geneid | 50650 |
---|---|
ensemblid | ENSG00000163947.12 |
hgncid | 683 |
symbol | ARHGEF3 |
name | Rho guanine nucleotide exchange factor 3 |
refseq_nuc | NM_019555.3 |
refseq_prot | NP_062455.1 |
ensembl_nuc | ENST00000296315.8 |
ensembl_prot | ENSP00000296315.3 |
mane_status | MANE Select |
chr | chr3 |
start | 56727420 |
end | 56801949 |
strand | - |
ver | v1.2 |
region | chr3:56727420-56801949 |
region5000 | chr3:56722420-56806949 |
regionname0 | ARHGEF3_chr3_56727420_56801949 |
regionname5000 | ARHGEF3_chr3_56722420_56806949 |
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 | 526 | 209 | 37 | 33 | 99 | 10 | 29 | 80 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002 | 0/1 | 526 | 145 | 44 | 21 | 60 | 6 | 13 | 48 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0003 | 0/0 | 526 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0004 | 0/0 | 526 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0005 | 0/0 | 526 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
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 | 1581 | 108 | 43 | 10 | 47 | 1 | 7 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0002 | 0/0 | 1581 | 81 | 19 | 4 | 46 | 0 | 12 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0003 | 1/0 | 1581 | 55 | 7 | 14 | 26 | 4 | 3 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0004 | 0/1 | 1581 | 37 | 1 | 11 | 13 | 5 | 6 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0005 | 0/0 | 1581 | 25 | 1 | 6 | 10 | 5 | 3 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0006 | 0/0 | 1581 | 23 | 1 | 3 | 9 | 1 | 9 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0007 | 0/0 | 1581 | 19 | 7 | 5 | 5 | 0 | 2 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0008 | 0/0 | 1581 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0009 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0010 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0011 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0012 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0013 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0014 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
c0015 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
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 | 1/0 | 2002 | 169 | 51 | 34 | 61 | 12 | 10 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0002 | 0/0 | 2002 | 97 | 12 | 7 | 56 | 1 | 21 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0003 | 0/1 | 2002 | 59 | 6 | 7 | 34 | 3 | 8 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0004 | 0/0 | 2002 | 14 | 0 | 5 | 7 | 0 | 2 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0005 | 0/0 | 1998 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0006 | 0/0 | 2002 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0007 | 0/0 | 2002 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0008 | 0/0 | 1998 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0009 | 0/0 | 2002 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0010 | 0/0 | 2002 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0011 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0012 | 0/0 | 2002 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0013 | 0/0 | 2002 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0014 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0015 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0016 | 0/0 | 2002 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0017 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
t0018 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
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 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0326 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
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 | 0/0 | 1581 | 81 | 19 | 4 | 46 | 0 | 12 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0003 | 1/0 | 1581 | 55 | 7 | 14 | 26 | 4 | 3 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0005 | 0/0 | 1581 | 25 | 1 | 6 | 10 | 5 | 3 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0006 | 0/0 | 1581 | 23 | 1 | 3 | 9 | 1 | 9 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0007 | 0/0 | 1581 | 19 | 7 | 5 | 5 | 0 | 2 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0008 | 0/0 | 1581 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0009 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0012 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0013 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002c0001 | 0/0 | 1581 | 108 | 43 | 10 | 47 | 1 | 7 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002c0004 | 0/1 | 1581 | 37 | 1 | 11 | 13 | 5 | 6 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0003c0010 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0003c0014 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0004c0011 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0005c0015 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002 | 0/0 | 3582 | 73 | 11 | 4 | 46 | 0 | 12 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0002t0005 | 0/0 | 3578 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0002t0006 | 0/0 | 3582 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0002t0008 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0002t0010 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0002t0017 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0003t0001 | 1/0 | 3582 | 53 | 7 | 14 | 24 | 4 | 3 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0003t0011 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0003t0015 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0005t0001 | 0/0 | 3582 | 25 | 1 | 6 | 10 | 5 | 3 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0006t0002 | 0/0 | 3582 | 22 | 1 | 3 | 8 | 1 | 9 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0006t0018 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0007t0001 | 0/0 | 3582 | 8 | 7 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0007t0004 | 0/0 | 3582 | 11 | 0 | 4 | 5 | 0 | 2 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0008t0004 | 0/0 | 3582 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0009t0002 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0012t0001 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0001c0013t0001 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002c0001t0001 | 0/0 | 3582 | 69 | 33 | 8 | 25 | 1 | 2 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002c0001t0003 | 0/0 | 3582 | 34 | 6 | 2 | 22 | 0 | 4 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002c0001t0007 | 0/0 | 3582 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002c0001t0009 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002c0001t0013 | 0/0 | 3582 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002c0001t0016 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002c0004t0001 | 0/0 | 3582 | 12 | 1 | 5 | 2 | 2 | 2 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002c0004t0003 | 0/1 | 3582 | 23 | 0 | 5 | 10 | 3 | 4 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002c0004t0012 | 0/0 | 3582 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0002c0004t0014 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0003c0010t0003 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0003c0014t0003 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0004c0011t0008 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
a0005c0015t0002 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | copy fasta | chr3 | 56722420 | 56806949 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0017g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0011g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0015g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0018g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0008t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0008t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0008t0004g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0009t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0012t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0013t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0007g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0013g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0016g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0326 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0012g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0014g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0003c0010t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0003c0014t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0004c0011t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0005c0015t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0174 | EUR | GBR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0167 | EUR | GBR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00140 | hp1 | a0002 | c0004 | t0003 | g0310 | EUR | GBR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00140 | hp2 | a0001 | c0005 | t0001 | g0331 | EUR | GBR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0168 | EUR | FIN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00280 | hp2 | a0001 | c0006 | t0002 | g0005 | EUR | FIN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00323 | hp1 | a0001 | c0005 | t0001 | g0303 | EUR | FIN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00323 | hp2 | a0002 | c0004 | t0001 | g0351 | EUR | FIN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00544 | hp1 | a0002 | c0001 | t0003 | g0054 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0058 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00558 | hp2 | a0003 | c0014 | t0003 | g0320 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00597 | hp2 | a0002 | c0001 | t0003 | g0111 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00621 | hp2 | a0002 | c0004 | t0003 | g0348 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0127 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0169 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0207 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00642 | hp2 | a0001 | c0005 | t0001 | g0308 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00673 | hp2 | a0002 | c0001 | t0003 | g0262 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00733 | hp1 | a0002 | c0004 | t0012 | g0269 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00733 | hp2 | a0002 | c0004 | t0001 | g0004 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00738 | hp1 | a0001 | c0006 | t0002 | g0005 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00738 | hp2 | a0001 | c0005 | t0001 | g0304 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00741 | hp1 | a0001 | c0005 | t0001 | g0268 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0103 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01070 | hp1 | a0001 | c0007 | t0001 | g0162 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01070 | hp2 | a0002 | c0004 | t0001 | g0289 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0175 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01071 | hp2 | a0002 | c0004 | t0001 | g0004 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0085 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0185 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01106 | hp1 | a0001 | c0005 | t0001 | g0278 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01106 | hp2 | a0001 | c0005 | t0001 | g0330 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01109 | hp1 | a0002 | c0001 | t0001 | g0233 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0177 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01167 | hp2 | a0002 | c0001 | t0001 | g0153 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01169 | hp1 | a0002 | c0001 | t0001 | g0135 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0183 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01175 | hp1 | a0002 | c0004 | t0003 | g0312 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0187 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01256 | hp1 | a0001 | c0006 | t0002 | g0275 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0154 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01258 | hp1 | a0001 | c0006 | t0002 | g0276 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0178 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01261 | hp1 | a0002 | c0001 | t0003 | g0156 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0179 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01361 | hp1 | a0002 | c0004 | t0001 | g0318 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01361 | hp2 | a0001 | c0007 | t0004 | g0115 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0090 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01496 | hp2 | a0002 | c0004 | t0001 | g0286 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0172 | EUR | IBS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01515 | hp2 | a0002 | c0004 | t0003 | g0315 | EUR | IBS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01516 | hp1 | a0001 | c0005 | t0001 | g0332 | EUR | IBS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01516 | hp2 | a0001 | c0005 | t0001 | g0300 | EUR | IBS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01517 | hp1 | a0001 | c0005 | t0001 | g0299 | EUR | IBS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01517 | hp2 | a0002 | c0004 | t0003 | g0314 | EUR | IBS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01884 | hp1 | a0002 | c0001 | t0001 | g0094 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0099 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0258 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0142 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01928 | hp1 | a0001 | c0007 | t0004 | g0112 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01928 | hp2 | a0002 | c0004 | t0003 | g0339 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01934 | hp1 | a0002 | c0004 | t0003 | g0311 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01934 | hp2 | a0002 | c0001 | t0001 | g0097 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01952 | hp1 | a0001 | c0008 | t0004 | g0324 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01952 | hp2 | a0002 | c0001 | t0001 | g0116 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01975 | hp1 | a0002 | c0001 | t0001 | g0214 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01975 | hp2 | a0002 | c0001 | t0003 | g0114 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01981 | hp1 | a0001 | c0005 | t0001 | g0319 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0019 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02027 | hp2 | a0002 | c0004 | t0003 | g0284 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0259 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0252 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02055 | hp1 | a0001 | c0002 | t0005 | g0212 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0171 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02071 | hp1 | a0001 | c0006 | t0002 | g0347 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02071 | hp2 | a0002 | c0001 | t0003 | g0231 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02074 | hp1 | a0002 | c0001 | t0003 | g0164 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02083 | hp1 | a0002 | c0004 | t0003 | g0283 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0123 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02135 | hp2 | a0002 | c0004 | t0003 | g0270 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02145 | hp1 | a0001 | c0006 | t0002 | g0296 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02155 | hp1 | a0002 | c0004 | t0003 | g0285 | EAS | CDX | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | CDX | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | CDX | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0173 | EAS | CDX | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02257 | hp1 | a0001 | c0005 | t0001 | g0305 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02257 | hp2 | a0002 | c0001 | t0003 | g0205 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02258 | hp1 | a0002 | c0001 | t0003 | g0088 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02258 | hp2 | a0001 | c0002 | t0010 | g0009 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02273 | hp1 | a0001 | c0007 | t0004 | g0027 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02273 | hp2 | a0002 | c0001 | t0001 | g0260 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02280 | hp1 | a0001 | c0007 | t0001 | g0092 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0082 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02293 | hp1 | a0001 | c0007 | t0004 | g0113 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02293 | hp2 | a0002 | c0004 | t0003 | g0325 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02300 | hp1 | a0002 | c0004 | t0003 | g0309 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0155 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02451 | hp1 | a0002 | c0001 | t0007 | g0001 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02451 | hp2 | a0002 | c0001 | t0001 | g0016 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02523 | hp1 | a0001 | c0007 | t0004 | g0063 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02523 | hp2 | a0001 | c0005 | t0001 | g0297 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02572 | hp1 | a0002 | c0001 | t0016 | g0138 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02572 | hp2 | a0002 | c0001 | t0001 | g0143 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02602 | hp1 | a0001 | c0006 | t0002 | g0337 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02602 | hp2 | a0001 | c0007 | t0004 | g0110 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02615 | hp1 | a0002 | c0001 | t0001 | g0232 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02615 | hp2 | a0002 | c0001 | t0001 | g0160 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02622 | hp1 | a0002 | c0001 | t0001 | g0102 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02622 | hp2 | a0002 | c0001 | t0001 | g0083 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0249 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02630 | hp2 | a0002 | c0001 | t0001 | g0250 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02647 | hp1 | a0004 | c0011 | t0008 | g0072 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02647 | hp2 | a0002 | c0001 | t0003 | g0140 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0180 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02683 | hp2 | a0001 | c0006 | t0002 | g0335 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02698 | hp1 | a0002 | c0001 | t0001 | g0267 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02698 | hp2 | a0001 | c0005 | t0001 | g0280 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02723 | hp1 | a0001 | c0002 | t0006 | g0008 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02723 | hp2 | a0002 | c0001 | t0001 | g0014 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0197 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02818 | hp1 | a0002 | c0001 | t0001 | g0144 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02818 | hp2 | a0002 | c0001 | t0001 | g0159 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0076 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02886 | hp2 | a0002 | c0001 | t0001 | g0098 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0266 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02896 | hp2 | a0002 | c0001 | t0001 | g0141 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0265 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02897 | hp2 | a0002 | c0001 | t0003 | g0263 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02922 | hp1 | a0002 | c0001 | t0001 | g0080 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02922 | hp2 | a0002 | c0001 | t0001 | g0010 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02965 | hp1 | a0002 | c0001 | t0001 | g0176 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02965 | hp2 | a0001 | c0007 | t0001 | g0073 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02976 | hp1 | a0001 | c0002 | t0005 | g0152 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02976 | hp2 | a0002 | c0001 | t0007 | g0001 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0040 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03017 | hp2 | a0001 | c0006 | t0002 | g0271 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03098 | hp1 | a0001 | c0002 | t0017 | g0161 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03098 | hp2 | a0002 | c0001 | t0001 | g0203 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03139 | hp1 | a0001 | c0007 | t0001 | g0093 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03195 | hp1 | a0002 | c0001 | t0001 | g0074 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03195 | hp2 | a0002 | c0001 | t0003 | g0079 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03225 | hp1 | a0002 | c0001 | t0001 | g0234 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03225 | hp2 | a0002 | c0001 | t0001 | g0096 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03239 | hp1 | a0002 | c0001 | t0003 | g0020 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03239 | hp2 | a0001 | c0006 | t0002 | g0334 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0148 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03486 | hp2 | a0002 | c0001 | t0001 | g0087 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03490 | hp1 | a0002 | c0001 | t0001 | g0089 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0035 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0036 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03491 | hp2 | a0001 | c0006 | t0002 | g0329 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03516 | hp1 | a0002 | c0001 | t0001 | g0213 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03516 | hp2 | a0001 | c0013 | t0001 | g0150 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03540 | hp1 | a0001 | c0012 | t0001 | g0104 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03540 | hp2 | a0002 | c0001 | t0001 | g0151 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0223 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03579 | hp2 | a0002 | c0001 | t0001 | g0084 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03654 | hp1 | a0002 | c0004 | t0003 | g0340 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03654 | hp2 | a0002 | c0001 | t0013 | g0204 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0215 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03669 | hp2 | a0002 | c0001 | t0003 | g0206 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03688 | hp1 | a0002 | c0004 | t0003 | g0307 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03688 | hp2 | a0001 | c0005 | t0001 | g0317 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0125 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03704 | hp2 | a0001 | c0005 | t0001 | g0306 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03710 | hp1 | a0002 | c0004 | t0001 | g0290 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03710 | hp2 | a0002 | c0004 | t0003 | g0338 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0041 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0108 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03927 | hp1 | a0002 | c0001 | t0003 | g0227 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0091 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03942 | hp1 | a0002 | c0004 | t0003 | g0344 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03942 | hp2 | a0001 | c0006 | t0002 | g0336 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04115 | hp1 | a0001 | c0006 | t0002 | g0298 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04115 | hp2 | a0002 | c0004 | t0001 | g0341 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0195 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04184 | hp2 | a0001 | c0006 | t0002 | g0333 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0037 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0039 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04204 | hp1 | a0001 | c0006 | t0002 | g0342 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04204 | hp2 | a0001 | c0007 | t0004 | g0109 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0157 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04228 | hp2 | a0002 | c0001 | t0003 | g0248 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18522 | hp1 | a0001 | c0007 | t0001 | g0101 | AFR | YRI | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0077 | AFR | YRI | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18612 | hp1 | a0002 | c0001 | t0001 | g0238 | EAS | CHB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18612 | hp2 | a0001 | c0006 | t0002 | g0350 | EAS | CHB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18906 | hp1 | a0001 | c0002 | t0005 | g0211 | AFR | YRI | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18906 | hp2 | a0002 | c0001 | t0001 | g0137 | AFR | YRI | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18940 | hp2 | a0002 | c0001 | t0001 | g0066 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18942 | hp1 | a0002 | c0001 | t0001 | g0264 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18942 | hp2 | a0002 | c0001 | t0003 | g0105 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18944 | hp2 | a0002 | c0001 | t0003 | g0228 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18945 | hp1 | a0001 | c0005 | t0001 | g0292 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18945 | hp2 | a0002 | c0001 | t0001 | g0242 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18946 | hp1 | a0001 | c0008 | t0004 | g0322 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18950 | hp2 | a0001 | c0006 | t0002 | g0281 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18952 | hp2 | a0001 | c0005 | t0001 | g0273 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18953 | hp1 | a0001 | c0003 | t0001 | g0216 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18954 | hp1 | a0002 | c0004 | t0003 | g0282 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0251 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18956 | hp1 | a0001 | c0005 | t0001 | g0327 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18956 | hp2 | a0002 | c0001 | t0001 | g0218 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18960 | hp1 | a0001 | c0006 | t0002 | g0346 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18960 | hp2 | a0002 | c0001 | t0003 | g0050 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18961 | hp1 | a0001 | c0003 | t0001 | g0065 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18961 | hp2 | a0002 | c0001 | t0001 | g0237 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18962 | hp2 | a0002 | c0004 | t0014 | g0291 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18963 | hp1 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18963 | hp2 | a0001 | c0005 | t0001 | g0277 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18964 | hp1 | a0002 | c0004 | t0001 | g0349 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18964 | hp2 | a0002 | c0001 | t0001 | g0062 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18965 | hp1 | a0001 | c0003 | t0001 | g0186 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18965 | hp2 | a0001 | c0007 | t0004 | g0046 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18966 | hp1 | a0001 | c0006 | t0002 | g0288 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18967 | hp2 | a0002 | c0001 | t0003 | g0055 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18968 | hp2 | a0002 | c0001 | t0003 | g0067 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18970 | hp1 | a0001 | c0005 | t0001 | g0274 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18972 | hp1 | a0001 | c0006 | t0018 | g0353 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18972 | hp2 | a0002 | c0001 | t0003 | g0025 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18973 | hp1 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18973 | hp2 | a0002 | c0001 | t0003 | g0230 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18977 | hp1 | a0002 | c0001 | t0001 | g0209 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18977 | hp2 | a0001 | c0005 | t0001 | g0279 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18979 | hp1 | a0002 | c0001 | t0001 | g0253 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18980 | hp1 | a0001 | c0003 | t0001 | g0163 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18984 | hp1 | a0001 | c0003 | t0015 | g0107 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18986 | hp2 | a0002 | c0004 | t0003 | g0328 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18990 | hp1 | a0002 | c0001 | t0003 | g0049 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0254 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18994 | hp2 | a0002 | c0001 | t0001 | g0239 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18995 | hp1 | a0002 | c0001 | t0003 | g0202 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18999 | hp1 | a0001 | c0007 | t0004 | g0121 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18999 | hp2 | a0002 | c0001 | t0001 | g0245 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19000 | hp1 | a0002 | c0001 | t0001 | g0208 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19000 | hp2 | a0001 | c0006 | t0002 | g0345 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19001 | hp1 | a0002 | c0001 | t0001 | g0236 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19004 | hp1 | a0002 | c0001 | t0001 | g0241 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19006 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19006 | hp2 | a0001 | c0005 | t0001 | g0293 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19007 | hp2 | a0002 | c0001 | t0001 | g0217 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19012 | hp1 | a0002 | c0001 | t0001 | g0244 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19012 | hp2 | a0001 | c0008 | t0004 | g0323 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0149 | AFR | LWK | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19030 | hp2 | a0002 | c0001 | t0001 | g0134 | AFR | LWK | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19043 | hp1 | a0001 | c0007 | t0001 | g0100 | AFR | LWK | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0078 | AFR | LWK | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19054 | hp1 | a0001 | c0005 | t0001 | g0294 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19055 | hp1 | a0002 | c0001 | t0003 | g0064 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19055 | hp2 | a0001 | c0003 | t0011 | g0118 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19056 | hp1 | a0002 | c0001 | t0001 | g0235 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19056 | hp2 | a0005 | c0015 | t0002 | g0352 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19057 | hp2 | a0002 | c0001 | t0003 | g0189 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19060 | hp2 | a0002 | c0004 | t0003 | g0301 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19063 | hp1 | a0001 | c0007 | t0004 | g0124 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19063 | hp2 | a0001 | c0003 | t0001 | g0184 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19064 | hp1 | a0001 | c0005 | t0001 | g0302 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19064 | hp2 | a0001 | c0007 | t0004 | g0120 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19065 | hp2 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19066 | hp2 | a0002 | c0001 | t0001 | g0243 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19067 | hp1 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19067 | hp2 | a0001 | c0006 | t0002 | g0321 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19068 | hp1 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19068 | hp2 | a0002 | c0004 | t0003 | g0316 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19070 | hp1 | a0002 | c0001 | t0003 | g0201 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19070 | hp2 | a0002 | c0001 | t0001 | g0188 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19078 | hp1 | a0002 | c0001 | t0001 | g0210 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19078 | hp2 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19079 | hp1 | a0002 | c0001 | t0003 | g0226 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19079 | hp2 | a0002 | c0001 | t0001 | g0257 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19081 | hp1 | a0002 | c0004 | t0001 | g0272 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19084 | hp2 | a0002 | c0001 | t0003 | g0229 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19085 | hp2 | a0002 | c0001 | t0003 | g0024 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19086 | hp1 | a0001 | c0006 | t0002 | g0287 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19086 | hp2 | a0002 | c0004 | t0003 | g0313 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19088 | hp1 | a0002 | c0001 | t0001 | g0240 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19088 | hp2 | a0002 | c0001 | t0003 | g0043 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19090 | hp1 | a0003 | c0010 | t0003 | g0117 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19091 | hp1 | a0001 | c0009 | t0002 | g0017 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19091 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA20129 | hp1 | a0002 | c0001 | t0001 | g0133 | AFR | ASW | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA20129 | hp2 | a0002 | c0001 | t0001 | g0136 | AFR | ASW | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA20752 | hp1 | a0002 | c0004 | t0001 | g0295 | EUR | TSI | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0147 | EUR | TSI | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01123 | hp1 | a0002 | c0001 | t0001 | g0261 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0170 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02109 | hp1 | a0002 | c0001 | t0009 | g0007 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02109 | hp2 | a0002 | c0001 | t0001 | g0146 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02486 | hp1 | a0002 | c0001 | t0003 | g0081 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0126 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02559 | hp1 | a0001 | c0002 | t0008 | g0145 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02559 | hp2 | a0002 | c0001 | t0001 | g0132 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03471 | hp1 | a0002 | c0001 | t0001 | g0158 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03471 | hp2 | a0002 | c0001 | t0001 | g0095 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG06807 | hp1 | a0002 | c0001 | t0001 | g0015 | AFR | USA | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG06807 | hp2 | a0001 | c0007 | t0001 | g0165 | AFR | USA | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18955 | hp1 | a0002 | c0001 | t0003 | g0045 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA20300 | hp1 | a0001 | c0007 | t0001 | g0075 | AFR | USA | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA20300 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | USA | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0086 | AFR | LWK | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA21309 | hp2 | a0002 | c0004 | t0001 | g0343 | AFR | LWK | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
homoSapiens_chm13v2 | hp1 | a0002 | c0004 | t0003 | g0326 | REF | REF | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0139 | REF | REF | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:56729329
|
G | A | 1 | a0003 | 2 | HG00558.hp2 NA19090.hp1 |
missense_variant | MODERATE | c.1522C>T | p.Arg508Cys | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1673/3582 | 1522/1581 | 508/526 | chr3 | 56729329 | ||
chr3:56732325
|
C | T | 1 | a0004 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.1141G>A | p.Val381Met | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/10 | 1292/3582 | 1141/1581 | 381/526 | chr3 | 56732325 | ||
chr3:56737223
|
A | C | 2 | a0002a0003 | 147 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(144): Show |
missense_variant | MODERATE | c.1003T>G | p.Leu335Val | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/10 | 1154/3582 | 1003/1581 | 335/526 | chr3 | 56737223 | ||
chr3:56801761
|
T | C | 1 | a0005 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.38A>G | p.Lys13Arg | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/10 | 189/3582 | 38/1581 | 13/526 | chr3 | 56801761 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:56729288
|
G | A | 12 | a0001c0002a0001c0006a0001c0007others(9): Show | 277 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(274): Show |
synonymous_variant | LOW | c.1563C>T | p.His521His | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1714/3582 | 1563/1581 | 521/526 | chr3 | 56729288 | ||
chr3:56729300
|
T | C | 11 | a0001c0002a0001c0006a0001c0007others(8): Show | 276 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(273): Show |
synonymous_variant | LOW | c.1551A>G | p.Gly517Gly | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1702/3582 | 1551/1581 | 517/526 | chr3 | 56729300 | ||
chr3:56729497
|
A | G | 5 | a0001c0002a0001c0006a0001c0009others(2): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
synonymous_variant | LOW | c.1354T>C | p.Leu452Leu | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1505/3582 | 1354/1581 | 452/526 | chr3 | 56729497 | ||
chr3:56729507
|
T | C | 1 | a0001c0013 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1344A>G | p.Lys448Lys | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1495/3582 | 1344/1581 | 448/526 | chr3 | 56729507 | ||
chr3:56729591
|
A | G | 5 | a0001c0002a0001c0006a0001c0009others(2): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
synonymous_variant | LOW | c.1260T>C | p.Asn420Asn | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1411/3582 | 1260/1581 | 420/526 | chr3 | 56729591 | ||
chr3:56732407
|
C | G | 5 | a0001c0002a0001c0006a0001c0009others(2): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
synonymous_variant | LOW | c.1059G>C | p.Leu353Leu | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/10 | 1210/3582 | 1059/1581 | 353/526 | chr3 | 56732407 | ||
chr3:56773772
|
C | T | 1 | a0001c0009 | 1 | NA19091.hp1 | synonymous_variant | LOW | c.141G>A | p.Ser47Ser | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/10 | 292/3582 | 141/1581 | 47/526 | chr3 | 56773772 | ||
chr3:56801733
|
G | A | 5 | a0001c0005a0001c0006a0001c0008others(2): Show | 89 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
synonymous_variant | LOW | c.66C>T | p.Pro22Pro | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/10 | 217/3582 | 66/1581 | 22/526 | chr3 | 56801733 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:56727622
|
A | G | 7 | a0002c0001t0003a0002c0001t0013a0002c0004t0003others(4): Show | 62 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1648T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1648 | chr3 | 56727622 | |||||
chr3:56727665
|
G | C | 1 | a0002c0001t0013 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1605C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1605 | chr3 | 56727665 | |||||
chr3:56727687
|
G | A | 7 | a0001c0002t0002a0001c0002t0006a0001c0002t0010others(4): Show | 101 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1583C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1583 | chr3 | 56727687 | |||||
chr3:56727893
|
C | T | 1 | a0002c0004t0012 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1377G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1377 | chr3 | 56727893 | |||||
chr3:56728013
|
A | G | 2 | a0001c0002t0005a0001c0002t0017 | 4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1257T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1257 | chr3 | 56728013 | |||||
chr3:56728217
|
T | C | 11 | a0001c0002t0002a0001c0002t0005a0001c0002t0006others(8): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1053A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1053 | chr3 | 56728217 | |||||
chr3:56728221
|
C | T | 2 | a0001c0007t0004a0001c0008t0004 | 14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1049G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1049 | chr3 | 56728221 | |||||
chr3:56728307
|
G | A | 1 | a0002c0004t0014 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*963C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 963 | chr3 | 56728307 | |||||
chr3:56728449
|
C | T | 2 | a0001c0002t0008a0004c0011t0008 | 2 | HG02559.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*821G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 821 | chr3 | 56728449 | |||||
chr3:56728679
|
C | T | 1 | a0001c0003t0011 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*591G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 591 | chr3 | 56728679 | |||||
chr3:56728712
|
T | G | 1 | a0001c0003t0015 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*558A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 558 | chr3 | 56728712 | |||||
chr3:56728736
|
T | C | 4 | a0001c0002t0005a0001c0002t0008a0001c0002t0017others(1): Show | 6 | HG02055.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*534A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 534 | chr3 | 56728736 | |||||
chr3:56728737
|
G | A | 1 | a0001c0002t0017 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*533C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 533 | chr3 | 56728737 | |||||
chr3:56728746
|
C | G | 4 | a0001c0002t0005a0001c0002t0008a0001c0002t0017others(1): Show | 6 | HG02055.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*524G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 524 | chr3 | 56728746 | |||||
chr3:56728905
|
A | G | 1 | a0002c0001t0007 | 2 | HG02451.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*365T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 365 | chr3 | 56728905 | |||||
chr3:56728920
|
C | A | 1 | a0002c0001t0016 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*350G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 350 | chr3 | 56728920 | |||||
chr3:56728939
|
A | G | 11 | a0001c0002t0002a0001c0002t0005a0001c0002t0006others(8): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*331T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 331 | chr3 | 56728939 | |||||
chr3:56728940
|
A | G | 11 | a0001c0002t0002a0001c0002t0005a0001c0002t0006others(8): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*330T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 330 | chr3 | 56728940 | |||||
chr3:56728968
|
ATTCT | A | 4 | a0001c0002t0005a0001c0002t0008a0001c0002t0017others(1): Show | 6 | HG02055.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*298_*301delAGAA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 298 | chr3 | 56728968 | |||||
chr3:56729200
|
T | C | 7 | a0001c0002t0002a0001c0002t0006a0001c0002t0010others(4): Show | 101 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*70A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 70 | chr3 | 56729200 | |||||
chr3:56801868
|
A | G | 1 | a0001c0006t0018 | 1 | NA18972.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/10 | 70 | chr3 | 56801868 | |||||
chr3:56801873
|
G | C | 1 | a0001c0006t0018 | 1 | NA18972.hp1 | 5_prime_UTR_variant | MODIFIER | c.-75C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/10 | 75 | chr3 | 56801873 | |||||
chr3:56801919
|
C | T | 1 | a0001c0002t0010 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/10 | 121 | chr3 | 56801919 | |||||
chr3:56801933
|
C | T | 2 | a0001c0002t0006a0002c0001t0009 | 3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
5_prime_UTR_variant | MODIFIER | c.-135G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/10 | 135 | chr3 | 56801933 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:56729746
|
T | A | 2 | a0001c0007t0001g0093a0001c0007t0001g0165 | 2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1229-124A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729746 | ||||||
chr3:56729853
|
C | CTCTCAGA | 104 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(101): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-232_1229-231i others(9): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729853 | ||||||
chr3:56729855
|
G | A | 104 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(101): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-233C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729855 | ||||||
chr3:56729856
|
G | C | 104 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(101): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-234C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729856 | ||||||
chr3:56729857
|
T | C | 104 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(101): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-235A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729857 | ||||||
chr3:56729946
|
G | A | 2 | a0001c0002t0002g0157a0001c0003t0001g0187 | 2 | HG01175.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1229-324C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729946 | ||||||
chr3:56729947
|
G | T | 1 | a0001c0003t0001g0187 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1229-325C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729947 | ||||||
chr3:56729974
|
C | T | 104 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(101): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-352G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729974 | ||||||
chr3:56730102
|
G | A | 98 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(95): Show | 101 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1229-480C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730102 | ||||||
chr3:56730130
|
C | G | 2 | a0002c0001t0001g0143a0002c0001t0001g0144 | 2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1229-508G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730130 | ||||||
chr3:56730169
|
G | A | 1 | a0002c0001t0003g0025 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1229-547C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730169 | ||||||
chr3:56730301
|
C | T | 104 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(101): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-679G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730301 | ||||||
chr3:56730352
|
A | T | 1 | a0001c0002t0002g0197 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1229-730T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730352 | ||||||
chr3:56730365
|
A | G | 7 | a0001c0007t0001g0075a0001c0007t0001g0092a0001c0007t0001g0093others(4): Show | 7 | HG01070.hp1 HG02280.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1229-743T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730365 | ||||||
chr3:56730388
|
C | CT | 9 | a0001c0003t0001g0070a0001c0003t0001g0186a0001c0003t0001g0254others(6): Show | 9 | HG00597.hp2 HG02074.hp1 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.1229-767dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730388 | ||||||
chr3:56730388
|
CT | C | 18 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(15): Show | 19 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.1229-767delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730388 | ||||||
chr3:56730388
|
CTTTTTTT others(4): Show |
C | 98 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(95): Show | 101 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1229-777_1229-767d others(13): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730388 | ||||||
chr3:56730413
|
A | G | 104 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(101): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-791T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730413 | ||||||
chr3:56730447
|
C | T | 14 | a0001c0007t0004g0027a0001c0007t0004g0046a0001c0007t0004g0063others(11): Show | 14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1229-825G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730447 | ||||||
chr3:56730625
|
C | T | 1 | a0001c0007t0001g0162 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1229-1003G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730625 | ||||||
chr3:56730792
|
G | T | 3 | a0001c0007t0004g0046a0001c0007t0004g0063a0001c0008t0004g0323 | 3 | HG02523.hp1 NA18965.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1229-1170C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730792 | ||||||
chr3:56730816
|
A | G | 12 | a0001c0007t0004g0027a0001c0007t0004g0046a0001c0007t0004g0063others(9): Show | 12 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.1229-1194T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730816 | ||||||
chr3:56730825
|
G | A | 2 | a0001c0005t0001g0268a0001c0005t0001g0280 | 2 | HG00741.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1229-1203C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730825 | ||||||
chr3:56730903
|
C | T | 165 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(162): Show | 169 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.1229-1281G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730903 | ||||||
chr3:56730966
|
A | C | 1 | a0001c0002t0002g0219 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1228+1272T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730966 | ||||||
chr3:56730984
|
T | C | 6 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228+1254A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730984 | ||||||
chr3:56731008
|
T | C | 98 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(95): Show | 101 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1228+1230A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731008 | ||||||
chr3:56731156
|
G | A | 155 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(152): Show | 158 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.1228+1082C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731156 | ||||||
chr3:56731219
|
A | T | 98 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(95): Show | 101 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1228+1019T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731219 | ||||||
chr3:56731411
|
C | T | 104 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(101): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1228+827G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731411 | ||||||
chr3:56731449
|
T | C | 2 | a0002c0001t0003g0020a0002c0004t0003g0344 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1228+789A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731449 | ||||||
chr3:56731517
|
G | T | 155 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(152): Show | 158 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.1228+721C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731517 | ||||||
chr3:56731592
|
C | CCGGGTTT others(598): Show |
1 | a0001c0002t0008g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1228+645_1228+646i others(607): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | ||||||
chr3:56731592
|
C | CCGGGTTT others(609): Show |
1 | a0004c0011t0008g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1228+645_1228+646i others(618): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | ||||||
chr3:56731592
|
C | CCGGGTTT others(598): Show |
6 | a0001c0002t0002g0076a0001c0002t0002g0077a0001c0002t0002g0078others(3): Show | 6 | HG01099.hp1 HG02280.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228+645_1228+646i others(607): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | ||||||
chr3:56731592
|
C | CCGGGTTT others(612): Show |
1 | a0001c0002t0005g0152 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1228+645_1228+646i others(621): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | ||||||
chr3:56731592
|
C | CCGGGTTT others(613): Show |
2 | a0001c0002t0005g0211a0001c0002t0017g0161 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1228+645_1228+646i others(622): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | ||||||
chr3:56731592
|
C | CCGGGTTT others(614): Show |
1 | a0001c0002t0005g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1228+645_1228+646i others(623): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | ||||||
chr3:56731592
|
C | CCGGGTTT others(596): Show |
3 | a0001c0002t0002g0044a0001c0002t0002g0053a0001c0006t0002g0288 | 3 | NA18966.hp1 NA18968.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1228+645_1228+646i others(605): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | ||||||
chr3:56731592
|
C | CCGGGTTT others(597): Show |
62 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(59): Show | 64 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1228+645_1228+646i others(606): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | ||||||
chr3:56731592
|
C | CCGGGTTT others(598): Show |
24 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(21): Show | 25 | HG00621.hp1 HG00673.hp1 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.1228+645_1228+646i others(607): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | ||||||
chr3:56731592
|
C | CCGGGTTT others(599): Show |
1 | a0001c0002t0002g0190 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1228+645_1228+646i others(608): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | ||||||
chr3:56731592
|
C | CCGGGTTT others(599): Show |
2 | a0001c0002t0002g0194a0001c0002t0002g0256 | 2 | NA18953.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1228+645_1228+646i others(608): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | ||||||
chr3:56731594
|
G | A | 29 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(26): Show | 29 | HG00558.hp1 HG01106.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1228+644C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731594 | ||||||
chr3:56731621
|
G | A | 104 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(101): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1228+617C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731621 | ||||||
chr3:56731775
|
A | C | 1 | a0001c0003t0001g0168 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1228+463T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731775 | ||||||
chr3:56731778
|
T | G | 1 | a0002c0001t0001g0136 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1228+460A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731778 | ||||||
chr3:56731786
|
C | G | 1 | a0004c0011t0008g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1228+452G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731786 | ||||||
chr3:56731977
|
T | C | 4 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(1): Show | 4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228+261A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731977 | ||||||
chr3:56731978
|
G | A | 1 | a0001c0002t0017g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1228+260C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731978 | ||||||
chr3:56731986
|
T | G | 105 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(102): Show | 108 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1228+252A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731986 | ||||||
chr3:56732110
|
G | A | 29 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(26): Show | 29 | HG00558.hp1 HG01106.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1228+128C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56732110 | ||||||
chr3:56732655
|
C | T | 1 | a0002c0001t0001g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1042-231G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56732655 | ||||||
chr3:56732656
|
C | T | 1 | a0001c0003t0001g0163 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1042-232G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56732656 | ||||||
chr3:56732922
|
C | T | 1 | a0001c0012t0001g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1042-498G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56732922 | ||||||
chr3:56732951
|
T | C | 104 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(101): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1042-527A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56732951 | ||||||
chr3:56732997
|
A | G | 1 | a0001c0003t0001g0058 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1042-573T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56732997 | ||||||
chr3:56733066
|
C | T | 1 | a0001c0003t0001g0183 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1042-642G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733066 | ||||||
chr3:56733082
|
G | C | 2 | a0001c0003t0001g0012a0001c0003t0001g0223 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1042-658C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733082 | ||||||
chr3:56733140
|
G | A | 23 | a0001c0002t0002g0036a0001c0002t0002g0037a0001c0002t0002g0053others(20): Show | 24 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1042-716C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733140 | ||||||
chr3:56733152
|
G | A | 18 | a0001c0002t0002g0036a0001c0002t0002g0037a0001c0002t0002g0053others(15): Show | 19 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1042-728C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733152 | ||||||
chr3:56733258
|
G | C | 1 | a0001c0003t0001g0163 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1042-834C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733258 | ||||||
chr3:56733281
|
TA | T | 53 | a0001c0002t0002g0256a0001c0003t0001g0011a0001c0003t0001g0012others(50): Show | 53 | HG00558.hp1 HG01070.hp1 HG01106.hp2 others(50): Show |
intron_variant | MODIFIER | c.1042-858delT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733281 | ||||||
chr3:56733281
|
TAA | T | 103 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(100): Show | 106 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1042-859_1042-858d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733281 | ||||||
chr3:56733317
|
C | T | 3 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212 | 3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1042-893G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733317 | ||||||
chr3:56733319
|
A | G | 3 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212 | 3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1042-895T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733319 | ||||||
chr3:56733321
|
G | C | 3 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212 | 3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1042-897C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733321 | ||||||
chr3:56733322
|
T | G | 3 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212 | 3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1042-898A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733322 | ||||||
chr3:56733331
|
C | CG | 31 | a0001c0003t0001g0031a0001c0003t0001g0099a0001c0003t0001g0154others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.1042-908dupC | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733331 | ||||||
chr3:56733331
|
C | G | 2 | a0001c0002t0005g0211a0001c0002t0005g0212 | 2 | HG02055.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1042-907G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733331 | ||||||
chr3:56733331
|
CG | C | 96 | a0001c0002t0002g0003a0001c0002t0002g0026a0001c0002t0002g0028others(93): Show | 98 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1042-908delC | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733331 | ||||||
chr3:56733331
|
CGG | C | 50 | a0001c0002t0002g0002a0001c0002t0002g0018a0001c0002t0002g0019others(47): Show | 52 | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.1042-909_1042-908d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733331 | ||||||
chr3:56733331
|
CGGG | C | 30 | a0001c0002t0002g0051a0001c0002t0002g0076a0001c0002t0002g0082others(27): Show | 30 | HG00323.hp2 HG01099.hp1 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.1042-910_1042-908d others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733331 | ||||||
chr3:56733335
|
G | GC | 4 | a0002c0004t0003g0270a0002c0004t0003g0301a0002c0004t0003g0313others(1): Show | 4 | HG02135.hp2 NA19060.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-912_1042-911i others(3): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733335 | ||||||
chr3:56733336
|
G | C | 2 | a0002c0004t0003g0316a0003c0014t0003g0320 | 2 | HG00558.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1042-912C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733336 | ||||||
chr3:56733337
|
G | T | 1 | a0001c0002t0002g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1042-913C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733337 | ||||||
chr3:56733341
|
G | C | 2 | a0001c0006t0002g0345a0001c0006t0002g0346 | 2 | NA18960.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1042-917C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733341 | ||||||
chr3:56733345
|
G | T | 2 | a0001c0007t0001g0075a0001c0007t0001g0092 | 2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1042-921C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733345 | ||||||
chr3:56733346
|
G | A | 59 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(56): Show | 61 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1042-922C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733346 | ||||||
chr3:56733346
|
G | C | 4 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0017g0161others(1): Show | 4 | HG02647.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042-922C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733346 | ||||||
chr3:56733346
|
G | GA | 5 | a0001c0002t0002g0053a0001c0002t0002g0125a0001c0002t0002g0265others(2): Show | 5 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-923_1042-922i others(3): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733346 | ||||||
chr3:56733348
|
C | T | 1 | a0002c0001t0003g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1042-924G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733348 | ||||||
chr3:56733349
|
G | A | 1 | a0001c0002t0002g0149 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1042-925C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733349 | ||||||
chr3:56733425
|
C | A | 342 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(339): Show | 347 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.1042-1001G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733425 | ||||||
chr3:56733443
|
T | A | 1 | a0001c0002t0002g0149 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1042-1019A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733443 | ||||||
chr3:56733521
|
A | G | 7 | a0001c0007t0001g0075a0001c0007t0001g0092a0001c0007t0001g0093others(4): Show | 7 | HG01070.hp1 HG02280.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1042-1097T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733521 | ||||||
chr3:56733534
|
C | T | 1 | a0001c0012t0001g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1042-1110G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733534 | ||||||
chr3:56733606
|
G | A | 3 | a0002c0001t0001g0133a0002c0001t0001g0134a0002c0004t0001g0343 | 3 | NA19030.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1042-1182C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733606 | ||||||
chr3:56733645
|
G | C | 104 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(101): Show | 107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1042-1221C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733645 | ||||||
chr3:56733661
|
G | A | 3 | a0001c0003t0001g0099a0001c0003t0001g0258a0001c0005t0001g0330 | 3 | HG01106.hp2 HG01884.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1042-1237C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733661 | ||||||
chr3:56733667
|
G | C | 1 | a0001c0006t0002g0337 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1042-1243C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733667 | ||||||
chr3:56733752
|
G | A | 1 | a0001c0002t0002g0061 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1042-1328C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733752 | ||||||
chr3:56733810
|
C | T | 3 | a0002c0001t0001g0131a0002c0001t0001g0243a0002c0001t0001g0244 | 3 | NA19012.hp1 NA19066.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1042-1386G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733810 | ||||||
chr3:56733845
|
G | A | 3 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212 | 3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1042-1421C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733845 | ||||||
chr3:56733846
|
C | T | 2 | a0001c0007t0001g0093a0001c0007t0001g0165 | 2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1042-1422G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733846 | ||||||
chr3:56733870
|
G | A | 1 | a0001c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1042-1446C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733870 | ||||||
chr3:56733902
|
T | A | 1 | a0001c0002t0008g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1042-1478A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733902 | ||||||
chr3:56733963
|
G | A | 1 | a0004c0011t0008g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1042-1539C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733963 | ||||||
chr3:56733984
|
C | CA | 21 | a0001c0002t0002g0192a0001c0002t0010g0009a0001c0002t0017g0161others(18): Show | 21 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1042-1561dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733984 | ||||||
chr3:56733984
|
C | CAA | 70 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(67): Show | 72 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1042-1562_1042-156 others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733984 | ||||||
chr3:56733984
|
C | CAAA | 11 | a0001c0002t0002g0019a0001c0002t0002g0123a0001c0002t0002g0128others(8): Show | 11 | HG01981.hp2 HG02083.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1042-1563_1042-156 others(7): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733984 | ||||||
chr3:56733984
|
CA | C | 29 | a0001c0007t0001g0073a0001c0007t0001g0075a0001c0007t0001g0093others(26): Show | 29 | HG01070.hp1 HG01361.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.1042-1561delT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733984 | ||||||
chr3:56733984
|
CAA | C | 25 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(22): Show | 25 | HG00558.hp1 HG01106.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1042-1562_1042-156 others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733984 | ||||||
chr3:56733984
|
CAAAA | C | 18 | a0001c0002t0002g0036a0001c0002t0002g0037a0001c0002t0002g0053others(15): Show | 19 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1042-1564_1042-156 others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733984 | ||||||
chr3:56734010
|
G | C | 1 | a0001c0012t0001g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1042-1586C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734010 | ||||||
chr3:56734044
|
C | G | 28 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(25): Show | 28 | HG00558.hp1 HG01106.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1042-1620G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734044 | ||||||
chr3:56734214
|
C | T | 100 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(97): Show | 103 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1042-1790G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734214 | ||||||
chr3:56734231
|
C | G | 100 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(97): Show | 103 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1042-1807G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734231 | ||||||
chr3:56734232
|
G | A | 1 | a0001c0005t0001g0308 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1042-1808C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734232 | ||||||
chr3:56734346
|
G | T | 119 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(116): Show | 122 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.1042-1922C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734346 | ||||||
chr3:56734376
|
T | C | 2 | a0001c0002t0002g0220a0001c0002t0002g0221 | 2 | NA18940.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1042-1952A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734376 | ||||||
chr3:56734443
|
G | A | 20 | a0001c0003t0001g0023a0001c0003t0001g0029a0001c0003t0001g0056others(17): Show | 20 | HG00558.hp1 HG01496.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.1042-2019C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734443 | ||||||
chr3:56734511
|
T | C | 1 | a0001c0012t0001g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1042-2087A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734511 | ||||||
chr3:56734833
|
G | C | 1 | a0001c0002t0002g0196 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1041+2352C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734833 | ||||||
chr3:56734896
|
T | G | 7 | a0002c0001t0001g0131a0002c0001t0001g0235a0002c0001t0001g0241others(4): Show | 7 | NA18945.hp2 NA19004.hp1 NA19012.hp1 others(4): Show |
intron_variant | MODIFIER | c.1041+2289A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734896 | ||||||
chr3:56734972
|
T | C | 152 | a0001c0007t0001g0075a0001c0007t0001g0092a0001c0007t0001g0093others(149): Show | 154 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.1041+2213A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734972 | ||||||
chr3:56735058
|
C | T | 1 | a0001c0003t0001g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1041+2127G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735058 | ||||||
chr3:56735235
|
G | C | 2 | a0001c0002t0006g0006a0001c0002t0006g0008 | 2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1041+1950C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735235 | ||||||
chr3:56735309
|
A | G | 4 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(1): Show | 4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+1876T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735309 | ||||||
chr3:56735392
|
C | G | 1 | a0001c0012t0001g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1041+1793G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735392 | ||||||
chr3:56735418
|
C | T | 100 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(97): Show | 103 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1041+1767G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735418 | ||||||
chr3:56735433
|
C | T | 4 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(1): Show | 4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+1752G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735433 | ||||||
chr3:56735483
|
A | C | 14 | a0001c0007t0004g0027a0001c0007t0004g0046a0001c0007t0004g0063others(11): Show | 14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1041+1702T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735483 | ||||||
chr3:56735519
|
T | A | 1 | a0001c0002t0008g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1041+1666A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735519 | ||||||
chr3:56735534
|
C | T | 2 | a0001c0002t0002g0126a0001c0002t0010g0009 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1041+1651G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735534 | ||||||
chr3:56735575
|
G | A | 1 | a0001c0003t0001g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1041+1610C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735575 | ||||||
chr3:56735603
|
G | C | 1 | a0004c0011t0008g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1041+1582C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735603 | ||||||
chr3:56735646
|
G | A | 1 | a0001c0002t0008g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1041+1539C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735646 | ||||||
chr3:56735688
|
T | C | 100 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(97): Show | 103 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1041+1497A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735688 | ||||||
chr3:56735820
|
C | T | 3 | a0001c0003t0001g0127a0001c0003t0001g0171a0001c0003t0001g0185 | 3 | HG00639.hp1 HG01099.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1041+1365G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735820 | ||||||
chr3:56735850
|
T | C | 100 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(97): Show | 103 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1041+1335A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735850 | ||||||
chr3:56735945
|
A | G | 1 | a0002c0004t0003g0282 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1041+1240T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735945 | ||||||
chr3:56736035
|
A | C | 2 | a0001c0007t0001g0100a0001c0007t0001g0101 | 2 | NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1041+1150T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736035 | ||||||
chr3:56736038
|
A | C | 1 | a0001c0003t0001g0183 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1041+1147T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736038 | ||||||
chr3:56736041
|
G | A | 1 | a0002c0004t0003g0340 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1041+1144C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736041 | ||||||
chr3:56736049
|
A | AAC | 3 | a0001c0003t0001g0091a0001c0003t0001g0177a0001c0005t0001g0302 | 3 | HG01167.hp1 HG03927.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1041+1134_1041+113 others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | ||||||
chr3:56736049
|
A | AACAC | 4 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(1): Show | 4 | HG02055.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+1132_1041+113 others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | ||||||
chr3:56736049
|
A | AACACAC | 5 | a0001c0002t0017g0161a0001c0003t0001g0011a0001c0003t0001g0012others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041+1130_1041+113 others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | ||||||
chr3:56736049
|
AAC | A | 7 | a0001c0003t0001g0249a0001c0005t0001g0305a0001c0013t0001g0150others(4): Show | 7 | HG01975.hp1 HG02257.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+1134_1041+113 others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | ||||||
chr3:56736049
|
AACAC | A | 83 | a0001c0003t0001g0029a0001c0003t0001g0056a0001c0003t0001g0057others(80): Show | 84 | HG00323.hp2 HG00558.hp1 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.1041+1132_1041+113 others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | ||||||
chr3:56736049
|
AACACAC | A | 81 | a0001c0007t0001g0075a0001c0007t0001g0092a0001c0007t0001g0093others(78): Show | 82 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1041+1130_1041+113 others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | ||||||
chr3:56736049
|
AACACACA others(7): Show |
A | 100 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(97): Show | 103 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1041+1122_1041+113 others(18): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | ||||||
chr3:56736063
|
C | CACAA | 14 | a0001c0007t0004g0027a0001c0007t0004g0046a0001c0007t0004g0063others(11): Show | 14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1041+1121_1041+112 others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736063 | ||||||
chr3:56736341
|
A | G | 102 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(99): Show | 105 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1041+844T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736341 | ||||||
chr3:56736454
|
A | T | 3 | a0001c0002t0002g0126a0001c0002t0002g0149a0001c0002t0010g0009 | 3 | HG02258.hp2 HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1041+731T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736454 | ||||||
chr3:56736575
|
C | T | 1 | a0001c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1041+610G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736575 | ||||||
chr3:56736645
|
A | G | 1 | a0001c0003t0001g0163 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1041+540T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736645 | ||||||
chr3:56736774
|
T | C | 8 | a0002c0001t0001g0010a0002c0001t0001g0135a0002c0001t0001g0136others(5): Show | 9 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1041+411A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736774 | ||||||
chr3:56736808
|
G | A | 1 | a0002c0004t0003g0282 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1041+377C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736808 | ||||||
chr3:56736818
|
C | T | 1 | a0001c0002t0002g0042 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1041+367G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736818 | ||||||
chr3:56736986
|
T | C | 1 | a0001c0007t0004g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1041+199A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736986 | ||||||
chr3:56737414
|
G | T | 2 | a0001c0002t0002g0076a0001c0002t0002g0085 | 2 | HG01099.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.871-59C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737414 | ||||||
chr3:56737427
|
A | T | 1 | a0001c0002t0002g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.871-72T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737427 | ||||||
chr3:56737484
|
T | C | 9 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0094others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-129A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737484 | ||||||
chr3:56737495
|
G | GA | 271 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(268): Show | 276 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(273): Show |
intron_variant | MODIFIER | c.871-141dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737495 | ||||||
chr3:56737527
|
C | G | 1 | a0001c0002t0017g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.871-172G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737527 | ||||||
chr3:56737677
|
C | T | 1 | a0001c0002t0008g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.871-322G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737677 | ||||||
chr3:56737706
|
A | G | 1 | a0001c0002t0002g0157 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.871-351T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737706 | ||||||
chr3:56737803
|
C | G | 2 | a0001c0002t0006g0006a0001c0002t0006g0008 | 2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.871-448G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737803 | ||||||
chr3:56737938
|
A | G | 108 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(105): Show | 111 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.871-583T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737938 | ||||||
chr3:56737971
|
C | T | 96 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(93): Show | 99 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.871-616G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737971 | ||||||
chr3:56738052
|
T | C | 1 | a0001c0002t0002g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.871-697A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738052 | ||||||
chr3:56738087
|
A | G | 1 | a0001c0003t0001g0175 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.871-732T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738087 | ||||||
chr3:56738097
|
G | A | 21 | a0002c0001t0003g0114a0002c0001t0003g0156a0002c0001t0003g0164others(18): Show | 21 | HG00140.hp1 HG00558.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.871-742C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738097 | ||||||
chr3:56738146
|
T | G | 1 | a0002c0001t0001g0089 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.871-791A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738146 | ||||||
chr3:56738287
|
C | A | 4 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(1): Show | 4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-932G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738287 | ||||||
chr3:56738311
|
T | C | 2 | a0001c0002t0002g0042a0001c0002t0002g0191 | 2 | HG02027.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.871-956A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738311 | ||||||
chr3:56738395
|
C | T | 1 | a0001c0002t0017g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.871-1040G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738395 | ||||||
chr3:56738685
|
G | A | 7 | a0001c0007t0001g0075a0001c0007t0001g0092a0001c0007t0001g0093others(4): Show | 7 | HG01070.hp1 HG02280.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-1330C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738685 | ||||||
chr3:56738806
|
C | T | 4 | a0001c0002t0002g0169a0001c0006t0002g0275a0001c0006t0002g0276others(1): Show | 4 | HG00639.hp2 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-1451G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738806 | ||||||
chr3:56738882
|
G | C | 7 | a0001c0007t0001g0075a0001c0007t0001g0092a0001c0007t0001g0093others(4): Show | 7 | HG01070.hp1 HG02280.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-1527C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738882 | ||||||
chr3:56738981
|
G | C | 1 | a0001c0005t0001g0297 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.871-1626C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738981 | ||||||
chr3:56738985
|
C | T | 1 | a0002c0001t0001g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.871-1630G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738985 | ||||||
chr3:56739146
|
T | C | 1 | a0001c0006t0002g0337 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.871-1791A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739146 | ||||||
chr3:56739205
|
T | C | 1 | a0001c0007t0001g0162 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.871-1850A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739205 | ||||||
chr3:56739232
|
G | A | 1 | a0001c0003t0001g0174 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.871-1877C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739232 | ||||||
chr3:56739309
|
G | C | 1 | a0001c0005t0001g0294 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.871-1954C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739309 | ||||||
chr3:56739377
|
T | C | 2 | a0001c0007t0001g0075a0001c0007t0001g0092 | 2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.871-2022A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739377 | ||||||
chr3:56739395
|
C | T | 267 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(264): Show | 272 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.871-2040G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739395 | ||||||
chr3:56739396
|
CT | C | 288 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(285): Show | 293 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.871-2042delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739396 | ||||||
chr3:56739659
|
C | T | 2 | a0001c0002t0002g0126a0001c0002t0010g0009 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.871-2304G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739659 | ||||||
chr3:56739675
|
C | T | 8 | a0002c0001t0001g0010a0002c0001t0001g0135a0002c0001t0001g0136others(5): Show | 9 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.871-2320G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739675 | ||||||
chr3:56739679
|
T | C | 2 | a0001c0002t0002g0126a0001c0002t0010g0009 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.871-2324A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739679 | ||||||
chr3:56739848
|
T | C | 2 | a0001c0002t0002g0126a0001c0002t0010g0009 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.871-2493A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739848 | ||||||
chr3:56739851
|
T | C | 2 | a0001c0002t0002g0126a0001c0002t0010g0009 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.871-2496A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739851 | ||||||
chr3:56739872
|
T | C | 2 | a0001c0002t0002g0126a0001c0002t0010g0009 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.871-2517A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739872 | ||||||
chr3:56739891
|
A | G | 2 | a0001c0007t0001g0093a0001c0007t0001g0165 | 2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.871-2536T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739891 | ||||||
chr3:56739901
|
A | AT | 77 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0021others(74): Show | 79 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.871-2547dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739901 | ||||||
chr3:56739911
|
T | C | 2 | a0001c0002t0002g0126a0001c0002t0010g0009 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.871-2556A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739911 | ||||||
chr3:56739994
|
G | A | 1 | a0004c0011t0008g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.871-2639C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739994 | ||||||
chr3:56740000
|
A | C | 14 | a0001c0007t0004g0027a0001c0007t0004g0046a0001c0007t0004g0063others(11): Show | 14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.871-2645T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740000 | ||||||
chr3:56740041
|
G | A | 108 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(105): Show | 111 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.871-2686C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740041 | ||||||
chr3:56740125
|
C | A | 1 | a0001c0002t0017g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.871-2770G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740125 | ||||||
chr3:56740132
|
G | A | 9 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0094others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-2777C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740132 | ||||||
chr3:56740183
|
C | T | 1 | a0001c0007t0004g0110 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.871-2828G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740183 | ||||||
chr3:56740187
|
C | CA | 148 | a0001c0002t0002g0028a0001c0002t0002g0044a0001c0005t0001g0297others(145): Show | 150 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.871-2833dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740187 | ||||||
chr3:56740270
|
T | TA | 263 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(260): Show | 268 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.871-2916dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740270 | ||||||
chr3:56740270
|
T | TAA | 7 | a0001c0007t0001g0075a0001c0007t0001g0092a0001c0007t0001g0093others(4): Show | 7 | HG01070.hp1 HG02280.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-2917_871-2916d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740270 | ||||||
chr3:56740281
|
A | AC | 4 | a0002c0004t0003g0270a0002c0004t0003g0301a0002c0004t0003g0313others(1): Show | 4 | HG02135.hp2 NA19060.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2927dupG | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740281 | ||||||
chr3:56740569
|
G | A | 1 | a0001c0002t0002g0149 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.871-3214C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740569 | ||||||
chr3:56740620
|
C | T | 1 | a0004c0011t0008g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.871-3265G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740620 | ||||||
chr3:56740621
|
T | C | 1 | a0002c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.871-3266A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740621 | ||||||
chr3:56740833
|
G | A | 1 | a0002c0001t0001g0106 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.871-3478C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740833 | ||||||
chr3:56740957
|
T | C | 14 | a0001c0007t0004g0027a0001c0007t0004g0046a0001c0007t0004g0063others(11): Show | 14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.871-3602A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740957 | ||||||
chr3:56741184
|
C | CCTT | 4 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0094others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-3830_871-3829i others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741184 | ||||||
chr3:56741184
|
C | CCTTT | 5 | a0002c0001t0001g0146a0002c0001t0001g0147a0002c0001t0001g0158others(2): Show | 5 | HG02109.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-3830_871-3829i others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741184 | ||||||
chr3:56741184
|
C | CT | 10 | a0001c0002t0002g0051a0001c0002t0008g0145a0001c0002t0017g0161others(7): Show | 10 | HG01070.hp1 HG01175.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.871-3830dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741184 | ||||||
chr3:56741184
|
C | CTT | 137 | a0001c0002t0002g0028a0001c0002t0002g0044a0001c0005t0001g0297others(134): Show | 139 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.871-3831_871-3830d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741184 | ||||||
chr3:56741215
|
C | T | 11 | a0001c0003t0001g0091a0001c0003t0001g0154a0001c0003t0001g0155others(8): Show | 11 | HG00140.hp2 HG00280.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.871-3860G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741215 | ||||||
chr3:56741427
|
G | A | 1 | a0004c0011t0008g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.870+3778C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741427 | ||||||
chr3:56741482
|
C | T | 1 | a0002c0001t0001g0260 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.870+3723G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741482 | ||||||
chr3:56741496
|
C | CT | 192 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(189): Show | 195 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.870+3708dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741496 | ||||||
chr3:56741496
|
C | CTT | 33 | a0001c0002t0002g0061a0001c0002t0002g0129a0001c0002t0002g0169others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.870+3707_870+3708d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741496 | ||||||
chr3:56741496
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0002g0195a0001c0012t0001g0104 | 2 | HG03540.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.870+3698_870+3708d others(13): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741496 | ||||||
chr3:56741496
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0001t0001g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.870+3697_870+3708d others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741496 | ||||||
chr3:56741532
|
G | A | 1 | a0004c0011t0008g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.870+3673C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741532 | ||||||
chr3:56741659
|
A | G | 3 | a0002c0001t0001g0232a0002c0001t0001g0233a0002c0001t0001g0234 | 3 | HG01109.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.870+3546T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741659 | ||||||
chr3:56741689
|
G | C | 1 | a0001c0005t0001g0297 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.870+3516C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741689 | ||||||
chr3:56741694
|
G | A | 1 | a0002c0001t0001g0066 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.870+3511C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741694 | ||||||
chr3:56741707
|
G | C | 3 | a0001c0002t0002g0026a0001c0002t0002g0200a0001c0006t0002g0281 | 3 | NA18950.hp2 NA18995.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.870+3498C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741707 | ||||||
chr3:56742214
|
G | A | 1 | a0001c0005t0001g0302 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.870+2991C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56742214 | ||||||
chr3:56742215
|
G | A | 2 | a0001c0005t0001g0303a0001c0005t0001g0306 | 2 | HG00323.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.870+2990C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56742215 | ||||||
chr3:56742391
|
T | C | 4 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(1): Show | 4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+2814A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56742391 | ||||||
chr3:56742818
|
C | T | 2 | a0001c0002t0002g0126a0001c0002t0010g0009 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.870+2387G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56742818 | ||||||
chr3:56742823
|
T | C | 2 | a0001c0002t0002g0126a0001c0002t0010g0009 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.870+2382A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56742823 | ||||||
chr3:56742880
|
T | C | 146 | a0001c0002t0002g0082a0001c0002t0002g0148a0002c0001t0001g0010others(143): Show | 148 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.870+2325A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56742880 | ||||||
chr3:56743025
|
G | T | 1 | a0001c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.870+2180C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743025 | ||||||
chr3:56743086
|
A | G | 2 | a0001c0002t0002g0126a0001c0002t0010g0009 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.870+2119T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743086 | ||||||
chr3:56743189
|
G | T | 3 | a0001c0002t0002g0126a0001c0002t0010g0009a0001c0007t0001g0092 | 3 | HG02258.hp2 HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.870+2016C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743189 | ||||||
chr3:56743232
|
C | T | 2 | a0001c0002t0002g0126a0001c0002t0010g0009 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.870+1973G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743232 | ||||||
chr3:56743265
|
T | C | 2 | a0001c0002t0002g0126a0001c0002t0010g0009 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.870+1940A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743265 | ||||||
chr3:56743369
|
C | A | 1 | a0001c0002t0008g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.870+1836G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743369 | ||||||
chr3:56743390
|
T | C | 2 | a0001c0002t0005g0152a0001c0002t0005g0211 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.870+1815A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743390 | ||||||
chr3:56743468
|
T | A | 16 | a0002c0001t0001g0062a0002c0001t0001g0066a0002c0001t0001g0188others(13): Show | 16 | NA18612.hp1 NA18940.hp2 NA18942.hp1 others(13): Show |
intron_variant | MODIFIER | c.870+1737A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743468 | ||||||
chr3:56743474
|
T | C | 1 | a0001c0006t0018g0353 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.870+1731A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743474 | ||||||
chr3:56743493
|
T | C | 1 | a0001c0003t0001g0058 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.870+1712A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743493 | ||||||
chr3:56743557
|
G | C | 3 | a0001c0003t0001g0068a0001c0003t0001g0069a0001c0003t0001g0070 | 3 | NA18941.hp1 NA18955.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.870+1648C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743557 | ||||||
chr3:56743581
|
T | C | 8 | a0002c0001t0001g0010a0002c0001t0001g0135a0002c0001t0001g0136others(5): Show | 9 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.870+1624A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743581 | ||||||
chr3:56743583
|
T | G | 8 | a0002c0001t0001g0010a0002c0001t0001g0135a0002c0001t0001g0136others(5): Show | 9 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.870+1622A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743583 | ||||||
chr3:56743753
|
A | AT | 3 | a0001c0002t0002g0126a0001c0002t0010g0009a0004c0011t0008g0072 | 3 | HG02258.hp2 HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.870+1451dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743753 | ||||||
chr3:56743758
|
TGTCCCAG | T | 3 | a0001c0002t0002g0126a0001c0002t0010g0009a0004c0011t0008g0072 | 3 | HG02258.hp2 HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.870+1440_870+1446d others(9): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743758 | ||||||
chr3:56743785
|
C | T | 2 | a0001c0002t0002g0026a0001c0006t0002g0281 | 2 | NA18950.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.870+1420G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743785 | ||||||
chr3:56743854
|
A | C | 107 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(104): Show | 110 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.870+1351T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743854 | ||||||
chr3:56743965
|
A | G | 5 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.870+1240T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743965 | ||||||
chr3:56744067
|
C | T | 2 | a0001c0007t0001g0100a0002c0001t0001g0097 | 2 | HG01934.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.870+1138G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744067 | ||||||
chr3:56744082
|
T | C | 14 | a0001c0007t0004g0027a0001c0007t0004g0046a0001c0007t0004g0063others(11): Show | 14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.870+1123A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744082 | ||||||
chr3:56744222
|
G | C | 1 | a0002c0001t0001g0176 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.870+983C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744222 | ||||||
chr3:56744299
|
C | T | 1 | a0001c0002t0002g0036 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.870+906G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744299 | ||||||
chr3:56744320
|
C | T | 2 | a0001c0002t0002g0126a0004c0011t0008g0072 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.870+885G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744320 | ||||||
chr3:56744397
|
CT | C | 265 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(262): Show | 270 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.870+807delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744397 | ||||||
chr3:56744397
|
CTT | C | 15 | a0001c0007t0004g0027a0001c0007t0004g0046a0001c0007t0004g0063others(12): Show | 15 | HG01261.hp1 HG01361.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.870+806_870+807del others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744397 | ||||||
chr3:56744475
|
T | G | 9 | a0002c0001t0001g0074a0002c0001t0001g0135a0002c0001t0001g0136others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.870+730A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744475 | ||||||
chr3:56744519
|
T | C | 2 | a0001c0002t0002g0126a0004c0011t0008g0072 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.870+686A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744519 | ||||||
chr3:56744555
|
C | T | 4 | a0001c0007t0001g0075a0001c0007t0001g0092a0001c0007t0001g0100others(1): Show | 4 | HG01934.hp2 HG02280.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+650G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744555 | ||||||
chr3:56744736
|
T | G | 1 | a0001c0006t0002g0347 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.870+469A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744736 | ||||||
chr3:56744760
|
A | G | 1 | a0001c0002t0002g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.870+445T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744760 | ||||||
chr3:56744861
|
AT | A | 37 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(34): Show | 38 | HG00544.hp2 HG00597.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.870+343delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744861 | ||||||
chr3:56744889
|
T | C | 4 | a0001c0002t0002g0149a0001c0002t0008g0145a0001c0002t0010g0009others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+316A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744889 | ||||||
chr3:56744945
|
T | C | 2 | a0001c0002t0002g0076a0001c0002t0002g0085 | 2 | HG01099.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.870+260A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744945 | ||||||
chr3:56744983
|
G | A | 139 | a0001c0002t0002g0082a0001c0007t0001g0101a0002c0001t0001g0014others(136): Show | 141 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.870+222C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744983 | ||||||
chr3:56745142
|
C | A | 1 | a0001c0005t0001g0330 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.870+63G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56745142 | ||||||
chr3:56745467
|
G | A | 1 | a0001c0005t0001g0279 | 1 | NA18977.hp2 | splice_region_variant&intron_variant | LOW | c.613-5C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56745467 | ||||||
chr3:56745792
|
C | A | 2 | a0002c0001t0001g0235a0002c0001t0001g0257 | 2 | NA19056.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.613-330G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56745792 | ||||||
chr3:56745975
|
C | T | 126 | a0001c0002t0002g0082a0001c0007t0001g0101a0002c0001t0001g0014others(123): Show | 127 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.613-513G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56745975 | ||||||
chr3:56746115
|
C | T | 1 | a0002c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.613-653G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56746115 | ||||||
chr3:56746467
|
C | A | 2 | a0001c0007t0001g0075a0001c0007t0001g0092 | 2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.613-1005G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56746467 | ||||||
chr3:56746512
|
A | C | 1 | a0001c0002t0002g0086 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.613-1050T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56746512 | ||||||
chr3:56746547
|
T | C | 4 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(1): Show | 4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-1085A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56746547 | ||||||
chr3:56746663
|
G | A | 1 | a0001c0002t0002g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.613-1201C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56746663 | ||||||
chr3:56746996
|
T | C | 1 | a0001c0002t0002g0048 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.613-1534A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56746996 | ||||||
chr3:56747055
|
A | G | 1 | a0001c0002t0002g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.613-1593T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747055 | ||||||
chr3:56747064
|
C | CAG | 9 | a0001c0003t0001g0127a0001c0003t0001g0171a0001c0005t0001g0330others(6): Show | 9 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.613-1604_613-1603d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | ||||||
chr3:56747064
|
C | CAGAG | 3 | a0001c0002t0005g0211a0001c0002t0005g0212a0001c0002t0017g0161 | 3 | HG02055.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.613-1606_613-1603d others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | ||||||
chr3:56747064
|
C | CAGAGAGA others(15): Show |
1 | a0001c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.613-1624_613-1603d others(24): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | ||||||
chr3:56747064
|
C | G | 16 | a0001c0007t0004g0027a0001c0007t0004g0046a0001c0007t0004g0063others(13): Show | 16 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.613-1602G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | ||||||
chr3:56747064
|
CAG | C | 109 | a0001c0002t0002g0082a0001c0007t0001g0101a0002c0001t0001g0014others(106): Show | 110 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.613-1604_613-1603d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | ||||||
chr3:56747064
|
CAGAG | C | 12 | a0001c0002t0002g0076a0001c0002t0002g0077a0001c0002t0002g0078others(9): Show | 12 | HG01070.hp1 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.613-1606_613-1603d others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | ||||||
chr3:56747064
|
CAGAGAG | C | 34 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(31): Show | 35 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.613-1608_613-1603d others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | ||||||
chr3:56747064
|
CAGAGAGA others(9): Show |
C | 64 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(61): Show | 66 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.613-1618_613-1603d others(18): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | ||||||
chr3:56747066
|
G | C | 4 | a0001c0003t0001g0068a0001c0003t0001g0069a0001c0003t0001g0070others(1): Show | 4 | HG03710.hp2 NA18941.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-1604C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747066 | ||||||
chr3:56747068
|
G | C | 1 | a0002c0001t0013g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.613-1606C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747068 | ||||||
chr3:56747112
|
C | CG | 64 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(61): Show | 66 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.613-1651_613-1650i others(3): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747112 | ||||||
chr3:56747216
|
A | G | 4 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(1): Show | 4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-1754T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747216 | ||||||
chr3:56747440
|
G | C | 3 | a0002c0001t0003g0114a0002c0004t0003g0325a0002c0004t0003g0339 | 3 | HG01928.hp2 HG01975.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.613-1978C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747440 | ||||||
chr3:56747497
|
C | T | 2 | a0002c0001t0001g0214a0002c0001t0001g0260 | 2 | HG01975.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.613-2035G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747497 | ||||||
chr3:56747568
|
T | C | 4 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(1): Show | 4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-2106A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747568 | ||||||
chr3:56747631
|
T | C | 1 | a0001c0005t0001g0331 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.613-2169A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747631 | ||||||
chr3:56748060
|
G | C | 4 | a0001c0007t0001g0075a0001c0007t0001g0092a0001c0007t0001g0100others(1): Show | 4 | HG01934.hp2 HG02280.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-2598C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748060 | ||||||
chr3:56748201
|
T | C | 1 | a0001c0002t0002g0061 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.613-2739A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748201 | ||||||
chr3:56748549
|
A | AT | 11 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(8): Show | 11 | HG00323.hp1 HG01109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.612+2506dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748549 | ||||||
chr3:56748549
|
AT | A | 8 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(5): Show | 8 | HG02055.hp1 HG02965.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+2506delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748549 | ||||||
chr3:56748549
|
ATT | A | 222 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(219): Show | 226 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.612+2505_612+2506d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748549 | ||||||
chr3:56748549
|
ATTT | A | 34 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(31): Show | 35 | HG00621.hp1 HG00673.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.612+2504_612+2506d others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748549 | ||||||
chr3:56748551
|
T | A | 1 | a0002c0001t0001g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.612+2505A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748551 | ||||||
chr3:56748784
|
C | T | 2 | a0001c0007t0001g0093a0002c0001t0001g0074 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.612+2272G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748784 | ||||||
chr3:56748785
|
G | A | 138 | a0001c0002t0002g0082a0001c0002t0010g0009a0001c0007t0001g0101others(135): Show | 140 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.612+2271C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748785 | ||||||
chr3:56748921
|
C | T | 3 | a0002c0001t0001g0132a0002c0001t0001g0159a0002c0001t0001g0160 | 3 | HG02559.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.612+2135G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748921 | ||||||
chr3:56749020
|
G | A | 3 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212 | 3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.612+2036C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749020 | ||||||
chr3:56749213
|
C | T | 1 | a0002c0001t0003g0263 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.612+1843G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749213 | ||||||
chr3:56749329
|
G | A | 1 | a0001c0002t0002g0018 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.612+1727C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749329 | ||||||
chr3:56749490
|
T | A | 1 | a0001c0002t0002g0149 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.612+1566A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749490 | ||||||
chr3:56749563
|
C | T | 2 | a0001c0007t0001g0075a0001c0007t0001g0092 | 2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.612+1493G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749563 | ||||||
chr3:56749604
|
C | T | 1 | a0001c0002t0002g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.612+1452G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749604 | ||||||
chr3:56749777
|
C | A | 33 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(30): Show | 34 | HG00621.hp1 HG00673.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.612+1279G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749777 | ||||||
chr3:56749778
|
T | C | 265 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(262): Show | 270 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.612+1278A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749778 | ||||||
chr3:56749855
|
T | C | 2 | a0001c0005t0001g0277a0001c0005t0001g0279 | 2 | NA18963.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.612+1201A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749855 | ||||||
chr3:56749873
|
T | C | 1 | a0001c0007t0001g0162 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.612+1183A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749873 | ||||||
chr3:56749902
|
T | TAAAACTT others(32): Show |
1 | a0001c0002t0010g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.612+1153_612+1154i others(41): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749902 | ||||||
chr3:56749902
|
T | TAAAACTT others(56): Show |
1 | a0002c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.612+1153_612+1154i others(65): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749902 | ||||||
chr3:56749902
|
T | TAAAACTT others(65): Show |
2 | a0002c0001t0001g0015a0002c0001t0001g0016 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.612+1153_612+1154i others(74): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749902 | ||||||
chr3:56749902
|
T | TAAAACTT others(66): Show |
1 | a0002c0001t0001g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.612+1153_612+1154i others(75): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749902 | ||||||
chr3:56749908
|
T | C | 2 | a0002c0001t0001g0135a0002c0001t0001g0153 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.612+1148A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749908 | ||||||
chr3:56750670
|
GT | G | 6 | a0001c0005t0001g0306a0001c0007t0001g0075a0001c0007t0001g0092others(3): Show | 6 | HG01261.hp1 HG01934.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.612+385delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56750670 | ||||||
chr3:56750820
|
C | G | 209 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(206): Show | 212 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.612+236G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56750820 | ||||||
chr3:56751023
|
T | G | 1 | a0001c0002t0010g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.612+33A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56751023 | ||||||
chr3:56751148
|
C | T | 1 | a0001c0003t0001g0182 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.536-16G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 5/9 | chr3 | 56751148 | ||||||
chr3:56751213
|
T | C | 1 | a0001c0007t0001g0162 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.536-81A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 5/9 | chr3 | 56751213 | ||||||
chr3:56751528
|
C | T | 213 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(210): Show | 217 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(214): Show |
intron_variant | MODIFIER | c.439-132G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56751528 | ||||||
chr3:56751849
|
A | G | 2 | a0001c0007t0004g0063a0002c0001t0003g0230 | 2 | HG02523.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.439-453T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56751849 | ||||||
chr3:56752082
|
CT | C | 212 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(209): Show | 216 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(213): Show |
intron_variant | MODIFIER | c.439-687delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752082 | ||||||
chr3:56752117
|
T | C | 9 | a0002c0001t0001g0074a0002c0001t0001g0135a0002c0001t0001g0136others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.439-721A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752117 | ||||||
chr3:56752167
|
C | T | 1 | a0001c0007t0001g0092 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.439-771G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752167 | ||||||
chr3:56752170
|
C | T | 1 | a0001c0002t0002g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.439-774G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752170 | ||||||
chr3:56752172
|
C | T | 1 | a0002c0001t0001g0208 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.439-776G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752172 | ||||||
chr3:56752192
|
A | G | 24 | a0001c0002t0002g0215a0001c0003t0001g0168a0001c0003t0001g0259others(21): Show | 24 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.439-796T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752192 | ||||||
chr3:56752214
|
C | T | 7 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(4): Show | 7 | HG01934.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.439-818G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752214 | ||||||
chr3:56752227
|
T | C | 162 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(159): Show | 166 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.439-831A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752227 | ||||||
chr3:56752325
|
C | T | 212 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(209): Show | 216 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(213): Show |
intron_variant | MODIFIER | c.439-929G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752325 | ||||||
chr3:56752346
|
C | T | 1 | a0001c0002t0002g0076 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.439-950G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752346 | ||||||
chr3:56752348
|
G | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.439-952C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752348 | ||||||
chr3:56752354
|
G | A | 1 | a0002c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.439-958C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752354 | ||||||
chr3:56752602
|
G | A | 5 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(2): Show | 5 | HG01934.hp2 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+902C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752602 | ||||||
chr3:56752702
|
T | C | 2 | a0001c0006t0002g0298a0001c0006t0002g0329 | 2 | HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.438+802A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752702 | ||||||
chr3:56752808
|
G | C | 1 | a0002c0001t0001g0208 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.438+696C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752808 | ||||||
chr3:56752944
|
T | C | 1 | a0001c0005t0001g0297 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.438+560A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752944 | ||||||
chr3:56752954
|
G | C | 1 | a0001c0002t0002g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.438+550C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752954 | ||||||
chr3:56752982
|
G | T | 1 | a0001c0007t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.438+522C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752982 | ||||||
chr3:56753005
|
G | C | 7 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(4): Show | 7 | HG01934.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.438+499C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56753005 | ||||||
chr3:56753423
|
C | T | 291 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(288): Show | 296 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.438+81G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56753423 | ||||||
chr3:56753441
|
T | C | 1 | a0001c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.438+63A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56753441 | ||||||
chr3:56753664
|
A | G | 127 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0149others(124): Show | 130 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.376-98T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56753664 | ||||||
chr3:56753686
|
G | A | 1 | a0002c0004t0003g0270 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.376-120C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56753686 | ||||||
chr3:56753949
|
T | C | 1 | a0001c0002t0002g0148 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.376-383A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56753949 | ||||||
chr3:56754008
|
C | T | 1 | a0002c0001t0001g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.376-442G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56754008 | ||||||
chr3:56754037
|
T | C | 2 | a0002c0001t0001g0066a0002c0001t0001g0237 | 2 | NA18940.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.376-471A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56754037 | ||||||
chr3:56754047
|
C | T | 1 | a0002c0001t0013g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.376-481G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56754047 | ||||||
chr3:56754149
|
C | T | 1 | a0001c0002t0002g0222 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.376-583G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56754149 | ||||||
chr3:56754368
|
T | C | 291 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(288): Show | 296 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.375+613A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56754368 | ||||||
chr3:56754417
|
G | A | 7 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(4): Show | 7 | HG01934.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.375+564C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56754417 | ||||||
chr3:56755311
|
C | T | 1 | a0001c0007t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.205-160G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755311 | ||||||
chr3:56755427
|
G | A | 1 | a0001c0005t0001g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.205-276C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755427 | ||||||
chr3:56755434
|
G | A | 2 | a0002c0001t0001g0143a0002c0001t0001g0144 | 2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.205-283C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755434 | ||||||
chr3:56755619
|
T | C | 1 | a0002c0001t0001g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-468A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755619 | ||||||
chr3:56755706
|
T | TA | 14 | a0001c0002t0002g0047a0001c0007t0004g0027a0001c0007t0004g0046others(11): Show | 14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.205-556dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755706 | ||||||
chr3:56755708
|
C | T | 26 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0003t0001g0011others(23): Show | 26 | HG00558.hp1 HG01109.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.205-557G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755708 | ||||||
chr3:56755715
|
A | C | 28 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0017g0161others(25): Show | 28 | HG00558.hp1 HG01109.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.205-564T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755715 | ||||||
chr3:56755715
|
A | G | 142 | a0001c0002t0002g0047a0001c0002t0002g0061a0001c0002t0002g0082others(139): Show | 145 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.205-564T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755715 | ||||||
chr3:56755778
|
G | A | 1 | a0001c0002t0002g0170 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.205-627C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755778 | ||||||
chr3:56755848
|
G | A | 3 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212 | 3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.205-697C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755848 | ||||||
chr3:56755876
|
G | A | 1 | a0002c0004t0003g0307 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.205-725C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755876 | ||||||
chr3:56755965
|
T | C | 1 | a0001c0002t0002g0190 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.205-814A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755965 | ||||||
chr3:56756034
|
C | G | 1 | a0001c0005t0001g0331 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.205-883G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756034 | ||||||
chr3:56756545
|
C | CT | 41 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(38): Show | 42 | HG00544.hp2 HG00597.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.205-1395dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756545 | ||||||
chr3:56756545
|
C | CTT | 6 | a0001c0002t0002g0026a0001c0002t0002g0221a0001c0002t0002g0222others(3): Show | 6 | HG03491.hp2 HG03942.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-1396_205-1395d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756545 | ||||||
chr3:56756545
|
CT | C | 65 | a0001c0002t0002g0047a0001c0002t0002g0053a0001c0002t0002g0077others(62): Show | 66 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.205-1395delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756545 | ||||||
chr3:56756545
|
CTT | C | 44 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(41): Show | 45 | HG00621.hp1 HG00673.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.205-1396_205-1395d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756545 | ||||||
chr3:56756545
|
CTTT | C | 22 | a0001c0002t0002g0036a0001c0002t0002g0044a0001c0002t0002g0059others(19): Show | 22 | HG00558.hp1 HG01109.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.205-1397_205-1395d others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756545 | ||||||
chr3:56756546
|
T | TTTTTTTT others(2621): Show |
3 | a0002c0004t0001g0004a0002c0004t0001g0286a0002c0004t0001g0289 | 4 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-1396_205-1395i others(2630): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756546 | ||||||
chr3:56756651
|
G | A | 1 | a0002c0001t0003g0248 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.205-1500C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756651 | ||||||
chr3:56756680
|
G | T | 1 | a0002c0001t0003g0025 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.205-1529C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756680 | ||||||
chr3:56756875
|
C | T | 1 | a0001c0002t0002g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.205-1724G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756875 | ||||||
chr3:56756966
|
T | G | 2 | a0001c0002t0017g0161a0002c0001t0001g0151 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.205-1815A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756966 | ||||||
chr3:56757014
|
C | T | 1 | a0001c0002t0002g0190 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.205-1863G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757014 | ||||||
chr3:56757097
|
T | C | 2 | a0001c0007t0001g0075a0001c0007t0001g0092 | 2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.205-1946A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757097 | ||||||
chr3:56757128
|
A | G | 2 | a0002c0001t0001g0095a0002c0001t0001g0096 | 2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.205-1977T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757128 | ||||||
chr3:56757185
|
G | C | 5 | a0001c0002t0002g0077a0001c0002t0002g0078a0001c0002t0006g0006others(2): Show | 5 | HG02723.hp1 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-2034C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757185 | ||||||
chr3:56757213
|
C | T | 111 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0157others(108): Show | 113 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.205-2062G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757213 | ||||||
chr3:56757335
|
G | A | 1 | a0002c0001t0003g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.205-2184C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757335 | ||||||
chr3:56757452
|
C | T | 1 | a0001c0006t0002g0337 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.205-2301G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757452 | ||||||
chr3:56757470
|
G | A | 1 | a0001c0007t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.205-2319C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757470 | ||||||
chr3:56757476
|
G | C | 7 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(4): Show | 7 | HG01934.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-2325C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757476 | ||||||
chr3:56757715
|
T | A | 1 | a0002c0001t0003g0043 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.205-2564A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757715 | ||||||
chr3:56757761
|
C | T | 1 | a0002c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.205-2610G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757761 | ||||||
chr3:56757816
|
G | A | 7 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(4): Show | 7 | HG01934.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-2665C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757816 | ||||||
chr3:56757849
|
A | G | 1 | a0001c0006t0002g0333 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.205-2698T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757849 | ||||||
chr3:56757906
|
A | T | 352 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(349): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.205-2755T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757906 | ||||||
chr3:56757908
|
A | G | 352 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(349): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.205-2757T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757908 | ||||||
chr3:56758016
|
G | A | 1 | a0002c0001t0001g0176 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.205-2865C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758016 | ||||||
chr3:56758017
|
C | T | 1 | a0001c0006t0002g0350 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.205-2866G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758017 | ||||||
chr3:56758048
|
C | T | 2 | a0001c0007t0001g0075a0001c0007t0001g0092 | 2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.205-2897G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758048 | ||||||
chr3:56758123
|
C | CA | 29 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0017g0161others(26): Show | 29 | HG00558.hp1 HG01109.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.205-2973dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758123 | ||||||
chr3:56758158
|
G | T | 5 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(2): Show | 5 | HG01934.hp2 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-3007C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758158 | ||||||
chr3:56758243
|
T | C | 1 | a0002c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.205-3092A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758243 | ||||||
chr3:56758619
|
T | C | 1 | a0001c0008t0004g0324 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.205-3468A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758619 | ||||||
chr3:56758727
|
C | G | 126 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0149others(123): Show | 129 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.205-3576G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758727 | ||||||
chr3:56758757
|
G | A | 22 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0003t0001g0023others(19): Show | 22 | HG00558.hp1 HG01496.hp1 HG02523.hp2 others(19): Show |
intron_variant | MODIFIER | c.205-3606C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758757 | ||||||
chr3:56758955
|
C | G | 2 | a0001c0007t0001g0093a0001c0007t0001g0165 | 2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.205-3804G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758955 | ||||||
chr3:56759174
|
A | AT | 65 | a0001c0002t0002g0037a0001c0002t0002g0039a0001c0002t0002g0053others(62): Show | 65 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.205-4024dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759174 | ||||||
chr3:56759174
|
A | ATT | 7 | a0001c0003t0001g0071a0001c0003t0011g0118a0001c0006t0002g0275others(4): Show | 7 | HG01175.hp1 HG01256.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-4025_205-4024d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759174 | ||||||
chr3:56759174
|
AT | A | 22 | a0001c0002t0002g0047a0001c0002t0002g0086a0001c0002t0008g0145others(19): Show | 22 | HG01361.hp2 HG01884.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.205-4024delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759174 | ||||||
chr3:56759326
|
C | T | 9 | a0002c0001t0001g0074a0002c0001t0001g0135a0002c0001t0001g0136others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.205-4175G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759326 | ||||||
chr3:56759331
|
C | G | 1 | a0001c0006t0002g0288 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.205-4180G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759331 | ||||||
chr3:56759428
|
C | T | 5 | a0001c0002t0002g0077a0001c0002t0002g0078a0001c0002t0006g0006others(2): Show | 5 | HG02723.hp1 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-4277G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759428 | ||||||
chr3:56759594
|
C | T | 29 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0017g0161others(26): Show | 29 | HG00558.hp1 HG01109.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.205-4443G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759594 | ||||||
chr3:56759694
|
A | G | 213 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(210): Show | 217 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(214): Show |
intron_variant | MODIFIER | c.205-4543T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759694 | ||||||
chr3:56759773
|
T | C | 14 | a0001c0002t0002g0047a0001c0007t0004g0027a0001c0007t0004g0046others(11): Show | 14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.205-4622A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759773 | ||||||
chr3:56759968
|
A | G | 1 | a0002c0001t0001g0066 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205-4817T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759968 | ||||||
chr3:56759969
|
A | G | 140 | a0001c0002t0002g0047a0001c0002t0002g0061a0001c0002t0002g0082others(137): Show | 143 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.205-4818T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759969 | ||||||
chr3:56760047
|
A | T | 7 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212others(4): Show | 7 | HG01934.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-4896T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760047 | ||||||
chr3:56760301
|
AGG | A | 3 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0203 | 3 | HG02451.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.205-5152_205-5151d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760301 | ||||||
chr3:56760305
|
T | TATAATAA others(17): Show |
3 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0203 | 3 | HG02451.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.205-5155_205-5154i others(26): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760305 | ||||||
chr3:56760414
|
G | A | 2 | a0001c0002t0002g0224a0001c0002t0002g0225 | 2 | NA19005.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.205-5263C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760414 | ||||||
chr3:56760626
|
A | G | 1 | a0002c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.205-5475T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760626 | ||||||
chr3:56760684
|
C | T | 3 | a0001c0002t0002g0255a0001c0002t0002g0256a0001c0006t0002g0321 | 3 | NA18967.hp1 NA18982.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.205-5533G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760684 | ||||||
chr3:56760991
|
T | C | 7 | a0002c0001t0001g0080a0002c0001t0001g0087a0002c0001t0001g0213others(4): Show | 7 | HG01109.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-5840A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760991 | ||||||
chr3:56761051
|
T | A | 1 | a0001c0006t0002g0334 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.205-5900A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761051 | ||||||
chr3:56761099
|
C | T | 1 | a0004c0011t0008g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.205-5948G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761099 | ||||||
chr3:56761159
|
G | A | 138 | a0001c0002t0002g0047a0001c0002t0002g0061a0001c0002t0002g0082others(135): Show | 140 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.205-6008C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761159 | ||||||
chr3:56761192
|
A | C | 291 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(288): Show | 296 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.205-6041T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761192 | ||||||
chr3:56761328
|
G | C | 1 | a0001c0003t0001g0090 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.205-6177C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761328 | ||||||
chr3:56761790
|
C | T | 1 | a0002c0001t0003g0111 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.205-6639G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761790 | ||||||
chr3:56761912
|
G | A | 1 | a0001c0002t0002g0026 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.205-6761C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761912 | ||||||
chr3:56761996
|
G | A | 1 | a0002c0001t0003g0248 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.205-6845C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761996 | ||||||
chr3:56761998
|
C | T | 181 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(178): Show | 184 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.205-6847G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761998 | ||||||
chr3:56762152
|
C | T | 104 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0157others(101): Show | 105 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.205-7001G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762152 | ||||||
chr3:56762271
|
G | A | 1 | a0002c0001t0003g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.205-7120C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762271 | ||||||
chr3:56762378
|
G | C | 2 | a0002c0004t0001g0318a0002c0004t0001g0351 | 2 | HG00323.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.205-7227C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762378 | ||||||
chr3:56762507
|
G | T | 2 | a0001c0003t0001g0103a0001c0005t0001g0280 | 2 | HG00741.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.205-7356C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762507 | ||||||
chr3:56762510
|
C | T | 1 | a0001c0003t0001g0030 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.205-7359G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762510 | ||||||
chr3:56762511
|
G | A | 1 | a0001c0006t0002g0335 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.205-7360C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762511 | ||||||
chr3:56762593
|
C | T | 1 | a0002c0001t0003g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.205-7442G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762593 | ||||||
chr3:56762594
|
G | A | 1 | a0001c0002t0002g0193 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.205-7443C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762594 | ||||||
chr3:56762710
|
T | C | 39 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(36): Show | 41 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.205-7559A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762710 | ||||||
chr3:56762718
|
C | A | 1 | a0002c0001t0001g0080 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.205-7567G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762718 | ||||||
chr3:56762973
|
G | A | 4 | a0001c0002t0002g0076a0001c0002t0002g0085a0001c0002t0002g0086others(1): Show | 4 | HG01099.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-7822C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762973 | ||||||
chr3:56763039
|
C | T | 1 | a0002c0004t0003g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.205-7888G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763039 | ||||||
chr3:56763049
|
A | T | 5 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-7898T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763049 | ||||||
chr3:56763078
|
A | G | 16 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0007t0004g0027others(13): Show | 16 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.205-7927T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763078 | ||||||
chr3:56763092
|
A | G | 10 | a0001c0007t0001g0100a0002c0001t0001g0074a0002c0001t0001g0135others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.205-7941T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763092 | ||||||
chr3:56763102
|
T | C | 1 | a0001c0002t0002g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.205-7951A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763102 | ||||||
chr3:56763159
|
C | G | 34 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(31): Show | 35 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(32): Show |
intron_variant | MODIFIER | c.205-8008G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763159 | ||||||
chr3:56763345
|
A | C | 352 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(349): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.205-8194T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763345 | ||||||
chr3:56763661
|
T | G | 10 | a0001c0007t0001g0100a0002c0001t0001g0074a0002c0001t0001g0135others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.205-8510A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763661 | ||||||
chr3:56763686
|
C | T | 16 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0007t0004g0027others(13): Show | 16 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.205-8535G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763686 | ||||||
chr3:56763740
|
T | G | 219 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(216): Show | 222 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.205-8589A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763740 | ||||||
chr3:56763760
|
G | A | 290 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(287): Show | 295 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.205-8609C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763760 | ||||||
chr3:56763802
|
T | C | 73 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0003t0001g0249others(70): Show | 75 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.205-8651A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763802 | ||||||
chr3:56763957
|
G | A | 34 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(31): Show | 35 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(32): Show |
intron_variant | MODIFIER | c.205-8806C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763957 | ||||||
chr3:56763991
|
G | A | 1 | a0002c0001t0003g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.205-8840C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763991 | ||||||
chr3:56764067
|
T | TAA | 113 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0002g0128others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.205-8918_205-8917d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764067 | ||||||
chr3:56764101
|
T | C | 113 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0002g0128others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.205-8950A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764101 | ||||||
chr3:56764278
|
C | T | 112 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0002g0128others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.205-9127G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764278 | ||||||
chr3:56764467
|
C | T | 7 | a0001c0003t0001g0168a0002c0001t0003g0164a0002c0004t0003g0309others(4): Show | 7 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+9242G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764467 | ||||||
chr3:56764525
|
G | A | 2 | a0002c0001t0001g0239a0002c0001t0001g0240 | 2 | NA18994.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.204+9184C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764525 | ||||||
chr3:56764637
|
C | CGATATGA others(9): Show |
1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+9056_204+9071d others(18): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764637 | ||||||
chr3:56764676
|
C | G | 73 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0003t0001g0249others(70): Show | 75 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.204+9033G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764676 | ||||||
chr3:56764721
|
A | G | 113 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(110): Show | 116 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.204+8988T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764721 | ||||||
chr3:56764746
|
T | C | 113 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0002g0128others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.204+8963A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764746 | ||||||
chr3:56764756
|
A | AT | 106 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0002g0128others(103): Show | 106 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.204+8952dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764756 | ||||||
chr3:56764756
|
AT | A | 95 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(92): Show | 97 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.204+8952delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764756 | ||||||
chr3:56764756
|
ATT | A | 10 | a0001c0002t0002g0040a0002c0001t0001g0074a0002c0001t0001g0135others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.204+8951_204+8952d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764756 | ||||||
chr3:56764919
|
G | A | 16 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0007t0004g0027others(13): Show | 16 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.204+8790C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764919 | ||||||
chr3:56765091
|
A | G | 113 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0002g0128others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.204+8618T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56765091 | ||||||
chr3:56765296
|
C | T | 1 | a0001c0002t0002g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.204+8413G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56765296 | ||||||
chr3:56765297
|
G | A | 4 | a0002c0001t0003g0079a0002c0001t0003g0081a0002c0001t0003g0088others(1): Show | 4 | HG02258.hp1 HG02486.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+8412C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56765297 | ||||||
chr3:56765389
|
C | T | 1 | a0001c0003t0001g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.204+8320G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56765389 | ||||||
chr3:56765764
|
G | C | 4 | a0001c0002t0002g0219a0001c0002t0002g0220a0001c0002t0002g0221others(1): Show | 4 | HG00597.hp1 NA18940.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+7945C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56765764 | ||||||
chr3:56765860
|
T | A | 1 | a0001c0002t0002g0019 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.204+7849A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56765860 | ||||||
chr3:56766193
|
A | G | 1 | a0002c0004t0003g0283 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.204+7516T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56766193 | ||||||
chr3:56766536
|
A | G | 2 | a0001c0002t0006g0006a0001c0002t0006g0008 | 2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.204+7173T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56766536 | ||||||
chr3:56766574
|
A | T | 1 | a0001c0002t0010g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.204+7135T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56766574 | ||||||
chr3:56766593
|
T | C | 1 | a0002c0001t0001g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.204+7116A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56766593 | ||||||
chr3:56766626
|
G | A | 2 | a0001c0007t0001g0075a0001c0007t0001g0092 | 2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.204+7083C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56766626 | ||||||
chr3:56766739
|
T | C | 3 | a0001c0003t0001g0167a0001c0005t0001g0299a0001c0005t0001g0300 | 3 | HG00099.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.204+6970A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56766739 | ||||||
chr3:56767020
|
A | C | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6689T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767020 | ||||||
chr3:56767021
|
G | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6688C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767021 | ||||||
chr3:56767027
|
T | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6682A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767027 | ||||||
chr3:56767028
|
G | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6681C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767028 | ||||||
chr3:56767029
|
G | T | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6680C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767029 | ||||||
chr3:56767031
|
G | C | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6678C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767031 | ||||||
chr3:56767036
|
G | T | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6673C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767036 | ||||||
chr3:56767037
|
T | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6672A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767037 | ||||||
chr3:56767039
|
G | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6670C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767039 | ||||||
chr3:56767040
|
T | C | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6669A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767040 | ||||||
chr3:56767045
|
C | G | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6664G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767045 | ||||||
chr3:56767048
|
G | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6661C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767048 | ||||||
chr3:56767049
|
C | G | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6660G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767049 | ||||||
chr3:56767066
|
T | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6643A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767066 | ||||||
chr3:56767067
|
TGGGAGGC others(5): Show |
T | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6630_204+6641d others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767067 | ||||||
chr3:56767081
|
G | T | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6628C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767081 | ||||||
chr3:56767082
|
G | T | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6627C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767082 | ||||||
chr3:56767088
|
C | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6621G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767088 | ||||||
chr3:56767090
|
G | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6619C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767090 | ||||||
chr3:56767091
|
C | T | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6618G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767091 | ||||||
chr3:56767093
|
T | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6616A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767093 | ||||||
chr3:56767094
|
G | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6615C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767094 | ||||||
chr3:56767096
|
G | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6613C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767096 | ||||||
chr3:56767097
|
G | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6612C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767097 | ||||||
chr3:56767098
|
C | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6611G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767098 | ||||||
chr3:56767102
|
G | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6607C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767102 | ||||||
chr3:56767104
|
G | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6605C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767104 | ||||||
chr3:56767105
|
T | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6604A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767105 | ||||||
chr3:56767107
|
T | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6602A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767107 | ||||||
chr3:56767108
|
G | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6601C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767108 | ||||||
chr3:56767110
|
G | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6599C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767110 | ||||||
chr3:56767111
|
A | T | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6598T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767111 | ||||||
chr3:56767113
|
C | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6596G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767113 | ||||||
chr3:56767119
|
G | T | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6590C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767119 | ||||||
chr3:56767120
|
G | T | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6589C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767120 | ||||||
chr3:56767122
|
C | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6587G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767122 | ||||||
chr3:56767125
|
C | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6584G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767125 | ||||||
chr3:56767126
|
A | C | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6583T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767126 | ||||||
chr3:56767141
|
T | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6568A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767141 | ||||||
chr3:56767144
|
C | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6565G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767144 | ||||||
chr3:56767145
|
T | C | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6564A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767145 | ||||||
chr3:56767188
|
G | C | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6521C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767188 | ||||||
chr3:56767189
|
A | G | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6520T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767189 | ||||||
chr3:56767190
|
C | A | 1 | a0002c0001t0001g0218 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6519G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767190 | ||||||
chr3:56767280
|
T | C | 2 | a0001c0007t0001g0093a0001c0007t0001g0165 | 2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.204+6429A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767280 | ||||||
chr3:56767300
|
C | T | 1 | a0004c0011t0008g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.204+6409G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767300 | ||||||
chr3:56767310
|
C | T | 17 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0007t0004g0027others(14): Show | 17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.204+6399G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767310 | ||||||
chr3:56767441
|
G | A | 33 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(30): Show | 35 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.204+6268C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767441 | ||||||
chr3:56767583
|
C | CA | 108 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(105): Show | 112 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.204+6125dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767583 | ||||||
chr3:56767583
|
C | CAA | 53 | a0001c0002t0002g0034a0001c0002t0002g0039a0001c0002t0002g0040others(50): Show | 53 | HG00544.hp2 HG00621.hp1 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.204+6124_204+6125d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767583 | ||||||
chr3:56767583
|
C | CAAA | 9 | a0001c0002t0002g0122a0001c0002t0002g0126a0001c0007t0004g0112others(6): Show | 9 | HG01361.hp2 HG01928.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.204+6123_204+6125d others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767583 | ||||||
chr3:56767583
|
CAAAAAAA | C | 110 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0002g0128others(107): Show | 110 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.204+6119_204+6125d others(9): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767583 | ||||||
chr3:56767999
|
C | T | 36 | a0001c0002t0002g0128a0001c0002t0002g0129a0001c0002t0002g0130others(33): Show | 36 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.204+5710G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767999 | ||||||
chr3:56768117
|
C | G | 2 | a0001c0002t0017g0161a0002c0001t0001g0151 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.204+5592G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768117 | ||||||
chr3:56768257
|
C | A | 1 | a0001c0003t0001g0183 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.204+5452G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768257 | ||||||
chr3:56768581
|
C | A | 2 | a0001c0002t0002g0126a0004c0011t0008g0072 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+5128G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768581 | ||||||
chr3:56768667
|
C | CA | 15 | a0001c0002t0002g0034a0001c0002t0002g0040a0001c0002t0002g0048others(12): Show | 15 | HG00544.hp2 HG01099.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.204+5041dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768667 | ||||||
chr3:56768667
|
CA | C | 32 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0003t0001g0011others(29): Show | 33 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.204+5041delT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768667 | ||||||
chr3:56768683
|
AG | A | 100 | a0001c0002t0002g0002a0001c0002t0002g0033a0001c0002t0002g0042others(97): Show | 102 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(99): Show |
intron_variant | MODIFIER | c.204+5025delC | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768683 | ||||||
chr3:56768684
|
G | A | 159 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(156): Show | 161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.204+5025C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768684 | ||||||
chr3:56768753
|
A | G | 1 | a0001c0002t0002g0190 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.204+4956T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768753 | ||||||
chr3:56768941
|
A | G | 9 | a0002c0001t0001g0074a0002c0001t0001g0135a0002c0001t0001g0136others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+4768T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768941 | ||||||
chr3:56769038
|
G | A | 2 | a0001c0002t0002g0126a0004c0011t0008g0072 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+4671C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769038 | ||||||
chr3:56769147
|
A | G | 76 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0008g0145others(73): Show | 77 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.204+4562T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769147 | ||||||
chr3:56769271
|
G | A | 3 | a0001c0005t0001g0330a0001c0007t0001g0162a0002c0001t0001g0102 | 3 | HG01070.hp1 HG01106.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.204+4438C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769271 | ||||||
chr3:56769454
|
A | G | 1 | a0001c0002t0002g0032 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.204+4255T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769454 | ||||||
chr3:56769488
|
G | A | 1 | a0002c0001t0001g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.204+4221C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769488 | ||||||
chr3:56769832
|
G | A | 17 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0007t0004g0027others(14): Show | 17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.204+3877C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769832 | ||||||
chr3:56769929
|
A | G | 2 | a0001c0002t0002g0219a0002c0001t0003g0045 | 2 | HG00597.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.204+3780T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769929 | ||||||
chr3:56770025
|
T | G | 10 | a0001c0007t0001g0100a0002c0001t0001g0074a0002c0001t0001g0135others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.204+3684A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770025 | ||||||
chr3:56770069
|
C | T | 2 | a0001c0002t0002g0126a0004c0011t0008g0072 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+3640G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770069 | ||||||
chr3:56770096
|
C | G | 15 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(12): Show | 16 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.204+3613G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770096 | ||||||
chr3:56770229
|
T | A | 113 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0002g0128others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.204+3480A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770229 | ||||||
chr3:56770239
|
G | A | 5 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+3470C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770239 | ||||||
chr3:56770361
|
G | C | 5 | a0001c0007t0004g0027a0001c0007t0004g0112a0001c0007t0004g0113others(2): Show | 5 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+3348C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770361 | ||||||
chr3:56770404
|
T | C | 4 | a0001c0002t0002g0219a0001c0002t0002g0220a0001c0002t0002g0221others(1): Show | 4 | HG00597.hp1 NA18940.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+3305A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770404 | ||||||
chr3:56770411
|
A | AAAATT | 106 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0002g0061others(103): Show | 109 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.204+3293_204+3297d others(7): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770411 | ||||||
chr3:56770411
|
A | AAAATTAA others(3): Show |
4 | a0001c0002t0002g0126a0001c0002t0010g0009a0001c0007t0001g0100others(1): Show | 4 | HG02258.hp2 HG02486.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+3288_204+3297d others(12): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770411 | ||||||
chr3:56770411
|
A | AAAATTAA others(8): Show |
1 | a0002c0001t0003g0263 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.204+3283_204+3297d others(17): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770411 | ||||||
chr3:56770411
|
AAAATT | A | 8 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(5): Show | 8 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+3293_204+3297d others(7): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770411 | ||||||
chr3:56770411
|
AAAATTAA others(3): Show |
A | 20 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0002t0002g0142others(17): Show | 20 | HG01361.hp2 HG01891.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+3288_204+3297d others(12): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770411 | ||||||
chr3:56770518
|
T | C | 3 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0203 | 3 | HG02451.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.204+3191A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770518 | ||||||
chr3:56770645
|
G | C | 1 | a0002c0004t0001g0343 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.204+3064C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770645 | ||||||
chr3:56770772
|
G | A | 2 | a0001c0002t0002g0149a0002c0001t0001g0146 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.204+2937C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770772 | ||||||
chr3:56770933
|
G | A | 2 | a0002c0001t0003g0064a0002c0004t0003g0284 | 2 | HG02027.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.204+2776C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770933 | ||||||
chr3:56770937
|
C | G | 3 | a0002c0001t0001g0014a0002c0001t0001g0095a0002c0001t0001g0096 | 3 | HG02723.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.204+2772G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770937 | ||||||
chr3:56770982
|
G | A | 205 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0002g0061others(202): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.204+2727C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770982 | ||||||
chr3:56771110
|
T | C | 2 | a0001c0003t0001g0249a0001c0013t0001g0150 | 2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.204+2599A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771110 | ||||||
chr3:56771113
|
C | CAA | 6 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+2594_204+2595d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771113 | ||||||
chr3:56771184
|
C | A | 2 | a0001c0002t0002g0149a0002c0001t0001g0146 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.204+2525G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771184 | ||||||
chr3:56771204
|
C | T | 5 | a0001c0003t0001g0108a0001c0003t0001g0167a0001c0003t0001g0183others(2): Show | 5 | HG00099.hp2 HG01169.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+2505G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771204 | ||||||
chr3:56771288
|
T | C | 2 | a0001c0002t0002g0032a0001c0002t0002g0190 | 2 | HG02080.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.204+2421A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771288 | ||||||
chr3:56771328
|
G | A | 1 | a0002c0004t0001g0349 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.204+2381C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771328 | ||||||
chr3:56771348
|
A | G | 124 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(121): Show | 128 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.204+2361T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771348 | ||||||
chr3:56771392
|
G | A | 1 | a0001c0002t0002g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.204+2317C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771392 | ||||||
chr3:56771610
|
G | C | 2 | a0001c0006t0002g0281a0002c0004t0014g0291 | 2 | NA18950.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.204+2099C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771610 | ||||||
chr3:56771613
|
C | T | 9 | a0002c0001t0001g0074a0002c0001t0001g0135a0002c0001t0001g0136others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+2096G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771613 | ||||||
chr3:56771615
|
C | T | 4 | a0001c0002t0002g0076a0001c0002t0002g0085a0001c0002t0002g0086others(1): Show | 4 | HG01099.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+2094G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771615 | ||||||
chr3:56771672
|
T | C | 1 | a0002c0001t0001g0176 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.204+2037A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771672 | ||||||
chr3:56771678
|
C | T | 10 | a0001c0007t0001g0100a0002c0001t0001g0074a0002c0001t0001g0135others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.204+2031G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771678 | ||||||
chr3:56771792
|
A | C | 1 | a0001c0005t0001g0293 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.204+1917T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771792 | ||||||
chr3:56771817
|
A | T | 2 | a0001c0002t0002g0126a0004c0011t0008g0072 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+1892T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771817 | ||||||
chr3:56771989
|
G | A | 1 | a0002c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.204+1720C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771989 | ||||||
chr3:56771989
|
G | T | 1 | a0001c0002t0002g0148 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.204+1720C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771989 | ||||||
chr3:56772117
|
A | G | 157 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(154): Show | 162 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.204+1592T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772117 | ||||||
chr3:56772144
|
G | C | 27 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(24): Show | 28 | HG00621.hp1 HG00673.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.204+1565C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772144 | ||||||
chr3:56772159
|
G | A | 5 | a0001c0003t0001g0091a0001c0003t0001g0177a0001c0003t0001g0178others(2): Show | 5 | HG01167.hp1 HG01258.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+1550C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772159 | ||||||
chr3:56772175
|
T | C | 93 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0126others(90): Show | 96 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.204+1534A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772175 | ||||||
chr3:56772409
|
C | T | 1 | a0001c0012t0001g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.204+1300G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772409 | ||||||
chr3:56772648
|
C | T | 1 | a0001c0002t0002g0198 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.204+1061G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772648 | ||||||
chr3:56772739
|
A | G | 1 | a0002c0001t0001g0147 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.204+970T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772739 | ||||||
chr3:56772747
|
G | T | 1 | a0002c0001t0001g0147 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.204+962C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772747 | ||||||
chr3:56772752
|
C | T | 1 | a0002c0001t0001g0188 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.204+957G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772752 | ||||||
chr3:56772914
|
A | T | 1 | a0002c0004t0003g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.204+795T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772914 | ||||||
chr3:56773198
|
T | A | 4 | a0002c0001t0003g0206a0002c0004t0003g0326a0002c0004t0003g0340others(1): Show | 4 | HG03654.hp1 HG03669.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+511A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56773198 | ||||||
chr3:56773302
|
A | G | 4 | a0002c0001t0003g0079a0002c0001t0003g0081a0002c0001t0003g0088others(1): Show | 4 | HG02258.hp1 HG02486.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+407T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56773302 | ||||||
chr3:56773500
|
C | T | 1 | a0001c0002t0002g0215 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.204+209G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56773500 | ||||||
chr3:56773662
|
G | A | 2 | a0001c0007t0001g0075a0001c0007t0001g0092 | 2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.204+47C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56773662 | ||||||
chr3:56773826
|
T | A | 1 | a0002c0004t0003g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.97-10A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56773826 | ||||||
chr3:56773961
|
T | C | 1 | a0002c0004t0001g0349 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.97-145A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56773961 | ||||||
chr3:56774127
|
C | A | 6 | a0001c0003t0001g0154a0001c0003t0001g0155a0001c0005t0001g0331others(3): Show | 6 | HG00140.hp2 HG01256.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-311G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774127 | ||||||
chr3:56774222
|
C | G | 17 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0007t0004g0027others(14): Show | 17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-406G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774222 | ||||||
chr3:56774414
|
C | T | 1 | a0002c0001t0001g0097 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.97-598G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774414 | ||||||
chr3:56774450
|
C | T | 2 | a0001c0007t0001g0075a0001c0007t0001g0092 | 2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.97-634G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774450 | ||||||
chr3:56774563
|
G | A | 1 | a0001c0002t0002g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.97-747C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774563 | ||||||
chr3:56774714
|
A | G | 70 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0003t0001g0249others(67): Show | 71 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.97-898T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774714 | ||||||
chr3:56774742
|
T | C | 113 | a0001c0002t0002g0036a0001c0002t0002g0051a0001c0002t0002g0059others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.97-926A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774742 | ||||||
chr3:56774825
|
G | C | 1 | a0002c0001t0001g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.97-1009C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774825 | ||||||
chr3:56774881
|
C | T | 9 | a0001c0002t0002g0078a0002c0001t0001g0135a0002c0001t0001g0136others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-1065G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774881 | ||||||
chr3:56774926
|
C | A | 2 | a0001c0007t0001g0075a0001c0007t0001g0092 | 2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.97-1110G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774926 | ||||||
chr3:56774926
|
C | CA | 10 | a0001c0002t0002g0077a0001c0002t0002g0149a0001c0003t0001g0030others(7): Show | 10 | HG03540.hp1 HG06807.hp2 NA18522.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-1111dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774926 | ||||||
chr3:56774928
|
A | AC | 170 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(167): Show | 173 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.97-1113_97-1112ins others(1): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774928 | ||||||
chr3:56774929
|
A | C | 76 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0126others(73): Show | 77 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.97-1113T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774929 | ||||||
chr3:56774931
|
A | C | 1 | a0001c0003t0001g0246 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.97-1115T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774931 | ||||||
chr3:56774947
|
G | A | 2 | a0001c0002t0017g0161a0002c0001t0001g0151 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.97-1131C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774947 | ||||||
chr3:56775221
|
G | A | 1 | a0002c0004t0001g0290 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.97-1405C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775221 | ||||||
chr3:56775262
|
T | C | 2 | a0002c0004t0001g0318a0002c0004t0001g0351 | 2 | HG00323.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.97-1446A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775262 | ||||||
chr3:56775600
|
A | G | 258 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(255): Show | 262 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.97-1784T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775600 | ||||||
chr3:56775722
|
A | G | 2 | a0001c0002t0002g0199a0001c0002t0002g0200 | 2 | NA19057.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.97-1906T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775722 | ||||||
chr3:56775768
|
C | A | 28 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(25): Show | 29 | HG00621.hp1 HG00673.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-1952G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775768 | ||||||
chr3:56775777
|
TACACACA others(19): Show |
T | 3 | a0001c0002t0005g0152a0001c0002t0005g0211a0001c0002t0005g0212 | 3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.97-1987_97-1962del others(26): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775777 | ||||||
chr3:56775791
|
C | T | 2 | a0001c0006t0002g0281a0002c0004t0014g0291 | 2 | NA18950.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.97-1975G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775791 | ||||||
chr3:56775792
|
A | G | 197 | a0001c0002t0002g0036a0001c0002t0002g0041a0001c0002t0002g0059others(194): Show | 199 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.97-1976T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775792 | ||||||
chr3:56775794
|
G | A | 14 | a0001c0002t0002g0019a0001c0002t0002g0026a0001c0002t0002g0038others(11): Show | 14 | HG00597.hp1 HG01109.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-1978C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775794 | ||||||
chr3:56775796
|
G | A | 10 | a0001c0002t0002g0078a0002c0001t0001g0074a0002c0001t0001g0135others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-1980C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775796 | ||||||
chr3:56775800
|
G | GCA | 185 | a0001c0002t0002g0036a0001c0002t0002g0040a0001c0002t0002g0041others(182): Show | 187 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.97-1986_97-1985dup others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775800 | ||||||
chr3:56775800
|
G | GCACA | 7 | a0001c0005t0001g0268a0002c0001t0001g0131a0002c0001t0001g0235others(4): Show | 7 | HG00741.hp1 NA18945.hp2 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-1988_97-1985dup others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775800 | ||||||
chr3:56775800
|
G | GCACACAC others(3): Show |
1 | a0001c0003t0001g0184 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.97-1994_97-1985dup others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775800 | ||||||
chr3:56775800
|
GCA | G | 17 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0007t0004g0027others(14): Show | 17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-1986_97-1985del others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775800 | ||||||
chr3:56775800
|
GCACACA | G | 5 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-1990_97-1985del others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775800 | ||||||
chr3:56776451
|
C | A | 3 | a0002c0001t0001g0014a0002c0001t0001g0095a0002c0001t0001g0096 | 3 | HG02723.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.97-2635G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776451 | ||||||
chr3:56776476
|
G | A | 1 | a0001c0002t0002g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.97-2660C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776476 | ||||||
chr3:56776481
|
T | C | 2 | a0001c0002t0017g0161a0002c0001t0001g0151 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.97-2665A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776481 | ||||||
chr3:56776643
|
G | T | 1 | a0001c0003t0001g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.97-2827C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776643 | ||||||
chr3:56776722
|
G | A | 2 | a0001c0007t0001g0093a0001c0007t0001g0165 | 2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.97-2906C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776722 | ||||||
chr3:56776737
|
G | A | 1 | a0001c0007t0004g0027 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.97-2921C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776737 | ||||||
chr3:56776841
|
C | T | 5 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-3025G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776841 | ||||||
chr3:56777290
|
A | C | 1 | a0001c0006t0002g0335 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.97-3474T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56777290 | ||||||
chr3:56777314
|
G | A | 1 | a0001c0005t0001g0327 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.97-3498C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56777314 | ||||||
chr3:56777317
|
G | A | 17 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0007t0004g0027others(14): Show | 17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-3501C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56777317 | ||||||
chr3:56777383
|
T | G | 1 | a0002c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-3567A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56777383 | ||||||
chr3:56777617
|
T | G | 1 | a0001c0003t0001g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.97-3801A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56777617 | ||||||
chr3:56777665
|
C | T | 5 | a0001c0002t0002g0077a0001c0002t0002g0078a0001c0002t0006g0006others(2): Show | 5 | HG02723.hp1 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-3849G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56777665 | ||||||
chr3:56778034
|
C | G | 1 | a0001c0007t0004g0124 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.97-4218G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778034 | ||||||
chr3:56778131
|
T | C | 30 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(27): Show | 31 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-4315A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778131 | ||||||
chr3:56778206
|
A | T | 112 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0002g0128others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.97-4390T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778206 | ||||||
chr3:56778394
|
T | C | 2 | a0001c0002t0002g0126a0004c0011t0008g0072 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.97-4578A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778394 | ||||||
chr3:56778422
|
T | C | 179 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(176): Show | 181 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.97-4606A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778422 | ||||||
chr3:56778710
|
A | T | 179 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(176): Show | 181 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.97-4894T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778710 | ||||||
chr3:56778983
|
T | C | 2 | a0001c0007t0001g0093a0001c0007t0001g0165 | 2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.97-5167A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778983 | ||||||
chr3:56779029
|
A | G | 1 | a0001c0002t0005g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.97-5213T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779029 | ||||||
chr3:56779115
|
C | G | 2 | a0001c0003t0001g0090a0001c0005t0001g0317 | 2 | HG01496.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.97-5299G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779115 | ||||||
chr3:56779142
|
C | T | 2 | a0001c0002t0017g0161a0002c0001t0001g0151 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.97-5326G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779142 | ||||||
chr3:56779203
|
T | G | 178 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(175): Show | 180 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.97-5387A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779203 | ||||||
chr3:56779253
|
A | AAT | 76 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0126others(73): Show | 78 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.97-5439_97-5438dup others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779253 | ||||||
chr3:56779294
|
G | A | 1 | a0001c0007t0004g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.97-5478C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779294 | ||||||
chr3:56779372
|
T | C | 1 | a0001c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.97-5556A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779372 | ||||||
chr3:56779482
|
T | A | 1 | a0002c0001t0001g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-5666A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779482 | ||||||
chr3:56779486
|
A | AT | 11 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(8): Show | 11 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-5671dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779486 | ||||||
chr3:56779495
|
T | G | 271 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(268): Show | 275 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.97-5679A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779495 | ||||||
chr3:56779528
|
TG | T | 5 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0021others(2): Show | 6 | HG02165.hp1 NA18950.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-5713delC | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779528 | ||||||
chr3:56779544
|
G | A | 12 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(9): Show | 12 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-5728C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779544 | ||||||
chr3:56779555
|
C | T | 6 | a0002c0001t0001g0135a0002c0001t0001g0136a0002c0001t0001g0143others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-5739G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779555 | ||||||
chr3:56779600
|
G | C | 17 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0007t0004g0027others(14): Show | 17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-5784C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779600 | ||||||
chr3:56779719
|
T | C | 2 | a0001c0002t0002g0224a0001c0002t0002g0225 | 2 | NA19005.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.97-5903A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779719 | ||||||
chr3:56779727
|
G | T | 2 | a0001c0002t0017g0161a0002c0001t0001g0151 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.97-5911C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779727 | ||||||
chr3:56780085
|
G | A | 2 | a0001c0003t0001g0023a0001c0003t0001g0029 | 2 | NA18963.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.97-6269C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56780085 | ||||||
chr3:56780129
|
C | G | 112 | a0001c0002t0002g0036a0001c0002t0002g0059a0001c0002t0002g0128others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.97-6313G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56780129 | ||||||
chr3:56780130
|
A | G | 181 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(178): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.97-6314T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56780130 | ||||||
chr3:56780303
|
T | G | 2 | a0002c0001t0003g0201a0002c0001t0003g0202 | 2 | NA18995.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.97-6487A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56780303 | ||||||
chr3:56780632
|
T | TTGTC | 69 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(66): Show | 72 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.97-6820_97-6817dup others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56780632 | ||||||
chr3:56780872
|
C | T | 1 | a0001c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.97-7056G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56780872 | ||||||
chr3:56781023
|
G | C | 2 | a0001c0005t0001g0331a0001c0005t0001g0332 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.97-7207C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781023 | ||||||
chr3:56781243
|
CT | C | 115 | a0001c0002t0002g0047a0001c0002t0002g0061a0001c0002t0002g0082others(112): Show | 117 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(114): Show |
intron_variant | MODIFIER | c.97-7428delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781243 | ||||||
chr3:56781305
|
T | C | 1 | a0001c0002t0002g0038 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.97-7489A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781305 | ||||||
chr3:56781385
|
TACAGGAG others(3): Show |
T | 1 | a0002c0001t0003g0263 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97-7579_97-7570del others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781385 | ||||||
chr3:56781445
|
C | T | 3 | a0002c0001t0001g0132a0002c0001t0001g0159a0002c0001t0001g0160 | 3 | HG02559.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.97-7629G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781445 | ||||||
chr3:56781446
|
C | CGA | 181 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(178): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.97-7631_97-7630ins others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781446 | ||||||
chr3:56781486
|
T | G | 3 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0203 | 3 | HG02451.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.97-7670A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781486 | ||||||
chr3:56781592
|
C | A | 276 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(273): Show | 280 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.97-7776G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781592 | ||||||
chr3:56781747
|
G | A | 6 | a0001c0002t0002g0061a0002c0001t0001g0217a0002c0001t0001g0218others(3): Show | 6 | NA18942.hp1 NA18956.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-7931C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781747 | ||||||
chr3:56781823
|
A | G | 38 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(35): Show | 40 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.97-8007T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781823 | ||||||
chr3:56781966
|
C | T | 291 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(288): Show | 296 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.97-8150G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781966 | ||||||
chr3:56782009
|
T | C | 1 | a0002c0001t0003g0050 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.97-8193A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782009 | ||||||
chr3:56782100
|
T | C | 1 | a0002c0004t0003g0340 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.97-8284A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782100 | ||||||
chr3:56782217
|
C | G | 181 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(178): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.97-8401G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782217 | ||||||
chr3:56782468
|
G | A | 1 | a0001c0007t0004g0120 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.97-8652C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782468 | ||||||
chr3:56782548
|
G | A | 95 | a0001c0002t0002g0047a0001c0002t0002g0061a0001c0002t0002g0082others(92): Show | 96 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(93): Show |
intron_variant | MODIFIER | c.97-8732C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782548 | ||||||
chr3:56782649
|
T | TA | 28 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(25): Show | 29 | HG00621.hp1 HG00673.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-8834dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782649 | ||||||
chr3:56782649
|
TA | T | 77 | a0001c0002t0002g0036a0001c0002t0002g0037a0001c0002t0002g0053others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.97-8834delT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782649 | ||||||
chr3:56782649
|
TAA | T | 96 | a0001c0002t0002g0047a0001c0002t0002g0061a0001c0002t0002g0082others(93): Show | 97 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(94): Show |
intron_variant | MODIFIER | c.97-8835_97-8834del others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782649 | ||||||
chr3:56782671
|
G | GTTTGT | 181 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(178): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.97-8860_97-8856dup others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782671 | ||||||
chr3:56782709
|
C | T | 10 | a0001c0007t0001g0100a0002c0001t0001g0074a0002c0001t0001g0135others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-8893G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782709 | ||||||
chr3:56782814
|
C | A | 93 | a0001c0002t0002g0128a0001c0002t0002g0129a0001c0002t0002g0130others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.97-8998G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782814 | ||||||
chr3:56783126
|
C | T | 1 | a0002c0001t0009g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.97-9310G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56783126 | ||||||
chr3:56783368
|
G | A | 1 | a0001c0007t0001g0100 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-9552C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56783368 | ||||||
chr3:56783400
|
G | A | 32 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(29): Show | 33 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-9584C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56783400 | ||||||
chr3:56783776
|
C | T | 1 | a0001c0007t0001g0100 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-9960G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56783776 | ||||||
chr3:56783996
|
A | G | 1 | a0001c0007t0004g0121 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.97-10180T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56783996 | ||||||
chr3:56784114
|
C | T | 2 | a0002c0001t0001g0135a0002c0001t0001g0153 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97-10298G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784114 | ||||||
chr3:56784128
|
G | C | 2 | a0002c0001t0001g0143a0002c0001t0001g0144 | 2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.97-10312C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784128 | ||||||
chr3:56784216
|
G | A | 2 | a0001c0002t0002g0126a0004c0011t0008g0072 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.97-10400C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784216 | ||||||
chr3:56784321
|
G | A | 5 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-10505C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784321 | ||||||
chr3:56784356
|
G | A | 1 | a0001c0007t0004g0124 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.97-10540C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784356 | ||||||
chr3:56784625
|
G | C | 1 | a0001c0002t0002g0148 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-10809C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784625 | ||||||
chr3:56784767
|
G | C | 3 | a0001c0002t0002g0128a0001c0002t0002g0129a0001c0002t0002g0130 | 3 | HG02080.hp1 HG02135.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.97-10951C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784767 | ||||||
chr3:56784801
|
T | C | 2 | a0001c0002t0002g0149a0002c0001t0001g0146 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-10985A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784801 | ||||||
chr3:56785107
|
A | T | 17 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0007t0004g0027others(14): Show | 17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-11291T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785107 | ||||||
chr3:56785246
|
G | C | 1 | a0004c0011t0008g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.97-11430C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785246 | ||||||
chr3:56785303
|
T | C | 1 | a0001c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.97-11487A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785303 | ||||||
chr3:56785349
|
T | C | 5 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-11533A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785349 | ||||||
chr3:56785412
|
C | T | 17 | a0001c0002t0002g0047a0001c0002t0002g0125a0001c0007t0004g0027others(14): Show | 17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-11596G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785412 | ||||||
chr3:56785436
|
C | T | 1 | a0001c0005t0001g0278 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.97-11620G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785436 | ||||||
chr3:56785668
|
T | G | 124 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(121): Show | 125 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.97-11852A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785668 | ||||||
chr3:56785715
|
G | A | 10 | a0001c0007t0001g0100a0002c0001t0001g0074a0002c0001t0001g0135others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-11899C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785715 | ||||||
chr3:56785839
|
G | A | 1 | a0001c0002t0002g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.97-12023C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785839 | ||||||
chr3:56786097
|
C | A | 1 | a0002c0001t0001g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-12281G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786097 | ||||||
chr3:56786164
|
A | G | 123 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(120): Show | 124 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.97-12348T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786164 | ||||||
chr3:56786290
|
C | G | 94 | a0001c0002t0002g0047a0001c0002t0002g0061a0001c0002t0002g0082others(91): Show | 95 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(92): Show |
intron_variant | MODIFIER | c.97-12474G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786290 | ||||||
chr3:56786328
|
A | T | 75 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0126others(72): Show | 76 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.97-12512T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786328 | ||||||
chr3:56786805
|
C | T | 96 | a0001c0002t0002g0041a0001c0002t0002g0128a0001c0002t0002g0129others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.97-12989G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786805 | ||||||
chr3:56786834
|
G | A | 1 | a0001c0007t0001g0100 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-13018C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786834 | ||||||
chr3:56786903
|
T | TA | 93 | a0001c0002t0002g0041a0001c0002t0002g0129a0001c0002t0002g0130others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.97-13088dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786903 | ||||||
chr3:56787072
|
A | G | 1 | a0002c0001t0003g0088 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.97-13256T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787072 | ||||||
chr3:56787080
|
C | T | 2 | a0002c0001t0003g0114a0002c0004t0003g0339 | 2 | HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.97-13264G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787080 | ||||||
chr3:56787084
|
T | C | 2 | a0002c0001t0001g0084a0002c0001t0001g0141 | 2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.97-13268A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787084 | ||||||
chr3:56787290
|
T | C | 96 | a0001c0002t0002g0041a0001c0002t0002g0128a0001c0002t0002g0129others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.97-13474A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787290 | ||||||
chr3:56787327
|
A | G | 1 | a0002c0001t0001g0133 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.97-13511T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787327 | ||||||
chr3:56787349
|
C | A | 3 | a0001c0002t0002g0076a0001c0002t0002g0085a0001c0002t0002g0086 | 3 | HG01099.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.97-13533G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787349 | ||||||
chr3:56787372
|
C | T | 8 | a0001c0002t0002g0126a0001c0002t0008g0145a0001c0002t0010g0009others(5): Show | 8 | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-13556G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787372 | ||||||
chr3:56787374
|
T | C | 81 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0017g0161others(78): Show | 83 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.97-13558A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787374 | ||||||
chr3:56787497
|
T | C | 303 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(300): Show | 308 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.97-13681A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787497 | ||||||
chr3:56787498
|
G | A | 291 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(288): Show | 296 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.97-13682C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787498 | ||||||
chr3:56787516
|
A | C | 291 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(288): Show | 296 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.97-13700T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787516 | ||||||
chr3:56787685
|
G | C | 96 | a0001c0002t0002g0041a0001c0002t0002g0128a0001c0002t0002g0129others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.97-13869C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787685 | ||||||
chr3:56787718
|
G | GATAATA | 4 | a0001c0002t0002g0157a0001c0002t0017g0161a0001c0007t0001g0100others(1): Show | 4 | HG03098.hp1 HG03540.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-13908_97-13903d others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787718 | ||||||
chr3:56787718
|
G | GATAATAA others(5): Show |
34 | a0001c0002t0002g0082a0001c0003t0001g0011a0001c0003t0001g0012others(31): Show | 34 | HG01109.hp1 HG01109.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.97-13914_97-13903d others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787718 | ||||||
chr3:56787718
|
G | GATAATAA others(8): Show |
38 | a0001c0002t0002g0061a0001c0003t0001g0254a0001c0006t0002g0287others(35): Show | 39 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.97-13917_97-13903d others(17): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787718 | ||||||
chr3:56787718
|
G | GATAATAA others(11): Show |
1 | a0001c0006t0002g0288 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.97-13920_97-13903d others(20): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787718 | ||||||
chr3:56787718
|
G | GATAATAA others(14): Show |
1 | a0002c0001t0001g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.97-13903_97-13902i others(23): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787718 | ||||||
chr3:56787864
|
A | G | 96 | a0001c0002t0002g0041a0001c0002t0002g0128a0001c0002t0002g0129others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.96+13839T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787864 | ||||||
chr3:56788154
|
T | C | 132 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(129): Show | 134 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.96+13549A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788154 | ||||||
chr3:56788213
|
C | T | 1 | a0001c0006t0002g0350 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.96+13490G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788213 | ||||||
chr3:56788229
|
G | A | 26 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(23): Show | 27 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.96+13474C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788229 | ||||||
chr3:56788289
|
A | G | 6 | a0001c0003t0001g0154a0001c0003t0001g0155a0001c0005t0001g0331others(3): Show | 6 | HG00140.hp2 HG01256.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+13414T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788289 | ||||||
chr3:56788349
|
T | C | 94 | a0001c0002t0002g0041a0001c0002t0002g0128a0001c0002t0002g0129others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.96+13354A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788349 | ||||||
chr3:56788463
|
A | G | 1 | a0001c0007t0004g0110 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.96+13240T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788463 | ||||||
chr3:56788499
|
A | G | 1 | a0002c0001t0001g0236 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.96+13204T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788499 | ||||||
chr3:56788500
|
G | A | 1 | a0002c0001t0001g0236 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.96+13203C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788500 | ||||||
chr3:56788597
|
A | G | 4 | a0001c0002t0002g0076a0001c0002t0002g0085a0001c0002t0002g0086others(1): Show | 4 | HG01099.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+13106T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788597 | ||||||
chr3:56788697
|
T | G | 1 | a0001c0003t0001g0187 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.96+13006A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788697 | ||||||
chr3:56788873
|
G | C | 1 | a0001c0007t0001g0162 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.96+12830C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788873 | ||||||
chr3:56788964
|
C | T | 8 | a0001c0002t0002g0126a0001c0002t0008g0145a0001c0002t0010g0009others(5): Show | 8 | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+12739G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788964 | ||||||
chr3:56789020
|
A | ATGC | 34 | a0001c0002t0002g0126a0001c0002t0002g0157a0001c0002t0002g0215others(31): Show | 34 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.96+12680_96+12682d others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | ||||||
chr3:56789020
|
A | ATGCTGC | 42 | a0001c0002t0002g0123a0001c0002t0002g0125a0001c0002t0002g0128others(39): Show | 43 | HG00544.hp1 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.96+12677_96+12682d others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | ||||||
chr3:56789020
|
A | ATGCTGCT others(2): Show |
9 | a0001c0002t0002g0047a0001c0002t0002g0122a0001c0002t0002g0129others(6): Show | 9 | HG02074.hp2 HG02135.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+12674_96+12682d others(11): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | ||||||
chr3:56789020
|
A | ATGCTGCT others(17): Show |
1 | a0001c0003t0001g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.96+12659_96+12682d others(26): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | ||||||
chr3:56789020
|
ATGC | A | 45 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(42): Show | 47 | HG00621.hp1 HG00673.hp1 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.96+12680_96+12682d others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | ||||||
chr3:56789020
|
ATGCTGC | A | 12 | a0001c0002t0002g0028a0001c0002t0002g0038a0001c0002t0002g0077others(9): Show | 12 | HG02055.hp1 HG02155.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.96+12677_96+12682d others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | ||||||
chr3:56789020
|
ATGCTGCT others(2): Show |
A | 46 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(43): Show | 47 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.96+12674_96+12682d others(11): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | ||||||
chr3:56789020
|
ATGCTGCT others(5): Show |
A | 1 | a0002c0001t0001g0066 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.96+12671_96+12682d others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | ||||||
chr3:56789020
|
ATGCTGCT others(8): Show |
A | 2 | a0001c0003t0001g0103a0001c0005t0001g0308 | 2 | HG00642.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.96+12668_96+12682d others(17): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | ||||||
chr3:56789020
|
ATGCTGCT others(11): Show |
A | 6 | a0001c0002t0008g0145a0001c0002t0010g0009a0002c0001t0001g0015others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+12665_96+12682d others(20): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | ||||||
chr3:56789020
|
ATGCTGCT others(14): Show |
A | 1 | a0001c0005t0001g0268 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.96+12662_96+12682d others(23): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | ||||||
chr3:56789020
|
ATGCTGCT others(17): Show |
A | 5 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+12659_96+12682d others(26): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | ||||||
chr3:56789083
|
G | A | 1 | a0001c0003t0001g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.96+12620C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789083 | ||||||
chr3:56789224
|
C | T | 1 | a0001c0003t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.96+12479G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789224 | ||||||
chr3:56789338
|
A | G | 291 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(288): Show | 296 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.96+12365T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789338 | ||||||
chr3:56789395
|
C | T | 3 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0203 | 3 | HG02451.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96+12308G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789395 | ||||||
chr3:56789618
|
A | G | 1 | a0001c0003t0001g0251 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.96+12085T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789618 | ||||||
chr3:56789619
|
G | C | 1 | a0001c0003t0001g0251 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.96+12084C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789619 | ||||||
chr3:56789754
|
G | A | 3 | a0002c0004t0003g0309a0002c0004t0003g0310a0002c0004t0003g0311 | 3 | HG00140.hp1 HG01934.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.96+11949C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789754 | ||||||
chr3:56789910
|
G | C | 1 | a0002c0001t0001g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.96+11793C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789910 | ||||||
chr3:56789978
|
G | A | 2 | a0001c0002t0002g0149a0002c0001t0001g0146 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+11725C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789978 | ||||||
chr3:56790173
|
C | T | 1 | a0001c0002t0002g0247 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.96+11530G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790173 | ||||||
chr3:56790174
|
G | A | 1 | a0002c0001t0001g0097 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.96+11529C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790174 | ||||||
chr3:56790317
|
T | A | 8 | a0001c0002t0002g0126a0001c0002t0008g0145a0001c0002t0010g0009others(5): Show | 8 | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+11386A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790317 | ||||||
chr3:56790471
|
C | T | 1 | a0001c0002t0002g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.96+11232G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790471 | ||||||
chr3:56790534
|
C | T | 19 | a0001c0002t0002g0047a0001c0002t0002g0122a0001c0002t0002g0123others(16): Show | 19 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.96+11169G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790534 | ||||||
chr3:56790594
|
T | C | 1 | a0002c0001t0001g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.96+11109A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790594 | ||||||
chr3:56790655
|
G | T | 3 | a0002c0001t0003g0024a0002c0001t0003g0049a0002c0001t0003g0050 | 3 | NA18960.hp2 NA18990.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.96+11048C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790655 | ||||||
chr3:56790773
|
G | A | 3 | a0001c0002t0002g0076a0001c0002t0002g0085a0001c0002t0002g0086 | 3 | HG01099.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.96+10930C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790773 | ||||||
chr3:56790798
|
T | C | 4 | a0002c0001t0003g0079a0002c0001t0003g0081a0002c0001t0003g0088others(1): Show | 4 | HG02258.hp1 HG02486.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+10905A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790798 | ||||||
chr3:56791062
|
C | T | 2 | a0001c0007t0001g0075a0001c0007t0001g0092 | 2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.96+10641G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791062 | ||||||
chr3:56791142
|
C | T | 36 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(33): Show | 37 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(34): Show |
intron_variant | MODIFIER | c.96+10561G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791142 | ||||||
chr3:56791459
|
A | G | 3 | a0002c0001t0003g0043a0002c0001t0003g0054a0002c0001t0003g0055 | 3 | HG00544.hp1 NA18967.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.96+10244T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791459 | ||||||
chr3:56791518
|
C | T | 2 | a0001c0007t0001g0075a0001c0007t0001g0092 | 2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.96+10185G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791518 | ||||||
chr3:56791542
|
A | C | 1 | a0001c0002t0010g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.96+10161T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791542 | ||||||
chr3:56791866
|
TA | T | 299 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(296): Show | 304 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.96+9836delT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791866 | ||||||
chr3:56791927
|
G | T | 2 | a0001c0002t0002g0082a0002c0001t0001g0083 | 2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.96+9776C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791927 | ||||||
chr3:56791969
|
G | A | 2 | a0001c0002t0005g0152a0001c0002t0005g0212 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.96+9734C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791969 | ||||||
chr3:56791969
|
G | C | 98 | a0001c0002t0002g0059a0001c0002t0002g0128a0001c0002t0002g0129others(95): Show | 98 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.96+9734C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791969 | ||||||
chr3:56791976
|
C | T | 1 | a0001c0002t0002g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.96+9727G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791976 | ||||||
chr3:56792093
|
G | A | 1 | a0002c0001t0001g0097 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.96+9610C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792093 | ||||||
chr3:56792103
|
C | CA | 38 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(35): Show | 39 | HG00544.hp2 HG00597.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.96+9599dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792103 | ||||||
chr3:56792103
|
C | CAAAAAA | 88 | a0001c0002t0002g0059a0001c0002t0002g0128a0001c0002t0002g0129others(85): Show | 88 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.96+9594_96+9599dup others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792103 | ||||||
chr3:56792113
|
A | AAAAAAAA others(4): Show |
1 | a0001c0006t0002g0335 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.96+9589_96+9590ins others(11): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | ||||||
chr3:56792113
|
A | AAAAAAAA others(3): Show |
3 | a0001c0002t0002g0032a0001c0002t0002g0190a0001c0006t0002g0334 | 3 | HG02080.hp2 HG03239.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.96+9589_96+9590ins others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | ||||||
chr3:56792113
|
A | AAAAAAAA others(8): Show |
1 | a0002c0001t0016g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.96+9589_96+9590ins others(15): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | ||||||
chr3:56792113
|
A | AAAAAAAA others(13): Show |
7 | a0002c0001t0001g0135a0002c0001t0001g0136a0002c0001t0001g0137others(4): Show | 8 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+9589_96+9590ins others(20): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | ||||||
chr3:56792113
|
A | AAAAAAG | 6 | a0001c0002t0002g0026a0001c0002t0002g0077a0001c0002t0002g0078others(3): Show | 6 | HG02723.hp1 HG03540.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+9589_96+9590ins others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | ||||||
chr3:56792113
|
AAAAAG | A | 20 | a0001c0002t0002g0047a0001c0002t0002g0122a0001c0002t0002g0123others(17): Show | 20 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.96+9585_96+9589del others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | ||||||
chr3:56792113
|
AAAAAGAA others(3): Show |
A | 2 | a0001c0007t0001g0093a0001c0007t0001g0165 | 2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.96+9580_96+9589del others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | ||||||
chr3:56792118
|
G | A | 22 | a0001c0002t0002g0002a0001c0002t0002g0033a0001c0002t0002g0042others(19): Show | 23 | HG00621.hp1 HG00673.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.96+9585C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792118 | ||||||
chr3:56792123
|
G | A | 1 | a0002c0001t0003g0231 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.96+9580C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792123 | ||||||
chr3:56792125
|
A | T | 1 | a0001c0005t0001g0319 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.96+9578T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792125 | ||||||
chr3:56792138
|
GAAAAGAA others(3): Show |
G | 7 | a0001c0002t0017g0161a0001c0007t0001g0100a0002c0001t0001g0014others(4): Show | 7 | HG02630.hp2 HG02723.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+9555_96+9564del others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792138 | ||||||
chr3:56792143
|
GAAAAT | G | 81 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0148others(78): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.96+9555_96+9559del others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792143 | ||||||
chr3:56792148
|
T | G | 8 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+9555A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792148 | ||||||
chr3:56792201
|
A | T | 1 | a0002c0001t0001g0188 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.96+9502T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792201 | ||||||
chr3:56792296
|
A | C | 131 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(128): Show | 133 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.96+9407T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792296 | ||||||
chr3:56792665
|
G | A | 94 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0148others(91): Show | 96 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.96+9038C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792665 | ||||||
chr3:56792737
|
T | A | 131 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(128): Show | 133 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.96+8966A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792737 | ||||||
chr3:56792763
|
T | C | 94 | a0001c0002t0002g0059a0001c0002t0002g0128a0001c0002t0002g0129others(91): Show | 94 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.96+8940A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792763 | ||||||
chr3:56792819
|
A | AT | 96 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0148others(93): Show | 98 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.96+8883dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792819 | ||||||
chr3:56792820
|
T | A | 131 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(128): Show | 133 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.96+8883A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792820 | ||||||
chr3:56792933
|
A | G | 1 | a0002c0004t0003g0344 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.96+8770T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792933 | ||||||
chr3:56792997
|
T | TG | 104 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(101): Show | 107 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.96+8705_96+8706ins others(1): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792997 | ||||||
chr3:56792998
|
T | G | 186 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(183): Show | 188 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(185): Show |
intron_variant | MODIFIER | c.96+8705A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792998 | ||||||
chr3:56793003
|
T | A | 1 | a0001c0006t0002g0342 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.96+8700A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793003 | ||||||
chr3:56793008
|
A | T | 1 | a0002c0001t0003g0164 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.96+8695T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793008 | ||||||
chr3:56793170
|
A | AT | 6 | a0001c0002t0002g0040a0001c0007t0004g0109a0002c0001t0001g0208others(3): Show | 6 | HG03017.hp1 HG04204.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+8532dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793170 | ||||||
chr3:56793170
|
A | ATT | 34 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(31): Show | 35 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(32): Show |
intron_variant | MODIFIER | c.96+8531_96+8532dup others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793170 | ||||||
chr3:56793170
|
AT | A | 138 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(135): Show | 140 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.96+8532delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793170 | ||||||
chr3:56793344
|
T | A | 1 | a0001c0007t0004g0120 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.96+8359A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793344 | ||||||
chr3:56793411
|
C | T | 36 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(33): Show | 37 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(34): Show |
intron_variant | MODIFIER | c.96+8292G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793411 | ||||||
chr3:56793416
|
G | A | 1 | a0002c0004t0001g0341 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.96+8287C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793416 | ||||||
chr3:56793424
|
T | C | 297 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(294): Show | 302 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.96+8279A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793424 | ||||||
chr3:56793484
|
G | T | 2 | a0001c0002t0002g0126a0004c0011t0008g0072 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.96+8219C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793484 | ||||||
chr3:56793510
|
C | T | 5 | a0001c0002t0002g0077a0001c0002t0002g0078a0001c0002t0006g0006others(2): Show | 5 | HG02723.hp1 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+8193G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793510 | ||||||
chr3:56793545
|
C | T | 1 | a0002c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.96+8158G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793545 | ||||||
chr3:56793566
|
G | A | 4 | a0001c0003t0001g0154a0001c0003t0001g0155a0001c0005t0001g0331others(1): Show | 4 | HG00140.hp2 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+8137C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793566 | ||||||
chr3:56793610
|
A | G | 4 | a0001c0003t0001g0249a0001c0007t0001g0101a0001c0013t0001g0150others(1): Show | 4 | HG02630.hp1 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+8093T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793610 | ||||||
chr3:56793611
|
T | A | 37 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(34): Show | 38 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.96+8092A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793611 | ||||||
chr3:56793633
|
A | G | 35 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(32): Show | 37 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.96+8070T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793633 | ||||||
chr3:56793739
|
C | A | 1 | a0001c0003t0001g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.96+7964G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793739 | ||||||
chr3:56793919
|
C | A | 2 | a0002c0004t0003g0314a0002c0004t0003g0315 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.96+7784G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793919 | ||||||
chr3:56794126
|
A | G | 1 | a0001c0002t0008g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.96+7577T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794126 | ||||||
chr3:56794285
|
C | T | 54 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(51): Show | 56 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.96+7418G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794285 | ||||||
chr3:56794290
|
C | G | 1 | a0001c0007t0001g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.96+7413G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794290 | ||||||
chr3:56794389
|
C | G | 294 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(291): Show | 299 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.96+7314G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794389 | ||||||
chr3:56794396
|
G | A | 89 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0148others(86): Show | 89 | HG00140.hp2 HG00323.hp2 HG01109.hp1 others(86): Show |
intron_variant | MODIFIER | c.96+7307C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794396 | ||||||
chr3:56794446
|
C | T | 2 | a0002c0001t0001g0208a0002c0001t0001g0209 | 2 | NA18977.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.96+7257G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794446 | ||||||
chr3:56794475
|
C | T | 58 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0003t0001g0246others(55): Show | 58 | HG00323.hp2 HG01109.hp1 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.96+7228G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794475 | ||||||
chr3:56794488
|
C | CA | 7 | a0001c0002t0002g0076a0001c0002t0002g0085a0001c0002t0002g0086others(4): Show | 7 | HG01099.hp1 HG02886.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+7214dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | ||||||
chr3:56794488
|
C | CAAAAAAA others(1): Show |
10 | a0001c0002t0002g0125a0001c0007t0004g0046a0001c0007t0004g0109others(7): Show | 10 | HG01928.hp1 HG02293.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+7207_96+7214dup others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | ||||||
chr3:56794488
|
C | CAAAAAAA others(2): Show |
6 | a0001c0002t0002g0047a0001c0002t0010g0009a0001c0007t0004g0110others(3): Show | 6 | HG01361.hp2 HG01952.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+7206_96+7214dup others(9): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | ||||||
chr3:56794488
|
C | CAAAAAAA others(3): Show |
1 | a0001c0007t0004g0121 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.96+7205_96+7214dup others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | ||||||
chr3:56794488
|
C | CAAAAAAA others(4): Show |
3 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0007t0001g0073 | 3 | HG02074.hp2 HG02083.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.96+7204_96+7214dup others(11): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | ||||||
chr3:56794488
|
C | CAAAAAAA others(5): Show |
1 | a0001c0002t0008g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.96+7203_96+7214dup others(12): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | ||||||
chr3:56794488
|
C | CAAAAAAA others(29): Show |
2 | a0002c0001t0001g0015a0002c0001t0001g0016 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96+7214_96+7215ins others(36): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | ||||||
chr3:56794488
|
C | CAAAAAAA others(32): Show |
1 | a0002c0001t0001g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+7214_96+7215ins others(39): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | ||||||
chr3:56794488
|
CAAAAA | C | 23 | a0001c0002t0002g0126a0001c0002t0002g0148a0001c0003t0001g0154others(20): Show | 23 | HG00140.hp2 HG01256.hp2 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.96+7210_96+7214del others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | ||||||
chr3:56794488
|
CAAAAAAA | C | 111 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(108): Show | 114 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.96+7208_96+7214del others(7): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | ||||||
chr3:56794488
|
CAAAAAAA others(1): Show |
C | 39 | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(36): Show | 41 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.96+7207_96+7214del others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | ||||||
chr3:56794488
|
CAAAAAAA others(2): Show |
C | 96 | a0001c0002t0002g0059a0001c0002t0002g0128a0001c0002t0002g0129others(93): Show | 96 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.96+7206_96+7214del others(9): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | ||||||
chr3:56794553
|
A | G | 1 | a0002c0001t0003g0079 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.96+7150T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794553 | ||||||
chr3:56794781
|
C | T | 1 | a0001c0002t0002g0042 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.96+6922G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794781 | ||||||
chr3:56794782
|
G | A | 92 | a0001c0002t0002g0059a0001c0002t0002g0128a0001c0002t0002g0129others(89): Show | 92 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.96+6921C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794782 | ||||||
chr3:56794909
|
G | C | 100 | a0001c0002t0002g0059a0001c0002t0002g0128a0001c0002t0002g0129others(97): Show | 100 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.96+6794C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794909 | ||||||
chr3:56794923
|
A | G | 4 | a0002c0001t0003g0024a0002c0001t0003g0025a0002c0001t0003g0049others(1): Show | 4 | NA18960.hp2 NA18972.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+6780T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794923 | ||||||
chr3:56794970
|
C | T | 1 | a0001c0002t0002g0035 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.96+6733G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794970 | ||||||
chr3:56795033
|
A | AT | 280 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(277): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.96+6669dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795033 | ||||||
chr3:56795033
|
A | ATT | 29 | a0001c0002t0002g0047a0001c0002t0002g0048a0001c0002t0002g0122others(26): Show | 29 | HG01109.hp1 HG01361.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.96+6668_96+6669dup others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795033 | ||||||
chr3:56795066
|
T | G | 19 | a0001c0002t0002g0047a0001c0002t0002g0122a0001c0002t0002g0123others(16): Show | 19 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.96+6637A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795066 | ||||||
chr3:56795095
|
G | A | 61 | a0001c0002t0002g0061a0001c0002t0002g0082a0001c0002t0002g0085others(58): Show | 61 | HG00323.hp2 HG01099.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.96+6608C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795095 | ||||||
chr3:56795224
|
T | C | 1 | a0001c0002t0002g0032 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.96+6479A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795224 | ||||||
chr3:56795401
|
C | T | 2 | a0001c0003t0001g0099a0001c0003t0001g0258 | 2 | HG01884.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.96+6302G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795401 | ||||||
chr3:56795580
|
A | G | 1 | a0001c0003t0001g0254 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.96+6123T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795580 | ||||||
chr3:56795585
|
G | A | 18 | a0001c0002t0002g0021a0001c0002t0002g0033a0001c0002t0002g0034others(15): Show | 18 | HG00544.hp2 HG00558.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.96+6118C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795585 | ||||||
chr3:56795633
|
A | G | 244 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(241): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.96+6070T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795633 | ||||||
chr3:56795635
|
T | C | 244 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(241): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.96+6068A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795635 | ||||||
chr3:56795655
|
C | CTCTTTTT others(3): Show |
9 | a0001c0002t0002g0197a0001c0002t0002g0198a0001c0002t0005g0152others(6): Show | 9 | HG00673.hp1 HG01169.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+6047_96+6048ins others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | ||||||
chr3:56795655
|
C | CTCTTTTT others(4): Show |
88 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0018others(85): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.96+6047_96+6048ins others(11): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | ||||||
chr3:56795655
|
C | CTCTTTTT others(5): Show |
19 | a0001c0002t0002g0042a0001c0002t0002g0191a0001c0005t0001g0268others(16): Show | 20 | HG00597.hp2 HG00733.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.96+6047_96+6048ins others(12): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | ||||||
chr3:56795655
|
C | CTCTTTTT others(7): Show |
1 | a0001c0007t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.96+6047_96+6048ins others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | ||||||
chr3:56795655
|
C | CTTTTTTT others(2): Show |
57 | a0001c0002t0002g0082a0001c0002t0002g0085a0001c0002t0002g0129others(54): Show | 57 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.96+6039_96+6047dup others(9): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | ||||||
chr3:56795655
|
C | CTTTTTTT others(3): Show |
3 | a0001c0002t0002g0128a0002c0001t0001g0217a0002c0001t0001g0218 | 3 | NA18956.hp2 NA19006.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.96+6038_96+6047dup others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | ||||||
chr3:56795655
|
C | CTTTTTTT others(4): Show |
7 | a0001c0002t0002g0215a0001c0003t0001g0091a0001c0005t0001g0277others(4): Show | 7 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+6037_96+6047dup others(11): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | ||||||
chr3:56795655
|
C | CTTTTTTT others(5): Show |
11 | a0001c0002t0002g0019a0001c0002t0002g0035a0001c0002t0002g0038others(8): Show | 11 | HG01981.hp2 HG02155.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.96+6036_96+6047dup others(12): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | ||||||
chr3:56795655
|
C | CTTTTTTT others(6): Show |
38 | a0001c0002t0002g0021a0001c0002t0002g0026a0001c0002t0002g0028others(35): Show | 38 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.96+6047_96+6048ins others(13): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | ||||||
chr3:56795655
|
C | CTTTTTTT others(7): Show |
1 | a0001c0003t0001g0023 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.96+6047_96+6048ins others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | ||||||
chr3:56795655
|
CT | C | 18 | a0001c0002t0002g0047a0001c0002t0002g0122a0001c0002t0002g0123others(15): Show | 18 | HG01952.hp1 HG02074.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.96+6047delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | ||||||
chr3:56795668
|
G | T | 2 | a0001c0002t0002g0022a0001c0002t0002g0040 | 2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.96+6035C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795668 | ||||||
chr3:56795707
|
G | A | 2 | a0001c0002t0002g0199a0001c0002t0002g0200 | 2 | NA19057.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.96+5996C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795707 | ||||||
chr3:56795737
|
G | C | 54 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0026others(51): Show | 54 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.96+5966C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795737 | ||||||
chr3:56795790
|
T | C | 76 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0026others(73): Show | 76 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+5913A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795790 | ||||||
chr3:56795798
|
C | T | 1 | a0001c0002t0002g0019 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.96+5905G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795798 | ||||||
chr3:56795801
|
C | A | 1 | a0001c0002t0002g0038 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.96+5902G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795801 | ||||||
chr3:56795830
|
T | C | 2 | a0001c0005t0001g0327a0002c0004t0003g0328 | 2 | NA18956.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.96+5873A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795830 | ||||||
chr3:56795842
|
G | A | 1 | a0001c0002t0008g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.96+5861C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795842 | ||||||
chr3:56795864
|
C | T | 157 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0022others(154): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.96+5839G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795864 | ||||||
chr3:56795915
|
C | T | 1 | a0002c0001t0003g0043 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.96+5788G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795915 | ||||||
chr3:56795916
|
G | A | 2 | a0001c0002t0002g0149a0001c0007t0001g0100 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.96+5787C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795916 | ||||||
chr3:56795977
|
T | TA | 58 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0022others(55): Show | 58 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.96+5725dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795977 | ||||||
chr3:56795977
|
TA | T | 133 | a0001c0002t0002g0002a0001c0002t0002g0076a0001c0002t0002g0082others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.96+5725delT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795977 | ||||||
chr3:56796059
|
C | T | 223 | a0001c0002t0002g0002a0001c0002t0002g0076a0001c0002t0002g0077others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.96+5644G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796059 | ||||||
chr3:56796068
|
G | A | 22 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0125others(19): Show | 22 | HG00597.hp2 HG01361.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+5635C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796068 | ||||||
chr3:56796360
|
T | C | 1 | a0001c0003t0001g0187 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.96+5343A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796360 | ||||||
chr3:56796375
|
T | C | 24 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0125others(21): Show | 24 | HG00597.hp2 HG01070.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.96+5328A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796375 | ||||||
chr3:56796431
|
C | T | 57 | a0001c0002t0002g0219a0001c0002t0002g0220a0001c0002t0002g0221others(54): Show | 57 | HG00597.hp1 HG00673.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.96+5272G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796431 | ||||||
chr3:56796471
|
G | A | 2 | a0002c0001t0003g0201a0002c0001t0003g0202 | 2 | NA18995.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.96+5232C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796471 | ||||||
chr3:56796538
|
G | A | 15 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0003t0001g0119others(12): Show | 15 | HG00597.hp2 HG01361.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+5165C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796538 | ||||||
chr3:56796551
|
G | A | 42 | a0001c0002t0002g0002a0001c0002t0002g0040a0001c0002t0002g0128others(39): Show | 43 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.96+5152C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796551 | ||||||
chr3:56797043
|
C | T | 4 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(1): Show | 4 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+4660G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797043 | ||||||
chr3:56797094
|
C | A | 59 | a0001c0002t0002g0219a0001c0002t0002g0220a0001c0002t0002g0221others(56): Show | 59 | HG00597.hp1 HG00673.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.96+4609G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797094 | ||||||
chr3:56797239
|
T | C | 91 | a0001c0002t0002g0041a0001c0005t0001g0268a0001c0005t0001g0273others(88): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.96+4464A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797239 | ||||||
chr3:56797242
|
T | A | 1 | a0001c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.96+4461A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797242 | ||||||
chr3:56797285
|
C | A | 1 | a0002c0004t0001g0272 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.96+4418G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797285 | ||||||
chr3:56797366
|
C | T | 18 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0190others(15): Show | 19 | HG00621.hp1 HG00673.hp1 HG02735.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+4337G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797366 | ||||||
chr3:56797391
|
C | A | 1 | a0001c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.96+4312G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797391 | ||||||
chr3:56797479
|
G | A | 2 | a0002c0001t0001g0015a0002c0001t0001g0016 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96+4224C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797479 | ||||||
chr3:56797520
|
G | A | 208 | a0001c0002t0002g0002a0001c0002t0002g0019a0001c0002t0002g0021others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.96+4183C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797520 | ||||||
chr3:56797530
|
C | A | 1 | a0001c0002t0002g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.96+4173G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797530 | ||||||
chr3:56797608
|
T | C | 2 | a0001c0005t0001g0273a0001c0005t0001g0274 | 2 | NA18952.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.96+4095A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797608 | ||||||
chr3:56797676
|
A | G | 1 | a0002c0001t0001g0188 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.96+4027T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797676 | ||||||
chr3:56798342
|
A | G | 1 | a0001c0003t0001g0163 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.96+3361T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798342 | ||||||
chr3:56798503
|
A | C | 1 | a0001c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.96+3200T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798503 | ||||||
chr3:56798536
|
CGTT | C | 3 | a0001c0003t0001g0068a0001c0003t0001g0069a0001c0003t0001g0070 | 3 | NA18941.hp1 NA18955.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.96+3164_96+3166del others(3): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798536 | ||||||
chr3:56798537
|
GT | G | 112 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0019others(109): Show | 113 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.96+3165delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798537 | ||||||
chr3:56798537
|
GTT | G | 129 | a0001c0002t0002g0002a0001c0002t0002g0041a0001c0002t0002g0042others(126): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.96+3164_96+3165del others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798537 | ||||||
chr3:56798537
|
GTTT | G | 7 | a0001c0002t0002g0126a0001c0002t0002g0265a0001c0002t0002g0266others(4): Show | 7 | HG02486.hp2 HG02698.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+3163_96+3165del others(3): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798537 | ||||||
chr3:56798537
|
GTTTTTTT | G | 83 | a0001c0005t0001g0268a0001c0005t0001g0277a0001c0005t0001g0278others(80): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.96+3159_96+3165del others(7): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798537 | ||||||
chr3:56798562
|
C | A | 5 | a0001c0003t0001g0103a0001c0007t0001g0100a0001c0007t0001g0101others(2): Show | 5 | HG00741.hp2 HG02622.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+3141G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798562 | ||||||
chr3:56798563
|
C | A | 5 | a0001c0003t0001g0103a0001c0007t0001g0100a0001c0007t0001g0101others(2): Show | 5 | HG00741.hp2 HG02622.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+3140G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798563 | ||||||
chr3:56798564
|
T | C | 21 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0125others(18): Show | 21 | HG00597.hp2 HG01361.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.96+3139A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798564 | ||||||
chr3:56798676
|
C | T | 1 | a0002c0001t0001g0132 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.96+3027G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798676 | ||||||
chr3:56798996
|
T | C | 89 | a0001c0002t0002g0076a0001c0002t0002g0077a0001c0002t0002g0078others(86): Show | 89 | HG00597.hp1 HG00673.hp2 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.96+2707A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798996 | ||||||
chr3:56799162
|
A | G | 19 | a0001c0002t0002g0076a0001c0002t0002g0077a0001c0002t0002g0078others(16): Show | 19 | HG01099.hp1 HG01496.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.96+2541T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799162 | ||||||
chr3:56799406
|
G | A | 1 | a0001c0002t0002g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.96+2297C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799406 | ||||||
chr3:56799686
|
G | A | 4 | a0001c0003t0001g0103a0001c0007t0001g0101a0001c0012t0001g0104others(1): Show | 4 | HG00741.hp2 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+2017C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799686 | ||||||
chr3:56799734
|
C | A | 22 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0125others(19): Show | 22 | HG00597.hp2 HG01361.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+1969G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799734 | ||||||
chr3:56799738
|
T | C | 170 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0022others(167): Show | 170 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.96+1965A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799738 | ||||||
chr3:56799741
|
G | A | 88 | a0001c0005t0001g0268a0001c0005t0001g0273a0001c0005t0001g0274others(85): Show | 90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.96+1962C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799741 | ||||||
chr3:56799763
|
A | G | 4 | a0001c0002t0002g0128a0001c0002t0002g0129a0001c0002t0002g0130others(1): Show | 4 | HG02080.hp1 HG02135.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1940T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799763 | ||||||
chr3:56799829
|
T | C | 19 | a0001c0002t0002g0003a0001c0002t0002g0018a0001c0002t0002g0190others(16): Show | 20 | HG00621.hp1 HG00673.hp1 HG02735.hp2 others(17): Show |
intron_variant | MODIFIER | c.96+1874A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799829 | ||||||
chr3:56799947
|
C | T | 1 | a0002c0004t0012g0269 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.96+1756G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799947 | ||||||
chr3:56799951
|
T | C | 89 | a0001c0005t0001g0268a0001c0005t0001g0273a0001c0005t0001g0274others(86): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.96+1752A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799951 | ||||||
chr3:56800167
|
G | A | 3 | a0001c0002t0006g0006a0001c0002t0006g0008a0002c0001t0009g0007 | 3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.96+1536C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800167 | ||||||
chr3:56800170
|
G | A | 89 | a0001c0005t0001g0268a0001c0005t0001g0273a0001c0005t0001g0274others(86): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.96+1533C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800170 | ||||||
chr3:56800204
|
T | G | 3 | a0001c0002t0006g0006a0001c0002t0006g0008a0002c0001t0009g0007 | 3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.96+1499A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800204 | ||||||
chr3:56800255
|
C | T | 1 | a0001c0003t0001g0127 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.96+1448G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800255 | ||||||
chr3:56800261
|
A | G | 170 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0022others(167): Show | 170 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.96+1442T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800261 | ||||||
chr3:56800398
|
T | C | 5 | a0001c0003t0001g0207a0002c0001t0001g0203a0002c0001t0003g0205others(2): Show | 5 | HG00642.hp1 HG02257.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+1305A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800398 | ||||||
chr3:56800496
|
C | T | 89 | a0001c0005t0001g0268a0001c0005t0001g0273a0001c0005t0001g0274others(86): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.96+1207G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800496 | ||||||
chr3:56800771
|
C | T | 89 | a0001c0005t0001g0268a0001c0005t0001g0273a0001c0005t0001g0274others(86): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.96+932G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800771 | ||||||
chr3:56800899
|
T | C | 1 | a0002c0004t0001g0351 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.96+804A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800899 | ||||||
chr3:56800950
|
T | A | 60 | a0001c0002t0002g0215a0001c0002t0002g0219a0001c0002t0002g0220others(57): Show | 60 | HG00597.hp1 HG00673.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.96+753A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800950 | ||||||
chr3:56800955
|
C | T | 1 | a0004c0011t0008g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.96+748G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800955 | ||||||
chr3:56800984
|
C | T | 53 | a0001c0002t0002g0019a0001c0002t0002g0021a0001c0002t0002g0022others(50): Show | 53 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.96+719G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800984 | ||||||
chr3:56801050
|
A | G | 2 | a0001c0002t0002g0018a0001c0009t0002g0017 | 2 | NA18950.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.96+653T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56801050 | ||||||
chr3:56801051
|
T | C | 3 | a0001c0002t0006g0006a0001c0002t0006g0008a0002c0001t0009g0007 | 3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.96+652A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56801051 | ||||||
chr3:56801064
|
C | T | 1 | a0001c0005t0001g0268 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.96+639G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56801064 | ||||||
chr3:56801607
|
A | G | 8 | a0001c0002t0010g0009a0001c0003t0001g0011a0001c0003t0001g0012others(5): Show | 8 | HG01109.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+96T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56801607 |