 5 | a0001c0004a0001c0021a0004c0014others(2): Show | 12 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(9): Show |
synonymous_variant | LOW | c.141T>G | p.Ser47Ser | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/15 | 275/2967 | 141/2028 | 47/675 | chr20 | 38623362 | ||
chr20:38628947
|
C | G | 26 | a0001c0002a0001c0004a0001c0007others(23): Show | 122 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(119): Show |
synonymous_variant | LOW | c.579C>G | p.Gly193Gly | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/15 | 713/2967 | 579/2028 | 193/675 | chr20 | 38628947 | ||
chr20:38634664
|
A | C | 1 | a0008c0013 | 3 | HG01884.hp1 HG01891.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.828A>C | p.Gly276Gly | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/15 | 962/2967 | 828/2028 | 276/675 | chr20 | 38634664 | ||
chr20:38637784
|
G | A | 1 | a0001c0029 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1026G>A | p.Pro342Pro | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/15 | 1160/2967 | 1026/2028 | 342/675 | chr20 | 38637784 | ||
chr20:38643910
|
G | A | 1 | a0003c0036 | 1 | HG02809.hp1 | splice_region_variant&synonymous_variant | LOW | c.1569G>A | p.Thr523Thr | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/15 | 1703/2967 | 1569/2028 | 523/675 | chr20 | 38643910 | ||
chr20:38647043
|
C | T | 1 | a0015c0025 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.1797C>T | p.His599His | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/15 | 1931/2967 | 1797/2028 | 599/675 | chr20 | 38647043 | ||
chr20:38648658
|
G | A | 2 | a0001c0007a0001c0030 | 6 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
synonymous_variant | LOW | c.1896G>A | p.Glu632Glu | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/15 | 2030/2967 | 1896/2028 | 632/675 | chr20 | 38648658 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:38601843
|
C | A | 28 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(25): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
5_prime_UTR_variant | MODIFIER | c.-100C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/15 | 100 | chr20 | 38601843 | |||||
chr20:38649915
|
C | T | 18 | a0001c0001t0004a0001c0001t0005a0001c0002t0004others(15): Show | 67 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*67C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 67 | chr20 | 38649915 | |||||
chr20:38649926
|
A | C | 18 | a0001c0001t0004a0001c0001t0005a0001c0002t0004others(15): Show | 67 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*78A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 78 | chr20 | 38649926 | |||||
chr20:38649948
|
G | C | 7 | a0001c0002t0008a0006c0009t0013a0008c0013t0008others(4): Show | 10 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*100G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 100 | chr20 | 38649948 | |||||
chr20:38649969
|
T | A | 50 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(47): Show | 237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*121T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 121 | chr20 | 38649969 | |||||
chr20:38650011
|
CAG | C | 5 | a0001c0002t0008a0008c0013t0008a0008c0017t0008others(2): Show | 8 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*164_*165delAG | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 164 | chr20 | 38650011 | |||||
chr20:38650180
|
T | C | 47 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(44): Show | 232 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*332T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 332 | chr20 | 38650180 | |||||
chr20:38650303
|
T | C | 61 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(58): Show | 258 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*455T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 455 | chr20 | 38650303 | |||||
chr20:38650316
|
A | C | 1 | a0001c0004t0016 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 468 | chr20 | 38650316 | |||||
chr20:38650456
|
G | A | 1 | a0001c0002t0015 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*608G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 608 | chr20 | 38650456 | |||||
chr20:38650612
|
C | T | 62 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(59): Show | 259 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*764C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 15/15 | 764 | chr20 | 38650612 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:38602118
|
C | T | 1 | a0001c0001t0003g0314 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.137+39C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602118 | ||||||
chr20:38602124
|
A | G | 2 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137+45A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602124 | ||||||
chr20:38602185
|
G | T | 1 | a0009c0019t0007g0311 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.137+106G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602185 | ||||||
chr20:38602235
|
G | T | 2 | a0001c0008t0004g0309a0001c0038t0002g0310 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.137+156G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602235 | ||||||
chr20:38602403
|
G | T | 1 | a0001c0001t0003g0308 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.137+324G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602403 | ||||||
chr20:38602407
|
T | TAG | 292 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(289): Show | 323 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.137+331_137+332dup others(2): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38602407 | |||||
chr20:38602439
|
C | T | 9 | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(6): Show | 10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+360C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602439 | ||||||
chr20:38602442
|
G | C | 3 | a0001c0001t0006g0030a0004c0011t0004g0312a0004c0011t0004g0313 | 3 | HG00639.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137+363G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602442 | ||||||
chr20:38602470
|
T | A | 9 | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(6): Show | 10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+391T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602470 | ||||||
chr20:38602740
|
C | T | 2 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137+661C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602740 | ||||||
chr20:38602918
|
G | T | 1 | a0001c0007t0002g0280 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.137+839G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38602918 | ||||||
chr20:38603229
|
G | A | 2 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137+1150G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38603229 | ||||||
chr20:38603333
|
A | C | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(183): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.137+1254A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38603333 | ||||||
chr20:38603366
|
A | G | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(183): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.137+1287A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38603366 | ||||||
chr20:38603407
|
GTCTA | G | 56 | a0001c0001t0001g0279a0001c0001t0002g0009a0001c0001t0002g0049others(53): Show | 62 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.137+1382_137+1385d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603407 | |||||
chr20:38603407
|
GTCTATCT others(1): Show |
G | 39 | a0001c0001t0001g0099a0001c0001t0002g0003a0001c0001t0002g0079others(36): Show | 43 | HG00642.hp2 HG00738.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.137+1378_137+1385d others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603407 | |||||
chr20:38603407
|
GTCTATCT others(5): Show |
G | 19 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(16): Show | 22 | HG01167.hp1 HG01243.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.137+1374_137+1385d others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603407 | |||||
chr20:38603407
|
GTCTATCT others(9): Show |
G | 1 | a0004c0011t0004g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.137+1370_137+1385d others(18): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603407 | |||||
chr20:38603451
|
A | ATCTATCT others(9): Show |
1 | a0001c0001t0009g0115 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.137+1385_137+1386i others(18): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603451 | |||||
chr20:38603451
|
A | ATCTATCT others(5): Show |
31 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0001t0001g0119others(28): Show | 34 | HG00140.hp2 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.137+1383_137+1384i others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603451 | |||||
chr20:38603451
|
A | ATCTATCT others(1): Show |
50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0144others(47): Show | 55 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.137+1379_137+1380i others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603451 | |||||
chr20:38603451
|
A | ATCTG | 62 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0192others(59): Show | 66 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.137+1375_137+1376i others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603451 | |||||
chr20:38603451
|
A | G | 41 | a0001c0001t0001g0005a0001c0001t0001g0245a0001c0001t0001g0246others(38): Show | 48 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.137+1372A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38603451 | ||||||
chr20:38603517
|
CCATCTAT others(5): Show |
C | 4 | a0004c0011t0007g0292a0005c0006t0002g0029a0008c0013t0008g0028others(1): Show | 6 | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+1450_137+1461d others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603517 | |||||
chr20:38603584
|
ATCTC | A | 87 | a0001c0001t0001g0099a0001c0001t0002g0003a0001c0001t0002g0006others(84): Show | 97 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(94): Show |
intron_variant | MODIFIER | c.137+1513_137+1516d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603584 | |||||
chr20:38603596
|
GTCTC | G | 9 | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(6): Show | 10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+1526_137+1529d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38603596 | |||||
chr20:38603877
|
A | G | 9 | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(6): Show | 10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+1798A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38603877 | ||||||
chr20:38603965
|
A | G | 2 | a0001c0002t0008g0074a0001c0004t0002g0075 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.137+1886A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38603965 | ||||||
chr20:38604068
|
G | A | 2 | a0001c0001t0003g0143a0001c0001t0003g0191 | 2 | NA18950.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.137+1989G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604068 | ||||||
chr20:38604238
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.137+2159G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604238 | ||||||
chr20:38604291
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.137+2212G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604291 | ||||||
chr20:38604296
|
A | G | 15 | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0141others(12): Show | 17 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.137+2217A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604296 | ||||||
chr20:38604397
|
G | GT | 73 | a0001c0001t0001g0099a0001c0001t0002g0003a0001c0001t0002g0006others(70): Show | 80 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.137+2334dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38604397 | |||||
chr20:38604533
|
T | A | 3 | a0001c0001t0003g0145a0001c0001t0003g0193a0016c0028t0001g0116 | 3 | HG00408.hp1 NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.137+2454T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604533 | ||||||
chr20:38604540
|
C | T | 9 | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(6): Show | 10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+2461C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604540 | ||||||
chr20:38604549
|
C | T | 16 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(13): Show | 19 | HG01261.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.137+2470C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604549 | ||||||
chr20:38604615
|
C | T | 1 | a0001c0002t0004g0306 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.137+2536C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604615 | ||||||
chr20:38604976
|
A | G | 66 | a0001c0001t0001g0099a0001c0001t0002g0003a0001c0001t0002g0006others(63): Show | 71 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.137+2897A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38604976 | ||||||
chr20:38605432
|
A | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0024c0037t0001g0185 | 3 | HG02056.hp2 NA18954.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.137+3353A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605432 | ||||||
chr20:38605517
|
C | G | 1 | a0008c0017t0008g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.137+3438C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605517 | ||||||
chr20:38605531
|
T | C | 1 | a0001c0002t0005g0194 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.137+3452T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605531 | ||||||
chr20:38605643
|
C | T | 1 | a0001c0002t0001g0269 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.137+3564C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605643 | ||||||
chr20:38605702
|
T | A | 1 | a0001c0001t0003g0015 | 2 | HG03017.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.137+3623T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605702 | ||||||
chr20:38605718
|
G | C | 1 | a0001c0001t0003g0195 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.137+3639G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605718 | ||||||
chr20:38605889
|
C | CT | 9 | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(6): Show | 10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+3819dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38605889 | |||||
chr20:38605893
|
T | C | 2 | a0001c0002t0007g0052a0001c0002t0007g0081 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.137+3814T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605893 | ||||||
chr20:38605955
|
G | A | 4 | a0004c0011t0007g0292a0005c0006t0002g0029a0008c0013t0008g0028others(1): Show | 6 | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+3876G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38605955 | ||||||
chr20:38606204
|
A | G | 7 | a0001c0004t0004g0045a0003c0005t0002g0008a0003c0005t0002g0047others(4): Show | 8 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.137+4125A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38606204 | ||||||
chr20:38606385
|
A | G | 2 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137+4306A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38606385 | ||||||
chr20:38606495
|
A | G | 201 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(198): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.137+4416A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38606495 | ||||||
chr20:38606662
|
C | A | 70 | a0001c0001t0001g0099a0001c0001t0002g0003a0001c0001t0002g0006others(67): Show | 77 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.137+4583C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38606662 | ||||||
chr20:38606842
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.137+4763C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38606842 | ||||||
chr20:38606888
|
G | C | 201 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(198): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.137+4809G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38606888 | ||||||
chr20:38607050
|
T | G | 21 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(18): Show | 25 | HG00639.hp1 HG01261.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.137+4971T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607050 | ||||||
chr20:38607097
|
C | A | 70 | a0001c0001t0001g0099a0001c0001t0002g0003a0001c0001t0002g0006others(67): Show | 77 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.137+5018C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607097 | ||||||
chr20:38607098
|
A | G | 2 | a0001c0001t0003g0267a0001c0002t0005g0268 | 2 | HG02148.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.137+5019A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607098 | ||||||
chr20:38607174
|
G | A | 5 | a0001c0001t0006g0030a0001c0007t0001g0243a0003c0005t0001g0196others(2): Show | 6 | HG00639.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+5095G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607174 | ||||||
chr20:38607183
|
A | T | 1 | a0001c0001t0001g0279 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.137+5104A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607183 | ||||||
chr20:38607316
|
A | G | 1 | a0010c0012t0009g0239 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.137+5237A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607316 | ||||||
chr20:38607352
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.137+5273C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607352 | ||||||
chr20:38607364
|
C | A | 1 | a0004c0011t0004g0312 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.137+5285C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607364 | ||||||
chr20:38607442
|
G | A | 1 | a0008c0017t0008g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.137+5363G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607442 | ||||||
chr20:38607507
|
C | T | 1 | a0001c0007t0001g0189 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.137+5428C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607507 | ||||||
chr20:38607552
|
T | C | 7 | a0001c0002t0007g0007a0001c0002t0007g0044a0001c0004t0007g0287others(4): Show | 9 | HG00642.hp2 HG01069.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+5473T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607552 | ||||||
chr20:38607858
|
A | G | 66 | a0001c0001t0001g0099a0001c0001t0002g0003a0001c0001t0002g0006others(63): Show | 71 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.137+5779A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607858 | ||||||
chr20:38607939
|
T | A | 1 | a0001c0001t0003g0244 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.137+5860T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38607939 | ||||||
chr20:38608046
|
AT | A | 5 | a0001c0001t0006g0030a0001c0007t0001g0243a0003c0005t0001g0196others(2): Show | 6 | HG00639.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+5973delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38608046 | |||||
chr20:38608163
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.137+6084T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608163 | ||||||
chr20:38608226
|
A | ACTC | 292 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(289): Show | 323 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.137+6149_137+6150i others(5): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38608226 | |||||
chr20:38608262
|
C | T | 16 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(13): Show | 19 | HG01261.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.137+6183C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608262 | ||||||
chr20:38608311
|
T | G | 9 | a0001c0002t0008g0074a0001c0004t0002g0075a0001c0004t0004g0045others(6): Show | 10 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+6232T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608311 | ||||||
chr20:38608333
|
A | G | 1 | a0003c0005t0001g0138 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.137+6254A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608333 | ||||||
chr20:38608348
|
A | G | 3 | a0002c0003t0004g0080a0002c0024t0002g0051a0004c0011t0004g0114 | 3 | HG02055.hp1 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.137+6269A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608348 | ||||||
chr20:38608370
|
C | T | 1 | a0001c0002t0004g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.137+6291C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608370 | ||||||
chr20:38608449
|
C | T | 1 | a0001c0002t0005g0184 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.137+6370C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608449 | ||||||
chr20:38608504
|
T | C | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(187): Show | 209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.137+6425T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608504 | ||||||
chr20:38608660
|
G | A | 1 | a0001c0002t0005g0197 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.137+6581G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608660 | ||||||
chr20:38608745
|
T | C | 4 | a0001c0007t0001g0243a0003c0005t0001g0196a0004c0014t0005g0024others(1): Show | 5 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+6666T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608745 | ||||||
chr20:38608851
|
G | A | 9 | a0001c0002t0008g0074a0001c0004t0002g0075a0001c0004t0004g0045others(6): Show | 10 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+6772G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608851 | ||||||
chr20:38608854
|
G | T | 2 | a0001c0002t0008g0074a0001c0004t0002g0075 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.137+6775G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608854 | ||||||
chr20:38608858
|
A | G | 3 | a0001c0001t0002g0072a0001c0004t0007g0113a0006c0009t0013g0042 | 3 | HG00741.hp2 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.137+6779A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38608858 | ||||||
chr20:38609155
|
G | A | 16 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(13): Show | 19 | HG01261.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.137+7076G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609155 | ||||||
chr20:38609304
|
A | C | 2 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.137+7225A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609304 | ||||||
chr20:38609372
|
A | G | 7 | a0001c0004t0004g0045a0003c0005t0002g0008a0003c0005t0002g0047others(4): Show | 8 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.137+7293A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609372 | ||||||
chr20:38609671
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.137+7592C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609671 | ||||||
chr20:38609775
|
G | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0118others(17): Show | 22 | HG00423.hp1 HG01099.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.137+7696G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609775 | ||||||
chr20:38609903
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.137+7824A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609903 | ||||||
chr20:38609945
|
C | T | 4 | a0004c0011t0007g0292a0005c0006t0002g0029a0008c0013t0008g0028others(1): Show | 6 | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+7866C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38609945 | ||||||
chr20:38610060
|
C | T | 87 | a0001c0001t0001g0099a0001c0001t0002g0003a0001c0001t0002g0006others(84): Show | 97 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(94): Show |
intron_variant | MODIFIER | c.137+7981C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610060 | ||||||
chr20:38610110
|
C | T | 1 | a0001c0001t0003g0314 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.137+8031C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610110 | ||||||
chr20:38610134
|
C | T | 1 | a0004c0011t0004g0312 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.137+8055C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610134 | ||||||
chr20:38610135
|
G | A | 1 | a0001c0002t0010g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137+8056G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610135 | ||||||
chr20:38610171
|
C | T | 4 | a0001c0002t0004g0071a0006c0009t0006g0068a0006c0009t0006g0069others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+8092C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610171 | ||||||
chr20:38610251
|
C | T | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(181): Show | 203 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.137+8172C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610251 | ||||||
chr20:38610363
|
C | T | 1 | a0001c0029t0003g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.137+8284C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610363 | ||||||
chr20:38610446
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0005g0187 | 3 | HG03491.hp2 HG03492.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.137+8367A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610446 | ||||||
chr20:38610524
|
G | T | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(269): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.137+8445G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610524 | ||||||
chr20:38610543
|
G | A | 1 | a0001c0001t0003g0201 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.137+8464G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610543 | ||||||
chr20:38610568
|
T | C | 272 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(269): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.137+8489T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610568 | ||||||
chr20:38610664
|
A | C | 16 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(13): Show | 19 | HG01261.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.137+8585A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610664 | ||||||
chr20:38610710
|
G | A | 1 | a0004c0011t0004g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.137+8631G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610710 | ||||||
chr20:38610775
|
G | A | 1 | a0008c0017t0008g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.137+8696G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610775 | ||||||
chr20:38610883
|
C | CT | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(178): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.137+8815dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38610883 | |||||
chr20:38610894
|
T | C | 1 | a0001c0001t0006g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.137+8815T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610894 | ||||||
chr20:38610895
|
C | T | 2 | a0001c0001t0003g0266a0001c0002t0005g0155 | 2 | HG01168.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.137+8816C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610895 | ||||||
chr20:38610896
|
T | C | 1 | a0001c0002t0005g0155 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.137+8817T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610896 | ||||||
chr20:38610924
|
C | T | 1 | a0001c0002t0005g0197 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.137+8845C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610924 | ||||||
chr20:38610993
|
G | A | 9 | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(6): Show | 10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+8914G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38610993 | ||||||
chr20:38611106
|
T | A | 4 | a0004c0011t0007g0292a0005c0006t0002g0029a0008c0013t0008g0028others(1): Show | 6 | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+9027T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611106 | ||||||
chr20:38611166
|
G | A | 4 | a0004c0011t0007g0292a0005c0006t0002g0029a0008c0013t0008g0028others(1): Show | 6 | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+9087G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611166 | ||||||
chr20:38611293
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0002g0041 | 2 | HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.137+9214C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611293 | ||||||
chr20:38611401
|
G | A | 1 | a0013c0015t0005g0248 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.137+9322G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611401 | ||||||
chr20:38611413
|
C | CT | 248 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(245): Show | 275 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.137+9355dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38611413 | |||||
chr20:38611413
|
C | CTT | 6 | a0001c0001t0001g0200a0001c0001t0001g0237a0001c0001t0003g0265others(3): Show | 6 | HG03710.hp1 HG03831.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+9354_137+9355d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38611413 | |||||
chr20:38611504
|
A | C | 1 | a0010c0012t0007g0098 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.137+9425A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611504 | ||||||
chr20:38611555
|
C | T | 1 | a0011c0016t0004g0040 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137+9476C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611555 | ||||||
chr20:38611563
|
A | G | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(271): Show | 303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.137+9484A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611563 | ||||||
chr20:38611665
|
G | A | 185 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(182): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.137+9586G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611665 | ||||||
chr20:38611667
|
G | A | 9 | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(6): Show | 10 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+9588G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611667 | ||||||
chr20:38611672
|
C | T | 1 | a0008c0017t0008g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.137+9593C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611672 | ||||||
chr20:38611721
|
G | A | 5 | a0001c0001t0003g0249a0001c0001t0003g0250a0001c0001t0003g0265others(2): Show | 5 | HG02004.hp2 HG02273.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+9642G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611721 | ||||||
chr20:38611764
|
T | C | 1 | a0001c0001t0003g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.137+9685T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611764 | ||||||
chr20:38611796
|
G | C | 2 | a0001c0001t0003g0267a0001c0002t0005g0268 | 2 | HG02148.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.137+9717G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611796 | ||||||
chr20:38611825
|
C | T | 9 | a0001c0002t0008g0074a0001c0004t0002g0075a0001c0004t0004g0045others(6): Show | 10 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+9746C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38611825 | ||||||
chr20:38611894
|
A | AT | 16 | a0001c0001t0001g0147a0001c0001t0002g0006a0001c0001t0002g0038others(13): Show | 17 | HG00438.hp2 HG01106.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.137+9825dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38611894 | |||||
chr20:38612094
|
G | T | 283 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(280): Show | 313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.137+10015G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612094 | ||||||
chr20:38612123
|
A | G | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(271): Show | 303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.137+10044A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612123 | ||||||
chr20:38612234
|
T | A | 2 | a0001c0002t0007g0052a0001c0002t0007g0081 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.137+10155T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612234 | ||||||
chr20:38612597
|
G | A | 1 | a0004c0014t0005g0024 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137+10518G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612597 | ||||||
chr20:38612626
|
C | T | 1 | a0001c0001t0003g0183 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.137+10547C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612626 | ||||||
chr20:38612691
|
A | G | 3 | a0002c0003t0004g0080a0002c0024t0002g0051a0004c0011t0004g0114 | 3 | HG02055.hp1 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.137+10612A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612691 | ||||||
chr20:38612928
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.138-10431A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38612928 | ||||||
chr20:38613049
|
T | C | 1 | a0003c0005t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.138-10310T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613049 | ||||||
chr20:38613187
|
G | A | 7 | a0001c0002t0005g0121a0001c0002t0005g0157a0001c0002t0005g0184others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-10172G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613187 | ||||||
chr20:38613191
|
G | A | 2 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-10168G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613191 | ||||||
chr20:38613410
|
T | C | 3 | a0006c0026t0002g0086a0011c0016t0004g0040a0011c0016t0004g0085 | 3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.138-9949T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613410 | ||||||
chr20:38613488
|
G | T | 4 | a0001c0002t0004g0071a0006c0009t0006g0068a0006c0009t0006g0069others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-9871G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613488 | ||||||
chr20:38613557
|
C | T | 1 | a0001c0001t0003g0265 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.138-9802C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613557 | ||||||
chr20:38613577
|
C | A | 1 | a0001c0001t0002g0111 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.138-9782C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613577 | ||||||
chr20:38613844
|
C | G | 9 | a0001c0001t0002g0291a0001c0001t0002g0293a0001c0001t0002g0298others(6): Show | 9 | NA18941.hp1 NA18949.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-9515C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38613844 | ||||||
chr20:38614056
|
T | C | 291 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(288): Show | 322 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.138-9303T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614056 | ||||||
chr20:38614073
|
C | T | 1 | a0001c0001t0006g0302 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.138-9286C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614073 | ||||||
chr20:38614098
|
C | T | 1 | a0001c0002t0003g0276 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.138-9261C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614098 | ||||||
chr20:38614310
|
C | T | 1 | a0001c0001t0006g0062 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.138-9049C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614310 | ||||||
chr20:38614321
|
A | G | 290 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(287): Show | 320 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.138-9038A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614321 | ||||||
chr20:38614424
|
A | G | 44 | a0001c0001t0001g0099a0001c0001t0002g0003a0001c0001t0002g0009others(41): Show | 49 | HG00738.hp2 HG00741.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.138-8935A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614424 | ||||||
chr20:38614523
|
A | G | 1 | a0001c0007t0002g0280 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.138-8836A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614523 | ||||||
chr20:38614620
|
G | T | 8 | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(5): Show | 9 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-8739G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614620 | ||||||
chr20:38614628
|
A | G | 2 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-8731A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614628 | ||||||
chr20:38614952
|
G | T | 1 | a0001c0004t0002g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138-8407G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38614952 | ||||||
chr20:38615004
|
T | G | 1 | a0004c0011t0004g0312 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.138-8355T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615004 | ||||||
chr20:38615073
|
C | T | 15 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(12): Show | 18 | HG01261.hp1 HG02055.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.138-8286C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615073 | ||||||
chr20:38615106
|
C | G | 1 | a0001c0002t0007g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.138-8253C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615106 | ||||||
chr20:38615109
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.138-8250A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615109 | ||||||
chr20:38615129
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.138-8230C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615129 | ||||||
chr20:38615286
|
C | T | 1 | a0008c0017t0008g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.138-8073C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615286 | ||||||
chr20:38615287
|
G | A | 1 | a0001c0007t0001g0189 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.138-8072G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615287 | ||||||
chr20:38615298
|
T | G | 1 | a0003c0005t0002g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138-8061T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615298 | ||||||
chr20:38615360
|
C | A | 1 | a0003c0005t0001g0138 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.138-7999C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615360 | ||||||
chr20:38615480
|
G | A | 2 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-7879G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615480 | ||||||
chr20:38615737
|
A | T | 35 | a0001c0001t0001g0099a0001c0001t0002g0003a0001c0001t0002g0009others(32): Show | 39 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.138-7622A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615737 | ||||||
chr20:38615748
|
C | T | 1 | a0001c0001t0003g0134 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.138-7611C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615748 | ||||||
chr20:38615909
|
T | C | 1 | a0015c0025t0004g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-7450T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615909 | ||||||
chr20:38615945
|
A | G | 4 | a0001c0002t0004g0071a0006c0009t0006g0068a0006c0009t0006g0069others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-7414A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38615945 | ||||||
chr20:38616064
|
G | A | 1 | a0003c0005t0002g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138-7295G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616064 | ||||||
chr20:38616251
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.138-7108C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616251 | ||||||
chr20:38616270
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.138-7089G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616270 | ||||||
chr20:38616274
|
G | A | 2 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-7085G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616274 | ||||||
chr20:38616301
|
G | A | 1 | a0001c0002t0010g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.138-7058G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616301 | ||||||
chr20:38616327
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.138-7032C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616327 | ||||||
chr20:38616788
|
T | C | 1 | a0003c0005t0002g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138-6571T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616788 | ||||||
chr20:38616914
|
G | A | 13 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(10): Show | 16 | HG01261.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.138-6445G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616914 | ||||||
chr20:38616935
|
C | CTTTA | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(156): Show | 175 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.138-6400_138-6397d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38616935 | |||||
chr20:38616935
|
C | CTTTATTT others(1): Show |
57 | a0001c0001t0001g0122a0001c0001t0001g0159a0001c0001t0001g0160others(54): Show | 65 | HG00408.hp2 HG00423.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.138-6404_138-6397d others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38616935 | |||||
chr20:38616935
|
C | CTTTATTT others(5): Show |
45 | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0241others(42): Show | 49 | HG00140.hp2 HG00438.hp2 HG01256.hp2 others(46): Show |
intron_variant | MODIFIER | c.138-6408_138-6397d others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38616935 | |||||
chr20:38616935
|
C | CTTTATTT others(9): Show |
5 | a0001c0001t0002g0009a0001c0002t0002g0063a0001c0008t0004g0309others(2): Show | 6 | HG01106.hp1 HG01175.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-6412_138-6397d others(18): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38616935 | |||||
chr20:38616998
|
T | C | 1 | a0001c0007t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.138-6361T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38616998 | ||||||
chr20:38617235
|
C | T | 38 | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0241others(35): Show | 42 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.138-6124C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617235 | ||||||
chr20:38617273
|
G | A | 1 | a0003c0005t0002g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138-6086G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617273 | ||||||
chr20:38617315
|
A | G | 123 | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0209others(120): Show | 137 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.138-6044A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617315 | ||||||
chr20:38617395
|
C | T | 103 | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0209others(100): Show | 116 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.138-5964C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617395 | ||||||
chr20:38617577
|
CCACCTA | C | 8 | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(5): Show | 9 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-5781_138-5776d others(8): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617577 | ||||||
chr20:38617584
|
G | A | 8 | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(5): Show | 9 | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-5775G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617584 | ||||||
chr20:38617655
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0188others(1): Show | 4 | HG00558.hp2 NA18965.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-5704G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617655 | ||||||
chr20:38617672
|
C | T | 3 | a0001c0007t0002g0037a0001c0007t0002g0093a0001c0007t0002g0280 | 3 | HG02622.hp2 HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.138-5687C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617672 | ||||||
chr20:38617675
|
G | A | 1 | a0001c0004t0002g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138-5684G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617675 | ||||||
chr20:38617687
|
T | TC | 10 | a0001c0004t0002g0075a0001c0004t0004g0045a0003c0005t0001g0138others(7): Show | 11 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-5671dupC | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38617687 | |||||
chr20:38617708
|
C | T | 10 | a0001c0004t0002g0075a0001c0004t0004g0045a0003c0005t0001g0138others(7): Show | 11 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-5651C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617708 | ||||||
chr20:38617757
|
A | T | 1 | a0001c0001t0006g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.138-5602A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617757 | ||||||
chr20:38617763
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.138-5596G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617763 | ||||||
chr20:38617908
|
G | A | 2 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-5451G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617908 | ||||||
chr20:38617922
|
G | A | 5 | a0001c0002t0004g0071a0001c0002t0008g0074a0006c0009t0006g0068others(2): Show | 5 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-5437G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617922 | ||||||
chr20:38617951
|
T | A | 5 | a0001c0002t0004g0071a0001c0002t0008g0074a0006c0009t0006g0068others(2): Show | 5 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-5408T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617951 | ||||||
chr20:38617990
|
G | A | 3 | a0001c0007t0002g0037a0001c0007t0002g0093a0001c0007t0002g0280 | 3 | HG02622.hp2 HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.138-5369G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38617990 | ||||||
chr20:38618100
|
C | CTT | 7 | a0001c0002t0004g0071a0001c0002t0008g0074a0002c0003t0005g0120others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.138-5245_138-5244d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38618100 | |||||
chr20:38618100
|
CT | C | 13 | a0001c0001t0001g0209a0001c0001t0003g0214a0001c0001t0003g0253others(10): Show | 14 | HG01243.hp2 HG01361.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.138-5244delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38618100 | |||||
chr20:38618256
|
C | T | 1 | a0008c0017t0008g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.138-5103C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618256 | ||||||
chr20:38618267
|
T | G | 13 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(10): Show | 16 | HG01261.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.138-5092T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618267 | ||||||
chr20:38618299
|
G | A | 84 | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0209others(81): Show | 94 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.138-5060G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618299 | ||||||
chr20:38618342
|
T | C | 301 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(298): Show | 334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.138-5017T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618342 | ||||||
chr20:38618355
|
C | T | 2 | a0001c0002t0002g0053a0001c0002t0002g0112 | 2 | NA18966.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.138-5004C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618355 | ||||||
chr20:38618403
|
A | G | 124 | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0209others(121): Show | 138 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.138-4956A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618403 | ||||||
chr20:38618483
|
G | T | 10 | a0001c0004t0002g0075a0001c0004t0004g0045a0003c0005t0001g0138others(7): Show | 11 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-4876G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618483 | ||||||
chr20:38618489
|
C | G | 10 | a0001c0004t0002g0075a0001c0004t0004g0045a0003c0005t0001g0138others(7): Show | 11 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-4870C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618489 | ||||||
chr20:38618586
|
G | A | 5 | a0001c0002t0004g0071a0001c0002t0008g0074a0006c0009t0006g0068others(2): Show | 5 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-4773G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618586 | ||||||
chr20:38618848
|
C | T | 11 | a0001c0001t0006g0030a0001c0004t0002g0075a0001c0004t0004g0045others(8): Show | 12 | HG00639.hp1 HG01243.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.138-4511C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38618848 | ||||||
chr20:38619028
|
A | T | 1 | a0001c0001t0005g0236 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.138-4331A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619028 | ||||||
chr20:38619061
|
G | A | 16 | a0001c0002t0004g0071a0001c0002t0008g0074a0001c0004t0002g0075others(13): Show | 17 | HG01243.hp2 HG01361.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.138-4298G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619061 | ||||||
chr20:38619122
|
A | G | 17 | a0001c0002t0004g0071a0001c0002t0008g0074a0001c0004t0002g0075others(14): Show | 18 | HG01243.hp2 HG01361.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.138-4237A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619122 | ||||||
chr20:38619177
|
C | T | 1 | a0001c0020t0003g0204 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.138-4182C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619177 | ||||||
chr20:38619288
|
T | C | 1 | a0001c0001t0003g0134 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.138-4071T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619288 | ||||||
chr20:38619333
|
C | T | 1 | a0001c0001t0003g0178 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.138-4026C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619333 | ||||||
chr20:38619375
|
A | C | 22 | a0001c0001t0002g0107a0001c0001t0002g0291a0001c0001t0002g0293others(19): Show | 24 | HG00642.hp2 HG01167.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.138-3984A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619375 | ||||||
chr20:38619457
|
T | A | 1 | a0002c0003t0005g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.138-3902T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619457 | ||||||
chr20:38619527
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.138-3832T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619527 | ||||||
chr20:38619530
|
G | A | 1 | a0008c0013t0008g0028 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.138-3829G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619530 | ||||||
chr20:38619728
|
C | T | 1 | a0015c0025t0004g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-3631C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619728 | ||||||
chr20:38619729
|
G | A | 5 | a0001c0004t0002g0048a0004c0011t0004g0312a0004c0011t0004g0313others(2): Show | 5 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-3630G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619729 | ||||||
chr20:38619809
|
A | G | 3 | a0001c0004t0002g0048a0012c0018t0004g0078a0012c0018t0004g0088 | 3 | HG02647.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.138-3550A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619809 | ||||||
chr20:38619860
|
G | T | 7 | a0001c0002t0004g0071a0006c0009t0006g0068a0006c0009t0006g0069others(4): Show | 7 | HG02257.hp1 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.138-3499G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619860 | ||||||
chr20:38619881
|
C | T | 1 | a0001c0002t0010g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.138-3478C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619881 | ||||||
chr20:38619922
|
A | T | 1 | a0005c0006t0002g0108 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.138-3437A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619922 | ||||||
chr20:38619952
|
A | G | 7 | a0001c0002t0004g0073a0001c0008t0004g0026a0001c0008t0004g0309others(4): Show | 8 | HG02258.hp1 HG02572.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-3407A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619952 | ||||||
chr20:38619987
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.138-3372G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38619987 | ||||||
chr20:38620041
|
G | A | 1 | a0008c0013t0008g0028 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.138-3318G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38620041 | ||||||
chr20:38620210
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.138-3149C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38620210 | ||||||
chr20:38620442
|
C | T | 4 | a0001c0001t0002g0006a0001c0001t0002g0064a0001c0001t0002g0065others(1): Show | 5 | HG02155.hp2 NA18963.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-2917C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38620442 | ||||||
chr20:38620738
|
G | A | 2 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.138-2621G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38620738 | ||||||
chr20:38621066
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.138-2293G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621066 | ||||||
chr20:38621101
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.138-2258G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621101 | ||||||
chr20:38621295
|
T | A | 1 | a0001c0001t0002g0102 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.138-2064T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621295 | ||||||
chr20:38621298
|
T | G | 1 | a0001c0001t0002g0102 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.138-2061T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621298 | ||||||
chr20:38621655
|
G | A | 9 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(6): Show | 10 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-1704G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621655 | ||||||
chr20:38621683
|
A | G | 1 | a0001c0002t0001g0132 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.138-1676A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621683 | ||||||
chr20:38621749
|
T | A | 9 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(6): Show | 10 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-1610T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621749 | ||||||
chr20:38621783
|
A | G | 2 | a0004c0014t0005g0024a0022c0023t0011g0117 | 3 | HG02622.hp1 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.138-1576A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621783 | ||||||
chr20:38621827
|
G | A | 184 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(181): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.138-1532G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621827 | ||||||
chr20:38621881
|
C | G | 1 | a0021c0032t0005g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138-1478C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621881 | ||||||
chr20:38621986
|
C | T | 1 | a0017c0034t0007g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.138-1373C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38621986 | ||||||
chr20:38622053
|
C | CA | 9 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(6): Show | 10 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-1300dupA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38622053 | |||||
chr20:38622110
|
T | TA | 11 | a0001c0001t0003g0177a0001c0002t0004g0073a0001c0008t0004g0026others(8): Show | 12 | HG01109.hp1 HG02258.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138-1249_138-1248i others(3): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622110 | ||||||
chr20:38622111
|
T | A | 98 | a0001c0001t0001g0023a0001c0001t0001g0127a0001c0001t0001g0140others(95): Show | 102 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.138-1248T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622111 | ||||||
chr20:38622113
|
T | A | 13 | a0001c0002t0008g0074a0004c0011t0004g0114a0006c0009t0006g0068others(10): Show | 13 | HG01261.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.138-1246T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622113 | ||||||
chr20:38622119
|
T | A | 3 | a0001c0001t0001g0241a0001c0001t0003g0134a0001c0001t0003g0190 | 3 | NA18950.hp2 NA18964.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.138-1240T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622119 | ||||||
chr20:38622119
|
TA | T | 15 | a0001c0004t0002g0048a0001c0004t0002g0075a0001c0004t0004g0045others(12): Show | 17 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.138-1235delA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 38622119 | |||||
chr20:38622198
|
A | G | 1 | a0001c0001t0006g0296 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.138-1161A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622198 | ||||||
chr20:38622254
|
A | G | 3 | a0001c0002t0005g0128a0001c0002t0005g0155a0001c0002t0005g0222 | 3 | HG00639.hp2 HG00741.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.138-1105A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622254 | ||||||
chr20:38622321
|
T | C | 1 | a0001c0001t0003g0136 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.138-1038T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622321 | ||||||
chr20:38622325
|
G | T | 4 | a0008c0013t0008g0028a0008c0013t0008g0303a0008c0017t0008g0046others(1): Show | 5 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-1034G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622325 | ||||||
chr20:38622404
|
C | T | 1 | a0001c0002t0004g0058 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.138-955C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622404 | ||||||
chr20:38622421
|
A | C | 1 | a0001c0002t0005g0184 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.138-938A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622421 | ||||||
chr20:38622516
|
C | T | 2 | a0001c0021t0002g0282a0001c0021t0002g0285 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.138-843C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622516 | ||||||
chr20:38622519
|
G | A | 18 | a0002c0003t0003g0168a0002c0003t0004g0010a0002c0003t0004g0027others(15): Show | 20 | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.138-840G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622519 | ||||||
chr20:38622611
|
A | G | 1 | a0003c0005t0002g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138-748A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622611 | ||||||
chr20:38622614
|
G | C | 1 | a0004c0011t0004g0312 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.138-745G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622614 | ||||||
chr20:38622776
|
A | G | 3 | a0001c0004t0002g0048a0001c0004t0002g0075a0001c0004t0016g0231 | 3 | HG02486.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.138-583A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622776 | ||||||
chr20:38622886
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.138-473G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622886 | ||||||
chr20:38622894
|
T | G | 1 | a0001c0001t0006g0296 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.138-465T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622894 | ||||||
chr20:38622992
|
A | G | 11 | a0001c0004t0002g0048a0001c0004t0002g0075a0001c0004t0004g0045others(8): Show | 12 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.138-367A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38622992 | ||||||
chr20:38623045
|
G | A | 1 | a0015c0025t0004g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-314G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38623045 | ||||||
chr20:38623181
|
C | A | 1 | a0019c0039t0013g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.138-178C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38623181 | ||||||
chr20:38623183
|
C | G | 11 | a0001c0004t0002g0048a0001c0004t0002g0075a0001c0004t0004g0045others(8): Show | 12 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.138-176C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38623183 | ||||||
chr20:38623187
|
G | A | 1 | a0001c0002t0005g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.138-172G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38623187 | ||||||
chr20:38623282
|
G | A | 67 | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0275others(64): Show | 71 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.138-77G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38623282 | ||||||
chr20:38623305
|
C | G | 4 | a0001c0002t0008g0074a0004c0011t0004g0114a0004c0011t0007g0292others(1): Show | 4 | HG02559.hp1 HG02559.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-54C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | chr20 | 38623305 | ||||||
chr20:38623567
|
C | A | 83 | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0275others(80): Show | 89 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.337+9C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38623567 | ||||||
chr20:38623590
|
G | A | 4 | a0006c0009t0006g0068a0006c0009t0006g0069a0006c0009t0006g0070others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.337+32G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38623590 | ||||||
chr20:38623699
|
C | A | 85 | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0275others(82): Show | 91 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.337+141C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38623699 | ||||||
chr20:38623755
|
G | A | 2 | a0001c0001t0005g0219a0001c0001t0005g0254 | 2 | NA18969.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.337+197G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38623755 | ||||||
chr20:38623787
|
C | A | 1 | a0003c0005t0001g0138 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.337+229C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38623787 | ||||||
chr20:38624171
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.337+613A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624171 | ||||||
chr20:38624283
|
C | G | 9 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(6): Show | 10 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.337+725C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624283 | ||||||
chr20:38624294
|
G | A | 11 | a0001c0004t0002g0048a0001c0004t0002g0075a0001c0004t0004g0045others(8): Show | 12 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.337+736G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624294 | ||||||
chr20:38624548
|
C | T | 67 | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0275others(64): Show | 71 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.337+990C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624548 | ||||||
chr20:38624632
|
C | T | 8 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(5): Show | 9 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.337+1074C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624632 | ||||||
chr20:38624644
|
C | T | 1 | a0001c0021t0002g0282 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.337+1086C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624644 | ||||||
chr20:38624648
|
TG | T | 220 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(217): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.337+1092delG | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr20 | 38624648 | |||||
chr20:38624839
|
T | A | 5 | a0001c0004t0007g0113a0001c0004t0007g0287a0004c0014t0005g0024others(2): Show | 6 | HG01243.hp2 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+1281T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624839 | ||||||
chr20:38624845
|
C | A | 1 | a0004c0011t0004g0312 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.337+1287C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624845 | ||||||
chr20:38624895
|
A | G | 59 | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0275others(56): Show | 62 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.337+1337A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624895 | ||||||
chr20:38624992
|
C | T | 2 | a0001c0008t0004g0309a0001c0038t0002g0310 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.337+1434C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38624992 | ||||||
chr20:38625307
|
C | T | 57 | a0001c0001t0002g0084a0001c0002t0001g0025a0001c0002t0001g0125others(54): Show | 59 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.338-1688C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625307 | ||||||
chr20:38625345
|
G | T | 67 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(64): Show | 82 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.338-1650G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625345 | ||||||
chr20:38625390
|
G | GT | 33 | a0001c0001t0002g0072a0001c0001t0002g0097a0001c0002t0004g0090others(30): Show | 36 | HG00642.hp2 HG00741.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.338-1594dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr20 | 38625390 | |||||
chr20:38625503
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.338-1492C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625503 | ||||||
chr20:38625521
|
C | T | 1 | a0001c0001t0003g0153 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.338-1474C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625521 | ||||||
chr20:38625522
|
G | A | 1 | a0001c0004t0007g0113 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.338-1473G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625522 | ||||||
chr20:38625590
|
C | T | 3 | a0006c0009t0006g0068a0006c0009t0006g0069a0006c0009t0006g0070 | 3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.338-1405C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625590 | ||||||
chr20:38625670
|
T | G | 1 | a0001c0001t0002g0064 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.338-1325T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625670 | ||||||
chr20:38625700
|
T | A | 2 | a0005c0006t0002g0029a0005c0006t0002g0087 | 3 | HG02886.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.338-1295T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625700 | ||||||
chr20:38625736
|
G | A | 313 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(310): Show | 347 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.338-1259G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625736 | ||||||
chr20:38625803
|
G | C | 1 | a0007c0040t0004g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.338-1192G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625803 | ||||||
chr20:38625831
|
G | T | 8 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(5): Show | 9 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.338-1164G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625831 | ||||||
chr20:38625878
|
C | G | 18 | a0001c0001t0002g0072a0002c0003t0003g0168a0002c0003t0004g0010others(15): Show | 20 | HG00642.hp2 HG00741.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.338-1117C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625878 | ||||||
chr20:38625878
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.338-1117C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38625878 | ||||||
chr20:38626407
|
C | T | 1 | a0001c0002t0010g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.338-588C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626407 | ||||||
chr20:38626465
|
C | T | 1 | a0001c0001t0005g0236 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.338-530C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626465 | ||||||
chr20:38626615
|
C | T | 2 | a0012c0018t0004g0078a0012c0018t0004g0088 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.338-380C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626615 | ||||||
chr20:38626665
|
G | A | 3 | a0001c0004t0007g0113a0001c0004t0007g0287a0014c0022t0007g0101 | 3 | HG01243.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.338-330G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626665 | ||||||
chr20:38626723
|
C | T | 3 | a0006c0026t0002g0086a0011c0016t0004g0040a0011c0016t0004g0085 | 3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.338-272C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626723 | ||||||
chr20:38626727
|
C | T | 2 | a0001c0001t0003g0143a0001c0001t0003g0191 | 2 | NA18950.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.338-268C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626727 | ||||||
chr20:38626810
|
G | A | 73 | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0126others(70): Show | 78 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.338-185G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626810 | ||||||
chr20:38626820
|
G | A | 1 | a0001c0004t0016g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.338-175G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626820 | ||||||
chr20:38626940
|
G | A | 3 | a0006c0026t0002g0086a0011c0016t0004g0040a0011c0016t0004g0085 | 3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.338-55G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626940 | ||||||
chr20:38626942
|
G | C | 2 | a0001c0001t0003g0172a0001c0001t0006g0059 | 2 | NA19070.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.338-53G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2/14 | chr20 | 38626942 | ||||||
chr20:38627270
|
C | T | 2 | a0001c0002t0008g0074a0002c0024t0002g0051 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.558+55C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627270 | ||||||
chr20:38627352
|
A | ATGTGTGT others(5): Show |
72 | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0126others(69): Show | 77 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.558+139_558+150dup others(12): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627352 | |||||
chr20:38627375
|
GGTGTGTG others(9): Show |
G | 1 | a0002c0003t0004g0304 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.558+177_558+192del others(16): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627375 | |||||
chr20:38627377
|
T | G | 1 | a0001c0029t0003g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.558+162T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627377 | ||||||
chr20:38627422
|
T | G | 2 | a0001c0001t0003g0232a0001c0007t0002g0280 | 2 | HG02622.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.558+207T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627422 | ||||||
chr20:38627495
|
A | ATGTTGGT others(75): Show |
73 | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0126others(70): Show | 78 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.558+289_558+290ins others(82): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627495 | |||||
chr20:38627495
|
A | ATGTTGGT others(72): Show |
1 | a0001c0002t0001g0218 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.558+289_558+290ins others(79): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627495 | |||||
chr20:38627519
|
G | A | 1 | a0001c0002t0005g0215 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.558+304G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627519 | ||||||
chr20:38627531
|
ATG | A | 70 | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0126others(67): Show | 74 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.558+328_558+329del others(2): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627531 | |||||
chr20:38627531
|
ATGTG | A | 9 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(6): Show | 10 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.558+326_558+329del others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627531 | |||||
chr20:38627553
|
G | A | 2 | a0001c0021t0002g0282a0001c0021t0002g0285 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.558+338G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627553 | ||||||
chr20:38627594
|
GGTGTGCG others(7): Show |
G | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0188others(1): Show | 4 | HG00558.hp2 NA18965.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+385_558+398del others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627594 | |||||
chr20:38627600
|
C | T | 237 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(234): Show | 262 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.558+385C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627600 | ||||||
chr20:38627621
|
G | GTGTA | 110 | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0126others(107): Show | 118 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(115): Show |
intron_variant | MODIFIER | c.558+409_558+410ins others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627621 | |||||
chr20:38627625
|
G | A | 1 | a0019c0039t0013g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.558+410G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627625 | ||||||
chr20:38627628
|
TGTTGGGG others(10): Show |
T | 1 | a0019c0039t0013g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.558+416_558+432del others(17): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627628 | |||||
chr20:38627633
|
G | GGGTGTGT others(11): Show |
4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.558+426_558+427ins others(18): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627633 | |||||
chr20:38627633
|
G | GGGTGTGT others(13): Show |
70 | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0126others(67): Show | 74 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.558+431_558+432ins others(20): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627633 | |||||
chr20:38627655
|
T | G | 1 | a0019c0039t0013g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.558+440T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627655 | ||||||
chr20:38627673
|
GGTGTGTG others(4): Show |
G | 1 | a0001c0004t0016g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.558+471_558+481del others(11): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38627673 | |||||
chr20:38627682
|
GTT | G | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.558+468_558+469del others(2): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627682 | ||||||
chr20:38627993
|
A | G | 83 | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0126others(80): Show | 90 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.558+778A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38627993 | ||||||
chr20:38628074
|
C | T | 2 | a0001c0021t0002g0282a0001c0021t0002g0285 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.559-853C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628074 | ||||||
chr20:38628098
|
A | G | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-829A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628098 | ||||||
chr20:38628126
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.559-801T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628126 | ||||||
chr20:38628148
|
G | A | 1 | a0001c0001t0003g0260 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.559-779G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628148 | ||||||
chr20:38628309
|
C | CT | 83 | a0001c0001t0002g0293a0001c0001t0006g0035a0001c0001t0006g0083others(80): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.559-605dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38628309 | |||||
chr20:38628309
|
CT | C | 6 | a0001c0001t0001g0271a0001c0001t0002g0097a0005c0006t0002g0029others(3): Show | 7 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.559-605delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | 38628309 | |||||
chr20:38628310
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.559-617T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628310 | ||||||
chr20:38628324
|
A | C | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-603A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628324 | ||||||
chr20:38628333
|
C | T | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-594C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628333 | ||||||
chr20:38628351
|
CT | C | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-575delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628351 | ||||||
chr20:38628373
|
C | T | 1 | a0001c0002t0010g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.559-554C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628373 | ||||||
chr20:38628375
|
A | G | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-552A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628375 | ||||||
chr20:38628498
|
G | T | 9 | a0001c0002t0007g0007a0001c0002t0007g0011a0001c0002t0007g0044others(6): Show | 11 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.559-429G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628498 | ||||||
chr20:38628502
|
C | G | 2 | a0012c0018t0004g0078a0012c0018t0004g0088 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.559-425C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628502 | ||||||
chr20:38628636
|
T | A | 8 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(5): Show | 9 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.559-291T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628636 | ||||||
chr20:38628689
|
C | T | 3 | a0001c0002t0001g0126a0001c0002t0001g0166a0001c0002t0001g0167 | 3 | NA18968.hp1 NA19002.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.559-238C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628689 | ||||||
chr20:38628714
|
A | G | 4 | a0001c0021t0002g0282a0001c0021t0002g0285a0015c0025t0004g0054others(1): Show | 4 | HG01884.hp2 HG02976.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.559-213A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628714 | ||||||
chr20:38628741
|
A | G | 67 | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0126others(64): Show | 71 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.559-186A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628741 | ||||||
chr20:38628833
|
A | G | 1 | a0001c0004t0004g0045 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.559-94A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628833 | ||||||
chr20:38628893
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.559-34A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628893 | ||||||
chr20:38628921
|
G | A | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.559-6G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | 38628921 | ||||||
chr20:38629071
|
A | T | 3 | a0001c0004t0007g0113a0001c0004t0007g0287a0014c0022t0007g0101 | 3 | HG01243.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.634+69A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629071 | ||||||
chr20:38629201
|
T | A | 1 | a0001c0002t0001g0269 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.634+199T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629201 | ||||||
chr20:38629345
|
C | A | 3 | a0001c0001t0003g0145a0001c0001t0003g0193a0001c0001t0003g0262 | 3 | HG00408.hp1 NA19074.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.635-157C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629345 | ||||||
chr20:38629378
|
G | A | 1 | a0001c0002t0010g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.635-124G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629378 | ||||||
chr20:38629467
|
C | T | 1 | a0001c0002t0010g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.635-35C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629467 | ||||||
chr20:38629492
|
C | G | 2 | a0005c0006t0002g0106a0005c0006t0002g0108 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.635-10C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629492 | ||||||
chr20:38629497
|
C | T | 1 | a0001c0002t0001g0126 | 1 | NA19002.hp1 | splice_region_variant&intron_variant | LOW | c.635-5C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4/14 | chr20 | 38629497 | ||||||
chr20:38629675
|
G | A | 4 | a0001c0002t0005g0197a0001c0002t0005g0203a0001c0002t0005g0206others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+25G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38629675 | ||||||
chr20:38629686
|
C | T | 1 | a0015c0025t0004g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.783+36C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38629686 | ||||||
chr20:38629760
|
A | C | 1 | a0019c0039t0013g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.783+110A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38629760 | ||||||
chr20:38629946
|
A | G | 1 | a0001c0001t0003g0267 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.783+296A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38629946 | ||||||
chr20:38629982
|
CAGAG | C | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+338_783+341del others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38629982 | |||||
chr20:38630060
|
TTTTC | T | 5 | a0008c0013t0008g0028a0008c0013t0008g0303a0008c0017t0008g0046others(2): Show | 6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.783+430_783+433del others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630060 | |||||
chr20:38630068
|
C | CTTTCTTT others(3): Show |
2 | a0005c0006t0002g0029a0005c0006t0002g0087 | 3 | HG02886.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.783+420_783+429dup others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630068 | |||||
chr20:38630068
|
CTTTCTTT others(7): Show |
C | 8 | a0001c0001t0006g0083a0001c0001t0006g0091a0001c0001t0006g0092others(5): Show | 9 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.783+434_783+447del others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630068 | |||||
chr20:38630072
|
CTTTCTTT others(3): Show |
C | 2 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.783+434_783+443del others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630072 | |||||
chr20:38630080
|
CTTTT | C | 4 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0123others(1): Show | 8 | HG01433.hp1 HG01496.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+432_783+435del others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630080 | |||||
chr20:38630082
|
T | TTC | 2 | a0005c0006t0002g0029a0005c0006t0002g0087 | 3 | HG02886.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.783+433_783+434ins others(2): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630082 | |||||
chr20:38630082
|
T | TTCTTTCT others(7): Show |
2 | a0005c0006t0002g0106a0005c0006t0002g0108 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.783+433_783+434ins others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630082 | |||||
chr20:38630082
|
T | TTTTC | 3 | a0001c0001t0001g0023a0001c0001t0002g0084a0001c0001t0005g0187 | 4 | HG02602.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+448_783+451dup others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630082 | |||||
chr20:38630084
|
T | G | 58 | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0126others(55): Show | 61 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.783+434T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630084 | ||||||
chr20:38630085
|
TCTTTCTT others(16): Show |
T | 58 | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0126others(55): Show | 61 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.783+436_783+458del others(23): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630085 | ||||||
chr20:38630103
|
TTTTTC | T | 7 | a0004c0011t0004g0114a0004c0011t0004g0312a0004c0011t0004g0313others(4): Show | 8 | HG02145.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+462_783+466del others(5): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630103 | |||||
chr20:38630105
|
T | TTTCGTTT others(1): Show |
6 | a0001c0002t0004g0073a0001c0004t0016g0231a0001c0008t0004g0026others(3): Show | 7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+458_783+459ins others(8): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630105 | |||||
chr20:38630105
|
T | TTTCTTTT others(1): Show |
4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+458_783+465dup others(8): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630105 | |||||
chr20:38630118
|
TCTTTCTT others(2): Show |
T | 4 | a0006c0009t0006g0068a0006c0009t0006g0069a0006c0009t0006g0070others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+478_783+486del others(9): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630118 | |||||
chr20:38630147
|
T | TTCCC | 67 | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0126others(64): Show | 72 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.783+511_783+514dup others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630147 | |||||
chr20:38630161
|
CCCTT | C | 6 | a0001c0002t0004g0073a0001c0004t0016g0231a0001c0008t0004g0026others(3): Show | 7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+525_783+528del others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38630161 | |||||
chr20:38630238
|
GA | G | 6 | a0001c0002t0004g0073a0001c0004t0016g0231a0001c0008t0004g0026others(3): Show | 7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+589delA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630238 | ||||||
chr20:38630266
|
C | T | 1 | a0006c0009t0013g0042 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.783+616C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630266 | ||||||
chr20:38630299
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.783+649A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630299 | ||||||
chr20:38630558
|
G | T | 1 | a0001c0002t0010g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.783+908G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630558 | ||||||
chr20:38630793
|
G | A | 4 | a0006c0009t0006g0068a0006c0009t0006g0069a0006c0009t0006g0070others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+1143G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630793 | ||||||
chr20:38630802
|
T | A | 5 | a0001c0002t0010g0082a0008c0013t0008g0028a0008c0013t0008g0303others(2): Show | 6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.783+1152T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630802 | ||||||
chr20:38630874
|
C | T | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+1224C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630874 | ||||||
chr20:38630915
|
C | T | 3 | a0006c0026t0002g0086a0011c0016t0004g0040a0011c0016t0004g0085 | 3 | HG02257.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.783+1265C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630915 | ||||||
chr20:38630921
|
A | G | 2 | a0001c0002t0008g0074a0002c0024t0002g0051 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.783+1271A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630921 | ||||||
chr20:38630946
|
G | C | 1 | a0001c0002t0010g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.783+1296G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38630946 | ||||||
chr20:38631148
|
C | T | 1 | a0001c0002t0004g0090 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.783+1498C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631148 | ||||||
chr20:38631210
|
G | T | 6 | a0001c0002t0004g0073a0001c0004t0016g0231a0001c0008t0004g0026others(3): Show | 7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+1560G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631210 | ||||||
chr20:38631264
|
T | C | 2 | a0001c0002t0002g0053a0001c0002t0002g0112 | 2 | NA18966.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.783+1614T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631264 | ||||||
chr20:38631304
|
T | TA | 28 | a0001c0001t0002g0111a0001c0001t0003g0191a0001c0002t0005g0121others(25): Show | 29 | HG01070.hp1 HG01109.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.783+1675dupA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38631304 | |||||
chr20:38631304
|
T | TAA | 38 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(35): Show | 40 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.783+1674_783+1675d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38631304 | |||||
chr20:38631304
|
TA | T | 18 | a0001c0001t0001g0118a0001c0001t0001g0180a0001c0001t0002g0038others(15): Show | 20 | HG00323.hp1 HG00408.hp2 HG02523.hp2 others(17): Show |
intron_variant | MODIFIER | c.783+1675delA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38631304 | |||||
chr20:38631407
|
C | T | 1 | a0002c0003t0006g0043 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.783+1757C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631407 | ||||||
chr20:38631519
|
G | A | 47 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(44): Show | 50 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.783+1869G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631519 | ||||||
chr20:38631632
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.783+1982G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631632 | ||||||
chr20:38631787
|
T | C | 1 | a0001c0001t0006g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.783+2137T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631787 | ||||||
chr20:38631860
|
T | C | 5 | a0004c0011t0004g0114a0004c0011t0004g0312a0004c0011t0004g0313others(2): Show | 6 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.783+2210T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631860 | ||||||
chr20:38631971
|
T | G | 7 | a0001c0002t0008g0074a0001c0021t0002g0282a0001c0021t0002g0285others(4): Show | 7 | HG01884.hp2 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.783+2321T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631971 | ||||||
chr20:38631999
|
T | A | 6 | a0001c0002t0004g0073a0001c0004t0016g0231a0001c0008t0004g0026others(3): Show | 7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+2349T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38631999 | ||||||
chr20:38632186
|
A | C | 48 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(45): Show | 51 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.784-2434A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632186 | ||||||
chr20:38632259
|
C | A | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-2361C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632259 | ||||||
chr20:38632267
|
A | AT | 7 | a0001c0001t0001g0258a0001c0001t0002g0006a0001c0001t0002g0064others(4): Show | 8 | HG00438.hp2 HG01884.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-2340dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38632267 | |||||
chr20:38632267
|
AT | A | 60 | a0001c0001t0006g0091a0001c0002t0001g0125a0001c0002t0004g0033others(57): Show | 65 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.784-2340delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38632267 | |||||
chr20:38632349
|
G | A | 15 | a0001c0002t0008g0074a0001c0021t0002g0282a0001c0021t0002g0285others(12): Show | 17 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.784-2271G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632349 | ||||||
chr20:38632349
|
G | T | 1 | a0017c0034t0007g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.784-2271G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632349 | ||||||
chr20:38632357
|
G | C | 4 | a0008c0013t0008g0028a0008c0013t0008g0303a0008c0017t0008g0046others(1): Show | 5 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-2263G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632357 | ||||||
chr20:38632383
|
C | G | 1 | a0001c0004t0004g0045 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.784-2237C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632383 | ||||||
chr20:38632401
|
ACAGGCGC others(7): Show |
A | 3 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0275 | 3 | HG00140.hp2 HG01361.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.784-2216_784-2203d others(16): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38632401 | |||||
chr20:38632410
|
C | T | 42 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(39): Show | 44 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.784-2210C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632410 | ||||||
chr20:38632540
|
C | T | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-2080C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632540 | ||||||
chr20:38632550
|
C | T | 9 | a0001c0004t0004g0045a0001c0004t0007g0113a0001c0004t0007g0287others(6): Show | 9 | HG01109.hp1 HG01243.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.784-2070C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632550 | ||||||
chr20:38632686
|
C | T | 1 | a0001c0001t0003g0178 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.784-1934C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632686 | ||||||
chr20:38632754
|
T | C | 42 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(39): Show | 44 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.784-1866T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632754 | ||||||
chr20:38632888
|
C | T | 12 | a0001c0002t0007g0007a0001c0002t0007g0011a0001c0002t0007g0044others(9): Show | 14 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.784-1732C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632888 | ||||||
chr20:38632893
|
C | T | 3 | a0001c0002t0002g0034a0001c0002t0002g0039a0001c0002t0002g0063 | 3 | HG01106.hp1 HG01978.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.784-1727C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632893 | ||||||
chr20:38632923
|
G | A | 1 | a0001c0007t0001g0189 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.784-1697G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632923 | ||||||
chr20:38632942
|
G | A | 29 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(26): Show | 29 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.784-1678G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632942 | ||||||
chr20:38632982
|
G | T | 8 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(5): Show | 9 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.784-1638G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38632982 | ||||||
chr20:38633114
|
C | T | 4 | a0008c0013t0008g0028a0008c0013t0008g0303a0008c0017t0008g0046others(1): Show | 5 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-1506C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633114 | ||||||
chr20:38633117
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0188others(1): Show | 4 | HG00558.hp2 NA18965.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-1503C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633117 | ||||||
chr20:38633122
|
C | CA | 18 | a0001c0001t0002g0111a0001c0008t0004g0309a0004c0011t0004g0114others(15): Show | 21 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.784-1484dupA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38633122 | |||||
chr20:38633122
|
CA | C | 48 | a0001c0001t0003g0175a0001c0002t0004g0033a0001c0002t0004g0055others(45): Show | 50 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.784-1484delA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38633122 | |||||
chr20:38633136
|
A | AT | 4 | a0001c0002t0004g0073a0001c0008t0004g0026a0001c0008t0006g0286others(1): Show | 5 | HG02258.hp1 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-1483dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | 38633136 | |||||
chr20:38633138
|
A | G | 4 | a0001c0002t0004g0073a0001c0008t0004g0026a0001c0008t0006g0286others(1): Show | 5 | HG02258.hp1 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-1482A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633138 | ||||||
chr20:38633177
|
C | G | 2 | a0001c0021t0002g0282a0001c0021t0002g0285 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.784-1443C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633177 | ||||||
chr20:38633485
|
C | T | 46 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(43): Show | 49 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.784-1135C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633485 | ||||||
chr20:38633539
|
C | T | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-1081C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633539 | ||||||
chr20:38633570
|
A | G | 1 | a0001c0002t0001g0186 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.784-1050A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633570 | ||||||
chr20:38633593
|
C | T | 33 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(30): Show | 34 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.784-1027C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633593 | ||||||
chr20:38633621
|
G | A | 2 | a0001c0021t0002g0282a0001c0021t0002g0285 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.784-999G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633621 | ||||||
chr20:38633654
|
C | T | 7 | a0001c0007t0001g0189a0001c0007t0001g0243a0001c0007t0002g0037others(4): Show | 7 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-966C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38633654 | ||||||
chr20:38634146
|
G | T | 10 | a0001c0002t0004g0073a0001c0008t0004g0026a0001c0008t0004g0309others(7): Show | 12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.784-474G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38634146 | ||||||
chr20:38634314
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.784-306T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38634314 | ||||||
chr20:38634357
|
A | G | 5 | a0001c0002t0004g0090a0001c0002t0005g0197a0001c0002t0005g0203others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-263A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38634357 | ||||||
chr20:38634497
|
T | C | 1 | a0001c0002t0015g0274 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.784-123T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38634497 | ||||||
chr20:38634558
|
C | T | 1 | a0015c0025t0004g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.784-62C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | chr20 | 38634558 | ||||||
chr20:38634831
|
T | C | 1 | a0001c0002t0008g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.949+46T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38634831 | ||||||
chr20:38634846
|
G | A | 6 | a0001c0004t0004g0045a0007c0010t0010g0224a0007c0010t0010g0307others(3): Show | 6 | HG01109.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.949+61G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38634846 | ||||||
chr20:38634886
|
C | CT | 152 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(149): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.949+115dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr20 | 38634886 | |||||
chr20:38634914
|
G | A | 1 | a0011c0016t0004g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.949+129G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38634914 | ||||||
chr20:38634947
|
T | C | 3 | a0001c0002t0004g0073a0001c0008t0004g0026a0001c0008t0004g0309 | 4 | HG02258.hp1 HG02572.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.949+162T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38634947 | ||||||
chr20:38634974
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.949+189C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38634974 | ||||||
chr20:38634994
|
G | T | 1 | a0001c0002t0001g0167 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.949+209G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38634994 | ||||||
chr20:38635007
|
G | A | 1 | a0010c0012t0009g0239 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.949+222G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38635007 | ||||||
chr20:38635118
|
G | A | 1 | a0001c0002t0009g0149 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.949+333G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38635118 | ||||||
chr20:38635161
|
T | G | 1 | a0001c0001t0001g0246 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.949+376T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38635161 | ||||||
chr20:38635213
|
AT | A | 31 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(28): Show | 31 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.949+437delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr20 | 38635213 | |||||
chr20:38635366
|
ATAT | A | 10 | a0001c0002t0004g0073a0001c0008t0004g0026a0001c0008t0004g0309others(7): Show | 12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.949+585_949+587del others(3): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr20 | 38635366 | |||||
chr20:38635524
|
G | C | 11 | a0001c0002t0004g0073a0001c0002t0008g0074a0001c0008t0004g0026others(8): Show | 13 | HG02258.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.949+739G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38635524 | ||||||
chr20:38635540
|
C | G | 57 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(54): Show | 62 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.949+755C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38635540 | ||||||
chr20:38635895
|
C | A | 1 | a0001c0001t0002g0104 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.949+1110C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38635895 | ||||||
chr20:38636140
|
T | C | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.949+1355T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636140 | ||||||
chr20:38636237
|
C | A | 14 | a0002c0003t0003g0168a0002c0003t0004g0010a0002c0003t0004g0027others(11): Show | 16 | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.949+1452C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636237 | ||||||
chr20:38636264
|
A | T | 2 | a0001c0001t0006g0213a0001c0001t0006g0252 | 2 | HG02165.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.950-1444A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636264 | ||||||
chr20:38636264
|
AT | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0140a0001c0001t0001g0182others(5): Show | 9 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.950-1429delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr20 | 38636264 | |||||
chr20:38636267
|
T | A | 17 | a0001c0002t0004g0073a0001c0008t0004g0026a0001c0008t0004g0309others(14): Show | 20 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.950-1441T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636267 | ||||||
chr20:38636267
|
T | TA | 3 | a0001c0001t0001g0200a0001c0002t0009g0135a0001c0004t0004g0045 | 3 | HG02970.hp1 NA18995.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.950-1441_950-1440i others(3): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636267 | ||||||
chr20:38636268
|
T | A | 102 | a0001c0001t0001g0118a0001c0001t0001g0150a0001c0001t0001g0151others(99): Show | 106 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.950-1440T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636268 | ||||||
chr20:38636272
|
T | A | 24 | a0001c0001t0006g0296a0001c0001t0006g0305a0001c0002t0004g0033others(21): Show | 24 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.950-1436T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636272 | ||||||
chr20:38636384
|
G | A | 3 | a0002c0003t0004g0080a0002c0003t0004g0295a0009c0035t0011g0124 | 3 | HG02055.hp1 HG02602.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.950-1324G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636384 | ||||||
chr20:38636482
|
C | T | 10 | a0001c0002t0004g0073a0001c0008t0004g0026a0001c0008t0004g0309others(7): Show | 12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.950-1226C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636482 | ||||||
chr20:38636504
|
C | T | 5 | a0001c0007t0001g0189a0001c0007t0001g0243a0001c0007t0002g0037others(2): Show | 5 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.950-1204C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636504 | ||||||
chr20:38636538
|
C | T | 5 | a0001c0021t0002g0282a0001c0021t0002g0285a0012c0018t0004g0078others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.950-1170C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636538 | ||||||
chr20:38636777
|
G | A | 1 | a0001c0002t0010g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.950-931G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636777 | ||||||
chr20:38636787
|
G | T | 4 | a0008c0013t0008g0028a0008c0013t0008g0303a0008c0017t0008g0046others(1): Show | 5 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.950-921G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636787 | ||||||
chr20:38636793
|
A | G | 2 | a0004c0014t0005g0024a0022c0023t0011g0117 | 3 | HG02622.hp1 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.950-915A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636793 | ||||||
chr20:38636804
|
G | T | 57 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(54): Show | 62 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.950-904G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38636804 | ||||||
chr20:38637144
|
C | CT | 14 | a0001c0001t0003g0220a0001c0002t0010g0082a0001c0007t0001g0189others(11): Show | 15 | HG01891.hp1 HG02109.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.950-550dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr20 | 38637144 | |||||
chr20:38637158
|
T | C | 1 | a0001c0004t0002g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.950-550T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637158 | ||||||
chr20:38637200
|
C | T | 8 | a0006c0026t0002g0086a0007c0040t0004g0283a0008c0013t0008g0028others(5): Show | 9 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.950-508C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637200 | ||||||
chr20:38637241
|
A | T | 2 | a0008c0017t0008g0046a0008c0017t0008g0105 | 2 | HG01261.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.950-467A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637241 | ||||||
chr20:38637251
|
T | C | 8 | a0001c0002t0010g0082a0003c0005t0001g0138a0003c0005t0001g0196others(5): Show | 9 | HG01891.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.950-457T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637251 | ||||||
chr20:38637254
|
T | A | 3 | a0006c0009t0006g0068a0006c0009t0006g0069a0006c0009t0006g0070 | 3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.950-454T>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637254 | ||||||
chr20:38637289
|
A | G | 1 | a0001c0002t0008g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.950-419A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637289 | ||||||
chr20:38637355
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.950-353G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637355 | ||||||
chr20:38637391
|
C | T | 6 | a0001c0001t0001g0018a0001c0021t0002g0282a0001c0021t0002g0285others(3): Show | 7 | HG01099.hp1 HG01884.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.950-317C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637391 | ||||||
chr20:38637392
|
G | A | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.950-316G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637392 | ||||||
chr20:38637468
|
C | A | 5 | a0001c0021t0002g0282a0001c0021t0002g0285a0012c0018t0004g0078others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.950-240C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637468 | ||||||
chr20:38637562
|
C | A | 92 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(89): Show | 99 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(96): Show |
intron_variant | MODIFIER | c.950-146C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | chr20 | 38637562 | ||||||
chr20:38637918
|
T | C | 167 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(164): Show | 188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1041+119T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38637918 | ||||||
chr20:38637937
|
C | T | 8 | a0006c0026t0002g0086a0007c0040t0004g0283a0008c0013t0008g0028others(5): Show | 9 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1041+138C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38637937 | ||||||
chr20:38638014
|
T | C | 151 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(148): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1041+215T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638014 | ||||||
chr20:38638038
|
C | G | 167 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(164): Show | 188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1041+239C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638038 | ||||||
chr20:38638045
|
C | T | 2 | a0006c0009t0006g0069a0006c0009t0006g0070 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1041+246C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638045 | ||||||
chr20:38638050
|
C | T | 4 | a0007c0010t0010g0224a0007c0010t0010g0307a0007c0010t0012g0129others(1): Show | 4 | HG01109.hp1 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041+251C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638050 | ||||||
chr20:38638081
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1041+282G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638081 | ||||||
chr20:38638153
|
C | CA | 151 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(148): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1041+366dupA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr20 | 38638153 | |||||
chr20:38638166
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1041+367T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638166 | ||||||
chr20:38638172
|
G | A | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041+373G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638172 | ||||||
chr20:38638183
|
C | T | 1 | a0001c0001t0003g0225 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1041+384C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638183 | ||||||
chr20:38638192
|
G | A | 1 | a0001c0001t0003g0158 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1041+393G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638192 | ||||||
chr20:38638228
|
C | T | 1 | a0018c0031t0002g0290 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1041+429C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638228 | ||||||
chr20:38638231
|
T | C | 193 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(190): Show | 216 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.1041+432T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638231 | ||||||
chr20:38638232
|
G | A | 29 | a0001c0002t0004g0033a0001c0002t0004g0055a0001c0002t0004g0057others(26): Show | 29 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1041+433G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638232 | ||||||
chr20:38638272
|
G | A | 1 | a0001c0001t0003g0256 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1041+473G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638272 | ||||||
chr20:38638485
|
A | G | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-276A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638485 | ||||||
chr20:38638606
|
G | C | 7 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(4): Show | 8 | HG01891.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1042-155G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638606 | ||||||
chr20:38638724
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1042-37G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638724 | ||||||
chr20:38638726
|
T | G | 1 | a0001c0001t0002g0012 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1042-35T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 7/14 | chr20 | 38638726 | ||||||
chr20:38638929
|
G | A | 19 | a0001c0001t0001g0209a0001c0001t0003g0002a0001c0001t0003g0015others(16): Show | 24 | HG00408.hp2 HG00544.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.1119+91G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 8/14 | chr20 | 38638929 | ||||||
chr20:38639003
|
CAG | C | 3 | a0003c0005t0001g0138a0003c0005t0001g0196a0009c0019t0007g0311 | 3 | HG01891.hp1 HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1119+170_1119+171d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr20 | 38639003 | |||||
chr20:38639086
|
C | T | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-141C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 8/14 | chr20 | 38639086 | ||||||
chr20:38639108
|
G | A | 1 | a0001c0001t0003g0256 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1120-119G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 8/14 | chr20 | 38639108 | ||||||
chr20:38639215
|
G | A | 1 | a0001c0001t0005g0236 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1120-12G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 8/14 | chr20 | 38639215 | ||||||
chr20:38639478
|
C | T | 2 | a0001c0001t0005g0219a0001c0001t0005g0254 | 2 | NA18969.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1279+92C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639478 | ||||||
chr20:38639518
|
T | G | 4 | a0006c0026t0002g0086a0007c0040t0004g0283a0011c0016t0004g0040others(1): Show | 4 | HG02257.hp1 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+132T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639518 | ||||||
chr20:38639537
|
G | T | 11 | a0001c0002t0004g0073a0001c0004t0004g0045a0001c0008t0004g0026others(8): Show | 13 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1279+151G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639537 | ||||||
chr20:38639540
|
C | T | 5 | a0001c0007t0001g0189a0001c0007t0001g0243a0001c0007t0002g0037others(2): Show | 5 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+154C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639540 | ||||||
chr20:38639564
|
A | T | 5 | a0001c0007t0001g0189a0001c0007t0001g0243a0001c0007t0002g0037others(2): Show | 5 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+178A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639564 | ||||||
chr20:38639576
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0159a0001c0001t0001g0226 | 3 | HG02735.hp2 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1279+190G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639576 | ||||||
chr20:38639577
|
C | T | 1 | a0001c0008t0006g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1279+191C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639577 | ||||||
chr20:38639643
|
A | G | 1 | a0001c0002t0015g0274 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1279+257A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639643 | ||||||
chr20:38639852
|
A | G | 2 | a0001c0021t0002g0282a0001c0021t0002g0285 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1279+466A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639852 | ||||||
chr20:38639945
|
G | A | 4 | a0008c0013t0008g0028a0008c0013t0008g0303a0008c0017t0008g0046others(1): Show | 5 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+559G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639945 | ||||||
chr20:38639971
|
C | T | 1 | a0015c0025t0004g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1279+585C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639971 | ||||||
chr20:38639980
|
C | T | 51 | a0001c0002t0004g0073a0001c0002t0008g0074a0001c0002t0010g0082others(48): Show | 57 | HG00642.hp2 HG01261.hp1 HG01433.hp2 others(54): Show |
intron_variant | MODIFIER | c.1279+594C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38639980 | ||||||
chr20:38640060
|
C | T | 1 | a0001c0002t0005g0128 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1279+674C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640060 | ||||||
chr20:38640076
|
G | T | 46 | a0001c0002t0004g0073a0001c0002t0008g0074a0001c0002t0010g0082others(43): Show | 51 | HG00642.hp2 HG01261.hp1 HG01433.hp2 others(48): Show |
intron_variant | MODIFIER | c.1279+690G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640076 | ||||||
chr20:38640088
|
G | C | 1 | a0001c0001t0001g0259 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1279+702G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640088 | ||||||
chr20:38640091
|
C | G | 13 | a0001c0001t0001g0188a0001c0002t0004g0090a0001c0002t0005g0197others(10): Show | 13 | HG00558.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1279+705C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640091 | ||||||
chr20:38640101
|
TTCC | T | 15 | a0001c0002t0008g0074a0001c0002t0010g0082a0001c0007t0001g0189others(12): Show | 16 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1279+721_1279+723d others(5): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640101 | |||||
chr20:38640104
|
C | CTCTTCT | 31 | a0001c0002t0004g0073a0001c0004t0004g0045a0001c0004t0016g0231others(28): Show | 35 | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.1279+720_1279+721i others(8): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640104 | |||||
chr20:38640104
|
C | T | 176 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(173): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1279+718C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640104 | ||||||
chr20:38640121
|
C | CT | 34 | a0001c0002t0004g0073a0001c0002t0008g0074a0001c0004t0004g0045others(31): Show | 38 | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(35): Show |
intron_variant | MODIFIER | c.1279+737dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640121 | |||||
chr20:38640123
|
TCC | T | 154 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(151): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1279+738_1279+739d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640123 | ||||||
chr20:38640125
|
C | T | 34 | a0001c0002t0004g0073a0001c0002t0008g0074a0001c0004t0004g0045others(31): Show | 38 | HG00642.hp2 HG01433.hp2 HG01516.hp2 others(35): Show |
intron_variant | MODIFIER | c.1279+739C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640125 | ||||||
chr20:38640133
|
T | C | 154 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(151): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1279+747T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640133 | ||||||
chr20:38640134
|
C | T | 154 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(151): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1279+748C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640134 | ||||||
chr20:38640140
|
CT | C | 154 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(151): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1279+757delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640140 | |||||
chr20:38640141
|
T | C | 2 | a0001c0002t0008g0074a0007c0040t0004g0283 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1279+755T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640141 | ||||||
chr20:38640145
|
T | C | 156 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(153): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1279+759T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640145 | ||||||
chr20:38640145
|
T | TTCTTCC | 64 | a0001c0002t0010g0082a0001c0004t0004g0045a0001c0004t0007g0113others(61): Show | 70 | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(67): Show |
intron_variant | MODIFIER | c.1279+765_1279+770d others(8): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640145 | |||||
chr20:38640151
|
C | CTCTTCTT | 37 | a0001c0004t0016g0231a0001c0007t0001g0189a0001c0007t0001g0243others(34): Show | 41 | HG00642.hp2 HG01261.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.1279+780_1279+786d others(9): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640151 | |||||
chr20:38640151
|
C | T | 1 | a0007c0040t0004g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1279+765C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640151 | ||||||
chr20:38640156
|
CT | C | 2 | a0001c0002t0004g0073a0001c0008t0004g0026 | 3 | HG02258.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1279+773delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640156 | |||||
chr20:38640158
|
T | C | 2 | a0001c0002t0004g0073a0001c0008t0004g0026 | 3 | HG02258.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1279+772T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640158 | ||||||
chr20:38640167
|
C | CTTCTTCT | 7 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(4): Show | 8 | HG01891.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1279+791_1279+797d others(9): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640167 | |||||
chr20:38640173
|
C | T | 133 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(130): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1279+787C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640173 | ||||||
chr20:38640173
|
CTTTCTTC others(1): Show |
C | 8 | a0001c0004t0007g0113a0001c0004t0007g0287a0007c0010t0010g0224others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+806_1279+813d others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640173 | |||||
chr20:38640174
|
T | C | 133 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(130): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1279+788T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640174 | ||||||
chr20:38640180
|
CT | C | 133 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(130): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1279+798delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640180 | |||||
chr20:38640189
|
TTTTCTTC | T | 30 | a0001c0001t0001g0099a0001c0001t0001g0127a0001c0001t0001g0141others(27): Show | 31 | HG00558.hp2 HG00741.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.1279+824_1279+830d others(9): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640189 | |||||
chr20:38640196
|
C | CT | 133 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(130): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1279+813dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640196 | |||||
chr20:38640218
|
C | CT | 17 | a0001c0001t0001g0200a0001c0001t0003g0201a0001c0004t0007g0113others(14): Show | 18 | HG00544.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1279+847dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640218 | |||||
chr20:38640218
|
CT | C | 8 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0001g0199others(5): Show | 8 | HG01169.hp2 HG01515.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+847delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38640218 | |||||
chr20:38640220
|
T | G | 4 | a0007c0010t0010g0224a0007c0010t0010g0307a0007c0010t0012g0129others(1): Show | 4 | HG01109.hp1 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+834T>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640220 | ||||||
chr20:38640222
|
T | C | 1 | a0006c0026t0002g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1279+836T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640222 | ||||||
chr20:38640238
|
A | T | 1 | a0001c0001t0003g0251 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1279+852A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640238 | ||||||
chr20:38640251
|
C | G | 1 | a0001c0029t0003g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1279+865C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640251 | ||||||
chr20:38640376
|
C | T | 2 | a0001c0002t0002g0053a0001c0002t0002g0112 | 2 | NA18966.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1279+990C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640376 | ||||||
chr20:38640426
|
C | T | 1 | a0001c0001t0006g0212 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1279+1040C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640426 | ||||||
chr20:38640460
|
G | A | 21 | a0001c0001t0001g0023a0001c0001t0002g0038a0001c0001t0002g0084others(18): Show | 23 | HG00558.hp1 HG00673.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1279+1074G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640460 | ||||||
chr20:38640538
|
A | G | 1 | a0017c0034t0007g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1279+1152A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640538 | ||||||
chr20:38640588
|
T | C | 1 | a0001c0002t0008g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1280-1138T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640588 | ||||||
chr20:38640627
|
C | T | 5 | a0001c0007t0001g0189a0001c0007t0001g0243a0001c0007t0002g0037others(2): Show | 5 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1280-1099C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640627 | ||||||
chr20:38640670
|
C | T | 1 | a0001c0002t0005g0164 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1280-1056C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640670 | ||||||
chr20:38640809
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1280-917G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640809 | ||||||
chr20:38640846
|
G | A | 12 | a0001c0004t0007g0113a0001c0004t0007g0287a0007c0010t0010g0224others(9): Show | 12 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1280-880G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640846 | ||||||
chr20:38640867
|
C | A | 10 | a0001c0002t0004g0073a0001c0004t0004g0045a0001c0008t0004g0026others(7): Show | 12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1280-859C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640867 | ||||||
chr20:38640989
|
A | G | 1 | a0001c0020t0003g0204 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1280-737A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38640989 | ||||||
chr20:38641024
|
A | G | 6 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(3): Show | 7 | HG02109.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280-702A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641024 | ||||||
chr20:38641079
|
A | T | 1 | a0001c0001t0003g0251 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1280-647A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641079 | ||||||
chr20:38641079
|
AGGAG | A | 16 | a0001c0001t0005g0187a0001c0004t0016g0231a0002c0003t0004g0010others(13): Show | 18 | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.1280-629_1280-626d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 38641079 | |||||
chr20:38641097
|
G | C | 1 | a0001c0002t0002g0034 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1280-629G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641097 | ||||||
chr20:38641100
|
G | A | 5 | a0001c0001t0003g0173a0001c0001t0003g0233a0001c0001t0003g0253others(2): Show | 5 | HG00642.hp1 HG01243.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1280-626G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641100 | ||||||
chr20:38641136
|
C | T | 4 | a0001c0004t0007g0113a0001c0004t0007g0287a0009c0019t0007g0311others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1280-590C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641136 | ||||||
chr20:38641159
|
T | C | 3 | a0001c0002t0001g0126a0001c0002t0001g0166a0001c0002t0001g0167 | 3 | NA18968.hp1 NA19002.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1280-567T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641159 | ||||||
chr20:38641235
|
G | T | 2 | a0001c0021t0002g0282a0001c0021t0002g0285 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1280-491G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641235 | ||||||
chr20:38641290
|
G | A | 6 | a0001c0007t0001g0189a0001c0007t0001g0243a0001c0007t0002g0037others(3): Show | 6 | HG02451.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-436G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641290 | ||||||
chr20:38641342
|
A | C | 2 | a0001c0021t0002g0282a0001c0021t0002g0285 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1280-384A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641342 | ||||||
chr20:38641367
|
A | G | 161 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(158): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.1280-359A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641367 | ||||||
chr20:38641386
|
T | C | 14 | a0001c0004t0007g0113a0001c0004t0007g0287a0001c0021t0002g0282others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1280-340T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641386 | ||||||
chr20:38641403
|
G | C | 1 | a0001c0004t0007g0287 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1280-323G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641403 | ||||||
chr20:38641464
|
C | T | 1 | a0006c0026t0002g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1280-262C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641464 | ||||||
chr20:38641466
|
G | T | 1 | a0001c0004t0007g0287 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1280-260G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641466 | ||||||
chr20:38641469
|
C | T | 1 | a0015c0025t0004g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1280-257C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641469 | ||||||
chr20:38641603
|
G | A | 4 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280-123G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | 38641603 | ||||||
chr20:38641869
|
T | C | 4 | a0001c0004t0007g0113a0001c0004t0007g0287a0009c0019t0007g0311others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1362+61T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38641869 | ||||||
chr20:38642032
|
C | T | 1 | a0002c0003t0004g0031 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1362+224C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642032 | ||||||
chr20:38642147
|
A | G | 13 | a0001c0002t0010g0082a0001c0007t0001g0189a0001c0007t0001g0243others(10): Show | 14 | HG02109.hp2 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1362+339A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642147 | ||||||
chr20:38642245
|
G | T | 1 | a0001c0001t0002g0038 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1362+437G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642245 | ||||||
chr20:38642321
|
A | T | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(212): Show | 237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1362+513A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642321 | ||||||
chr20:38642346
|
C | T | 1 | a0001c0002t0004g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1362+538C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642346 | ||||||
chr20:38642495
|
A | G | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(154): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1362+687A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642495 | ||||||
chr20:38642509
|
C | T | 4 | a0001c0001t0005g0187a0002c0003t0004g0010a0002c0003t0004g0031others(1): Show | 5 | HG01516.hp2 HG01517.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1362+701C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642509 | ||||||
chr20:38642608
|
T | TCCTC | 9 | a0001c0021t0002g0282a0001c0021t0002g0285a0007c0010t0010g0224others(6): Show | 9 | HG01109.hp1 HG02257.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1362+814_1362+817d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 38642608 | |||||
chr20:38642653
|
C | T | 1 | a0004c0011t0007g0292 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1362+845C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642653 | ||||||
chr20:38642714
|
ATCCATCC others(9): Show |
A | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(154): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1362+922_1362+937d others(18): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 38642714 | |||||
chr20:38642765
|
C | T | 5 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(2): Show | 6 | HG02630.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1363-939C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642765 | ||||||
chr20:38642911
|
C | T | 48 | a0001c0001t0005g0187a0001c0001t0005g0255a0001c0002t0004g0073others(45): Show | 54 | HG00642.hp2 HG01261.hp1 HG01516.hp2 others(51): Show |
intron_variant | MODIFIER | c.1363-793C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642911 | ||||||
chr20:38642939
|
G | C | 2 | a0012c0018t0004g0078a0012c0018t0004g0088 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1363-765G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642939 | ||||||
chr20:38642970
|
G | A | 3 | a0001c0001t0006g0083a0001c0001t0006g0091a0001c0001t0006g0092 | 3 | HG00738.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1363-734G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38642970 | ||||||
chr20:38643008
|
G | A | 12 | a0001c0007t0001g0189a0001c0007t0001g0243a0001c0007t0002g0037others(9): Show | 13 | HG02109.hp2 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1363-696G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643008 | ||||||
chr20:38643023
|
C | T | 1 | a0001c0002t0010g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1363-681C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643023 | ||||||
chr20:38643031
|
C | T | 13 | a0001c0002t0007g0007a0001c0002t0007g0011a0001c0002t0007g0044others(10): Show | 15 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1363-673C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643031 | ||||||
chr20:38643145
|
C | CAA | 6 | a0006c0009t0013g0042a0008c0013t0008g0028a0008c0013t0008g0303others(3): Show | 7 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1363-547_1363-546d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 38643145 | |||||
chr20:38643145
|
CA | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0226a0001c0002t0004g0033others(4): Show | 7 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1363-546delA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 38643145 | |||||
chr20:38643145
|
CAA | C | 149 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(146): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1363-547_1363-546d others(4): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 38643145 | |||||
chr20:38643145
|
CAAAA | C | 7 | a0007c0010t0010g0224a0007c0010t0010g0307a0007c0010t0012g0129others(4): Show | 7 | HG01109.hp1 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1363-549_1363-546d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 38643145 | |||||
chr20:38643223
|
T | C | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(212): Show | 237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1363-481T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643223 | ||||||
chr20:38643551
|
G | A | 6 | a0001c0001t0001g0146a0001c0001t0001g0170a0001c0001t0002g0003others(3): Show | 8 | HG01074.hp1 HG01192.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.1363-153G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643551 | ||||||
chr20:38643566
|
C | T | 35 | a0001c0001t0005g0187a0001c0001t0005g0255a0001c0002t0004g0073others(32): Show | 40 | HG00642.hp2 HG01261.hp1 HG01516.hp2 others(37): Show |
intron_variant | MODIFIER | c.1363-138C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643566 | ||||||
chr20:38643572
|
C | A | 1 | a0006c0009t0013g0042 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1363-132C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643572 | ||||||
chr20:38643657
|
G | A | 7 | a0001c0004t0004g0045a0004c0011t0004g0114a0004c0011t0004g0312others(4): Show | 8 | HG02559.hp1 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1363-47G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | chr20 | 38643657 | ||||||
chr20:38643946
|
G | A | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(154): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1569+36G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38643946 | ||||||
chr20:38644027
|
G | T | 1 | a0001c0002t0010g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1569+117G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644027 | ||||||
chr20:38644127
|
G | C | 5 | a0001c0001t0002g0013a0001c0001t0002g0049a0001c0001t0002g0079others(2): Show | 6 | HG02280.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1569+217G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644127 | ||||||
chr20:38644150
|
C | T | 4 | a0007c0010t0010g0224a0007c0010t0010g0307a0007c0010t0012g0129others(1): Show | 4 | HG01109.hp1 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569+240C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644150 | ||||||
chr20:38644326
|
A | C | 1 | a0001c0001t0001g0235 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1569+416A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644326 | ||||||
chr20:38644333
|
A | G | 1 | a0006c0009t0013g0042 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1569+423A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644333 | ||||||
chr20:38644389
|
T | C | 1 | a0006c0009t0013g0042 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1569+479T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644389 | ||||||
chr20:38644533
|
A | G | 1 | a0017c0034t0007g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1569+623A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644533 | ||||||
chr20:38644569
|
A | G | 58 | a0001c0001t0005g0187a0001c0001t0005g0255a0001c0002t0004g0073others(55): Show | 64 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(61): Show |
intron_variant | MODIFIER | c.1569+659A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644569 | ||||||
chr20:38644613
|
GTCACCCA others(5): Show |
G | 10 | a0001c0002t0004g0073a0001c0004t0004g0045a0001c0008t0004g0026others(7): Show | 12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1569+716_1569+727d others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr20 | 38644613 | |||||
chr20:38644636
|
A | C | 1 | a0015c0025t0004g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1569+726A>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644636 | ||||||
chr20:38644709
|
T | C | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(212): Show | 237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1569+799T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644709 | ||||||
chr20:38644888
|
T | C | 16 | a0001c0001t0005g0187a0001c0001t0005g0255a0001c0004t0016g0231others(13): Show | 18 | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.1569+978T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644888 | ||||||
chr20:38644925
|
T | TC | 10 | a0001c0002t0004g0073a0001c0004t0004g0045a0001c0008t0004g0026others(7): Show | 12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1569+1018dupC | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr20 | 38644925 | |||||
chr20:38644929
|
T | C | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(209): Show | 234 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1569+1019T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644929 | ||||||
chr20:38644931
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1569+1021T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38644931 | ||||||
chr20:38645149
|
C | CT | 34 | a0001c0001t0004g0050a0001c0001t0005g0219a0001c0001t0005g0254others(31): Show | 34 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.1570-886dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr20 | 38645149 | |||||
chr20:38645149
|
CT | C | 17 | a0001c0001t0003g0191a0001c0002t0004g0073a0001c0004t0004g0045others(14): Show | 20 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.1570-886delT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr20 | 38645149 | |||||
chr20:38645174
|
G | A | 1 | a0006c0026t0002g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1570-873G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645174 | ||||||
chr20:38645233
|
G | A | 1 | a0018c0031t0002g0290 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1570-814G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645233 | ||||||
chr20:38645267
|
T | C | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(212): Show | 237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1570-780T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645267 | ||||||
chr20:38645607
|
C | A | 7 | a0001c0007t0001g0189a0001c0007t0001g0243a0001c0007t0002g0037others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1570-440C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645607 | ||||||
chr20:38645663
|
C | A | 1 | a0001c0001t0003g0143 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1570-384C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645663 | ||||||
chr20:38645677
|
C | G | 216 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(213): Show | 238 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.1570-370C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645677 | ||||||
chr20:38645832
|
C | A | 49 | a0001c0001t0005g0187a0001c0001t0005g0236a0001c0001t0005g0255others(46): Show | 53 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.1570-215C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645832 | ||||||
chr20:38645916
|
C | CA | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(154): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1570-129dupA | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr20 | 38645916 | |||||
chr20:38645965
|
G | A | 10 | a0001c0002t0004g0073a0001c0004t0004g0045a0001c0008t0004g0026others(7): Show | 12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1570-82G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38645965 | ||||||
chr20:38646021
|
G | A | 1 | a0001c0004t0016g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1570-26G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | chr20 | 38646021 | ||||||
chr20:38646218
|
A | G | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(154): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1710+31A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646218 | ||||||
chr20:38646231
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1710+44A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646231 | ||||||
chr20:38646319
|
G | C | 5 | a0008c0013t0008g0028a0008c0013t0008g0303a0008c0017t0008g0046others(2): Show | 6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1710+132G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646319 | ||||||
chr20:38646359
|
C | A | 10 | a0001c0002t0004g0073a0001c0004t0004g0045a0001c0008t0004g0026others(7): Show | 12 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1710+172C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646359 | ||||||
chr20:38646447
|
C | T | 5 | a0008c0013t0008g0028a0008c0013t0008g0303a0008c0017t0008g0046others(2): Show | 6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1710+260C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646447 | ||||||
chr20:38646511
|
C | T | 19 | a0001c0002t0007g0007a0001c0002t0007g0011a0001c0002t0007g0044others(16): Show | 22 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1710+324C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646511 | ||||||
chr20:38646514
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0159 | 2 | HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1710+327G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646514 | ||||||
chr20:38646653
|
A | G | 2 | a0001c0002t0004g0306a0001c0002t0015g0274 | 2 | HG02071.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1711-304A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 12/14 | chr20 | 38646653 | ||||||
chr20:38647275
|
A | G | 1 | a0001c0001t0006g0302 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1880+149A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647275 | ||||||
chr20:38647290
|
C | T | 9 | a0001c0002t0008g0074a0006c0009t0013g0042a0008c0013t0008g0028others(6): Show | 10 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1880+164C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647290 | ||||||
chr20:38647374
|
CTGTTGGT others(1): Show |
C | 7 | a0001c0007t0001g0189a0001c0007t0001g0243a0001c0007t0002g0037others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1880+253_1880+260d others(10): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | 38647374 | |||||
chr20:38647375
|
TGTTG | T | 200 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(197): Show | 221 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.1880+253_1880+256d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | 38647375 | |||||
chr20:38647379
|
G | GGTTT | 4 | a0001c0001t0003g0232a0001c0001t0003g0272a0001c0002t0007g0007others(1): Show | 5 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1880+278_1880+281d others(6): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | 38647379 | |||||
chr20:38647379
|
G | T | 9 | a0001c0002t0010g0082a0001c0004t0016g0231a0003c0005t0001g0138others(6): Show | 10 | HG02109.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1880+253G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647379 | ||||||
chr20:38647557
|
A | AT | 33 | a0001c0001t0004g0050a0001c0001t0005g0219a0001c0001t0005g0254others(30): Show | 33 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1880+438dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | 38647557 | |||||
chr20:38647592
|
T | C | 216 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(213): Show | 238 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.1880+466T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647592 | ||||||
chr20:38647714
|
T | C | 3 | a0001c0002t0004g0073a0001c0008t0004g0026a0001c0008t0004g0309 | 4 | HG02258.hp1 HG02572.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1880+588T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647714 | ||||||
chr20:38647744
|
C | T | 17 | a0001c0002t0004g0073a0001c0004t0004g0045a0001c0007t0001g0189others(14): Show | 19 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1880+618C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647744 | ||||||
chr20:38647797
|
G | C | 17 | a0001c0001t0005g0187a0001c0001t0005g0236a0001c0001t0005g0255others(14): Show | 19 | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.1880+671G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647797 | ||||||
chr20:38647802
|
G | A | 26 | a0001c0001t0005g0187a0001c0001t0005g0236a0001c0001t0005g0255others(23): Show | 29 | HG00642.hp2 HG01261.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.1880+676G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647802 | ||||||
chr20:38647930
|
G | T | 1 | a0010c0012t0007g0098 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1881-713G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647930 | ||||||
chr20:38647992
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1881-651T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38647992 | ||||||
chr20:38648152
|
G | C | 13 | a0001c0002t0007g0007a0001c0002t0007g0011a0001c0002t0007g0044others(10): Show | 15 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1881-491G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648152 | ||||||
chr20:38648393
|
C | T | 4 | a0001c0004t0004g0045a0004c0011t0004g0114a0004c0011t0004g0312others(1): Show | 4 | HG02559.hp1 HG02630.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1881-250C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648393 | ||||||
chr20:38648455
|
C | T | 2 | a0006c0009t0013g0042a0019c0039t0013g0284 | 2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1881-188C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648455 | ||||||
chr20:38648499
|
G | T | 3 | a0007c0010t0010g0224a0007c0010t0010g0307a0007c0010t0012g0129 | 3 | HG01109.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1881-144G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648499 | ||||||
chr20:38648505
|
ATGC | A | 5 | a0008c0013t0008g0028a0008c0013t0008g0303a0008c0017t0008g0046others(2): Show | 6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1881-133_1881-131d others(5): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | 38648505 | |||||
chr20:38648510
|
G | T | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(208): Show | 232 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1881-133G>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648510 | ||||||
chr20:38648571
|
C | T | 3 | a0001c0002t0005g0203a0001c0002t0005g0206a0001c0002t0005g0215 | 3 | HG01069.hp1 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1881-72C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648571 | ||||||
chr20:38648613
|
G | GT | 10 | a0001c0001t0002g0084a0001c0002t0008g0074a0006c0009t0013g0042others(7): Show | 11 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1881-20dupT | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | 38648613 | |||||
chr20:38648622
|
T | C | 1 | a0001c0001t0003g0123 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1881-21T>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648622 | ||||||
chr20:38648626
|
C | T | 16 | a0001c0001t0005g0187a0001c0001t0005g0236a0001c0001t0005g0255others(13): Show | 18 | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.1881-17C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648626 | ||||||
chr20:38648628
|
C | T | 199 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(196): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.1881-15C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | chr20 | 38648628 | ||||||
chr20:38648733
|
G | C | 17 | a0001c0002t0004g0073a0001c0004t0004g0045a0001c0007t0001g0189others(14): Show | 19 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1936+35G>C | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38648733 | ||||||
chr20:38648758
|
A | G | 2 | a0001c0001t0003g0172a0001c0001t0006g0059 | 2 | NA19070.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1936+60A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38648758 | ||||||
chr20:38648920
|
G | A | 17 | a0001c0002t0004g0073a0001c0004t0004g0045a0001c0007t0001g0189others(14): Show | 19 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1936+222G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38648920 | ||||||
chr20:38648975
|
A | G | 233 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(230): Show | 257 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1936+277A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38648975 | ||||||
chr20:38649144
|
C | A | 9 | a0001c0002t0004g0073a0001c0004t0004g0045a0001c0008t0004g0026others(6): Show | 11 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1936+446C>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649144 | ||||||
chr20:38649269
|
C | T | 2 | a0005c0006t0002g0106a0005c0006t0002g0108 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1937-488C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649269 | ||||||
chr20:38649364
|
A | G | 6 | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(3): Show | 7 | HG02109.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1937-393A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649364 | ||||||
chr20:38649422
|
C | T | 5 | a0008c0013t0008g0028a0008c0013t0008g0303a0008c0017t0008g0046others(2): Show | 6 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1937-335C>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649422 | ||||||
chr20:38649464
|
A | T | 234 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(231): Show | 258 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1937-293A>T | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649464 | ||||||
chr20:38649480
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0275 | 3 | HG00140.hp2 HG01361.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1937-277G>A | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649480 | ||||||
chr20:38649542
|
C | G | 1 | a0017c0034t0007g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1937-215C>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649542 | ||||||
chr20:38649553
|
C | CG | 33 | a0001c0001t0004g0050a0001c0001t0005g0219a0001c0001t0005g0254others(30): Show | 33 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1937-204_1937-203i others(3): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649553 | ||||||
chr20:38649554
|
A | G | 312 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(309): Show | 346 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.1937-203A>G | ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 14/14 | chr20 | 38649554 |