geneid | 9138 |
---|---|
ensemblid | ENSG00000076928.20 |
hgncid | 681 |
symbol | ARHGEF1 |
name | Rho guanine nucleotide exchange factor 1 |
refseq_nuc | NM_004706.4 |
refseq_prot | NP_004697.2 |
ensembl_nuc | ENST00000354532.8 |
ensembl_prot | ENSP00000346532.3 |
mane_status | MANE Select |
chr | chr19 |
start | 41883184 |
end | 41907452 |
strand | + |
ver | v1.2 |
region | chr19:41883184-41907452 |
region5000 | chr19:41878184-41912452 |
regionname0 | ARHGEF1_chr19_41883184_41907452 |
regionname5000 | ARHGEF1_chr19_41878184_41912452 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 912 | 224 | 65 | 42 | 82 | 8 | 25 | 53 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0002 | 0/0 | 912 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0003 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0004 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0005 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0006 | 0/0 | 907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0007 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0008 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2739 | 140 | 18 | 37 | 57 | 7 | 19 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
c0002 | 0/0 | 2739 | 74 | 40 | 5 | 23 | 0 | 6 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
c0003 | 0/0 | 2739 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
c0004 | 0/0 | 2739 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
c0005 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
c0006 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
c0007 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
c0008 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
c0009 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
c0010 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
c0011 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
c0012 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
c0013 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 491 | 230 | 65 | 46 | 84 | 8 | 25 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
t0002 | 0/0 | 491 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
t0003 | 0/0 | 491 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
t0004 | 0/0 | 491 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
t0005 | 0/0 | 491 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 0 | 0 | 10 | 0 | 2 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0002 | 0/0 | 10 | 1 | 3 | 6 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0003 | 0/0 | 9 | 0 | 2 | 2 | 1 | 4 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0004 | 0/0 | 8 | 0 | 3 | 4 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0005 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0009 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2739 | 140 | 18 | 37 | 57 | 7 | 19 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0002 | 0/0 | 2739 | 74 | 40 | 5 | 23 | 0 | 6 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0003 | 0/0 | 2739 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0006 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0007 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0013 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0002c0004 | 0/0 | 2739 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0003c0012 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0004c0010 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0005c0009 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0006c0005 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0007c0008 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0008c0011 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3229 | 139 | 18 | 37 | 56 | 7 | 19 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0001t0003 | 0/0 | 3229 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0002t0001 | 0/0 | 3229 | 71 | 39 | 5 | 22 | 0 | 5 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0002t0002 | 0/0 | 3229 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0002t0004 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0002t0005 | 0/0 | 3229 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0003t0001 | 0/0 | 3229 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0006t0001 | 0/0 | 3229 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0007t0001 | 0/0 | 3229 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0001c0013t0001 | 0/0 | 3229 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0002c0004t0001 | 0/0 | 3229 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0003c0012t0001 | 0/0 | 3229 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0004c0010t0001 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0005c0009t0001 | 0/0 | 3229 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0006c0005t0001 | 0/0 | 3214 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0007c0008t0001 | 0/0 | 3229 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
a0008c0011t0001 | 0/0 | 3229 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | copy fasta | chr19 | 41878184 | 41912452 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 10 | 1 | 3 | 6 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0003 | 0/0 | 9 | 0 | 2 | 2 | 1 | 4 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 2 | 4 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0005 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0009 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0001 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0002t0005g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0006t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0007t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0001c0013t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0002c0004t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0002c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0002c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0003c0012t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0004c0010t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0005c0009t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0006c0005t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0007c0008t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
a0008c0011t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00099 | hp2 | a0001 | c0006 | t0001 | g0159 | EUR | GBR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00639 | hp1 | a0003 | c0012 | t0001 | g0160 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00738 | hp2 | a0006 | c0005 | t0001 | g0089 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01361 | hp1 | a0005 | c0009 | t0001 | g0004 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02004 | hp1 | a0007 | c0008 | t0001 | g0006 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02040 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | CDX | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02572 | hp2 | a0001 | c0002 | t0004 | g0057 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0062 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0050 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03831 | hp1 | a0008 | c0011 | t0001 | g0167 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0010 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0046 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | YRI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | YRI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | CHB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | YRI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | YRI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18940 | hp2 | a0002 | c0004 | t0001 | g0047 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18950 | hp2 | a0001 | c0007 | t0001 | g0014 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA18998 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | LWK | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | LWK | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19079 | hp2 | a0001 | c0013 | t0001 | g0001 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19091 | hp1 | a0002 | c0004 | t0001 | g0048 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0071 | AFR | YRI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0119 | AFR | YRI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0026 | AFR | ASW | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | TSI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA20905 | hp1 | a0001 | c0002 | t0005 | g0001 | SAS | GIH | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | GIH | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02109 | hp2 | a0004 | c0010 | t0001 | g0020 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | USA | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0019 | AFR | LWK | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0152 | REF | REF | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0093 | REF | REF | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41888066
|
C | T | 1 | a0001 | 1 | NA20905.hp1 | splice_region_variant | LOW | c.-17C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 2/29 | chr19 | 41888066 | ||||||
chr19:41892690
|
G | T | 1 | a0003 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.455G>T | p.Arg152Leu | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 7/29 | 580/3229 | 455/2739 | 152/912 | chr19 | 41892690 | ||
chr19:41894463
|
C | T | 1 | a0008 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.757C>T | p.Arg253Trp | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 10/29 | 882/3229 | 757/2739 | 253/912 | chr19 | 41894463 | ||
chr19:41898444
|
C | T | 1 | a0002 | 4 | HG02040.hp1 NA18940.hp2 NA18998.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1124C>T | p.Pro375Leu | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/29 | 1249/3229 | 1124/2739 | 375/912 | chr19 | 41898444 | ||
chr19:41898460
|
G | T | 1 | a0004 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1140G>T | p.Glu380Asp | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/29 | 1265/3229 | 1140/2739 | 380/912 | chr19 | 41898460 | ||
chr19:41898477
|
C | T | 1 | a0005 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1157C>T | p.Ser386Leu | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/29 | 1282/3229 | 1157/2739 | 386/912 | chr19 | 41898477 | ||
chr19:41903765
|
CTATGCTG others(8): Show |
C | 1 | a0006 | 1 | HG00738.hp2 | disruptive_inframe_deletion | MODERATE | c.1899_1913delTATGCT others(9): Show |
p.Met634_Phe638del | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 20/29 | 2024/3229 | 1899/2739 | 633/912 | chr19 | 41903765 | ||
chr19:41903767
|
A | G | 1 | a0007 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.1900A>G | p.Met634Val | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 20/29 | 2025/3229 | 1900/2739 | 634/912 | chr19 | 41903767 | ||
chr19:41905015
|
A | C | 1 | a0006 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.2228A>C | p.Gln743Pro | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 23/29 | 2353/3229 | 2228/2739 | 743/912 | chr19 | 41905015 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41888239
|
C | T | 3 | a0001c0002a0001c0013a0002c0004 | 79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
synonymous_variant | LOW | c.72C>T | p.Ile24Ile | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/29 | 197/3229 | 72/2739 | 24/912 | chr19 | 41888239 | ||
chr19:41902293
|
G | A | 1 | a0004c0010 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.1434G>A | p.Leu478Leu | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 16/29 | 1559/3229 | 1434/2739 | 478/912 | chr19 | 41902293 | ||
chr19:41904274
|
G | A | 2 | a0001c0003a0004c0010 | 8 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(5): Show |
synonymous_variant | LOW | c.2052G>A | p.Arg684Arg | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 22/29 | 2177/3229 | 2052/2739 | 684/912 | chr19 | 41904274 | ||
chr19:41904956
|
A | G | 1 | a0001c0007 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.2169A>G | p.Lys723Lys | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 23/29 | 2294/3229 | 2169/2739 | 723/912 | chr19 | 41904956 | ||
chr19:41905208
|
C | A | 1 | a0001c0013 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.2283C>A | p.Ser761Ser | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/29 | 2408/3229 | 2283/2739 | 761/912 | chr19 | 41905208 | ||
chr19:41905814
|
G | A | 1 | a0001c0006 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.2391G>A | p.Thr797Thr | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 25/29 | 2516/3229 | 2391/2739 | 797/912 | chr19 | 41905814 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41883263
|
C | A | 1 | a0001c0002t0002 | 1 | NA18965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/29 | 4820 | chr19 | 41883263 | |||||
chr19:41907226
|
G | A | 1 | a0001c0002t0002 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*139G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 29/29 | 440 | chr19 | 41907226 | |||||
chr19:41907310
|
A | T | 1 | a0001c0002t0004 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*223A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 29/29 | 524 | chr19 | 41907310 | |||||
chr19:41907439
|
A | C | 1 | a0001c0001t0003 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*352A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 29/29 | 653 | chr19 | 41907439 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41883427
|
T | C | 2 | a0001c0003t0001g0019a0004c0010t0001g0020 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-20+138T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41883427 | ||||||
chr19:41883736
|
A | G | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(59): Show | 79 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-20+447A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41883736 | ||||||
chr19:41884115
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-20+826G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41884115 | ||||||
chr19:41884158
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-20+869C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41884158 | ||||||
chr19:41884574
|
C | A | 2 | a0001c0003t0001g0022a0001c0003t0001g0023 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-20+1285C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41884574 | ||||||
chr19:41885063
|
T | C | 6 | a0001c0003t0001g0022a0001c0003t0001g0023a0001c0003t0001g0024others(3): Show | 6 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+1774T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41885063 | ||||||
chr19:41885094
|
C | T | 6 | a0001c0003t0001g0022a0001c0003t0001g0023a0001c0003t0001g0024others(3): Show | 6 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+1805C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41885094 | ||||||
chr19:41885213
|
A | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(56): Show | 76 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.-20+1924A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41885213 | ||||||
chr19:41885347
|
C | G | 8 | a0001c0003t0001g0019a0001c0003t0001g0022a0001c0003t0001g0023others(5): Show | 8 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20+2058C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41885347 | ||||||
chr19:41885454
|
T | TTTTA | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(59): Show | 79 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-20+2185_-20+2188d others(6): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 41885454 | |||||
chr19:41885524
|
C | T | 6 | a0001c0003t0001g0022a0001c0003t0001g0023a0001c0003t0001g0024others(3): Show | 6 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+2235C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41885524 | ||||||
chr19:41885912
|
C | G | 3 | a0001c0002t0001g0017a0001c0002t0001g0119a0001c0002t0001g0120 | 4 | HG02572.hp1 HG02622.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-2152C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41885912 | ||||||
chr19:41886134
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-19-1930T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886134 | ||||||
chr19:41886170
|
T | C | 6 | a0001c0002t0001g0017a0001c0002t0001g0028a0001c0002t0001g0029others(3): Show | 7 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-1894T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886170 | ||||||
chr19:41886176
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-19-1888G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886176 | ||||||
chr19:41886253
|
T | C | 12 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(9): Show | 12 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-1811T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886253 | ||||||
chr19:41886396
|
C | T | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-19-1668C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886396 | ||||||
chr19:41886405
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-19-1659G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886405 | ||||||
chr19:41886864
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-19-1200G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886864 | ||||||
chr19:41886957
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-1107G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886957 | ||||||
chr19:41887008
|
G | A | 11 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(8): Show | 11 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-1056G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887008 | ||||||
chr19:41887180
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0116a0001c0001t0001g0117others(1): Show | 6 | HG01884.hp2 HG02145.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-884C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887180 | ||||||
chr19:41887335
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-729C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887335 | ||||||
chr19:41887339
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-19-725C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887339 | ||||||
chr19:41887354
|
G | A | 66 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(63): Show | 79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-19-710G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887354 | ||||||
chr19:41887394
|
C | CTGAGAGG others(38): Show |
1 | a0001c0001t0003g0131 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-19-666_-19-665ins others(45): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 41887394 | |||||
chr19:41887536
|
G | A | 2 | a0001c0002t0001g0033a0001c0002t0001g0034 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-528G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887536 | ||||||
chr19:41887542
|
T | G | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-522T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887542 | ||||||
chr19:41887614
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-19-450G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887614 | ||||||
chr19:41887643
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-19-421C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887643 | ||||||
chr19:41887686
|
T | G | 11 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(8): Show | 11 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-378T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887686 | ||||||
chr19:41887753
|
A | T | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-311A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887753 | ||||||
chr19:41887754
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-310G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887754 | ||||||
chr19:41887755
|
G | T | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-309G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887755 | ||||||
chr19:41887756
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-308C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887756 | ||||||
chr19:41887758
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-306C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887758 | ||||||
chr19:41887759
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-305C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887759 | ||||||
chr19:41887760
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-304C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887760 | ||||||
chr19:41887761
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-303A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887761 | ||||||
chr19:41887762
|
G | T | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-302G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887762 | ||||||
chr19:41887763
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-301C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887763 | ||||||
chr19:41887764
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-300C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887764 | ||||||
chr19:41887765
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-299C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887765 | ||||||
chr19:41887766
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-298C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887766 | ||||||
chr19:41887767
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-297C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887767 | ||||||
chr19:41888059
|
T | C | 72 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(69): Show | 85 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(82): Show |
splice_region_variant&intron_variant | LOW | c.-19-5T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41888059 | ||||||
chr19:41888133
|
C | G | 10 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.24+27C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 2/28 | chr19 | 41888133 | ||||||
chr19:41888299
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.111+21A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888299 | ||||||
chr19:41888370
|
T | C | 74 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(71): Show | 87 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.111+92T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888370 | ||||||
chr19:41888420
|
C | T | 1 | a0001c0002t0001g0078 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.111+142C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888420 | ||||||
chr19:41888427
|
G | A | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.111+149G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888427 | ||||||
chr19:41888459
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.111+181C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888459 | ||||||
chr19:41888483
|
C | T | 4 | a0001c0003t0001g0024a0001c0003t0001g0025a0001c0003t0001g0026others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+205C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888483 | ||||||
chr19:41888510
|
C | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+232C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888510 | ||||||
chr19:41888651
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.112-101A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888651 | ||||||
chr19:41888748
|
C | G | 11 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(8): Show | 11 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.112-4C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888748 | ||||||
chr19:41888881
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.225+16G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41888881 | ||||||
chr19:41889043
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.225+178C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889043 | ||||||
chr19:41889179
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.225+314A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889179 | ||||||
chr19:41889182
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.225+317G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889182 | ||||||
chr19:41889215
|
A | G | 77 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(74): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.225+350A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889215 | ||||||
chr19:41889269
|
G | A | 1 | a0001c0002t0001g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.225+404G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889269 | ||||||
chr19:41889332
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.225+467C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889332 | ||||||
chr19:41889633
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.225+768T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889633 | ||||||
chr19:41889664
|
A | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.225+799A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889664 | ||||||
chr19:41889675
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.225+810T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889675 | ||||||
chr19:41889747
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.225+882C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889747 | ||||||
chr19:41889975
|
G | A | 7 | a0001c0001t0001g0122a0001c0003t0001g0022a0001c0003t0001g0023others(4): Show | 7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+1110G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889975 | ||||||
chr19:41889980
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.225+1115C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889980 | ||||||
chr19:41890015
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.225+1150G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890015 | ||||||
chr19:41890030
|
T | G | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.225+1165T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890030 | ||||||
chr19:41890149
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.225+1284G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890149 | ||||||
chr19:41890187
|
T | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0085a0001c0001t0001g0086others(2): Show | 5 | NA18950.hp2 NA18980.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+1322T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890187 | ||||||
chr19:41890239
|
C | T | 10 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(7): Show | 10 | HG02109.hp1 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.225+1374C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890239 | ||||||
chr19:41890411
|
T | A | 66 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(63): Show | 79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.225+1546T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890411 | ||||||
chr19:41890578
|
C | T | 1 | a0001c0003t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.226-1447C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890578 | ||||||
chr19:41890760
|
G | GA | 35 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0084others(32): Show | 37 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.226-1249dupA | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 41890760 | |||||
chr19:41890794
|
T | C | 1 | a0001c0003t0001g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.226-1231T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890794 | ||||||
chr19:41890821
|
G | GAGGCTGA others(3): Show |
1 | a0001c0002t0001g0078 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.226-1200_226-1191d others(12): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 41890821 | |||||
chr19:41890943
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.226-1082A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890943 | ||||||
chr19:41890944
|
G | T | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.226-1081G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890944 | ||||||
chr19:41890945
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.226-1080T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890945 | ||||||
chr19:41891070
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.226-955T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891070 | ||||||
chr19:41891223
|
C | T | 2 | a0001c0003t0001g0022a0001c0003t0001g0023 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.226-802C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891223 | ||||||
chr19:41891244
|
C | G | 77 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(74): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.226-781C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891244 | ||||||
chr19:41891336
|
G | A | 67 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(64): Show | 80 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.226-689G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891336 | ||||||
chr19:41891349
|
C | T | 1 | a0001c0002t0001g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.226-676C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891349 | ||||||
chr19:41891446
|
A | G | 77 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(74): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.226-579A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891446 | ||||||
chr19:41891481
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.226-544G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891481 | ||||||
chr19:41891597
|
A | AACTATAC others(6): Show |
1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.226-427_226-426ins others(13): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 41891597 | |||||
chr19:41891599
|
G | T | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.226-426G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891599 | ||||||
chr19:41891600
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.226-425C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891600 | ||||||
chr19:41891623
|
G | A | 68 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(65): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.226-402G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891623 | ||||||
chr19:41891686
|
G | A | 1 | a0001c0003t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.226-339G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891686 | ||||||
chr19:41891689
|
G | A | 1 | a0001c0003t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.226-336G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891689 | ||||||
chr19:41891699
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.226-326C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891699 | ||||||
chr19:41891726
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.226-299T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891726 | ||||||
chr19:41891793
|
C | T | 7 | a0001c0001t0001g0122a0001c0003t0001g0022a0001c0003t0001g0023others(4): Show | 7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.226-232C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891793 | ||||||
chr19:41891899
|
G | A | 66 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(63): Show | 79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.226-126G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891899 | ||||||
chr19:41891929
|
A | G | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.226-96A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891929 | ||||||
chr19:41891997
|
G | A | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.226-28G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891997 | ||||||
chr19:41892195
|
G | A | 77 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(74): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.324+72G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 5/28 | chr19 | 41892195 | ||||||
chr19:41892222
|
C | T | 1 | a0001c0002t0001g0076 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.324+99C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 5/28 | chr19 | 41892222 | ||||||
chr19:41892438
|
G | C | 7 | a0001c0001t0001g0122a0001c0003t0001g0022a0001c0003t0001g0023others(4): Show | 7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.367+65G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 6/28 | chr19 | 41892438 | ||||||
chr19:41892513
|
A | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0090others(5): Show | 10 | HG00642.hp1 HG01169.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.368-90A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 6/28 | chr19 | 41892513 | ||||||
chr19:41892876
|
G | A | 1 | a0001c0001t0001g0018 | 2 | NA18970.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.614+27G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 7/28 | chr19 | 41892876 | ||||||
chr19:41893106
|
A | C | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.615-168A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 7/28 | chr19 | 41893106 | ||||||
chr19:41893328
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.644+25G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893328 | ||||||
chr19:41893332
|
TCCTGGGT others(70): Show |
T | 1 | a0001c0002t0002g0039 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.644+37_644+113delT others(76): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893332 | |||||
chr19:41893340
|
T | C | 23 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0036others(20): Show | 32 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.644+37T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893340 | ||||||
chr19:41893357
|
TGAGGGCC others(71): Show |
T | 23 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0036others(20): Show | 32 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.644+56_644+133delA others(77): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893357 | |||||
chr19:41893366
|
G | GGACGCCT others(32): Show |
1 | a0001c0001t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.644+66_644+67insGC others(37): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893366 | |||||
chr19:41893370
|
T | G | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.644+67T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893370 | ||||||
chr19:41893391
|
A | G | 2 | a0001c0001t0001g0127a0001c0002t0001g0075 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.644+88A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893391 | ||||||
chr19:41893410
|
C | CCTGGGTC others(31): Show |
41 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(38): Show | 45 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.644+136_644+137ins others(38): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893410 | |||||
chr19:41893410
|
C | CCTGGGTC others(70): Show |
1 | a0001c0003t0001g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.644+136_644+137ins others(77): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893410 | |||||
chr19:41893434
|
TG | T | 10 | a0001c0001t0001g0122a0001c0002t0001g0029a0001c0002t0001g0073others(7): Show | 10 | HG02109.hp1 HG02486.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.644+137delG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893434 | |||||
chr19:41893444
|
A | G | 78 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(75): Show | 91 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.644+141A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893444 | ||||||
chr19:41893445
|
G | A | 34 | a0001c0001t0001g0122a0001c0002t0001g0001a0001c0002t0001g0010others(31): Show | 43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.644+142G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893445 | ||||||
chr19:41893449
|
C | T | 34 | a0001c0001t0001g0122a0001c0002t0001g0001a0001c0002t0001g0010others(31): Show | 43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.644+146C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893449 | ||||||
chr19:41893464
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.644+161G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893464 | ||||||
chr19:41893474
|
G | GGGGTCCT others(68): Show |
1 | a0001c0001t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.644+174_644+175ins others(75): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893474 | |||||
chr19:41893484
|
G | A | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02109.hp2 HG02818.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+181G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893484 | ||||||
chr19:41893487
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.644+184G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893487 | ||||||
chr19:41893488
|
C | T | 10 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.644+185C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893488 | ||||||
chr19:41893506
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.644+203G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893506 | ||||||
chr19:41893527
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.644+224C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893527 | ||||||
chr19:41893551
|
T | TG | 37 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(34): Show | 46 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.644+252dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893551 | |||||
chr19:41893556
|
T | G | 77 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(74): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.644+253T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893556 | ||||||
chr19:41893561
|
G | A | 38 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(35): Show | 42 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.644+258G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893561 | ||||||
chr19:41893565
|
C | T | 39 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(36): Show | 43 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.644+262C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893565 | ||||||
chr19:41893583
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.644+280G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893583 | ||||||
chr19:41893589
|
T | TG | 48 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(45): Show | 52 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.644+291dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893589 | |||||
chr19:41893589
|
T | TGGGGGGC others(227): Show |
1 | a0001c0003t0001g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.644+291_644+292ins others(234): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893589 | |||||
chr19:41893590
|
GGGGGCCT others(30): Show |
G | 1 | a0001c0001t0001g0147 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.644+292_644+328del others(37): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893590 | |||||
chr19:41893599
|
G | A | 3 | a0001c0002t0001g0029a0001c0002t0001g0073a0001c0002t0001g0083 | 3 | HG02486.hp2 HG02723.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.644+296G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893599 | ||||||
chr19:41893603
|
C | T | 3 | a0001c0002t0001g0029a0001c0002t0001g0073a0001c0002t0001g0083 | 3 | HG02486.hp2 HG02723.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.644+300C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893603 | ||||||
chr19:41893627
|
T | TG | 45 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(42): Show | 49 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.644+329dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893627 | |||||
chr19:41893640
|
T | G | 74 | a0001c0001t0001g0122a0001c0001t0001g0147a0001c0002t0001g0001others(71): Show | 87 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.644+337T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893640 | ||||||
chr19:41893641
|
C | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0147a0001c0003t0001g0022others(4): Show | 7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.644+338C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893641 | ||||||
chr19:41893644
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.644+341G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893644 | ||||||
chr19:41893645
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.644+342G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893645 | ||||||
chr19:41893661
|
A | G | 49 | a0001c0001t0001g0122a0001c0002t0001g0011a0001c0002t0001g0012others(46): Show | 53 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.644+358A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893661 | ||||||
chr19:41893661
|
AGGCTGGG others(70): Show |
A | 1 | a0001c0002t0001g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.644+368_644+444del others(77): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893661 | |||||
chr19:41893665
|
T | TG | 70 | a0001c0001t0001g0122a0001c0002t0001g0001a0001c0002t0001g0010others(67): Show | 83 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.644+367dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893665 | |||||
chr19:41893677
|
C | T | 24 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0036others(21): Show | 33 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.644+374C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893677 | ||||||
chr19:41893678
|
T | G | 76 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(73): Show | 89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.644+375T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893678 | ||||||
chr19:41893679
|
C | T | 10 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(7): Show | 10 | HG02109.hp1 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.644+376C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893679 | ||||||
chr19:41893697
|
A | AGGGGCTG others(185): Show |
1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.644+405_644+406ins others(192): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893697 | |||||
chr19:41893697
|
A | G | 75 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(72): Show | 88 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.644+394A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893697 | ||||||
chr19:41893703
|
TG | T | 37 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(34): Show | 41 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.644+406delG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893703 | |||||
chr19:41893717
|
GTCTGGGT others(109): Show |
G | 23 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0036others(20): Show | 32 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.644+415_645-374del | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893717 | ||||||
chr19:41893718
|
T | C | 49 | a0001c0001t0001g0122a0001c0002t0001g0011a0001c0002t0001g0012others(46): Show | 53 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.644+415T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893718 | ||||||
chr19:41893721
|
GGGTCTGA others(108): Show |
G | 1 | a0001c0002t0001g0043 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.644+421_645-369del | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893721 | |||||
chr19:41893742
|
TG | T | 41 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(38): Show | 45 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.644+445delG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893742 | |||||
chr19:41893755
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.644+452C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893755 | ||||||
chr19:41893756
|
G | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.645-451G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893756 | ||||||
chr19:41893760
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.645-447G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893760 | ||||||
chr19:41893777
|
G | A | 38 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(35): Show | 42 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.645-430G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893777 | ||||||
chr19:41893781
|
T | TGGGGGCC others(32): Show |
1 | a0001c0002t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.645-421_645-420ins others(39): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893781 | |||||
chr19:41893782
|
G | GGGGGCCT others(30): Show |
1 | a0001c0002t0001g0083 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.645-421_645-420ins others(37): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893782 | |||||
chr19:41893788
|
T | C | 53 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(50): Show | 57 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.645-419T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893788 | ||||||
chr19:41893794
|
C | T | 40 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(37): Show | 44 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.645-413C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893794 | ||||||
chr19:41893795
|
T | G | 50 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0002t0001g0011others(47): Show | 54 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.645-412T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893795 | ||||||
chr19:41893799
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.645-408G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893799 | ||||||
chr19:41893814
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.645-393G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893814 | ||||||
chr19:41893814
|
G | GGGGGCTG others(31): Show |
1 | a0001c0001t0001g0148 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.645-355_645-318dup others(38): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893814 | |||||
chr19:41893814
|
GGGGGCTG others(31): Show |
G | 1 | a0001c0002t0001g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.645-355_645-318del others(38): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893814 | |||||
chr19:41893816
|
G | A | 1 | a0001c0002t0001g0073 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.645-391G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893816 | ||||||
chr19:41893817
|
G | A | 1 | a0001c0003t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.645-390G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893817 | ||||||
chr19:41893820
|
T | TG | 49 | a0001c0001t0001g0122a0001c0002t0001g0011a0001c0002t0001g0012others(46): Show | 53 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.645-382dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893820 | |||||
chr19:41893832
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.645-375C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893832 | ||||||
chr19:41893833
|
T | G | 43 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(40): Show | 47 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.645-374T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893833 | ||||||
chr19:41893834
|
C | CCTAGGTC others(186): Show |
6 | a0001c0001t0001g0122a0001c0003t0001g0022a0001c0003t0001g0023others(3): Show | 6 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.645-371_645-370ins others(193): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893834 | |||||
chr19:41893852
|
A | G | 12 | a0001c0001t0001g0107a0001c0001t0001g0122a0001c0001t0001g0123others(9): Show | 12 | HG01099.hp2 HG02109.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.645-355A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893852 | ||||||
chr19:41893854
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.645-353G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893854 | ||||||
chr19:41893858
|
T | TG | 7 | a0001c0001t0001g0122a0001c0002t0001g0073a0001c0003t0001g0022others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.645-344dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893858 | |||||
chr19:41893858
|
T | TGGGGGGC others(226): Show |
1 | a0001c0003t0001g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.645-344_645-343ins others(233): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893858 | |||||
chr19:41893864
|
C | CCTGGACG others(110): Show |
3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.645-337_645-336ins others(117): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893864 | |||||
chr19:41893864
|
C | G | 1 | a0001c0002t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.645-343C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893864 | ||||||
chr19:41893871
|
T | G | 8 | a0001c0001t0001g0122a0001c0002t0001g0073a0001c0003t0001g0022others(5): Show | 8 | HG02109.hp1 HG02723.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.645-336T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893871 | ||||||
chr19:41893890
|
G | A | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 6 | HG02109.hp2 HG02155.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-317G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893890 | ||||||
chr19:41893892
|
G | C | 32 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(29): Show | 42 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.645-315G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893892 | ||||||
chr19:41893896
|
T | TG | 7 | a0001c0001t0001g0122a0001c0003t0001g0022a0001c0003t0001g0023others(4): Show | 7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.645-306dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893896 | |||||
chr19:41893902
|
C | T | 7 | a0001c0001t0001g0122a0001c0003t0001g0022a0001c0003t0001g0023others(4): Show | 7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.645-305C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893902 | ||||||
chr19:41893928
|
G | A | 7 | a0001c0001t0001g0122a0001c0003t0001g0022a0001c0003t0001g0023others(4): Show | 7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.645-279G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893928 | ||||||
chr19:41894006
|
A | G | 1 | a0001c0002t0001g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.645-201A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894006 | ||||||
chr19:41894062
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.645-145G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894062 | ||||||
chr19:41894121
|
A | AGAGAGAG others(101): Show |
1 | a0001c0001t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.645-83_645-82insAG others(106): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894121 | |||||
chr19:41894123
|
A | AGAGAGAG others(101): Show |
1 | a0001c0003t0001g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.645-83_645-82insAG others(106): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | |||||
chr19:41894123
|
A | AGAGAGAG others(107): Show |
4 | a0001c0003t0001g0024a0001c0003t0001g0025a0001c0003t0001g0026others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.645-83_645-82insAG others(112): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | |||||
chr19:41894123
|
A | AGAGAGAG others(102): Show |
1 | a0001c0003t0001g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.645-83_645-82insAG others(107): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | |||||
chr19:41894123
|
A | AGAGAGAG others(101): Show |
1 | a0001c0001t0001g0124 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.645-83_645-82insAG others(106): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | |||||
chr19:41894123
|
A | AGAGAGAG others(104): Show |
1 | a0001c0001t0001g0125 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.645-83_645-82insAG others(109): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | |||||
chr19:41894123
|
A | AGAGAGAG others(103): Show |
1 | a0001c0001t0001g0123 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.645-83_645-82insAG others(108): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | |||||
chr19:41894123
|
AGTGTGTG others(7): Show |
A | 2 | a0001c0002t0001g0033a0001c0002t0001g0034 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.645-72_645-59delAG others(12): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | |||||
chr19:41894131
|
T | A | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02818.hp2 HG02897.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.645-76T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894131 | ||||||
chr19:41894135
|
A | AGT | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02735.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.645-41_645-40dupGT | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | |||||
chr19:41894135
|
A | AGTGT | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(57): Show | 89 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.645-43_645-40dupGT others(2): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | |||||
chr19:41894135
|
A | AGTGTGT | 38 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0102others(35): Show | 44 | HG00438.hp2 HG00609.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.645-45_645-40dupGT others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | |||||
chr19:41894135
|
A | AGTGTGTG others(1): Show |
16 | a0001c0001t0001g0127a0001c0001t0001g0134a0001c0001t0001g0143others(13): Show | 17 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.645-47_645-40dupGT others(6): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | |||||
chr19:41894135
|
A | AGTGTGTG others(3): Show |
34 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0029others(31): Show | 43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.645-49_645-40dupGT others(8): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | |||||
chr19:41894135
|
A | AGTGTGTG others(5): Show |
7 | a0001c0002t0001g0012a0001c0002t0001g0053a0001c0002t0001g0066others(4): Show | 8 | HG00738.hp1 HG02027.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.645-51_645-40dupGT others(10): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | |||||
chr19:41894135
|
A | AGTGTGTG others(7): Show |
9 | a0001c0002t0001g0013a0001c0002t0001g0042a0001c0002t0001g0055others(6): Show | 10 | HG02109.hp2 HG02145.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.645-53_645-40dupGT others(12): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | |||||
chr19:41894135
|
A | T | 5 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(2): Show | 5 | HG02818.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.645-72A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894135 | ||||||
chr19:41894137
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.645-70T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894137 | ||||||
chr19:41894163
|
T | TGTGTGTG others(4): Show |
1 | a0001c0002t0001g0043 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.645-40_645-39insGT others(9): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894163 | |||||
chr19:41894168
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.645-39C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894168 | ||||||
chr19:41894173
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.645-34T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894173 | ||||||
chr19:41894180
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.645-27T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894180 | ||||||
chr19:41894181
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.645-26G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894181 | ||||||
chr19:41894185
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.645-22C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894185 | ||||||
chr19:41894187
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.645-20T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894187 | ||||||
chr19:41894199
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | splice_region_variant&intron_variant | LOW | c.645-8C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894199 | ||||||
chr19:41894321
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.744+15G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 9/28 | chr19 | 41894321 | ||||||
chr19:41894322
|
C | A | 1 | a0001c0001t0003g0131 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.744+16C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 9/28 | chr19 | 41894322 | ||||||
chr19:41894322
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.744+16C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 9/28 | chr19 | 41894322 | ||||||
chr19:41894377
|
T | C | 74 | a0001c0001t0001g0122a0001c0002t0001g0001a0001c0002t0001g0010others(71): Show | 87 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.744+71T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 9/28 | chr19 | 41894377 | ||||||
chr19:41894609
|
A | T | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.842-17A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 10/28 | chr19 | 41894609 | ||||||
chr19:41894610
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.842-16T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 10/28 | chr19 | 41894610 | ||||||
chr19:41894612
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.842-14C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 10/28 | chr19 | 41894612 | ||||||
chr19:41894619
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00438.hp2 | splice_region_variant&intron_variant | LOW | c.842-7G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 10/28 | chr19 | 41894619 | ||||||
chr19:41894732
|
GTCTGAGG others(29): Show |
G | 64 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(61): Show | 77 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.877+88_877+123delC others(35): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 41894732 | |||||
chr19:41894747
|
G | A | 10 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(7): Show | 10 | HG02109.hp1 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.877+86G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894747 | ||||||
chr19:41894749
|
C | A | 2 | a0001c0002t0001g0083a0004c0010t0001g0020 | 2 | HG02109.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.877+88C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894749 | ||||||
chr19:41894751
|
GGGACCTG others(28): Show |
G | 1 | a0001c0002t0001g0083 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.877+93_877+127delA others(34): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 41894751 | |||||
chr19:41894754
|
A | G | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.877+93A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894754 | ||||||
chr19:41894762
|
G | A | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.877+101G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894762 | ||||||
chr19:41894768
|
T | C | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.877+107T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894768 | ||||||
chr19:41894799
|
ACCTGGGT others(270): Show |
A | 4 | a0001c0003t0001g0024a0001c0003t0001g0025a0001c0003t0001g0026others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+170_878-242del | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 41894799 | |||||
chr19:41894856
|
TGGGCCTG others(97): Show |
T | 72 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(69): Show | 85 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.877+215_877+318del | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 41894856 | |||||
chr19:41894924
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.877+263G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894924 | ||||||
chr19:41894925
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.877+264C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894925 | ||||||
chr19:41894999
|
C | G | 1 | a0001c0002t0001g0082 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.877+338C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894999 | ||||||
chr19:41895067
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.878-282G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41895067 | ||||||
chr19:41895163
|
A | C | 1 | a0001c0001t0001g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.878-186A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41895163 | ||||||
chr19:41895556
|
G | A | 66 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(63): Show | 79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1015+70G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41895556 | ||||||
chr19:41895561
|
C | T | 65 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(62): Show | 78 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1015+75C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41895561 | ||||||
chr19:41895618
|
T | G | 1 | a0001c0002t0001g0074 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1015+132T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41895618 | ||||||
chr19:41895741
|
C | T | 2 | a0001c0006t0001g0159a0003c0012t0001g0160 | 2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.1015+255C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41895741 | ||||||
chr19:41895868
|
C | G | 65 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(62): Show | 78 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1015+382C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41895868 | ||||||
chr19:41895973
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1016-404C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41895973 | ||||||
chr19:41896034
|
A | G | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1016-343A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41896034 | ||||||
chr19:41896185
|
T | G | 4 | a0001c0001t0001g0122a0001c0003t0001g0019a0001c0003t0001g0022others(1): Show | 4 | HG02976.hp2 HG03195.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016-192T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41896185 | ||||||
chr19:41896234
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1016-143C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41896234 | ||||||
chr19:41896261
|
C | A | 1 | a0001c0002t0001g0078 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1016-116C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41896261 | ||||||
chr19:41896333
|
G | GC | 77 | a0001c0001t0001g0087a0001c0001t0001g0101a0001c0001t0001g0141others(74): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1016-42dupC | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr19 | 41896333 | |||||
chr19:41896336
|
G | A | 1 | a0001c0002t0001g0046 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1016-41G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41896336 | ||||||
chr19:41896342
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1016-35G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41896342 | ||||||
chr19:41896528
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1121+46G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896528 | ||||||
chr19:41896619
|
G | C | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1121+137G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896619 | ||||||
chr19:41896656
|
C | G | 7 | a0001c0003t0001g0019a0001c0003t0001g0022a0001c0003t0001g0023others(4): Show | 7 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+174C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896656 | ||||||
chr19:41896716
|
C | T | 3 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0172 | 3 | HG01109.hp2 HG01192.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1121+234C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896716 | ||||||
chr19:41896766
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1121+284A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896766 | ||||||
chr19:41896787
|
T | TCCCCCTC others(48): Show |
1 | a0001c0002t0001g0066 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1121+327_1121+328i others(57): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | |||||
chr19:41896787
|
T | TCCCCCTC others(105): Show |
3 | a0001c0002t0001g0012a0001c0002t0001g0054a0001c0002t0001g0077 | 4 | HG01884.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121+327_1121+328i others(114): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | |||||
chr19:41896787
|
T | TCCCCCTC others(143): Show |
1 | a0001c0002t0001g0078 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1121+327_1121+328i others(152): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | |||||
chr19:41896787
|
T | TCCCCCTC others(272): Show |
1 | a0001c0002t0001g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1121+327_1121+328i others(281): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | |||||
chr19:41896787
|
T | TCCCCCTC others(31): Show |
1 | a0001c0002t0001g0130 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+310_1121+347d others(40): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | |||||
chr19:41896787
|
T | TCCCCCTC others(143): Show |
1 | a0001c0001t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1121+420_1121+421i others(152): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | |||||
chr19:41896787
|
T | TCCCCCTC others(217): Show |
2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1121+347_1121+348i others(226): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | |||||
chr19:41896787
|
T | TCCCCTCC others(49): Show |
1 | a0001c0003t0001g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1121+309_1121+310i others(58): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | |||||
chr19:41896787
|
T | TCCCCTCC others(199): Show |
2 | a0001c0003t0001g0024a0001c0003t0001g0026 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1121+309_1121+310i others(208): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | |||||
chr19:41896791
|
C | CCTCCTCT others(162): Show |
12 | a0001c0002t0001g0013a0001c0002t0001g0017a0001c0002t0001g0028others(9): Show | 14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1121+327_1121+328i others(171): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896791 | |||||
chr19:41896791
|
C | CCTCCTCT others(445): Show |
1 | a0001c0002t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1121+327_1121+328i others(454): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896791 | |||||
chr19:41896791
|
C | CCTCCTCT others(86): Show |
1 | a0001c0001t0001g0132 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1121+332_1121+424d others(95): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896791 | |||||
chr19:41896791
|
C | CT | 7 | a0001c0002t0001g0011a0001c0002t0001g0035a0001c0002t0001g0041others(4): Show | 8 | HG01109.hp1 HG01243.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1121+309_1121+310i others(3): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896791 | ||||||
chr19:41896791
|
CCTCCTCT others(12): Show |
C | 1 | a0001c0003t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1121+328_1121+346d others(21): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896791 | |||||
chr19:41896792
|
C | CTCCTCTC others(107): Show |
1 | a0001c0001t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1121+327_1121+328i others(116): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896792 | |||||
chr19:41896792
|
CTCCTCTC others(31): Show |
C | 4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0113others(1): Show | 4 | HG00099.hp1 HG01099.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121+328_1121+365d others(40): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896792 | |||||
chr19:41896796
|
T | TCTCTCAC others(48): Show |
1 | a0001c0001t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1121+327_1121+328i others(57): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896796 | |||||
chr19:41896805
|
T | TCCCCTCT others(13): Show |
1 | a0001c0002t0001g0078 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1121+328_1121+347d others(22): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896805 | |||||
chr19:41896810
|
T | C | 2 | a0001c0001t0001g0127a0001c0002t0001g0077 | 2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1121+328T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896810 | ||||||
chr19:41896810
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1121+328T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896810 | ||||||
chr19:41896811
|
CTCCTCTC others(12): Show |
C | 2 | a0001c0001t0001g0032a0001c0002t0001g0065 | 2 | HG01261.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1121+348_1121+366d others(21): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896811 | |||||
chr19:41896814
|
C | CTCTCTCA others(203): Show |
1 | a0001c0003t0001g0027 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1121+347_1121+348i others(212): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896814 | |||||
chr19:41896814
|
C | T | 2 | a0001c0003t0001g0024a0001c0003t0001g0026 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1121+332C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896814 | ||||||
chr19:41896829
|
C | T | 2 | a0001c0002t0001g0130a0004c0010t0001g0020 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1121+347C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896829 | ||||||
chr19:41896830
|
A | ATCCTCTC others(31): Show |
1 | a0001c0001t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1121+366_1121+367i others(40): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896830 | |||||
chr19:41896830
|
A | ATCCTCTC others(12): Show |
2 | a0001c0001t0001g0171a0001c0001t0001g0176 | 2 | NA19001.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1121+362_1121+380d others(21): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896830 | |||||
chr19:41896830
|
A | ATCCTCTC others(86): Show |
1 | a0001c0001t0001g0125 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1121+381_1121+473d others(95): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896830 | |||||
chr19:41896830
|
A | ATCCTCTC others(86): Show |
6 | a0001c0002t0001g0040a0001c0002t0001g0063a0001c0002t0001g0064others(3): Show | 6 | HG02055.hp2 HG02723.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121+380_1121+381i others(95): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896830 | |||||
chr19:41896830
|
A | ATCCTCTC others(124): Show |
1 | a0001c0001t0001g0123 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1121+365_1121+366i others(133): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896830 | |||||
chr19:41896830
|
A | C | 2 | a0001c0002t0001g0130a0004c0010t0001g0020 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1121+348A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896830 | ||||||
chr19:41896832
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1121+350C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896832 | ||||||
chr19:41896844
|
C | CCCCCCTC others(85): Show |
1 | a0001c0001t0001g0124 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1121+368_1121+459d others(94): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896844 | |||||
chr19:41896844
|
C | T | 1 | a0001c0002t0001g0012 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1121+362C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896844 | ||||||
chr19:41896849
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1121+367C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896849 | ||||||
chr19:41896849
|
C | CTCCTCTC others(102): Show |
1 | a0001c0003t0001g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1121+401_1121+402i others(111): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896849 | |||||
chr19:41896850
|
T | C | 1 | a0001c0002t0001g0036 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1121+368T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896850 | ||||||
chr19:41896851
|
C | T | 1 | a0001c0002t0001g0036 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1121+369C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896851 | ||||||
chr19:41896862
|
TAC | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0117a0001c0001t0001g0118 | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121+381_1121+382d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896862 | ||||||
chr19:41896863
|
A | C | 3 | a0001c0002t0001g0033a0001c0002t0001g0034a0004c0010t0001g0020 | 3 | HG02109.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1121+381A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896863 | ||||||
chr19:41896869
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1121+387T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896869 | ||||||
chr19:41896870
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1121+388C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896870 | ||||||
chr19:41896870
|
CCTCTCAC others(46): Show |
C | 3 | a0001c0001t0001g0008a0001c0001t0001g0117a0001c0001t0001g0118 | 5 | HG02145.hp1 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121+389_1121+441d others(55): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896870 | ||||||
chr19:41896884
|
G | C | 5 | a0001c0003t0001g0019a0001c0003t0001g0024a0001c0003t0001g0025others(2): Show | 5 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+402G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896884 | ||||||
chr19:41896886
|
T | C | 1 | a0001c0003t0001g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1121+404T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896886 | ||||||
chr19:41896889
|
T | C | 1 | a0001c0003t0001g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1121+407T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896889 | ||||||
chr19:41896891
|
T | C | 1 | a0001c0003t0001g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1121+409T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896891 | ||||||
chr19:41896936
|
T | C | 3 | a0001c0002t0001g0036a0002c0004t0001g0047a0002c0004t0001g0048 | 3 | NA18940.hp2 NA18961.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1121+454T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896936 | ||||||
chr19:41896937
|
C | T | 1 | a0001c0002t0001g0036 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1121+455C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896937 | ||||||
chr19:41896943
|
T | G | 2 | a0002c0004t0001g0047a0002c0004t0001g0048 | 2 | NA18940.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1121+461T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896943 | ||||||
chr19:41896989
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1121+507C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896989 | ||||||
chr19:41897106
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1121+624C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897106 | ||||||
chr19:41897123
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0170 | 2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1121+641C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897123 | ||||||
chr19:41897132
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1121+650G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897132 | ||||||
chr19:41897348
|
G | C | 1 | a0001c0001t0001g0150 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1121+866G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897348 | ||||||
chr19:41897617
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1122-825C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897617 | ||||||
chr19:41897626
|
A | T | 1 | a0001c0002t0001g0036 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1122-816A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897626 | ||||||
chr19:41897755
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1122-687G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897755 | ||||||
chr19:41898021
|
G | T | 1 | a0001c0001t0001g0018 | 2 | NA18970.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1122-421G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41898021 | ||||||
chr19:41898117
|
T | TGTCAACC others(275): Show |
1 | a0001c0001t0001g0133 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1122-323_1122-42du others(283): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41898117 | |||||
chr19:41898134
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1122-308C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41898134 | ||||||
chr19:41899057
|
A | C | 1 | a0001c0001t0001g0156 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1267+470A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899057 | ||||||
chr19:41899058
|
T | A | 1 | a0001c0001t0001g0156 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1267+471T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899058 | ||||||
chr19:41899367
|
A | G | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1267+780A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899367 | ||||||
chr19:41899458
|
T | G | 80 | a0001c0001t0001g0086a0001c0001t0001g0122a0001c0001t0001g0123others(77): Show | 93 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1267+871T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899458 | ||||||
chr19:41899505
|
CT | C | 74 | a0001c0001t0001g0088a0001c0001t0001g0097a0001c0001t0001g0109others(71): Show | 86 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1267+939delT | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41899505 | |||||
chr19:41899505
|
CTT | C | 6 | a0001c0002t0001g0010a0001c0002t0001g0066a0001c0002t0001g0071others(3): Show | 7 | HG00738.hp1 HG02897.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.1267+938_1267+939d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41899505 | |||||
chr19:41899526
|
T | A | 1 | a0001c0001t0001g0102 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1267+939T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899526 | ||||||
chr19:41899533
|
G | C | 1 | a0001c0002t0001g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1267+946G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899533 | ||||||
chr19:41899573
|
A | G | 77 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(74): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1267+986A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899573 | ||||||
chr19:41899920
|
T | TA | 67 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0098others(64): Show | 80 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1267+1348dupA | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41899920 | |||||
chr19:41899920
|
TA | T | 7 | a0001c0001t0001g0116a0001c0002t0001g0040a0001c0002t0001g0063others(4): Show | 7 | HG01884.hp2 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1267+1348delA | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41899920 | |||||
chr19:41900132
|
G | A | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1267+1545G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41900132 | ||||||
chr19:41900191
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 218 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.1267+1604A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41900191 | ||||||
chr19:41900786
|
G | GT | 27 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0014others(24): Show | 32 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1268-1077dupT | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41900786 | |||||
chr19:41900786
|
GT | G | 8 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0099others(5): Show | 8 | HG01257.hp2 HG01515.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1268-1077delT | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41900786 | |||||
chr19:41900786
|
GTT | G | 13 | a0001c0002t0001g0033a0001c0002t0001g0036a0001c0002t0001g0045others(10): Show | 13 | HG00438.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1268-1078_1268-107 others(6): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41900786 | |||||
chr19:41900786
|
GTTT | G | 51 | a0001c0001t0001g0122a0001c0002t0001g0001a0001c0002t0001g0010others(48): Show | 64 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1268-1079_1268-107 others(7): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41900786 | |||||
chr19:41900786
|
GTTTT | G | 9 | a0001c0002t0001g0038a0001c0002t0001g0076a0001c0002t0001g0130others(6): Show | 9 | HG02027.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1268-1080_1268-107 others(8): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41900786 | |||||
chr19:41900852
|
G | A | 1 | a0002c0004t0001g0047 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1268-1035G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41900852 | ||||||
chr19:41900853
|
T | C | 76 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(73): Show | 89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1268-1034T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41900853 | ||||||
chr19:41900860
|
C | G | 73 | a0001c0001t0001g0122a0001c0002t0001g0001a0001c0002t0001g0010others(70): Show | 86 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1268-1027C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41900860 | ||||||
chr19:41900939
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1268-948C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41900939 | ||||||
chr19:41901051
|
A | C | 1 | a0001c0001t0001g0164 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1268-836A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41901051 | ||||||
chr19:41901086
|
G | T | 76 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(73): Show | 89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1268-801G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41901086 | ||||||
chr19:41901224
|
A | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1268-663A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41901224 | ||||||
chr19:41901245
|
G | A | 1 | a0008c0011t0001g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1268-642G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41901245 | ||||||
chr19:41901298
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1268-589C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41901298 | ||||||
chr19:41901573
|
C | T | 1 | a0001c0003t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1268-314C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41901573 | ||||||
chr19:41902376
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1497+20C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 16/28 | chr19 | 41902376 | ||||||
chr19:41902415
|
C | T | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1497+59C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 16/28 | chr19 | 41902415 | ||||||
chr19:41902419
|
T | A | 2 | a0001c0002t0001g0061a0001c0002t0001g0069 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1497+63T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 16/28 | chr19 | 41902419 | ||||||
chr19:41902444
|
C | T | 1 | a0001c0003t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1497+88C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 16/28 | chr19 | 41902444 | ||||||
chr19:41902493
|
T | C | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1498-40T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 16/28 | chr19 | 41902493 | ||||||
chr19:41903093
|
G | GT | 10 | a0001c0002t0001g0011a0001c0002t0001g0035a0001c0002t0001g0041others(7): Show | 11 | HG01109.hp1 HG01243.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1739-203dupT | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 41903093 | |||||
chr19:41903093
|
GTT | G | 8 | a0001c0001t0001g0122a0001c0003t0001g0022a0001c0003t0001g0023others(5): Show | 8 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1739-204_1739-203d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 41903093 | |||||
chr19:41903111
|
G | A | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1739-196G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 18/28 | chr19 | 41903111 | ||||||
chr19:41903119
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1739-188G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 18/28 | chr19 | 41903119 | ||||||
chr19:41903217
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1739-90C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 18/28 | chr19 | 41903217 | ||||||
chr19:41903527
|
C | CTG | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 233 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1839+124_1839+125d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr19 | 41903527 | |||||
chr19:41903606
|
G | A | 1 | a0001c0002t0001g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1840-101G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 19/28 | chr19 | 41903606 | ||||||
chr19:41903817
|
C | G | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1917+33C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 20/28 | chr19 | 41903817 | ||||||
chr19:41904000
|
C | A | 1 | a0006c0005t0001g0089 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1918-35C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 20/28 | chr19 | 41904000 | ||||||
chr19:41904033
|
A | T | 1 | a0006c0005t0001g0089 | 1 | HG00738.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1918-2A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 20/28 | chr19 | 41904033 | ||||||
chr19:41904212
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02735.hp1 | splice_region_variant&intron_variant | LOW | c.1994-4G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 21/28 | chr19 | 41904212 | ||||||
chr19:41904444
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2161+61T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 22/28 | chr19 | 41904444 | ||||||
chr19:41904639
|
G | C | 1 | a0001c0001t0001g0085 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2161+256G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 22/28 | chr19 | 41904639 | ||||||
chr19:41904724
|
C | T | 74 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(71): Show | 87 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.2162-225C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 22/28 | chr19 | 41904724 | ||||||
chr19:41904797
|
G | T | 1 | a0001c0002t0001g0058 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2162-152G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 22/28 | chr19 | 41904797 | ||||||
chr19:41904887
|
T | C | 77 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(74): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.2162-62T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 22/28 | chr19 | 41904887 | ||||||
chr19:41905075
|
G | A | 6 | a0001c0001t0001g0122a0001c0003t0001g0022a0001c0003t0001g0023others(3): Show | 6 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2249+39G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 23/28 | chr19 | 41905075 | ||||||
chr19:41905379
|
G | A | 8 | a0001c0001t0001g0122a0001c0003t0001g0022a0001c0003t0001g0023others(5): Show | 8 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2336+118G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905379 | ||||||
chr19:41905381
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0090a0001c0001t0001g0109others(1): Show | 6 | HG01943.hp1 HG01978.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2336+120G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905381 | ||||||
chr19:41905391
|
ATG | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0176 | 2 | NA19001.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2336+136_2336+137d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | 41905391 | |||||
chr19:41905426
|
CATAT | C | 2 | a0001c0003t0001g0022a0001c0003t0001g0023 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2336+169_2336+172d others(6): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | 41905426 | |||||
chr19:41905440
|
GTA | G | 4 | a0001c0003t0001g0024a0001c0003t0001g0025a0001c0003t0001g0026others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2336+181_2336+182d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | 41905440 | |||||
chr19:41905442
|
A | G | 7 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.2336+181A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905442 | ||||||
chr19:41905457
|
C | T | 6 | a0001c0001t0001g0095a0001c0001t0001g0103a0001c0001t0001g0123others(3): Show | 6 | HG01257.hp1 HG01258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2336+196C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905457 | ||||||
chr19:41905460
|
G | A | 1 | a0001c0002t0001g0049 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2336+199G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905460 | ||||||
chr19:41905473
|
C | T | 1 | a0001c0003t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2336+212C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905473 | ||||||
chr19:41905480
|
GGT | G | 9 | a0001c0001t0001g0098a0001c0001t0001g0122a0001c0003t0001g0022others(6): Show | 9 | HG00423.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2336+228_2336+229d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | 41905480 | |||||
chr19:41905542
|
T | C | 1 | a0004c0010t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2337-218T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905542 | ||||||
chr19:41905545
|
G | A | 1 | a0001c0002t0001g0082 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2337-215G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905545 | ||||||
chr19:41905642
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2337-118C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905642 | ||||||
chr19:41905710
|
G | A | 9 | a0001c0001t0001g0122a0001c0003t0001g0019a0001c0003t0001g0022others(6): Show | 9 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.2337-50G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905710 | ||||||
chr19:41905872
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2404+45C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 25/28 | chr19 | 41905872 | ||||||
chr19:41905934
|
T | C | 8 | a0001c0001t0001g0122a0001c0003t0001g0022a0001c0003t0001g0023others(5): Show | 8 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.2405-5T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 25/28 | chr19 | 41905934 | ||||||
chr19:41906174
|
T | G | 1 | a0001c0001t0001g0172 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2491+149T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 26/28 | chr19 | 41906174 | ||||||
chr19:41906179
|
G | A | 65 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(62): Show | 78 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.2491+154G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 26/28 | chr19 | 41906179 | ||||||
chr19:41906354
|
A | C | 1 | a0006c0005t0001g0089 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2492-103A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 26/28 | chr19 | 41906354 | ||||||
chr19:41906831
|
G | GCTGTCCT others(85): Show |
1 | a0006c0005t0001g0089 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.*17+41_*17+42insGA others(90): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr19 | 41906831 | |||||
chr19:41906920
|
A | T | 66 | a0001c0002t0001g0001a0001c0002t0001g0010a0001c0002t0001g0011others(63): Show | 79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.*17+117A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 28/28 | chr19 | 41906920 |