geneid | 7984 |
---|---|
ensemblid | ENSG00000050327.15 |
hgncid | 13209 |
symbol | ARHGEF5 |
name | Rho guanine nucleotide exchange factor 5 |
refseq_nuc | NM_005435.4 |
refseq_prot | NP_005426.2 |
ensembl_nuc | ENST00000056217.10 |
ensembl_prot | ENSP00000056217.5 |
mane_status | MANE Select |
chr | chr7 |
start | 144355402 |
end | 144380632 |
strand | + |
ver | v1.2 |
region | chr7:144355402-144380632 |
region5000 | chr7:144350402-144385632 |
regionname0 | ARHGEF5_chr7_144355402_144380632 |
regionname5000 | ARHGEF5_chr7_144350402_144385632 |
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 | 1/0 | 1597 | 49 | 9 | 11 | 18 | 2 | 8 | 16 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0002 | 0/0 | 1597 | 47 | 1 | 15 | 24 | 1 | 6 | 13 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0003 | 0/1 | 1597 | 35 | 9 | 10 | 4 | 4 | 7 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0004 | 0/0 | 1597 | 25 | 1 | 11 | 2 | 4 | 7 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0005 | 0/0 | 1597 | 17 | 4 | 0 | 5 | 2 | 6 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0006 | 0/0 | 1597 | 17 | 2 | 1 | 11 | 2 | 1 | 9 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0007 | 0/0 | 1597 | 17 | 16 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0008 | 0/0 | 1597 | 11 | 9 | 1 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009 | 0/0 | 10 | 9 | 1 | 1 | 7 | 0 | 0 | 7 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0010 | 0/0 | 1597 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0011 | 0/0 | 1597 | 5 | 3 | 0 | 2 | 0 | 0 | 2 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0012 | 0/0 | 1597 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0013 | 0/0 | 1597 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0014 | 0/0 | 1597 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0015 | 0/0 | 817 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0016 | 0/0 | 817 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0017 | 0/0 | 1597 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0018 | 0/0 | 1597 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0019 | 0/0 | 817 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0020 | 0/0 | 1597 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0021 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0022 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0023 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0024 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0025 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0026 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0027 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0028 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0029 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0030 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0031 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0032 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0033 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0034 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0035 | 0/0 | 1597 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0036 | 0/0 | 817 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0037 | 0/0 | 817 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0038 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0039 | 0/0 | 1597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0040 | 0/0 | 1597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0041 | 0/0 | 1597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0042 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0043 | 0/0 | 817 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0044 | 0/0 | 817 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0045 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0046 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0047 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0048 | 0/0 | 1597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
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 | 0/0 | 4794 | 41 | 1 | 13 | 21 | 1 | 5 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0002 | 1/0 | 4794 | 37 | 3 | 10 | 16 | 2 | 5 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0003 | 0/0 | 4794 | 25 | 1 | 11 | 2 | 4 | 7 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0004 | 0/1 | 4794 | 25 | 1 | 8 | 4 | 4 | 7 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0005 | 0/0 | 4794 | 17 | 2 | 1 | 11 | 2 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0006 | 0/0 | 4794 | 17 | 4 | 0 | 5 | 2 | 6 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0007 | 0/0 | 4794 | 10 | 10 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0008 | 0/0 | 4794 | 10 | 8 | 1 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0009 | 0/0 | 4794 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0010 | 0/0 | 4794 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0011 | 0/0 | 4794 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0012 | 0/0 | 4794 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0013 | 0/0 | 4794 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0014 | 0/0 | 4794 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0015 | 0/0 | 4794 | 3 | 0 | 1 | 0 | 2 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0016 | 0/0 | 4794 | 3 | 0 | 1 | 1 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0017 | 0/0 | 4794 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0018 | 0/0 | 4794 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0019 | 0/0 | 4795 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0020 | 0/0 | 4794 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0021 | 0/0 | 4794 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0022 | 0/0 | 4794 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0023 | 0/0 | 4794 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0024 | 0/0 | 4795 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0025 | 0/0 | 4794 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0026 | 0/0 | 4816 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0027 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0028 | 0/0 | 4795 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0029 | 0/0 | 4795 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0030 | 0/0 | 4794 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0031 | 0/0 | 4795 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0032 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0033 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0034 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0035 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0036 | 0/0 | 4794 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0037 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0038 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0039 | 0/0 | 4794 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0040 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0041 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0042 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0043 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0044 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0045 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0046 | 0/0 | 4795 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0047 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0048 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0049 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0050 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0051 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0052 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0053 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0054 | 0/0 | 4795 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0055 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0056 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0057 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0058 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0059 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0060 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0061 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0062 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0063 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0064 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0065 | 0/0 | 4795 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0066 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0067 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0068 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0069 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0070 | 0/0 | 4816 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0071 | 0/0 | 4816 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0072 | 0/0 | 4816 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0073 | 0/0 | 4817 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0074 | 0/0 | 4816 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0075 | 0/0 | 4816 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
c0076 | 0/0 | 4816 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
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 | 689 | 162 | 31 | 32 | 66 | 10 | 23 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
t0002 | 1/1 | 689 | 112 | 34 | 28 | 26 | 7 | 15 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
t0003 | 0/0 | 689 | 11 | 11 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
t0004 | 0/0 | 689 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
t0005 | 0/0 | 689 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
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 | 16 | 1 | 6 | 5 | 0 | 4 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0002 | 0/0 | 13 | 2 | 4 | 1 | 3 | 3 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0003 | 0/0 | 12 | 0 | 7 | 4 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0004 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0007 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0008 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0009 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0011 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 1/0 | 4794 | 37 | 3 | 10 | 16 | 2 | 5 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0001c0010 | 0/0 | 4794 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0001c0020 | 0/0 | 4794 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0001c0021 | 0/0 | 4794 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0001c0036 | 0/0 | 4794 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0001c0039 | 0/0 | 4794 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0002c0001 | 0/0 | 4794 | 41 | 1 | 13 | 21 | 1 | 5 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0002c0016 | 0/0 | 4794 | 3 | 0 | 1 | 1 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0002c0061 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0002c0063 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0002c0064 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0003c0004 | 0/1 | 4794 | 25 | 1 | 8 | 4 | 4 | 7 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0003c0012 | 0/0 | 4794 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0003c0014 | 0/0 | 4794 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0003c0032 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0003c0047 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0004c0003 | 0/0 | 4794 | 25 | 1 | 11 | 2 | 4 | 7 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0005c0006 | 0/0 | 4794 | 17 | 4 | 0 | 5 | 2 | 6 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0006c0005 | 0/0 | 4794 | 17 | 2 | 1 | 11 | 2 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0007c0007 | 0/0 | 4794 | 10 | 10 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0007c0011 | 0/0 | 4794 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0007c0041 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0007c0042 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0008c0008 | 0/0 | 4794 | 10 | 8 | 1 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0008c0055 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0026 | 0/0 | 4816 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0070 | 0/0 | 4816 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0071 | 0/0 | 4816 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0072 | 0/0 | 4816 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0073 | 0/0 | 4817 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0074 | 0/0 | 4816 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0075 | 0/0 | 4816 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0076 | 0/0 | 4816 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0010c0009 | 0/0 | 4794 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0011c0023 | 0/0 | 4794 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0011c0043 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0011c0044 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0011c0045 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0012c0013 | 0/0 | 4794 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0013c0017 | 0/0 | 4794 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0014c0015 | 0/0 | 4794 | 3 | 0 | 1 | 0 | 2 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0015c0024 | 0/0 | 4795 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0016c0054 | 0/0 | 4795 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0016c0065 | 0/0 | 4795 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0017c0025 | 0/0 | 4794 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0018c0022 | 0/0 | 4794 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0019c0019 | 0/0 | 4795 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0020c0018 | 0/0 | 4794 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0021c0053 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0022c0058 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0023c0059 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0024c0057 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0025c0062 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0026c0060 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0027c0056 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0028c0052 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0029c0051 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0030c0050 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0031c0066 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0032c0067 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0033c0068 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0034c0027 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0035c0030 | 0/0 | 4794 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0036c0029 | 0/0 | 4795 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0037c0028 | 0/0 | 4795 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0038c0040 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0039c0038 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0040c0034 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0041c0037 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0042c0035 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0043c0031 | 0/0 | 4795 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0044c0046 | 0/0 | 4795 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0045c0033 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0046c0048 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0047c0049 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0048c0069 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002 | 1/0 | 5482 | 35 | 3 | 8 | 16 | 2 | 5 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0001c0002t0004 | 0/0 | 5482 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0001c0010t0002 | 0/0 | 5482 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0001c0020t0002 | 0/0 | 5482 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0001c0021t0002 | 0/0 | 5482 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0001c0036t0002 | 0/0 | 5482 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0001c0039t0002 | 0/0 | 5482 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0002c0001t0001 | 0/0 | 5482 | 41 | 1 | 13 | 21 | 1 | 5 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0002c0016t0001 | 0/0 | 5482 | 3 | 0 | 1 | 1 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0002c0061t0001 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0002c0063t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0002c0064t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0003c0004t0002 | 0/1 | 5482 | 24 | 1 | 8 | 4 | 3 | 7 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0003c0004t0005 | 0/0 | 5482 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0003c0012t0002 | 0/0 | 5482 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0003c0014t0002 | 0/0 | 5482 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0003c0032t0002 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0003c0047t0002 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0004c0003t0001 | 0/0 | 5482 | 25 | 1 | 11 | 2 | 4 | 7 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0005c0006t0001 | 0/0 | 5482 | 17 | 4 | 0 | 5 | 2 | 6 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0006c0005t0001 | 0/0 | 5482 | 17 | 2 | 1 | 11 | 2 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0007c0007t0003 | 0/0 | 5482 | 10 | 10 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0007c0011t0002 | 0/0 | 5482 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0007c0041t0001 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0007c0042t0001 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0008c0008t0001 | 0/0 | 5482 | 10 | 8 | 1 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0008c0055t0001 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0026t0001 | 0/0 | 5504 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0070t0001 | 0/0 | 5504 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0071t0001 | 0/0 | 5504 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0072t0001 | 0/0 | 5504 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0073t0001 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0074t0001 | 0/0 | 5504 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0075t0002 | 0/0 | 5504 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0009c0076t0001 | 0/0 | 5504 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0010c0009t0001 | 0/0 | 5482 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0011c0023t0002 | 0/0 | 5482 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0011c0043t0002 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0011c0044t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0011c0045t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0012c0013t0002 | 0/0 | 5482 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0013c0017t0001 | 0/0 | 5482 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0014c0015t0002 | 0/0 | 5482 | 3 | 0 | 1 | 0 | 2 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0015c0024t0001 | 0/0 | 5483 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0016c0054t0001 | 0/0 | 5483 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0016c0065t0001 | 0/0 | 5483 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0017c0025t0001 | 0/0 | 5482 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0018c0022t0002 | 0/0 | 5482 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0019c0019t0002 | 0/0 | 5483 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0020c0018t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0020c0018t0002 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0021c0053t0001 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0022c0058t0001 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0023c0059t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0024c0057t0001 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0025c0062t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0026c0060t0001 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0027c0056t0001 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0028c0052t0001 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0029c0051t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0030c0050t0001 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0031c0066t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0032c0067t0001 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0033c0068t0001 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0034c0027t0002 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0035c0030t0001 | 0/0 | 5482 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0036c0029t0001 | 0/0 | 5483 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0037c0028t0001 | 0/0 | 5483 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0038c0040t0002 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0039c0038t0002 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0040c0034t0002 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0041c0037t0002 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0042c0035t0002 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0043c0031t0003 | 0/0 | 5483 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0044c0046t0002 | 0/0 | 5483 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0045c0033t0002 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0046c0048t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0047c0049t0002 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
a0048c0069t0002 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | copy fasta | chr7 | 144350402 | 144385632 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002g0003 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0010t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0010t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0010t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0010t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0010t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0010t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0020t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0020t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0021t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0036t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0039t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0001 | 0/0 | 10 | 0 | 6 | 2 | 0 | 2 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0016t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0016t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0016t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0061t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0063t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0064t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0004 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0005g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0012t0002g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0012t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0014t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0014t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0032t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0047t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0002 | 0/0 | 12 | 1 | 4 | 1 | 3 | 3 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0007 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0006t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0005t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0005t0001g0009 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0005t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0005t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0005t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0011t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0011t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0041t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0042t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0055t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0026t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0026t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0070t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0071t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0072t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0073t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0074t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0075t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0076t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0010c0009t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0010c0009t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0010c0009t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0010c0009t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0010c0009t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0011c0023t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0011c0023t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0011c0043t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0011c0044t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0011c0045t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0012c0013t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0012c0013t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0012c0013t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0012c0013t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0013c0017t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0013c0017t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0013c0017t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0014c0015t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0014c0015t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0015c0024t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0015c0024t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0016c0054t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0016c0065t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0017c0025t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0018c0022t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0019c0019t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0019c0019t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0020c0018t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0020c0018t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0021c0053t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0022c0058t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0023c0059t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0024c0057t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0025c0062t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0026c0060t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0027c0056t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0028c0052t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0029c0051t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0030c0050t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0031c0066t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0032c0067t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0033c0068t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0034c0027t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0035c0030t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0036c0029t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0037c0028t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0038c0040t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0039c0038t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0040c0034t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0041c0037t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0042c0035t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0043c0031t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0044c0046t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0045c0033t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0046c0048t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0047c0049t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0048c0069t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0171 | EUR | GBR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00099 | hp2 | a0006 | c0005 | t0001 | g0009 | EUR | GBR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00140 | hp1 | a0003 | c0004 | t0002 | g0165 | EUR | GBR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00140 | hp2 | a0004 | c0003 | t0001 | g0002 | EUR | GBR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0172 | EUR | FIN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00280 | hp2 | a0004 | c0003 | t0001 | g0002 | EUR | FIN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00323 | hp1 | a0006 | c0005 | t0001 | g0161 | EUR | FIN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00323 | hp2 | a0004 | c0003 | t0001 | g0180 | EUR | FIN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00423 | hp1 | a0006 | c0005 | t0001 | g0008 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00423 | hp2 | a0019 | c0019 | t0002 | g0005 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00438 | hp2 | a0002 | c0001 | t0001 | g0088 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00544 | hp1 | a0005 | c0006 | t0001 | g0028 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00544 | hp2 | a0002 | c0001 | t0001 | g0091 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00558 | hp1 | a0002 | c0001 | t0001 | g0090 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00558 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00597 | hp1 | a0013 | c0017 | t0001 | g0163 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00597 | hp2 | a0024 | c0057 | t0001 | g0028 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00621 | hp1 | a0002 | c0001 | t0001 | g0110 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00621 | hp2 | a0005 | c0006 | t0001 | g0099 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00639 | hp1 | a0004 | c0003 | t0001 | g0002 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00639 | hp2 | a0018 | c0022 | t0002 | g0031 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00642 | hp1 | a0004 | c0003 | t0001 | g0041 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00642 | hp2 | a0039 | c0038 | t0002 | g0032 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00673 | hp1 | a0030 | c0050 | t0001 | g0027 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00673 | hp2 | a0031 | c0066 | t0001 | g0001 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00735 | hp1 | a0008 | c0008 | t0001 | g0030 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00735 | hp2 | a0001 | c0020 | t0002 | g0143 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00741 | hp1 | a0002 | c0061 | t0001 | g0093 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00741 | hp2 | a0044 | c0046 | t0002 | g0015 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01069 | hp1 | a0017 | c0025 | t0001 | g0009 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01071 | hp1 | a0006 | c0005 | t0001 | g0025 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01071 | hp2 | a0017 | c0025 | t0001 | g0009 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01074 | hp1 | a0003 | c0004 | t0002 | g0004 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01074 | hp2 | a0040 | c0034 | t0002 | g0173 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01099 | hp1 | a0014 | c0015 | t0002 | g0004 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01099 | hp2 | a0018 | c0022 | t0002 | g0031 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01167 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01167 | hp2 | a0004 | c0003 | t0001 | g0043 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01168 | hp1 | a0003 | c0004 | t0002 | g0015 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01168 | hp2 | a0002 | c0001 | t0001 | g0029 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01169 | hp1 | a0002 | c0001 | t0001 | g0029 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01169 | hp2 | a0001 | c0002 | t0004 | g0003 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01192 | hp1 | a0002 | c0001 | t0001 | g0104 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01192 | hp2 | a0003 | c0004 | t0002 | g0011 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01243 | hp1 | a0019 | c0019 | t0002 | g0003 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01243 | hp2 | a0004 | c0003 | t0001 | g0040 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01255 | hp1 | a0002 | c0001 | t0001 | g0012 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01255 | hp2 | a0003 | c0032 | t0002 | g0059 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01256 | hp1 | a0003 | c0004 | t0002 | g0004 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01258 | hp1 | a0003 | c0004 | t0002 | g0004 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01258 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01261 | hp1 | a0003 | c0004 | t0002 | g0058 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01261 | hp2 | a0003 | c0047 | t0002 | g0004 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01346 | hp2 | a0004 | c0003 | t0001 | g0002 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01361 | hp1 | a0004 | c0003 | t0001 | g0002 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01361 | hp2 | a0048 | c0069 | t0002 | g0166 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01433 | hp1 | a0003 | c0004 | t0002 | g0021 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01433 | hp2 | a0004 | c0003 | t0001 | g0002 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01496 | hp1 | a0009 | c0071 | t0001 | g0182 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01496 | hp2 | a0004 | c0003 | t0001 | g0154 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01515 | hp1 | a0014 | c0015 | t0002 | g0004 | EUR | IBS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01515 | hp2 | a0002 | c0001 | t0001 | g0086 | EUR | IBS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01516 | hp1 | a0003 | c0004 | t0002 | g0018 | EUR | IBS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01516 | hp2 | a0005 | c0006 | t0001 | g0083 | EUR | IBS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01517 | hp1 | a0014 | c0015 | t0002 | g0019 | EUR | IBS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01517 | hp2 | a0005 | c0006 | t0001 | g0007 | EUR | IBS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01884 | hp1 | a0012 | c0013 | t0002 | g0122 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01884 | hp2 | a0009 | c0076 | t0001 | g0047 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01891 | hp1 | a0007 | c0007 | t0003 | g0034 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01891 | hp2 | a0008 | c0008 | t0001 | g0116 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01928 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01934 | hp1 | a0003 | c0004 | t0002 | g0066 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01934 | hp2 | a0002 | c0016 | t0001 | g0105 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01975 | hp1 | a0002 | c0001 | t0001 | g0100 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01975 | hp2 | a0041 | c0037 | t0002 | g0145 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01993 | hp1 | a0004 | c0003 | t0001 | g0181 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01993 | hp2 | a0002 | c0001 | t0001 | g0095 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02004 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0148 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02015 | hp1 | a0004 | c0003 | t0001 | g0002 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02015 | hp2 | a0006 | c0005 | t0001 | g0084 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02027 | hp1 | a0038 | c0040 | t0002 | g0003 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02027 | hp2 | a0002 | c0001 | t0001 | g0042 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02040 | hp1 | a0042 | c0035 | t0002 | g0146 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02040 | hp2 | a0002 | c0064 | t0001 | g0071 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02074 | hp1 | a0013 | c0017 | t0001 | g0112 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02083 | hp1 | a0003 | c0004 | t0002 | g0167 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02083 | hp2 | a0002 | c0001 | t0001 | g0024 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02132 | hp1 | a0023 | c0059 | t0001 | g0080 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02132 | hp2 | a0002 | c0001 | t0001 | g0042 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02135 | hp1 | a0005 | c0006 | t0001 | g0070 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02135 | hp2 | a0020 | c0018 | t0001 | g0156 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02145 | hp1 | a0003 | c0004 | t0002 | g0060 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02145 | hp2 | a0001 | c0010 | t0002 | g0130 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02148 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02148 | hp2 | a0007 | c0042 | t0001 | g0179 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02165 | hp1 | a0003 | c0004 | t0002 | g0063 | EAS | CDX | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02165 | hp2 | a0013 | c0017 | t0001 | g0113 | EAS | CDX | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02258 | hp1 | a0007 | c0011 | t0002 | g0010 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02258 | hp2 | a0001 | c0010 | t0002 | g0121 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02273 | hp1 | a0002 | c0001 | t0001 | g0186 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02293 | hp1 | a0004 | c0003 | t0001 | g0041 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02293 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02300 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02451 | hp1 | a0003 | c0012 | t0002 | g0006 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02451 | hp2 | a0032 | c0067 | t0001 | g0178 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02622 | hp1 | a0005 | c0006 | t0001 | g0096 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02622 | hp2 | a0007 | c0007 | t0003 | g0014 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02630 | hp1 | a0005 | c0006 | t0001 | g0008 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02630 | hp2 | a0007 | c0007 | t0003 | g0119 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02647 | hp1 | a0007 | c0007 | t0003 | g0014 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02647 | hp2 | a0020 | c0018 | t0002 | g0061 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02683 | hp1 | a0006 | c0005 | t0001 | g0159 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02698 | hp1 | a0004 | c0003 | t0001 | g0002 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02698 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02723 | hp1 | a0007 | c0007 | t0003 | g0033 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02723 | hp2 | a0045 | c0033 | t0002 | g0135 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02735 | hp1 | a0004 | c0003 | t0001 | g0170 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02735 | hp2 | a0001 | c0020 | t0002 | g0141 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02738 | hp1 | a0036 | c0029 | t0001 | g0001 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02738 | hp2 | a0003 | c0004 | t0002 | g0021 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02809 | hp1 | a0003 | c0014 | t0002 | g0022 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02809 | hp2 | a0011 | c0043 | t0002 | g0062 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02818 | hp1 | a0007 | c0011 | t0002 | g0010 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02818 | hp2 | a0007 | c0007 | t0003 | g0014 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02886 | hp1 | a0006 | c0005 | t0001 | g0009 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02886 | hp2 | a0003 | c0014 | t0002 | g0020 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02895 | hp1 | a0005 | c0006 | t0001 | g0109 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02895 | hp2 | a0008 | c0008 | t0001 | g0026 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02897 | hp1 | a0008 | c0008 | t0001 | g0026 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02897 | hp2 | a0010 | c0009 | t0001 | g0017 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02922 | hp2 | a0011 | c0023 | t0002 | g0067 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02965 | hp1 | a0010 | c0009 | t0001 | g0054 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02965 | hp2 | a0003 | c0012 | t0002 | g0006 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02970 | hp1 | a0007 | c0011 | t0002 | g0164 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02970 | hp2 | a0012 | c0013 | t0002 | g0125 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02976 | hp1 | a0007 | c0007 | t0003 | g0124 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02976 | hp2 | a0021 | c0053 | t0001 | g0118 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03017 | hp1 | a0005 | c0006 | t0001 | g0081 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03017 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03041 | hp1 | a0006 | c0005 | t0001 | g0069 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03041 | hp2 | a0001 | c0010 | t0002 | g0132 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03130 | hp2 | a0007 | c0007 | t0003 | g0123 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03139 | hp1 | a0008 | c0008 | t0001 | g0039 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03139 | hp2 | a0005 | c0006 | t0001 | g0097 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03195 | hp1 | a0008 | c0008 | t0001 | g0039 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03195 | hp2 | a0007 | c0011 | t0002 | g0010 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03209 | hp1 | a0022 | c0058 | t0001 | g0098 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03209 | hp2 | a0003 | c0012 | t0002 | g0006 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03239 | hp1 | a0003 | c0004 | t0002 | g0019 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03239 | hp2 | a0005 | c0006 | t0001 | g0007 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03453 | hp1 | a0010 | c0009 | t0001 | g0017 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03453 | hp2 | a0003 | c0012 | t0002 | g0065 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03486 | hp1 | a0012 | c0013 | t0002 | g0127 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03486 | hp2 | a0007 | c0007 | t0003 | g0033 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03490 | hp1 | a0005 | c0006 | t0001 | g0007 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03490 | hp2 | a0004 | c0003 | t0001 | g0040 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03491 | hp1 | a0005 | c0006 | t0001 | g0101 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03491 | hp2 | a0003 | c0004 | t0002 | g0023 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03492 | hp1 | a0005 | c0006 | t0001 | g0007 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03492 | hp2 | a0003 | c0004 | t0002 | g0023 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03516 | hp1 | a0037 | c0028 | t0001 | g0053 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03516 | hp2 | a0004 | c0003 | t0001 | g0002 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03540 | hp1 | a0008 | c0008 | t0001 | g0160 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03540 | hp2 | a0007 | c0011 | t0002 | g0010 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0128 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03579 | hp2 | a0001 | c0010 | t0002 | g0120 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03669 | hp1 | a0001 | c0036 | t0002 | g0003 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03669 | hp2 | a0035 | c0030 | t0001 | g0001 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0139 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03704 | hp2 | a0004 | c0003 | t0001 | g0155 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03710 | hp1 | a0003 | c0004 | t0002 | g0018 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03710 | hp2 | a0004 | c0003 | t0001 | g0169 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03831 | hp1 | a0002 | c0001 | t0001 | g0078 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03831 | hp2 | a0004 | c0003 | t0001 | g0002 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03834 | hp1 | a0003 | c0004 | t0002 | g0044 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0134 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03927 | hp1 | a0005 | c0006 | t0001 | g0108 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03927 | hp2 | a0016 | c0065 | t0001 | g0157 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0142 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG04184 | hp2 | a0001 | c0039 | t0002 | g0016 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG04204 | hp1 | a0003 | c0004 | t0002 | g0004 | SAS | STU | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG04204 | hp2 | a0002 | c0016 | t0001 | g0074 | SAS | STU | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG04228 | hp1 | a0002 | c0001 | t0001 | g0102 | SAS | STU | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | STU | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18522 | hp1 | a0007 | c0007 | t0003 | g0133 | AFR | YRI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18522 | hp2 | a0010 | c0009 | t0001 | g0055 | AFR | YRI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18612 | hp1 | a0003 | c0004 | t0002 | g0064 | EAS | CHB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18612 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | CHB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18747 | hp1 | a0005 | c0006 | t0001 | g0094 | EAS | CHB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18747 | hp2 | a0002 | c0001 | t0001 | g0087 | EAS | CHB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18906 | hp1 | a0007 | c0041 | t0001 | g0002 | AFR | YRI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18906 | hp2 | a0034 | c0027 | t0002 | g0056 | AFR | YRI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18939 | hp2 | a0002 | c0001 | t0001 | g0111 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18941 | hp2 | a0006 | c0005 | t0001 | g0103 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18944 | hp1 | a0002 | c0001 | t0001 | g0107 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18944 | hp2 | a0027 | c0056 | t0001 | g0079 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18945 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18951 | hp1 | a0009 | c0075 | t0002 | g0183 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18951 | hp2 | a0011 | c0045 | t0001 | g0151 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18962 | hp1 | a0025 | c0062 | t0001 | g0024 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18964 | hp1 | a0046 | c0048 | t0001 | g0153 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18970 | hp1 | a0029 | c0051 | t0001 | g0185 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18970 | hp2 | a0001 | c0021 | t0002 | g0038 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18971 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18977 | hp1 | a0009 | c0026 | t0001 | g0046 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18977 | hp2 | a0015 | c0024 | t0001 | g0092 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18982 | hp2 | a0002 | c0063 | t0001 | g0076 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18985 | hp1 | a0009 | c0073 | t0001 | g0049 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18985 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18986 | hp1 | a0002 | c0001 | t0001 | g0073 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18986 | hp2 | a0009 | c0070 | t0001 | g0184 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18990 | hp1 | a0002 | c0016 | t0001 | g0176 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18990 | hp2 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18999 | hp1 | a0006 | c0005 | t0001 | g0001 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18999 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19000 | hp2 | a0002 | c0001 | t0001 | g0077 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19001 | hp1 | a0003 | c0004 | t0002 | g0011 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19001 | hp2 | a0006 | c0005 | t0001 | g0085 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19002 | hp1 | a0004 | c0003 | t0001 | g0043 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19002 | hp2 | a0006 | c0005 | t0001 | g0001 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19010 | hp1 | a0002 | c0001 | t0001 | g0082 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19011 | hp1 | a0006 | c0005 | t0001 | g0115 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19012 | hp1 | a0033 | c0068 | t0001 | g0152 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19012 | hp2 | a0009 | c0074 | t0001 | g0048 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19030 | hp1 | a0028 | c0052 | t0001 | g0008 | AFR | LWK | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19030 | hp2 | a0008 | c0008 | t0001 | g0162 | AFR | LWK | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19055 | hp1 | a0009 | c0026 | t0001 | g0050 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19057 | hp1 | a0006 | c0005 | t0001 | g0013 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19065 | hp1 | a0006 | c0005 | t0001 | g0013 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19065 | hp2 | a0001 | c0021 | t0002 | g0038 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19083 | hp1 | a0015 | c0024 | t0001 | g0089 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19083 | hp2 | a0026 | c0060 | t0001 | g0177 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19084 | hp1 | a0009 | c0072 | t0001 | g0051 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19084 | hp2 | a0011 | c0044 | t0001 | g0150 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19088 | hp1 | a0005 | c0006 | t0001 | g0027 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19088 | hp2 | a0006 | c0005 | t0001 | g0013 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19091 | hp1 | a0006 | c0005 | t0001 | g0025 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19240 | hp1 | a0012 | c0013 | t0002 | g0126 | AFR | YRI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19240 | hp2 | a0043 | c0031 | t0003 | g0034 | AFR | YRI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20129 | hp1 | a0010 | c0009 | t0001 | g0057 | AFR | ASW | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20129 | hp2 | a0003 | c0014 | t0002 | g0020 | AFR | ASW | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20752 | hp1 | a0008 | c0008 | t0001 | g0158 | EUR | TSI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20752 | hp2 | a0003 | c0004 | t0005 | g0011 | EUR | TSI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20805 | hp1 | a0003 | c0004 | t0002 | g0015 | EUR | TSI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20805 | hp2 | a0004 | c0003 | t0001 | g0002 | EUR | TSI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20905 | hp1 | a0002 | c0001 | t0001 | g0045 | SAS | GIH | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20905 | hp2 | a0004 | c0003 | t0001 | g0002 | SAS | GIH | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01123 | hp1 | a0004 | c0003 | t0001 | g0168 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02109 | hp1 | a0001 | c0010 | t0002 | g0032 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02109 | hp2 | a0016 | c0054 | t0001 | g0030 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02486 | hp1 | a0003 | c0012 | t0002 | g0006 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02486 | hp2 | a0002 | c0001 | t0001 | g0008 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03471 | hp1 | a0008 | c0008 | t0001 | g0117 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03471 | hp2 | a0011 | c0023 | t0002 | g0068 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG06807 | hp1 | a0010 | c0009 | t0001 | g0052 | AFR | USA | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG06807 | hp2 | a0008 | c0055 | t0001 | g0001 | AFR | USA | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18955 | hp1 | a0002 | c0001 | t0001 | g0072 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18955 | hp2 | a0002 | c0001 | t0001 | g0175 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA21309 | hp1 | a0047 | c0049 | t0002 | g0022 | AFR | LWK | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA21309 | hp2 | a0001 | c0010 | t0002 | g0131 | AFR | LWK | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
homoSapiens_chm13v2 | hp1 | a0003 | c0004 | t0002 | g0129 | REF | REF | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0136 | REF | REF | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:144362670
|
A | ATGGAGGC others(15): Show |
1 | a0009 | 9 | HG01496.hp1 HG01884.hp2 NA18951.hp1 others(6): Show |
frameshift_variant&stop_gained | HIGH | c.7_28dupGCTGAGGAGGC others(11): Show |
p.Ala10fs | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 141/5482 | 29/4794 | 10/1597 | INFO_REALIGN_3_PRIME | chr7 | 144362670 | |
chr7:144362742
|
G | A | 1 | a0020 | 2 | HG02135.hp2 HG02647.hp2 |
missense_variant | MODERATE | c.73G>A | p.Glu25Lys | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 185/5482 | 73/4794 | 25/1597 | chr7 | 144362742 | ||
chr7:144362991
|
C | T | 1 | a0048 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.322C>T | p.Pro108Ser | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 434/5482 | 322/4794 | 108/1597 | chr7 | 144362991 | ||
chr7:144363042
|
T | C | 1 | a0012 | 4 | HG01884.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
missense_variant | MODERATE | c.373T>C | p.Trp125Arg | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 485/5482 | 373/4794 | 125/1597 | chr7 | 144363042 | ||
chr7:144363102
|
A | G | 22 | a0002a0005a0006others(19): Show | 116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
missense_variant | MODERATE | c.433A>G | p.Ser145Gly | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 545/5482 | 433/4794 | 145/1597 | chr7 | 144363102 | ||
chr7:144363193
|
A | G | 3 | a0033a0046a0047 | 3 | NA18964.hp1 NA19012.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.524A>G | p.Asp175Gly | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 636/5482 | 524/4794 | 175/1597 | chr7 | 144363193 | ||
chr7:144363264
|
T | G | 25 | a0002a0005a0006others(22): Show | 124 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(121): Show |
missense_variant | MODERATE | c.595T>G | p.Ser199Ala | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 707/5482 | 595/4794 | 199/1597 | chr7 | 144363264 | ||
chr7:144363303
|
C | T | 25 | a0002a0005a0006others(22): Show | 124 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(121): Show |
missense_variant | MODERATE | c.634C>T | p.Pro212Ser | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 746/5482 | 634/4794 | 212/1597 | chr7 | 144363303 | ||
chr7:144363352
|
A | C | 1 | a0013 | 3 | HG00597.hp1 HG02074.hp1 HG02165.hp2 |
missense_variant | MODERATE | c.683A>C | p.Gln228Pro | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 795/5482 | 683/4794 | 228/1597 | chr7 | 144363352 | ||
chr7:144363488
|
G | C | 1 | a0031 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.819G>C | p.Lys273Asn | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 931/5482 | 819/4794 | 273/1597 | chr7 | 144363488 | ||
chr7:144363594
|
G | A | 2 | a0029a0030 | 2 | HG00673.hp1 NA18970.hp1 |
missense_variant | MODERATE | c.925G>A | p.Asp309Asn | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1037/5482 | 925/4794 | 309/1597 | chr7 | 144363594 | ||
chr7:144363606
|
A | C | 1 | a0017 | 2 | HG01069.hp1 HG01071.hp2 |
missense_variant | MODERATE | c.937A>C | p.Lys313Gln | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1049/5482 | 937/4794 | 313/1597 | chr7 | 144363606 | ||
chr7:144363647
|
G | C | 1 | a0028 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.978G>C | p.Arg326Ser | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1090/5482 | 978/4794 | 326/1597 | chr7 | 144363647 | ||
chr7:144363709
|
C | T | 1 | a0009 | 7 | HG01496.hp1 HG01884.hp2 NA18951.hp1 others(4): Show |
missense_variant | MODERATE | c.1040C>T | p.Thr347Ile | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1152/5482 | 1040/4794 | 347/1597 | chr7 | 144363709 | ||
chr7:144363729
|
G | A | 1 | a0045 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1060G>A | p.Glu354Lys | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1172/5482 | 1060/4794 | 354/1597 | chr7 | 144363729 | ||
chr7:144363954
|
A | G | 32 | a0002a0003a0005others(29): Show | 172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
missense_variant | MODERATE | c.1285A>G | p.Met429Val | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1397/5482 | 1285/4794 | 429/1597 | chr7 | 144363954 | ||
chr7:144364024
|
C | T | 1 | a0020 | 2 | HG02135.hp2 HG02647.hp2 |
missense_variant | MODERATE | c.1355C>T | p.Ser452Leu | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1467/5482 | 1355/4794 | 452/1597 | chr7 | 144364024 | ||
chr7:144364111
|
A | G | 5 | a0003a0014a0034others(2): Show | 41 | HG00140.hp1 HG00741.hp2 HG01074.hp1 others(38): Show |
missense_variant | MODERATE | c.1442A>G | p.Gln481Arg | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1554/5482 | 1442/4794 | 481/1597 | chr7 | 144364111 | ||
chr7:144364129
|
A | G | 36 | a0002a0003a0004others(33): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
missense_variant | MODERATE | c.1460A>G | p.Glu487Gly | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1572/5482 | 1460/4794 | 487/1597 | chr7 | 144364129 | ||
chr7:144364321
|
G | A | 1 | a0009 | 2 | NA18985.hp1 NA19012.hp2 |
missense_variant | MODERATE | c.1652G>A | p.Arg551His | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1764/5482 | 1652/4794 | 551/1597 | chr7 | 144364321 | ||
chr7:144364393
|
C | A | 1 | a0004 | 25 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(22): Show |
missense_variant | MODERATE | c.1724C>A | p.Pro575Gln | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1836/5482 | 1724/4794 | 575/1597 | chr7 | 144364393 | ||
chr7:144364407
|
G | T | 16 | a0002a0005a0013others(13): Show | 81 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(78): Show |
missense_variant | MODERATE | c.1738G>T | p.Gly580Cys | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1850/5482 | 1738/4794 | 580/1597 | chr7 | 144364407 | ||
chr7:144364479
|
A | C | 1 | a0038 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1810A>C | p.Ser604Arg | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1922/5482 | 1810/4794 | 604/1597 | chr7 | 144364479 | ||
chr7:144364514
|
G | C | 13 | a0005a0008a0010others(10): Show | 47 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(44): Show |
missense_variant | MODERATE | c.1845G>C | p.Gln615His | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1957/5482 | 1845/4794 | 615/1597 | chr7 | 144364514 | ||
chr7:144364839
|
C | T | 1 | a0032 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.2170C>T | p.Pro724Ser | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2282/5482 | 2170/4794 | 724/1597 | chr7 | 144364839 | ||
chr7:144365046
|
T | A | 1 | a0026 | 1 | NA19083.hp2 | missense_variant | MODERATE | c.2377T>A | p.Ser793Thr | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2489/5482 | 2377/4794 | 793/1597 | chr7 | 144365046 | ||
chr7:144365108
|
A | AC | 14 | a0009a0015a0016others(11): Show | 17 | HG00423.hp2 HG00597.hp2 HG00673.hp1 others(14): Show |
frameshift_variant | HIGH | c.2444dupC | p.Thr816fs | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2557/5482 | 2445/4794 | 815/1597 | INFO_REALIGN_3_PRIME | chr7 | 144365108 | |
chr7:144365112
|
C | G | 2 | a0018a0039 | 3 | HG00639.hp2 HG00642.hp2 HG01099.hp2 |
missense_variant | MODERATE | c.2443C>G | p.Pro815Ala | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2555/5482 | 2443/4794 | 815/1597 | chr7 | 144365112 | ||
chr7:144365322
|
T | C | 1 | a0040 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.2653T>C | p.Trp885Arg | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2765/5482 | 2653/4794 | 885/1597 | chr7 | 144365322 | ||
chr7:144365350
|
G | T | 1 | a0023 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.2681G>T | p.Gly894Val | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2793/5482 | 2681/4794 | 894/1597 | chr7 | 144365350 | ||
chr7:144365352
|
C | T | 1 | a0041 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.2683C>T | p.Arg895Cys | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2795/5482 | 2683/4794 | 895/1597 | chr7 | 144365352 | ||
chr7:144365490
|
T | G | 1 | a0026 | 1 | NA19083.hp2 | missense_variant | MODERATE | c.2821T>G | p.Trp941Gly | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2933/5482 | 2821/4794 | 941/1597 | chr7 | 144365490 | ||
chr7:144365539
|
C | G | 1 | a0009 | 1 | HG01884.hp2 | stop_gained | HIGH | c.2870C>G | p.Ser957* | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2982/5482 | 2870/4794 | 957/1597 | chr7 | 144365539 | ||
chr7:144365640
|
C | G | 1 | a0014 | 3 | HG01099.hp1 HG01515.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.2971C>G | p.Pro991Ala | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 3083/5482 | 2971/4794 | 991/1597 | chr7 | 144365640 | ||
chr7:144365641
|
C | A | 1 | a0014 | 3 | HG01099.hp1 HG01515.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.2972C>A | p.Pro991Gln | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 3084/5482 | 2972/4794 | 991/1597 | chr7 | 144365641 | ||
chr7:144365751
|
G | T | 1 | a0039 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.3082G>T | p.Gly1028Trp | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 3194/5482 | 3082/4794 | 1028/1597 | chr7 | 144365751 | ||
chr7:144367261
|
T | C | 1 | a0045 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.3437T>C | p.Met1146Thr | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/15 | 3549/5482 | 3437/4794 | 1146/1597 | chr7 | 144367261 | ||
chr7:144367296
|
G | A | 1 | a0022 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.3472G>A | p.Val1158Met | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/15 | 3584/5482 | 3472/4794 | 1158/1597 | chr7 | 144367296 | ||
chr7:144371236
|
T | A | 1 | a0042 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.3607T>A | p.Ser1203Thr | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 6/15 | 3719/5482 | 3607/4794 | 1203/1597 | chr7 | 144371236 | ||
chr7:144379913
|
G | A | 1 | a0025 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.4651G>A | p.Val1551Met | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 15/15 | 4763/5482 | 4651/4794 | 1551/1597 | chr7 | 144379913 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:144363275
|
G | A | 2 | a0007c0007a0043c0031 | 11 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
synonymous_variant | LOW | c.606G>A | p.Gly202Gly | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 718/5482 | 606/4794 | 202/1597 | chr7 | 144363275 | ||
chr7:144363476
|
G | A | 29 | a0002c0001a0002c0016a0002c0061others(26): Show | 122 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
synonymous_variant | LOW | c.807G>A | p.Lys269Lys | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 919/5482 | 807/4794 | 269/1597 | chr7 | 144363476 | ||
chr7:144363575
|
C | T | 1 | a0002c0064 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.906C>T | p.Asp302Asp | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1018/5482 | 906/4794 | 302/1597 | chr7 | 144363575 | ||
chr7:144363677
|
T | C | 36 | a0001c0010a0002c0001a0002c0016others(33): Show | 134 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(131): Show |
synonymous_variant | LOW | c.1008T>C | p.Asn336Asn | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1120/5482 | 1008/4794 | 336/1597 | chr7 | 144363677 | ||
chr7:144363953
|
C | T | 5 | a0003c0004a0003c0032a0003c0047others(2): Show | 31 | HG00140.hp1 HG00741.hp2 HG01074.hp1 others(28): Show |
synonymous_variant | LOW | c.1284C>T | p.Leu428Leu | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1396/5482 | 1284/4794 | 428/1597 | chr7 | 144363953 | ||
chr7:144364026
|
C | T | 2 | a0004c0003a0007c0042 | 26 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(23): Show |
synonymous_variant | LOW | c.1357C>T | p.Leu453Leu | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1469/5482 | 1357/4794 | 453/1597 | chr7 | 144364026 | ||
chr7:144364436
|
G | A | 2 | a0004c0003a0007c0041 | 26 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(23): Show |
synonymous_variant | LOW | c.1767G>A | p.Pro589Pro | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1879/5482 | 1767/4794 | 589/1597 | chr7 | 144364436 | ||
chr7:144364691
|
A | G | 1 | a0001c0039 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.2022A>G | p.Gln674Gln | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2134/5482 | 2022/4794 | 674/1597 | chr7 | 144364691 | ||
chr7:144365369
|
G | A | 1 | a0002c0061 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.2700G>A | p.Pro900Pro | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2812/5482 | 2700/4794 | 900/1597 | chr7 | 144365369 | ||
chr7:144365498
|
G | A | 1 | a0032c0067 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.2829G>A | p.Pro943Pro | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2941/5482 | 2829/4794 | 943/1597 | chr7 | 144365498 | ||
chr7:144365546
|
C | T | 2 | a0003c0047a0014c0015 | 4 | HG01099.hp1 HG01261.hp2 HG01515.hp1 others(1): Show |
synonymous_variant | LOW | c.2877C>T | p.His959His | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2989/5482 | 2877/4794 | 959/1597 | chr7 | 144365546 | ||
chr7:144365600
|
C | G | 3 | a0001c0021a0011c0044a0011c0045 | 4 | NA18951.hp2 NA18970.hp2 NA19065.hp2 others(1): Show |
synonymous_variant | LOW | c.2931C>G | p.Ala977Ala | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 3043/5482 | 2931/4794 | 977/1597 | chr7 | 144365600 | ||
chr7:144373245
|
A | G | 48 | a0001c0020a0002c0001a0002c0061others(45): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(177): Show |
synonymous_variant | LOW | c.4101A>G | p.Glu1367Glu | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/15 | 4213/5482 | 4101/4794 | 1367/1597 | chr7 | 144373245 | ||
chr7:144374740
|
G | A | 1 | a0001c0036 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.4149G>A | p.Pro1383Pro | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 11/15 | 4261/5482 | 4149/4794 | 1383/1597 | chr7 | 144374740 | ||
chr7:144375547
|
C | T | 1 | a0008c0055 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.4332C>T | p.Pro1444Pro | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/15 | 4444/5482 | 4332/4794 | 1444/1597 | chr7 | 144375547 | ||
chr7:144379966
|
C | T | 1 | a0007c0011 | 5 | HG02258.hp1 HG02818.hp1 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.4704C>T | p.Phe1568Phe | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 15/15 | 4816/5482 | 4704/4794 | 1568/1597 | chr7 | 144379966 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:144380074
|
T | A | 1 | a0001c0002t0004 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*18T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 15/15 | 18 | chr7 | 144380074 | |||||
chr7:144380078
|
G | A | 2 | a0007c0007t0003a0043c0031t0003 | 11 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*22G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 15/15 | 22 | chr7 | 144380078 | |||||
chr7:144380496
|
C | T | 1 | a0003c0004t0005 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 15/15 | 440 | chr7 | 144380496 | |||||
chr7:144380523
|
T | C | 47 | a0002c0001t0001a0002c0016t0001a0002c0061t0001others(44): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*467T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 15/15 | 467 | chr7 | 144380523 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:144355651
|
G | T | 5 | a0002c0001t0001g0186a0009c0070t0001g0184a0009c0071t0001g0182others(2): Show | 5 | HG01496.hp1 HG02273.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+150G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144355651 | ||||||
chr7:144355660
|
C | G | 4 | a0004c0003t0001g0043a0004c0003t0001g0180a0004c0003t0001g0181others(1): Show | 5 | HG00323.hp2 HG01167.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+159C>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144355660 | ||||||
chr7:144355971
|
T | G | 1 | a0003c0004t0002g0044 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-13+470T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144355971 | ||||||
chr7:144355998
|
T | G | 1 | a0007c0042t0001g0179 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-13+497T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144355998 | ||||||
chr7:144356069
|
T | C | 17 | a0002c0001t0001g0045a0009c0026t0001g0046a0009c0026t0001g0050others(14): Show | 18 | HG01496.hp1 HG01884.hp2 HG02897.hp2 others(15): Show |
intron_variant | MODIFIER | c.-13+568T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356069 | ||||||
chr7:144356228
|
TC | T | 2 | a0010c0009t0001g0017a0010c0009t0001g0057 | 3 | HG02897.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-13+729delC | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144356228 | |||||
chr7:144356238
|
C | A | 24 | a0003c0004t0002g0004a0003c0004t0002g0011a0003c0004t0002g0018others(21): Show | 36 | HG01074.hp1 HG01099.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.-13+737C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356238 | ||||||
chr7:144356248
|
A | G | 1 | a0032c0067t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13+747A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356248 | ||||||
chr7:144356251
|
G | C | 2 | a0011c0023t0002g0067a0011c0023t0002g0068 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-13+750G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356251 | ||||||
chr7:144356267
|
C | T | 4 | a0002c0001t0001g0042a0002c0001t0001g0175a0002c0016t0001g0176others(1): Show | 5 | HG02027.hp2 HG02132.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+766C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356267 | ||||||
chr7:144356346
|
A | G | 1 | a0001c0002t0002g0174 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-13+845A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356346 | ||||||
chr7:144356422
|
C | A | 1 | a0006c0005t0001g0069 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-13+921C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356422 | ||||||
chr7:144356605
|
G | A | 76 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(73): Show | 98 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.-13+1104G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356605 | ||||||
chr7:144356648
|
A | G | 40 | a0001c0002t0002g0016a0001c0002t0002g0171a0001c0002t0002g0172others(37): Show | 62 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(59): Show |
intron_variant | MODIFIER | c.-13+1147A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356648 | ||||||
chr7:144356659
|
A | C | 1 | a0003c0004t0002g0023 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-13+1158A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356659 | ||||||
chr7:144356724
|
G | A | 2 | a0010c0009t0001g0017a0010c0009t0001g0057 | 3 | HG02897.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-13+1223G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356724 | ||||||
chr7:144356770
|
G | A | 2 | a0011c0044t0001g0150a0011c0045t0001g0151 | 2 | NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-13+1269G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356770 | ||||||
chr7:144356794
|
A | G | 1 | a0034c0027t0002g0056 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+1293A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356794 | ||||||
chr7:144356864
|
G | A | 9 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(6): Show | 9 | HG01496.hp1 HG01884.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+1363G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356864 | ||||||
chr7:144356902
|
G | A | 10 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(7): Show | 10 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+1401G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356902 | ||||||
chr7:144357116
|
G | A | 1 | a0003c0004t0002g0058 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-13+1615G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357116 | ||||||
chr7:144357123
|
C | T | 10 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(7): Show | 10 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+1622C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357123 | ||||||
chr7:144357124
|
C | T | 10 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(7): Show | 10 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+1623C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357124 | ||||||
chr7:144357178
|
G | A | 17 | a0004c0003t0001g0154a0004c0003t0001g0155a0005c0006t0001g0070others(14): Show | 17 | HG01496.hp1 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13+1677G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357178 | ||||||
chr7:144357191
|
A | C | 1 | a0034c0027t0002g0056 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+1690A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357191 | ||||||
chr7:144357210
|
T | C | 1 | a0001c0002t0002g0114 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-13+1709T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357210 | ||||||
chr7:144357221
|
T | C | 1 | a0032c0067t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13+1720T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357221 | ||||||
chr7:144357223
|
T | G | 165 | a0001c0002t0002g0128a0001c0010t0002g0032a0001c0010t0002g0120others(162): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-13+1722T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357223 | ||||||
chr7:144357378
|
G | A | 93 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(90): Show | 118 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-13+1877G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357378 | ||||||
chr7:144357390
|
T | C | 104 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(101): Show | 129 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-13+1889T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357390 | ||||||
chr7:144357410
|
C | T | 108 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(105): Show | 133 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-13+1909C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357410 | ||||||
chr7:144357425
|
G | A | 3 | a0013c0017t0001g0112a0013c0017t0001g0113a0013c0017t0001g0163 | 3 | HG00597.hp1 HG02074.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.-13+1924G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357425 | ||||||
chr7:144357588
|
A | G | 9 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(6): Show | 9 | HG01496.hp1 HG01884.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+2087A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357588 | ||||||
chr7:144357662
|
G | A | 10 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(7): Show | 10 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+2161G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357662 | ||||||
chr7:144357680
|
A | G | 1 | a0032c0067t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13+2179A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357680 | ||||||
chr7:144357767
|
A | G | 10 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(7): Show | 10 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+2266A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357767 | ||||||
chr7:144357835
|
G | A | 31 | a0004c0003t0001g0002a0004c0003t0001g0040a0004c0003t0001g0041others(28): Show | 48 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.-13+2334G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357835 | ||||||
chr7:144357861
|
G | A | 1 | a0004c0003t0001g0180 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-13+2360G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357861 | ||||||
chr7:144357959
|
C | T | 12 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(9): Show | 12 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(9): Show |
intron_variant | MODIFIER | c.-13+2458C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357959 | ||||||
chr7:144358071
|
C | T | 2 | a0009c0070t0001g0184a0009c0072t0001g0051 | 2 | NA18986.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-13+2570C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358071 | ||||||
chr7:144358227
|
C | T | 1 | a0002c0001t0001g0111 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-13+2726C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358227 | ||||||
chr7:144358434
|
G | A | 1 | a0034c0027t0002g0056 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+2933G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358434 | ||||||
chr7:144358444
|
A | G | 11 | a0002c0001t0001g0110a0009c0026t0001g0046a0009c0026t0001g0050others(8): Show | 11 | HG00621.hp1 HG01496.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+2943A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358444 | ||||||
chr7:144358460
|
C | T | 1 | a0032c0067t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13+2959C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358460 | ||||||
chr7:144358464
|
G | C | 1 | a0006c0005t0001g0115 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-13+2963G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358464 | ||||||
chr7:144358467
|
T | G | 1 | a0006c0005t0001g0115 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-13+2966T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358467 | ||||||
chr7:144358515
|
G | C | 2 | a0011c0023t0002g0067a0011c0023t0002g0068 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-13+3014G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358515 | ||||||
chr7:144358536
|
G | A | 2 | a0033c0068t0001g0152a0046c0048t0001g0153 | 2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-13+3035G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358536 | ||||||
chr7:144358633
|
C | A | 1 | a0032c0067t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13+3132C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358633 | ||||||
chr7:144358661
|
A | G | 1 | a0006c0005t0001g0013 | 3 | NA19057.hp1 NA19065.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-13+3160A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358661 | ||||||
chr7:144358745
|
G | A | 2 | a0011c0023t0002g0067a0011c0023t0002g0068 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-13+3244G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358745 | ||||||
chr7:144358758
|
A | AGT | 25 | a0001c0002t0002g0003a0001c0002t0002g0035a0001c0002t0002g0036others(22): Show | 35 | HG00323.hp1 HG00642.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-13+3300_-13+3301d others(4): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | |||||
chr7:144358758
|
A | AGTGT | 19 | a0001c0002t0002g0037a0001c0002t0002g0147a0001c0002t0002g0148others(16): Show | 26 | HG00741.hp2 HG01168.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.-13+3298_-13+3301d others(6): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | |||||
chr7:144358758
|
A | AGTGTGT | 6 | a0001c0010t0002g0132a0003c0004t0002g0004a0003c0004t0002g0063others(3): Show | 10 | HG01074.hp1 HG01099.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+3296_-13+3301d others(8): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | |||||
chr7:144358758
|
A | AGTGTGTG others(1): Show |
5 | a0003c0004t0002g0019a0003c0004t0002g0064a0003c0012t0002g0065others(2): Show | 6 | HG01517.hp1 HG02886.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+3294_-13+3301d others(10): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | |||||
chr7:144358758
|
A | AGTGTGTG others(3): Show |
3 | a0003c0004t0002g0021a0003c0014t0002g0022a0047c0049t0002g0022 | 4 | HG01433.hp1 HG02738.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+3292_-13+3301d others(12): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | |||||
chr7:144358758
|
A | AGTGTGTG others(5): Show |
1 | a0003c0004t0002g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-13+3290_-13+3301d others(14): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | |||||
chr7:144358758
|
AGT | A | 67 | a0001c0002t0002g0016a0001c0002t0002g0134a0001c0002t0002g0171others(64): Show | 91 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-13+3300_-13+3301d others(4): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | |||||
chr7:144358758
|
AGTGT | A | 13 | a0001c0010t0002g0120a0001c0010t0002g0121a0002c0001t0001g0082others(10): Show | 14 | HG00597.hp1 HG01891.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+3298_-13+3301d others(6): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | |||||
chr7:144358758
|
AGTGTGT | A | 6 | a0002c0001t0001g0077a0002c0001t0001g0078a0002c0063t0001g0076others(3): Show | 8 | HG02622.hp2 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+3296_-13+3301d others(8): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | |||||
chr7:144358758
|
AGTGTGTG others(1): Show |
A | 5 | a0002c0001t0001g0072a0002c0001t0001g0073a0002c0001t0001g0075others(2): Show | 5 | HG00558.hp2 HG02040.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+3294_-13+3301d others(10): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | |||||
chr7:144358758
|
AGTGTGTG others(3): Show |
A | 1 | a0007c0007t0003g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-13+3292_-13+3301d others(12): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | |||||
chr7:144358784
|
TGTGTGTG others(15): Show |
T | 12 | a0004c0003t0001g0002a0004c0003t0001g0040a0004c0003t0001g0041others(9): Show | 26 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.-13+3284_-13+3305d others(24): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358784 | ||||||
chr7:144358786
|
TGTGTGTG others(13): Show |
T | 1 | a0004c0003t0001g0170 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-13+3286_-13+3305d others(22): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358786 | ||||||
chr7:144358792
|
TGTGTGTG others(7): Show |
T | 5 | a0009c0026t0001g0046a0009c0071t0001g0182a0009c0073t0001g0049others(2): Show | 5 | HG01496.hp1 HG01884.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+3292_-13+3305d others(16): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358792 | ||||||
chr7:144358794
|
TGTGTGTG others(5): Show |
T | 4 | a0009c0026t0001g0050a0009c0070t0001g0184a0009c0072t0001g0051others(1): Show | 4 | NA18951.hp1 NA18986.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+3294_-13+3305d others(14): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358794 | ||||||
chr7:144358796
|
TGTGTGTA others(3): Show |
T | 1 | a0034c0027t0002g0056 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+3296_-13+3305d others(12): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358796 | ||||||
chr7:144358800
|
TGTACAC | T | 4 | a0007c0007t0003g0123a0011c0044t0001g0150a0011c0045t0001g0151others(1): Show | 4 | HG02451.hp2 HG03130.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+3300_-13+3305d others(8): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358800 | ||||||
chr7:144358803
|
A | G | 5 | a0007c0011t0002g0010a0007c0011t0002g0164a0010c0009t0001g0055others(2): Show | 8 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+3302A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358803 | ||||||
chr7:144358804
|
C | T | 5 | a0007c0011t0002g0010a0007c0011t0002g0164a0010c0009t0001g0055others(2): Show | 8 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+3303C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358804 | ||||||
chr7:144358805
|
A | G | 3 | a0007c0011t0002g0010a0007c0011t0002g0164a0010c0009t0001g0055 | 6 | HG02258.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+3304A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358805 | ||||||
chr7:144358806
|
C | T | 3 | a0007c0011t0002g0010a0007c0011t0002g0164a0010c0009t0001g0055 | 6 | HG02258.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+3305C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358806 | ||||||
chr7:144358812
|
G | A | 10 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(7): Show | 10 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+3311G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358812 | ||||||
chr7:144358884
|
G | A | 1 | a0034c0027t0002g0056 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+3383G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358884 | ||||||
chr7:144358929
|
G | T | 13 | a0004c0003t0001g0002a0004c0003t0001g0040a0004c0003t0001g0041others(10): Show | 27 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.-13+3428G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358929 | ||||||
chr7:144358970
|
T | C | 2 | a0011c0044t0001g0150a0011c0045t0001g0151 | 2 | NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-13+3469T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358970 | ||||||
chr7:144358988
|
G | A | 3 | a0020c0018t0001g0156a0033c0068t0001g0152a0046c0048t0001g0153 | 3 | HG02135.hp2 NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-13+3487G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358988 | ||||||
chr7:144358991
|
A | C | 1 | a0002c0001t0001g0075 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-13+3490A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358991 | ||||||
chr7:144359134
|
G | A | 12 | a0006c0005t0001g0103a0006c0005t0001g0115a0009c0026t0001g0046others(9): Show | 12 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12-3524G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359134 | ||||||
chr7:144359386
|
C | T | 97 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(94): Show | 122 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-12-3272C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359386 | ||||||
chr7:144359423
|
T | C | 6 | a0001c0002t0002g0139a0007c0011t0002g0164a0011c0044t0001g0150others(3): Show | 6 | HG02970.hp1 HG03704.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-3235T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359423 | ||||||
chr7:144359426
|
G | A | 108 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(105): Show | 133 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-12-3232G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359426 | ||||||
chr7:144359658
|
T | A | 1 | a0005c0006t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-12-3000T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359658 | ||||||
chr7:144359681
|
A | G | 2 | a0011c0044t0001g0150a0011c0045t0001g0151 | 2 | NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-12-2977A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359681 | ||||||
chr7:144359682
|
GA | G | 2 | a0006c0005t0001g0013a0046c0048t0001g0153 | 4 | NA18964.hp1 NA19057.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-2975delA | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359682 | ||||||
chr7:144359683
|
A | G | 5 | a0011c0044t0001g0150a0011c0045t0001g0151a0020c0018t0001g0156others(2): Show | 5 | HG02135.hp2 NA18906.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-2975A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359683 | ||||||
chr7:144359683
|
AG | A | 59 | a0003c0004t0002g0004a0003c0004t0002g0011a0003c0004t0002g0015others(56): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.-12-2967delG | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144359683 | |||||
chr7:144359691
|
G | A | 1 | a0026c0060t0001g0177 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-12-2967G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359691 | ||||||
chr7:144359692
|
A | T | 1 | a0026c0060t0001g0177 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-12-2966A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359692 | ||||||
chr7:144359693
|
T | G | 1 | a0026c0060t0001g0177 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-12-2965T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359693 | ||||||
chr7:144359752
|
G | A | 2 | a0033c0068t0001g0152a0046c0048t0001g0153 | 2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-12-2906G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359752 | ||||||
chr7:144359755
|
G | T | 1 | a0005c0006t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-12-2903G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359755 | ||||||
chr7:144359814
|
T | A | 1 | a0005c0006t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-12-2844T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359814 | ||||||
chr7:144359887
|
G | A | 100 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(97): Show | 125 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-12-2771G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359887 | ||||||
chr7:144359899
|
T | C | 1 | a0006c0005t0001g0084 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-12-2759T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359899 | ||||||
chr7:144359903
|
G | C | 1 | a0020c0018t0001g0156 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-12-2755G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359903 | ||||||
chr7:144360105
|
T | A | 129 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(126): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-12-2553T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360105 | ||||||
chr7:144360107
|
T | C | 2 | a0008c0008t0001g0030a0016c0054t0001g0030 | 2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-12-2551T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360107 | ||||||
chr7:144360148
|
G | A | 1 | a0020c0018t0001g0156 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-12-2510G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360148 | ||||||
chr7:144360149
|
A | T | 111 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(108): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-12-2509A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360149 | ||||||
chr7:144360202
|
T | A | 17 | a0004c0003t0001g0002a0004c0003t0001g0040a0004c0003t0001g0041others(14): Show | 34 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12-2456T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360202 | ||||||
chr7:144360209
|
AGGATCCC others(7): Show |
A | 111 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(108): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-12-2448_-12-2435d others(16): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360209 | ||||||
chr7:144360224
|
C | T | 111 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(108): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-12-2434C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360224 | ||||||
chr7:144360231
|
CT | C | 110 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(107): Show | 135 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-12-2426delT | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360231 | ||||||
chr7:144360236
|
G | A | 111 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(108): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-12-2422G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360236 | ||||||
chr7:144360298
|
A | C | 1 | a0026c0060t0001g0177 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-12-2360A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360298 | ||||||
chr7:144360350
|
A | G | 13 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(10): Show | 13 | HG01496.hp1 HG01884.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-2308A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360350 | ||||||
chr7:144360359
|
C | T | 1 | a0002c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12-2299C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360359 | ||||||
chr7:144360390
|
C | T | 162 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(159): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.-12-2268C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360390 | ||||||
chr7:144360476
|
T | C | 1 | a0011c0043t0002g0062 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-12-2182T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360476 | ||||||
chr7:144360584
|
G | C | 13 | a0007c0011t0002g0010a0007c0011t0002g0164a0009c0026t0001g0046others(10): Show | 16 | HG01496.hp1 HG01884.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-12-2074G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360584 | ||||||
chr7:144360609
|
G | A | 2 | a0033c0068t0001g0152a0046c0048t0001g0153 | 2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-12-2049G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360609 | ||||||
chr7:144360631
|
A | G | 97 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(94): Show | 122 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-12-2027A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360631 | ||||||
chr7:144360638
|
G | T | 1 | a0001c0002t0002g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-12-2020G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360638 | ||||||
chr7:144360689
|
T | C | 2 | a0033c0068t0001g0152a0046c0048t0001g0153 | 2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-12-1969T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360689 | ||||||
chr7:144360709
|
A | G | 1 | a0001c0002t0002g0149 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-12-1949A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360709 | ||||||
chr7:144360739
|
A | G | 96 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(93): Show | 121 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-12-1919A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360739 | ||||||
chr7:144360868
|
C | A | 9 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(6): Show | 9 | HG01496.hp1 HG01884.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-1790C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360868 | ||||||
chr7:144360884
|
A | T | 98 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(95): Show | 123 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.-12-1774A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360884 | ||||||
chr7:144360912
|
A | C | 2 | a0033c0068t0001g0152a0046c0048t0001g0153 | 2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-12-1746A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360912 | ||||||
chr7:144360957
|
T | C | 100 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(97): Show | 125 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-12-1701T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360957 | ||||||
chr7:144360958
|
G | A | 100 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(97): Show | 125 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-12-1700G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360958 | ||||||
chr7:144361001
|
G | T | 1 | a0032c0067t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-12-1657G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361001 | ||||||
chr7:144361014
|
G | A | 2 | a0033c0068t0001g0152a0046c0048t0001g0153 | 2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-12-1644G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361014 | ||||||
chr7:144361042
|
G | A | 100 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(97): Show | 125 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-12-1616G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361042 | ||||||
chr7:144361042
|
G | T | 1 | a0004c0003t0001g0170 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12-1616G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361042 | ||||||
chr7:144361107
|
A | G | 1 | a0010c0009t0001g0017 | 2 | HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-12-1551A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361107 | ||||||
chr7:144361142
|
G | C | 109 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(106): Show | 134 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-12-1516G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361142 | ||||||
chr7:144361143
|
G | T | 96 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(93): Show | 121 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-12-1515G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361143 | ||||||
chr7:144361157
|
A | G | 101 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(98): Show | 126 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.-12-1501A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361157 | ||||||
chr7:144361167
|
C | T | 1 | a0002c0001t0001g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-12-1491C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361167 | ||||||
chr7:144361188
|
C | T | 8 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(5): Show | 8 | HG01884.hp2 NA18951.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-1470C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361188 | ||||||
chr7:144361190
|
G | A | 4 | a0012c0013t0002g0122a0012c0013t0002g0125a0012c0013t0002g0126others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-1468G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361190 | ||||||
chr7:144361226
|
C | CA | 14 | a0001c0020t0002g0141a0002c0001t0001g0077a0002c0001t0001g0082others(11): Show | 19 | HG01192.hp1 HG01515.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12-1417dupA | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144361226 | |||||
chr7:144361232
|
AAAAAAAA others(3): Show |
A | 62 | a0003c0004t0002g0004a0003c0004t0002g0011a0003c0004t0002g0015others(59): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-12-1421_-12-1412d others(12): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144361232 | |||||
chr7:144361232
|
AAAAAAAA others(8): Show |
A | 1 | a0006c0005t0001g0084 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-12-1416_-12-1402d others(17): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144361232 | |||||
chr7:144361241
|
AG | A | 3 | a0002c0001t0001g0100a0006c0005t0001g0069a0020c0018t0001g0156 | 3 | HG01975.hp1 HG02135.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-12-1416delG | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361241 | ||||||
chr7:144361242
|
G | A | 96 | a0001c0002t0002g0140a0002c0001t0001g0001a0002c0001t0001g0008others(93): Show | 121 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-12-1416G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361242 | ||||||
chr7:144361247
|
G | A | 1 | a0005c0006t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-12-1411G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361247 | ||||||
chr7:144361247
|
GA | G | 4 | a0006c0005t0001g0009a0006c0005t0001g0159a0006c0005t0001g0161others(1): Show | 6 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1398delA | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144361247 | |||||
chr7:144361251
|
A | G | 67 | a0001c0002t0002g0140a0002c0001t0001g0102a0003c0004t0002g0004others(64): Show | 99 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.-12-1407A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361251 | ||||||
chr7:144361448
|
A | G | 25 | a0004c0003t0001g0002a0004c0003t0001g0040a0004c0003t0001g0041others(22): Show | 42 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.-12-1210A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361448 | ||||||
chr7:144361509
|
C | T | 2 | a0007c0007t0003g0034a0043c0031t0003g0034 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-12-1149C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361509 | ||||||
chr7:144361592
|
T | C | 35 | a0001c0002t0002g0128a0001c0010t0002g0032a0001c0010t0002g0120others(32): Show | 53 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.-12-1066T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361592 | ||||||
chr7:144361610
|
C | T | 1 | a0003c0032t0002g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-12-1048C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361610 | ||||||
chr7:144361702
|
G | A | 91 | a0001c0002t0002g0134a0002c0001t0001g0001a0002c0001t0001g0008others(88): Show | 114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-12-956G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361702 | ||||||
chr7:144361799
|
G | A | 1 | a0045c0033t0002g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-12-859G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361799 | ||||||
chr7:144362044
|
C | T | 37 | a0001c0002t0002g0128a0001c0010t0002g0032a0001c0010t0002g0120others(34): Show | 55 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.-12-614C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144362044 | ||||||
chr7:144362416
|
C | T | 9 | a0009c0026t0001g0046a0009c0026t0001g0050a0009c0070t0001g0184others(6): Show | 9 | HG01496.hp1 HG01884.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-242C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144362416 | ||||||
chr7:144362419
|
T | C | 16 | a0004c0003t0001g0002a0004c0003t0001g0040a0004c0003t0001g0041others(13): Show | 33 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.-12-239T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144362419 | ||||||
chr7:144362513
|
T | C | 11 | a0002c0001t0001g0012a0002c0001t0001g0024a0002c0001t0001g0087others(8): Show | 13 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12-145T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144362513 | ||||||
chr7:144365934
|
C | T | 2 | a0007c0011t0002g0010a0007c0011t0002g0164 | 5 | HG02258.hp1 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3154+111C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/14 | chr7 | 144365934 | ||||||
chr7:144366128
|
G | T | 1 | a0022c0058t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3155-227G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/14 | chr7 | 144366128 | ||||||
chr7:144366277
|
G | A | 1 | a0009c0070t0001g0184 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3155-78G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/14 | chr7 | 144366277 | ||||||
chr7:144366492
|
T | C | 1 | a0009c0070t0001g0184 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3212+80T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 3/14 | chr7 | 144366492 | ||||||
chr7:144366938
|
A | C | 167 | a0001c0021t0002g0038a0002c0001t0001g0001a0002c0001t0001g0008others(164): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.3277+28A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 4/14 | chr7 | 144366938 | ||||||
chr7:144367761
|
G | A | 1 | a0002c0064t0001g0071 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3531+406G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144367761 | ||||||
chr7:144367898
|
T | G | 2 | a0001c0010t0002g0130a0048c0069t0002g0166 | 2 | HG01361.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3531+543T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144367898 | ||||||
chr7:144368058
|
G | GAT | 1 | a0007c0007t0003g0014 | 3 | HG02622.hp2 HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3531+706_3531+707d others(4): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr7 | 144368058 | |||||
chr7:144368080
|
A | T | 188 | a0001c0002t0002g0003a0001c0002t0002g0005a0001c0002t0002g0016others(185): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.3531+725A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368080 | ||||||
chr7:144368178
|
C | T | 1 | a0003c0012t0002g0006 | 4 | HG02451.hp1 HG02486.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3531+823C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368178 | ||||||
chr7:144368179
|
G | C | 3 | a0009c0070t0001g0184a0026c0060t0001g0177a0046c0048t0001g0153 | 3 | NA18964.hp1 NA18986.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.3531+824G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368179 | ||||||
chr7:144368288
|
C | T | 1 | a0003c0012t0002g0006 | 4 | HG02451.hp1 HG02486.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3531+933C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368288 | ||||||
chr7:144368294
|
T | C | 1 | a0002c0061t0001g0093 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3531+939T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368294 | ||||||
chr7:144368386
|
C | T | 1 | a0009c0073t0001g0049 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3531+1031C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368386 | ||||||
chr7:144368497
|
A | G | 4 | a0009c0070t0001g0184a0015c0024t0001g0092a0026c0060t0001g0177others(1): Show | 4 | NA18977.hp2 NA18986.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.3531+1142A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368497 | ||||||
chr7:144368499
|
A | C | 3 | a0003c0004t0002g0060a0003c0004t0002g0129a0003c0032t0002g0059 | 3 | HG01255.hp2 HG02145.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3531+1144A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368499 | ||||||
chr7:144368750
|
A | T | 14 | a0004c0003t0001g0002a0004c0003t0001g0040a0004c0003t0001g0041others(11): Show | 28 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3531+1395A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368750 | ||||||
chr7:144368783
|
C | T | 213 | a0001c0002t0002g0003a0001c0002t0002g0005a0001c0002t0002g0016others(210): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.3531+1428C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368783 | ||||||
chr7:144368996
|
A | C | 101 | a0001c0021t0002g0038a0002c0001t0001g0001a0002c0001t0001g0008others(98): Show | 128 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.3531+1641A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368996 | ||||||
chr7:144369131
|
A | G | 28 | a0003c0004t0002g0004a0003c0004t0002g0011a0003c0004t0002g0015others(25): Show | 41 | HG00140.hp1 HG00741.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.3531+1776A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144369131 | ||||||
chr7:144369227
|
TC | T | 22 | a0003c0004t0002g0004a0003c0004t0002g0011a0003c0004t0002g0015others(19): Show | 31 | HG00140.hp1 HG00741.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.3531+1873delC | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144369227 | ||||||
chr7:144369465
|
C | T | 95 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(92): Show | 117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.3532-1696C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144369465 | ||||||
chr7:144369577
|
G | T | 166 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(163): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.3532-1584G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144369577 | ||||||
chr7:144369673
|
A | G | 1 | a0012c0013t0002g0127 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3532-1488A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144369673 | ||||||
chr7:144370024
|
G | T | 2 | a0005c0006t0001g0028a0024c0057t0001g0028 | 2 | HG00544.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.3532-1137G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370024 | ||||||
chr7:144370058
|
C | G | 1 | a0033c0068t0001g0152 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3532-1103C>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370058 | ||||||
chr7:144370059
|
T | A | 1 | a0006c0005t0001g0085 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3532-1102T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370059 | ||||||
chr7:144370121
|
C | T | 1 | a0001c0002t0002g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3532-1040C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370121 | ||||||
chr7:144370205
|
C | T | 1 | a0001c0002t0002g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3532-956C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370205 | ||||||
chr7:144370356
|
A | G | 1 | a0032c0067t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3532-805A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370356 | ||||||
chr7:144370468
|
A | T | 14 | a0004c0003t0001g0002a0004c0003t0001g0040a0004c0003t0001g0041others(11): Show | 28 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3532-693A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370468 | ||||||
chr7:144370483
|
T | C | 1 | a0003c0012t0002g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3532-678T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370483 | ||||||
chr7:144370664
|
C | G | 115 | a0001c0002t0002g0139a0001c0002t0002g0140a0001c0002t0002g0149others(112): Show | 141 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.3532-497C>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370664 | ||||||
chr7:144370667
|
C | T | 2 | a0002c0001t0001g0024a0025c0062t0001g0024 | 2 | HG02083.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.3532-494C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370667 | ||||||
chr7:144370668
|
G | A | 2 | a0007c0007t0003g0014a0007c0007t0003g0119 | 4 | HG02622.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3532-493G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370668 | ||||||
chr7:144370744
|
G | C | 1 | a0009c0073t0001g0049 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3532-417G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370744 | ||||||
chr7:144370955
|
C | T | 1 | a0005c0006t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3532-206C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370955 | ||||||
chr7:144371015
|
C | T | 17 | a0005c0006t0001g0007a0005c0006t0001g0027a0005c0006t0001g0028others(14): Show | 20 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.3532-146C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144371015 | ||||||
chr7:144371070
|
T | C | 66 | a0001c0002t0002g0139a0002c0001t0001g0008a0002c0016t0001g0176others(63): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.3532-91T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144371070 | ||||||
chr7:144371071
|
G | A | 2 | a0007c0011t0002g0010a0007c0011t0002g0164 | 5 | HG02258.hp1 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3532-90G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144371071 | ||||||
chr7:144371114
|
G | C | 1 | a0009c0026t0001g0050 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3532-47G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144371114 | ||||||
chr7:144371121
|
T | C | 27 | a0003c0004t0002g0004a0003c0004t0002g0011a0003c0004t0002g0015others(24): Show | 40 | HG00140.hp1 HG00741.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.3532-40T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144371121 | ||||||
chr7:144371383
|
T | C | 2 | a0007c0007t0003g0014a0007c0007t0003g0119 | 4 | HG02622.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3692+62T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 6/14 | chr7 | 144371383 | ||||||
chr7:144371387
|
G | A | 121 | a0001c0010t0002g0120a0002c0001t0001g0001a0002c0001t0001g0008others(118): Show | 148 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.3692+66G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 6/14 | chr7 | 144371387 | ||||||
chr7:144371480
|
G | A | 102 | a0002c0001t0001g0001a0002c0001t0001g0012a0002c0001t0001g0024others(99): Show | 129 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.3692+159G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 6/14 | chr7 | 144371480 | ||||||
chr7:144371561
|
G | C | 2 | a0011c0043t0002g0062a0020c0018t0002g0061 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3692+240G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 6/14 | chr7 | 144371561 | ||||||
chr7:144371721
|
G | A | 1 | a0008c0008t0001g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3693-156G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 6/14 | chr7 | 144371721 | ||||||
chr7:144372168
|
G | A | 1 | a0004c0003t0001g0041 | 2 | HG00642.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.3846-131G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 7/14 | chr7 | 144372168 | ||||||
chr7:144372517
|
C | T | 2 | a0001c0002t0002g0138a0001c0002t0002g0144 | 2 | NA19011.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.3975+89C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 8/14 | chr7 | 144372517 | ||||||
chr7:144372815
|
C | T | 2 | a0005c0006t0001g0096a0005c0006t0001g0097 | 2 | HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4050+58C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 9/14 | chr7 | 144372815 | ||||||
chr7:144372891
|
G | T | 3 | a0001c0020t0002g0143a0003c0012t0002g0006a0045c0033t0002g0135 | 6 | HG00735.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4050+134G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 9/14 | chr7 | 144372891 | ||||||
chr7:144372934
|
G | A | 1 | a0003c0012t0002g0006 | 4 | HG02451.hp1 HG02486.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4050+177G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 9/14 | chr7 | 144372934 | ||||||
chr7:144372979
|
C | A | 5 | a0001c0010t0002g0120a0001c0010t0002g0121a0007c0011t0002g0010others(2): Show | 8 | HG02258.hp1 HG02258.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.4051-216C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 9/14 | chr7 | 144372979 | ||||||
chr7:144372984
|
C | A | 121 | a0001c0010t0002g0120a0001c0010t0002g0121a0001c0020t0002g0143others(118): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.4051-211C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 9/14 | chr7 | 144372984 | ||||||
chr7:144373022
|
G | C | 8 | a0001c0002t0002g0037a0001c0020t0002g0143a0003c0012t0002g0006others(5): Show | 15 | HG00735.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4051-173G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 9/14 | chr7 | 144373022 | ||||||
chr7:144373291
|
C | T | 1 | a0002c0001t0001g0102 | 1 | HG04228.hp1 | splice_region_variant&intron_variant | LOW | c.4140+7C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373291 | ||||||
chr7:144373299
|
T | G | 1 | a0002c0001t0001g0088 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4140+15T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373299 | ||||||
chr7:144373472
|
T | A | 135 | a0001c0020t0002g0143a0002c0001t0001g0001a0002c0001t0001g0008others(132): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.4140+188T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373472 | ||||||
chr7:144373538
|
T | G | 11 | a0006c0005t0001g0009a0006c0005t0001g0159a0006c0005t0001g0161others(8): Show | 14 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.4140+254T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373538 | ||||||
chr7:144373547
|
G | A | 1 | a0032c0067t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4140+263G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373547 | ||||||
chr7:144373692
|
G | C | 13 | a0004c0003t0001g0002a0004c0003t0001g0040a0004c0003t0001g0041others(10): Show | 27 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.4140+408G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373692 | ||||||
chr7:144373757
|
G | T | 4 | a0007c0011t0002g0010a0007c0011t0002g0164a0009c0070t0001g0184others(1): Show | 7 | HG02258.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.4140+473G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373757 | ||||||
chr7:144373846
|
C | CT | 7 | a0002c0016t0001g0074a0002c0016t0001g0105a0002c0016t0001g0176others(4): Show | 10 | HG01934.hp2 HG02083.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.4140+576dupT | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 144373846 | |||||
chr7:144373880
|
G | A | 164 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(161): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.4140+596G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373880 | ||||||
chr7:144373912
|
G | C | 1 | a0005c0006t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4140+628G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373912 | ||||||
chr7:144374003
|
G | A | 1 | a0020c0018t0001g0156 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4140+719G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374003 | ||||||
chr7:144374054
|
C | T | 1 | a0032c0067t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4141-678C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374054 | ||||||
chr7:144374067
|
C | T | 1 | a0045c0033t0002g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4141-665C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374067 | ||||||
chr7:144374111
|
G | T | 118 | a0001c0002t0002g0171a0002c0001t0001g0001a0002c0001t0001g0008others(115): Show | 149 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.4141-621G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374111 | ||||||
chr7:144374118
|
AG | A | 4 | a0012c0013t0002g0122a0012c0013t0002g0125a0012c0013t0002g0126others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4141-612delG | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 144374118 | |||||
chr7:144374122
|
G | A | 6 | a0007c0007t0003g0033a0007c0007t0003g0034a0007c0007t0003g0123others(3): Show | 7 | HG01891.hp1 HG02723.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.4141-610G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374122 | ||||||
chr7:144374136
|
T | C | 171 | a0001c0002t0002g0137a0002c0001t0001g0001a0002c0001t0001g0008others(168): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.4141-596T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374136 | ||||||
chr7:144374197
|
A | T | 2 | a0011c0043t0002g0062a0020c0018t0002g0061 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4141-535A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374197 | ||||||
chr7:144374218
|
C | T | 1 | a0001c0002t0002g0174 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4141-514C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374218 | ||||||
chr7:144374238
|
A | T | 1 | a0005c0006t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4141-494A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374238 | ||||||
chr7:144374269
|
C | A | 2 | a0004c0003t0001g0168a0009c0070t0001g0184 | 2 | HG01123.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.4141-463C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374269 | ||||||
chr7:144374445
|
C | T | 1 | a0004c0003t0001g0040 | 2 | HG01243.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.4141-287C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374445 | ||||||
chr7:144374512
|
A | G | 112 | a0001c0002t0002g0142a0002c0001t0001g0001a0002c0001t0001g0008others(109): Show | 140 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.4141-220A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374512 | ||||||
chr7:144374626
|
G | A | 1 | a0003c0012t0002g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4141-106G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374626 | ||||||
chr7:144374670
|
G | A | 1 | a0001c0002t0002g0134 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4141-62G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374670 | ||||||
chr7:144375183
|
T | A | 2 | a0002c0001t0001g0106a0002c0016t0001g0176 | 2 | NA18990.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.4298+294T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 11/14 | chr7 | 144375183 | ||||||
chr7:144375232
|
G | T | 136 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(133): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.4299-282G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 11/14 | chr7 | 144375232 | ||||||
chr7:144375350
|
C | T | 3 | a0003c0004t0002g0063a0003c0004t0002g0064a0003c0004t0002g0066 | 3 | HG01934.hp1 HG02165.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.4299-164C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 11/14 | chr7 | 144375350 | ||||||
chr7:144375714
|
A | G | 2 | a0011c0043t0002g0062a0020c0018t0002g0061 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4460+39A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144375714 | ||||||
chr7:144375721
|
C | T | 2 | a0001c0002t0002g0036a0001c0002t0002g0142 | 3 | HG04184.hp1 NA18964.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.4460+46C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144375721 | ||||||
chr7:144375923
|
G | A | 1 | a0001c0020t0002g0141 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4460+248G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144375923 | ||||||
chr7:144376457
|
C | T | 1 | a0032c0067t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4461-663C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144376457 | ||||||
chr7:144376702
|
T | G | 1 | a0015c0024t0001g0089 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4461-418T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144376702 | ||||||
chr7:144376737
|
G | A | 13 | a0004c0003t0001g0002a0004c0003t0001g0040a0004c0003t0001g0041others(10): Show | 27 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.4461-383G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144376737 | ||||||
chr7:144376808
|
G | A | 1 | a0002c0001t0001g0090 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4461-312G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144376808 | ||||||
chr7:144376860
|
A | T | 132 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(129): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.4461-260A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144376860 | ||||||
chr7:144376902
|
T | G | 109 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(106): Show | 135 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.4461-218T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144376902 | ||||||
chr7:144377062
|
C | T | 1 | a0002c0001t0001g0095 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4461-58C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144377062 | ||||||
chr7:144377466
|
A | T | 8 | a0007c0007t0003g0014a0007c0007t0003g0033a0007c0007t0003g0034others(5): Show | 11 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.4531+276A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377466 | ||||||
chr7:144377536
|
A | G | 131 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(128): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.4531+346A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377536 | ||||||
chr7:144377630
|
G | A | 1 | a0021c0053t0001g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4531+440G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377630 | ||||||
chr7:144377677
|
A | C | 1 | a0002c0001t0001g0072 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4531+487A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377677 | ||||||
chr7:144377680
|
C | G | 2 | a0007c0007t0003g0033a0007c0007t0003g0133 | 3 | HG02723.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4531+490C>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377680 | ||||||
chr7:144377836
|
G | A | 27 | a0003c0004t0002g0004a0003c0004t0002g0011a0003c0004t0002g0015others(24): Show | 40 | HG00140.hp1 HG00741.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.4531+646G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377836 | ||||||
chr7:144377920
|
C | T | 14 | a0004c0003t0001g0002a0004c0003t0001g0040a0004c0003t0001g0041others(11): Show | 28 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.4531+730C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377920 | ||||||
chr7:144378024
|
A | G | 1 | a0008c0008t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4532-738A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144378024 | ||||||
chr7:144378544
|
C | G | 1 | a0001c0010t0002g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4532-218C>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144378544 | ||||||
chr7:144378578
|
A | G | 1 | a0001c0010t0002g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4532-184A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144378578 | ||||||
chr7:144378656
|
A | G | 131 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(128): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.4532-106A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144378656 | ||||||
chr7:144378895
|
C | T | 1 | a0002c0001t0001g0045 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4636+29C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144378895 | ||||||
chr7:144378899
|
G | T | 2 | a0003c0004t0002g0023a0003c0004t0002g0058 | 3 | HG01261.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4636+33G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144378899 | ||||||
chr7:144379338
|
G | A | 4 | a0012c0013t0002g0122a0012c0013t0002g0125a0012c0013t0002g0126others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4636+472G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379338 | ||||||
chr7:144379399
|
G | A | 1 | a0003c0004t0002g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4637-500G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379399 | ||||||
chr7:144379457
|
A | G | 135 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(132): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.4637-442A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379457 | ||||||
chr7:144379606
|
G | A | 1 | a0005c0006t0001g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4637-293G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379606 | ||||||
chr7:144379671
|
A | G | 133 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(130): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.4637-228A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379671 | ||||||
chr7:144379822
|
C | G | 131 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0012others(128): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.4637-77C>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379822 | ||||||
chr7:144379860
|
T | C | 1 | a0002c0001t0001g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.4637-39T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379860 |