geneid | 100271715 |
---|---|
ensemblid | ENSG00000214694.13 |
hgncid | 37252 |
symbol | ARHGEF33 |
name | Rho guanine nucleotide exchange factor 33 |
refseq_nuc | NM_001145451.5 |
refseq_prot | NP_001138923.2 |
ensembl_nuc | ENST00000409978.7 |
ensembl_prot | ENSP00000387020.1 |
mane_status | MANE Select |
chr | chr2 |
start | 38889875 |
end | 38975454 |
strand | + |
ver | v1.2 |
region | chr2:38889875-38975454 |
region5000 | chr2:38884875-38980454 |
regionname0 | ARHGEF33_chr2_38889875_38975454 |
regionname5000 | ARHGEF33_chr2_38884875_38980454 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 870 | 231 | 79 | 47 | 72 | 4 | 28 | 61 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0002 | 1/0 | 870 | 35 | 1 | 3 | 23 | 0 | 7 | 20 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0003 | 0/0 | 870 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0004 | 0/0 | 870 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0005 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0006 | 0/0 | 870 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0007 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0008 | 0/0 | 870 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0009 | 0/0 | 870 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0010 | 0/0 | 870 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0011 | 0/0 | 870 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2613 | 222 | 76 | 47 | 66 | 4 | 28 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0002 | 1/0 | 2613 | 35 | 1 | 3 | 23 | 0 | 7 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0003 | 0/0 | 2613 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0004 | 0/0 | 2613 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0005 | 0/0 | 2613 | 3 | 0 | 2 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0006 | 0/0 | 2613 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0007 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0008 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0009 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0010 | 0/0 | 2613 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0011 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0012 | 0/0 | 2613 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0013 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
c0014 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1882 | 130 | 17 | 26 | 64 | 3 | 20 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0002 | 1/0 | 1882 | 68 | 24 | 15 | 16 | 0 | 12 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0003 | 0/0 | 1882 | 23 | 23 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0004 | 0/0 | 1882 | 19 | 11 | 1 | 7 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0005 | 0/0 | 1882 | 11 | 1 | 7 | 0 | 1 | 2 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0006 | 0/0 | 1880 | 10 | 0 | 2 | 8 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0007 | 0/0 | 1884 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0008 | 0/0 | 1882 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0009 | 0/0 | 1882 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0010 | 0/0 | 1882 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0011 | 0/0 | 1882 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0012 | 0/0 | 1884 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0013 | 0/0 | 1882 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0014 | 0/0 | 1880 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0015 | 0/0 | 1882 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0016 | 0/0 | 1882 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0017 | 0/1 | 1882 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
t0018 | 0/0 | 1882 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2613 | 222 | 76 | 47 | 66 | 4 | 28 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0003 | 0/0 | 2613 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0004 | 0/0 | 2613 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0014 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0002c0002 | 1/0 | 2613 | 35 | 1 | 3 | 23 | 0 | 7 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0003c0005 | 0/0 | 2613 | 3 | 0 | 2 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0004c0006 | 0/0 | 2613 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0005c0008 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0006c0009 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0007c0011 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0008c0012 | 0/0 | 2613 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0009c0013 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0010c0010 | 0/0 | 2613 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0011c0007 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4494 | 93 | 16 | 22 | 39 | 3 | 13 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0002 | 0/0 | 4494 | 63 | 24 | 14 | 13 | 0 | 12 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0003 | 0/0 | 4494 | 23 | 23 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0004 | 0/0 | 4494 | 13 | 8 | 1 | 4 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0005 | 0/0 | 4494 | 8 | 1 | 4 | 0 | 1 | 2 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0006 | 0/0 | 4492 | 10 | 0 | 2 | 8 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0007 | 0/0 | 4496 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0008 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0009 | 0/0 | 4494 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0010 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0013 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0014 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0017 | 0/1 | 4494 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0001t0018 | 0/0 | 4494 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0003t0002 | 0/0 | 4494 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0003t0004 | 0/0 | 4494 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0003t0015 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0004t0004 | 0/0 | 4494 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0004t0011 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0001c0014t0002 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0002c0002t0001 | 0/0 | 4494 | 30 | 1 | 1 | 22 | 0 | 6 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0002c0002t0002 | 1/0 | 4494 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0002c0002t0004 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0002c0002t0005 | 0/0 | 4494 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0002c0002t0008 | 0/0 | 4494 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0003c0005t0001 | 0/0 | 4494 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0003c0005t0012 | 0/0 | 4496 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0004c0006t0001 | 0/0 | 4494 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0005c0008t0004 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0006c0009t0001 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0007c0011t0016 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0008c0012t0002 | 0/0 | 4494 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0009c0013t0001 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0010c0010t0005 | 0/0 | 4494 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
a0011c0007t0001 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | copy fasta | chr2 | 38884875 | 38980454 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0006g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0007g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0007g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0007g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0009g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0010g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0013g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0014g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0017g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0001t0018g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0003t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0003t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0003t0015g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0004t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0004t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0004t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0001c0014t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0002g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0002c0002t0008g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0003c0005t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0003c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0003c0005t0012g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0004c0006t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0004c0006t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0005c0008t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0006c0009t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0007c0011t0016g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0008c0012t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0009c0013t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0010c0010t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
a0011c0007t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | FIN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | CHS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00738 | hp1 | a0004 | c0006 | t0001 | g0102 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG00741 | hp2 | a0001 | c0001 | t0007 | g0064 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01069 | hp2 | a0002 | c0002 | t0005 | g0068 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01071 | hp1 | a0002 | c0002 | t0005 | g0067 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01081 | hp1 | a0001 | c0001 | t0007 | g0046 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01081 | hp2 | a0004 | c0006 | t0001 | g0100 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0251 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01167 | hp2 | a0001 | c0001 | t0007 | g0038 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01257 | hp1 | a0003 | c0005 | t0012 | g0002 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01258 | hp2 | a0003 | c0005 | t0001 | g0002 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0061 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01358 | hp2 | a0001 | c0001 | t0007 | g0032 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0212 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0194 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0065 | EUR | IBS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01978 | hp1 | a0008 | c0012 | t0002 | g0033 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01981 | hp1 | a0010 | c0010 | t0005 | g0063 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01993 | hp2 | a0001 | c0001 | t0006 | g0250 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | KHV | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | CDX | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02280 | hp1 | a0001 | c0001 | t0009 | g0005 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0267 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02602 | hp1 | a0001 | c0001 | t0018 | g0011 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0180 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02615 | hp2 | a0001 | c0004 | t0004 | g0076 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02622 | hp2 | a0001 | c0004 | t0004 | g0075 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02723 | hp2 | a0007 | c0011 | t0016 | g0210 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0010 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02809 | hp2 | a0001 | c0004 | t0011 | g0077 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0262 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0245 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02886 | hp2 | a0001 | c0001 | t0010 | g0213 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02976 | hp1 | a0001 | c0001 | t0008 | g0166 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03017 | hp2 | a0003 | c0005 | t0001 | g0139 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03710 | hp1 | a0002 | c0002 | t0008 | g0197 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | BEB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0185 | SAS | BEB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0181 | SAS | BEB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0176 | SAS | STU | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | STU | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0189 | SAS | STU | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | STU | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | STU | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | YRI | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | YRI | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | YRI | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0255 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18953 | hp2 | a0011 | c0007 | t0001 | g0170 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18956 | hp1 | a0001 | c0001 | t0006 | g0257 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18961 | hp1 | a0001 | c0001 | t0006 | g0258 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18964 | hp1 | a0001 | c0001 | t0013 | g0144 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18977 | hp2 | a0006 | c0009 | t0001 | g0129 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18982 | hp1 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18988 | hp2 | a0002 | c0002 | t0004 | g0206 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18991 | hp2 | a0001 | c0003 | t0002 | g0272 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18993 | hp2 | a0001 | c0003 | t0004 | g0204 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18997 | hp1 | a0001 | c0001 | t0006 | g0239 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19003 | hp2 | a0001 | c0001 | t0006 | g0254 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19012 | hp1 | a0001 | c0003 | t0015 | g0173 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | LWK | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | LWK | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19043 | hp2 | a0005 | c0008 | t0004 | g0214 | AFR | LWK | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19058 | hp1 | a0001 | c0001 | t0014 | g0094 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19060 | hp1 | a0001 | c0014 | t0002 | g0056 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19068 | hp2 | a0001 | c0001 | t0006 | g0256 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19077 | hp1 | a0001 | c0003 | t0004 | g0205 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19079 | hp1 | a0001 | c0003 | t0002 | g0271 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19083 | hp1 | a0001 | c0001 | t0006 | g0253 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | YRI | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | YRI | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | ASW | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ASW | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA20905 | hp1 | a0001 | c0001 | t0005 | g0013 | SAS | GIH | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | GIH | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18955 | hp1 | a0009 | c0013 | t0001 | g0186 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | USA | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0017 | g0042 | REF | REF | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0219 | REF | REF | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:38928925
|
G | A | 1 | a0011 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.94G>A | p.Glu32Lys | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/18 | 364/4494 | 94/2613 | 32/870 | chr2 | 38928925 | ||
chr2:38931156
|
C | G | 1 | a0003 | 3 | HG01257.hp1 HG01258.hp2 HG03017.hp2 |
missense_variant | MODERATE | c.410C>G | p.Ala137Gly | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/18 | 680/4494 | 410/2613 | 137/870 | chr2 | 38931156 | ||
chr2:38937535
|
G | A | 1 | a0005 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.766G>A | p.Val256Ile | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/18 | 1036/4494 | 766/2613 | 256/870 | chr2 | 38937535 | ||
chr2:38953177
|
T | C | 1 | a0006 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.1069T>C | p.Tyr357His | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/18 | 1339/4494 | 1069/2613 | 357/870 | chr2 | 38953177 | ||
chr2:38959867
|
G | C | 1 | a0010 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.1562G>C | p.Ser521Thr | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 1832/4494 | 1562/2613 | 521/870 | chr2 | 38959867 | ||
chr2:38960049
|
T | C | 9 | a0001a0003a0004others(6): Show | 242 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(239): Show |
missense_variant | MODERATE | c.1744T>C | p.Ser582Pro | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2014/4494 | 1744/2613 | 582/870 | chr2 | 38960049 | ||
chr2:38960076
|
G | T | 1 | a0004 | 2 | HG00738.hp1 HG01081.hp2 |
missense_variant | MODERATE | c.1771G>T | p.Val591Leu | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2041/4494 | 1771/2613 | 591/870 | chr2 | 38960076 | ||
chr2:38960196
|
G | A | 1 | a0009 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.1891G>A | p.Glu631Lys | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2161/4494 | 1891/2613 | 631/870 | chr2 | 38960196 | ||
chr2:38960551
|
C | G | 1 | a0008 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.2246C>G | p.Pro749Arg | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2516/4494 | 2246/2613 | 749/870 | chr2 | 38960551 | ||
chr2:38960581
|
C | T | 1 | a0007 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.2276C>T | p.Ala759Val | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2546/4494 | 2276/2613 | 759/870 | chr2 | 38960581 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:38928966
|
A | G | 1 | a0001c0014 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.135A>G | p.Ser45Ser | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/18 | 405/4494 | 135/2613 | 45/870 | chr2 | 38928966 | ||
chr2:38960378
|
A | G | 9 | a0001c0001a0001c0014a0003c0005others(6): Show | 233 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(230): Show |
synonymous_variant | LOW | c.2073A>G | p.Lys691Lys | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2343/4494 | 2073/2613 | 691/870 | chr2 | 38960378 | ||
chr2:38960450
|
G | C | 1 | a0001c0004 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.2145G>C | p.Ala715Ala | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2415/4494 | 2145/2613 | 715/870 | chr2 | 38960450 | ||
chr2:38960525
|
C | T | 1 | a0007c0011 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.2220C>T | p.Ala740Ala | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2490/4494 | 2220/2613 | 740/870 | chr2 | 38960525 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:38889976
|
G | A | 20 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(17): Show | 157 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(154): Show |
5_prime_UTR_variant | MODIFIER | c.-169G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/18 | 29472 | chr2 | 38889976 | |||||
chr2:38895800
|
A | C | 17 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(14): Show | 148 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(145): Show |
5_prime_UTR_variant | MODIFIER | c.-135A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/18 | 23648 | chr2 | 38895800 | |||||
chr2:38973911
|
A | AAT | 2 | a0001c0001t0007a0003c0005t0012 | 5 | HG00741.hp2 HG01081.hp1 HG01167.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*81_*82dupAT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 83 | INFO_REALIGN_3_PRIME | chr2 | 38973911 | ||||
chr2:38973928
|
A | G | 1 | a0001c0003t0015 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*85A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 85 | chr2 | 38973928 | |||||
chr2:38973932
|
CTA | C | 2 | a0001c0001t0006a0001c0001t0014 | 11 | HG01106.hp2 HG01993.hp2 NA18952.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*105_*106delAT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 105 | INFO_REALIGN_3_PRIME | chr2 | 38973932 | ||||
chr2:38973938
|
A | C | 1 | a0001c0001t0018 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*95A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 95 | chr2 | 38973938 | |||||
chr2:38974668
|
A | G | 1 | a0001c0001t0009 | 2 | HG02280.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*825A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 825 | chr2 | 38974668 | |||||
chr2:38974941
|
A | G | 1 | a0001c0001t0017 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1098A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 1098 | chr2 | 38974941 | |||||
chr2:38975241
|
A | G | 2 | a0001c0001t0008a0002c0002t0008 | 2 | HG02976.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1398A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 1398 | chr2 | 38975241 | |||||
chr2:38975340
|
T | G | 1 | a0007c0011t0016 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1497T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 1497 | chr2 | 38975340 | |||||
chr2:38975352
|
G | A | 1 | a0001c0001t0013 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1509G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 1509 | chr2 | 38975352 | |||||
chr2:38975378
|
C | T | 1 | a0001c0004t0011 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1535C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 1535 | chr2 | 38975378 | |||||
chr2:38975446
|
A | G | 4 | a0001c0001t0003a0001c0001t0006a0001c0001t0010others(1): Show | 35 | HG01106.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1603A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 1603 | chr2 | 38975446 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:38890048
|
T | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0007 | 2 | HG01109.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-159+62T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890048 | ||||||
chr2:38890059
|
C | G | 5 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0009g0005others(2): Show | 6 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-159+73C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890059 | ||||||
chr2:38890144
|
T | G | 66 | a0001c0001t0001g0066a0001c0001t0002g0006a0001c0001t0002g0007others(63): Show | 66 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.-159+158T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890144 | ||||||
chr2:38890164
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-159+178T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890164 | ||||||
chr2:38890225
|
C | T | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-159+239C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890225 | ||||||
chr2:38890266
|
A | G | 7 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0004g0261others(4): Show | 7 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-159+280A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890266 | ||||||
chr2:38890477
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(225): Show | 232 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(229): Show |
intron_variant | MODIFIER | c.-159+491T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890477 | ||||||
chr2:38890513
|
G | C | 4 | a0001c0001t0002g0004a0001c0001t0002g0215a0001c0001t0002g0216others(1): Show | 5 | HG01496.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+527G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890513 | ||||||
chr2:38890615
|
G | A | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-159+629G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890615 | ||||||
chr2:38890675
|
A | G | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-159+689A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890675 | ||||||
chr2:38890765
|
T | C | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-159+779T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890765 | ||||||
chr2:38890956
|
A | G | 3 | a0001c0001t0004g0211a0001c0001t0004g0212a0001c0001t0010g0213 | 3 | HG01361.hp2 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-159+970A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890956 | ||||||
chr2:38890962
|
C | G | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-159+976C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890962 | ||||||
chr2:38890968
|
G | GT | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(243): Show | 250 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(247): Show |
intron_variant | MODIFIER | c.-159+995dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38890968 | |||||
chr2:38890987
|
T | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-159+1001T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890987 | ||||||
chr2:38891064
|
A | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(268): Show | 276 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(273): Show |
intron_variant | MODIFIER | c.-159+1078A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891064 | ||||||
chr2:38891133
|
C | G | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-159+1147C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891133 | ||||||
chr2:38891247
|
T | C | 4 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0004g0261others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-159+1261T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891247 | ||||||
chr2:38891402
|
T | C | 63 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(60): Show | 63 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.-159+1416T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891402 | ||||||
chr2:38891427
|
A | G | 2 | a0001c0001t0003g0209a0007c0011t0016g0210 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-159+1441A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891427 | ||||||
chr2:38891537
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-159+1551T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891537 | ||||||
chr2:38891620
|
T | A | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-159+1634T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891620 | ||||||
chr2:38891850
|
T | A | 4 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-159+1864T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891850 | ||||||
chr2:38891877
|
C | T | 5 | a0001c0001t0003g0209a0001c0001t0004g0266a0001c0001t0004g0267others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+1891C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891877 | ||||||
chr2:38891925
|
C | T | 12 | a0001c0001t0003g0248a0001c0001t0003g0249a0001c0001t0006g0239others(9): Show | 12 | HG01106.hp2 HG01993.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-159+1939C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891925 | ||||||
chr2:38892056
|
T | C | 5 | a0001c0001t0001g0079a0002c0002t0001g0078a0002c0002t0001g0080others(2): Show | 5 | HG02135.hp2 NA18956.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+2070T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892056 | ||||||
chr2:38892075
|
A | T | 5 | a0001c0001t0003g0209a0001c0001t0004g0266a0001c0001t0004g0267others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+2089A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892075 | ||||||
chr2:38892408
|
G | A | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-159+2422G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892408 | ||||||
chr2:38892421
|
A | ATC | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(144): Show | 150 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.-159+2436_-159+243 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38892421 | |||||
chr2:38892585
|
T | A | 4 | a0001c0001t0003g0209a0001c0001t0004g0266a0001c0001t0004g0267others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-159+2599T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892585 | ||||||
chr2:38892647
|
A | G | 2 | a0001c0001t0003g0209a0007c0011t0016g0210 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-159+2661A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892647 | ||||||
chr2:38892712
|
A | G | 5 | a0001c0001t0001g0207a0001c0001t0004g0208a0001c0003t0004g0204others(2): Show | 5 | HG00558.hp1 NA18949.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.-159+2726A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892712 | ||||||
chr2:38892771
|
A | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-159+2785A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892771 | ||||||
chr2:38892920
|
TTCCTC | T | 3 | a0002c0002t0001g0085a0002c0002t0001g0086a0002c0002t0001g0087 | 3 | NA18945.hp2 NA18980.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-158-2855_-158-285 others(9): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38892920 | |||||
chr2:38892943
|
A | G | 4 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0004g0261others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158-2834A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892943 | ||||||
chr2:38893093
|
A | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-158-2684A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893093 | ||||||
chr2:38893157
|
CT | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(229): Show | 236 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(233): Show |
intron_variant | MODIFIER | c.-158-2604delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38893157 | |||||
chr2:38893157
|
CTT | C | 6 | a0001c0001t0001g0088a0001c0001t0002g0008a0001c0001t0004g0259others(3): Show | 6 | HG02818.hp2 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-158-2605_-158-260 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38893157 | |||||
chr2:38893263
|
A | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-158-2514A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893263 | ||||||
chr2:38893335
|
C | T | 5 | a0001c0001t0003g0209a0001c0001t0004g0266a0001c0001t0004g0267others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-2442C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893335 | ||||||
chr2:38893639
|
A | G | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-158-2138A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893639 | ||||||
chr2:38893662
|
A | G | 10 | a0001c0001t0006g0239a0001c0001t0006g0250a0001c0001t0006g0251others(7): Show | 10 | HG01106.hp2 HG01993.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.-158-2115A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893662 | ||||||
chr2:38893699
|
T | C | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-158-2078T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893699 | ||||||
chr2:38893712
|
A | C | 4 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158-2065A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893712 | ||||||
chr2:38893766
|
C | G | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-158-2011C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893766 | ||||||
chr2:38893785
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | NA18942.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-158-1992C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893785 | ||||||
chr2:38893829
|
A | G | 78 | a0001c0001t0001g0083a0001c0001t0002g0006a0001c0001t0002g0007others(75): Show | 79 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.-158-1948A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893829 | ||||||
chr2:38893890
|
G | A | 5 | a0001c0001t0003g0209a0001c0001t0004g0266a0001c0001t0004g0267others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-1887G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893890 | ||||||
chr2:38894001
|
A | G | 3 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0009g0005 | 4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-158-1776A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894001 | ||||||
chr2:38894044
|
C | A | 1 | a0001c0001t0002g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-158-1733C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894044 | ||||||
chr2:38894332
|
T | TA | 68 | a0001c0001t0001g0083a0001c0001t0002g0006a0001c0001t0002g0007others(65): Show | 68 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.-158-1433dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38894332 | |||||
chr2:38894423
|
G | GA | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(240): Show | 246 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.-158-1343dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38894423 | |||||
chr2:38894423
|
G | GAA | 6 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0006g0239others(3): Show | 7 | HG02280.hp1 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-158-1344_-158-134 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38894423 | |||||
chr2:38894438
|
T | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(223): Show | 230 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(227): Show |
intron_variant | MODIFIER | c.-158-1339T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894438 | ||||||
chr2:38894441
|
T | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA19012.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-158-1336T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894441 | ||||||
chr2:38894487
|
AAAAC | A | 7 | a0001c0001t0002g0222a0001c0001t0004g0259a0001c0001t0004g0260others(4): Show | 7 | HG01516.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-158-1271_-158-126 others(8): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38894487 | |||||
chr2:38894549
|
C | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-158-1228C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894549 | ||||||
chr2:38894593
|
C | A | 2 | a0001c0001t0003g0209a0007c0011t0016g0210 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-158-1184C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894593 | ||||||
chr2:38894716
|
C | G | 43 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(40): Show | 43 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-158-1061C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894716 | ||||||
chr2:38895202
|
A | G | 3 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0009g0005 | 4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-158-575A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895202 | ||||||
chr2:38895228
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA19012.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-158-549C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895228 | ||||||
chr2:38895313
|
C | T | 1 | a0001c0001t0004g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-158-464C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895313 | ||||||
chr2:38895316
|
T | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-158-461T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895316 | ||||||
chr2:38895316
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(222): Show | 229 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(226): Show |
intron_variant | MODIFIER | c.-158-461T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895316 | ||||||
chr2:38895485
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(134): Show | 140 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.-158-292C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895485 | ||||||
chr2:38895719
|
G | A | 5 | a0001c0001t0003g0209a0001c0001t0004g0266a0001c0001t0004g0267others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-58G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895719 | ||||||
chr2:38895754
|
GT | G | 6 | a0001c0001t0001g0202a0001c0001t0003g0209a0001c0001t0004g0266others(3): Show | 6 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.-158-5delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38895754 | |||||
chr2:38895758
|
T | TG | 6 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0006g0239others(3): Show | 7 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-158-19_-158-18ins others(1): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895758 | ||||||
chr2:38895759
|
T | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(232): Show | 238 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(235): Show |
intron_variant | MODIFIER | c.-158-18T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895759 | ||||||
chr2:38895760
|
T | G | 4 | a0001c0001t0001g0202a0001c0001t0004g0266a0001c0001t0004g0267others(1): Show | 4 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158-17T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895760 | ||||||
chr2:38895888
|
C | T | 4 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+39C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38895888 | ||||||
chr2:38896018
|
T | C | 1 | a0001c0001t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-86+169T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896018 | ||||||
chr2:38896048
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-86+199C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896048 | ||||||
chr2:38896079
|
G | A | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-86+230G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896079 | ||||||
chr2:38896098
|
A | G | 5 | a0001c0001t0003g0209a0001c0001t0004g0266a0001c0001t0004g0267others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+249A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896098 | ||||||
chr2:38896105
|
T | C | 20 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(17): Show | 20 | HG01106.hp2 HG01884.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.-86+256T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896105 | ||||||
chr2:38896110
|
A | C | 2 | a0002c0002t0001g0199a0002c0002t0001g0200 | 2 | NA18977.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-86+261A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896110 | ||||||
chr2:38896285
|
C | A | 1 | a0001c0001t0003g0249 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-86+436C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896285 | ||||||
chr2:38896340
|
G | A | 2 | a0001c0001t0006g0250a0001c0001t0006g0251 | 2 | HG01106.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-86+491G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896340 | ||||||
chr2:38896360
|
A | G | 20 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(17): Show | 20 | HG01106.hp2 HG01884.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.-86+511A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896360 | ||||||
chr2:38896397
|
G | A | 3 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0009g0005 | 4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+548G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896397 | ||||||
chr2:38896430
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-86+581G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896430 | ||||||
chr2:38896450
|
A | T | 1 | a0001c0001t0002g0060 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-86+601A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896450 | ||||||
chr2:38896452
|
T | A | 1 | a0001c0001t0002g0060 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-86+603T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896452 | ||||||
chr2:38896454
|
A | T | 1 | a0001c0001t0002g0060 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-86+605A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896454 | ||||||
chr2:38896572
|
G | T | 4 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+723G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896572 | ||||||
chr2:38896578
|
G | T | 4 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+729G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896578 | ||||||
chr2:38896649
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(244): Show | 251 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(248): Show |
intron_variant | MODIFIER | c.-86+800T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896649 | ||||||
chr2:38896685
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-86+836G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896685 | ||||||
chr2:38896907
|
G | A | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-86+1058G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896907 | ||||||
chr2:38897027
|
T | A | 2 | a0001c0001t0003g0209a0007c0011t0016g0210 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+1178T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897027 | ||||||
chr2:38897041
|
G | A | 2 | a0001c0001t0006g0252a0001c0001t0006g0253 | 2 | NA18982.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-86+1192G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897041 | ||||||
chr2:38897059
|
G | A | 3 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0009g0005 | 4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+1210G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897059 | ||||||
chr2:38897119
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(142): Show | 148 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.-86+1270T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897119 | ||||||
chr2:38897156
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(138): Show | 144 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.-86+1307C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897156 | ||||||
chr2:38897165
|
C | A | 1 | a0001c0001t0014g0094 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-86+1316C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897165 | ||||||
chr2:38897193
|
C | T | 1 | a0002c0002t0001g0198 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-86+1344C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897193 | ||||||
chr2:38897266
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-86+1417T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897266 | ||||||
chr2:38897328
|
T | C | 2 | a0001c0001t0003g0209a0007c0011t0016g0210 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+1479T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897328 | ||||||
chr2:38897368
|
A | G | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-86+1519A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897368 | ||||||
chr2:38897419
|
C | T | 1 | a0001c0001t0004g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-86+1570C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897419 | ||||||
chr2:38897586
|
G | A | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+1737G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897586 | ||||||
chr2:38897618
|
A | T | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+1769A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897618 | ||||||
chr2:38897677
|
C | T | 4 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+1828C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897677 | ||||||
chr2:38897814
|
T | C | 54 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(51): Show | 54 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.-86+1965T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897814 | ||||||
chr2:38897856
|
A | T | 1 | a0002c0002t0008g0197 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-86+2007A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897856 | ||||||
chr2:38897886
|
G | A | 1 | a0001c0001t0003g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-86+2037G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897886 | ||||||
chr2:38898135
|
A | G | 9 | a0001c0001t0001g0083a0001c0001t0005g0012a0001c0001t0005g0013others(6): Show | 9 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-86+2286A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898135 | ||||||
chr2:38898229
|
A | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+2380A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898229 | ||||||
chr2:38898342
|
A | G | 3 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | HG02717.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-86+2493A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898342 | ||||||
chr2:38898373
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-86+2524G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898373 | ||||||
chr2:38898413
|
C | T | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+2564C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898413 | ||||||
chr2:38898461
|
C | G | 1 | a0001c0001t0003g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-86+2612C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898461 | ||||||
chr2:38898473
|
C | T | 4 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0004g0261others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+2624C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898473 | ||||||
chr2:38898886
|
A | G | 1 | a0001c0001t0002g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-86+3037A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898886 | ||||||
chr2:38899027
|
AT | A | 7 | a0001c0001t0001g0202a0001c0001t0003g0209a0001c0004t0004g0075others(4): Show | 7 | HG02615.hp2 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+3188delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38899027 | |||||
chr2:38899107
|
T | C | 1 | a0001c0001t0002g0026 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-86+3258T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899107 | ||||||
chr2:38899121
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-86+3272C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899121 | ||||||
chr2:38899145
|
A | G | 7 | a0001c0001t0004g0208a0001c0001t0004g0263a0001c0001t0004g0264others(4): Show | 7 | NA18949.hp1 NA18961.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+3296A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899145 | ||||||
chr2:38899257
|
C | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(224): Show | 231 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(228): Show |
intron_variant | MODIFIER | c.-86+3408C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899257 | ||||||
chr2:38899284
|
A | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+3435A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899284 | ||||||
chr2:38899357
|
T | A | 2 | a0002c0002t0001g0096a0002c0002t0001g0198 | 2 | NA18986.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-86+3508T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899357 | ||||||
chr2:38899663
|
T | C | 1 | a0001c0001t0003g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-86+3814T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899663 | ||||||
chr2:38899698
|
G | T | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+3849G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899698 | ||||||
chr2:38899737
|
G | A | 2 | a0002c0002t0005g0067a0002c0002t0005g0068 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-86+3888G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899737 | ||||||
chr2:38899739
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-86+3890G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899739 | ||||||
chr2:38899879
|
G | A | 5 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0101others(2): Show | 5 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+4030G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899879 | ||||||
chr2:38900026
|
CA | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(163): Show | 169 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.-86+4187delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38900026 | |||||
chr2:38900106
|
T | C | 18 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(15): Show | 18 | HG01069.hp1 HG01070.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-86+4257T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900106 | ||||||
chr2:38900213
|
A | G | 40 | a0001c0001t0001g0079a0001c0001t0001g0178a0001c0001t0001g0183others(37): Show | 40 | HG00597.hp2 HG01123.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.-86+4364A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900213 | ||||||
chr2:38900350
|
C | T | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+4501C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900350 | ||||||
chr2:38900428
|
T | C | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+4579T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900428 | ||||||
chr2:38900606
|
T | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | NA18945.hp1 NA18952.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-86+4757T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900606 | ||||||
chr2:38900679
|
C | G | 20 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(17): Show | 20 | HG01106.hp2 HG01884.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.-86+4830C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900679 | ||||||
chr2:38900788
|
C | G | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-86+4939C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900788 | ||||||
chr2:38900969
|
C | G | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-86+5120C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900969 | ||||||
chr2:38901031
|
C | T | 1 | a0001c0001t0001g0003 | 2 | HG00738.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-86+5182C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901031 | ||||||
chr2:38901433
|
C | T | 1 | a0001c0001t0003g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-86+5584C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901433 | ||||||
chr2:38901469
|
C | T | 72 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(69): Show | 73 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.-86+5620C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901469 | ||||||
chr2:38901485
|
C | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(149): Show | 155 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.-86+5636C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901485 | ||||||
chr2:38901493
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-86+5644G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901493 | ||||||
chr2:38901578
|
C | T | 12 | a0001c0001t0003g0248a0001c0001t0003g0249a0001c0001t0006g0239others(9): Show | 12 | HG01106.hp2 HG01993.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-86+5729C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901578 | ||||||
chr2:38901798
|
C | T | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+5949C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901798 | ||||||
chr2:38902018
|
G | C | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-86+6169G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902018 | ||||||
chr2:38902071
|
C | T | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-86+6222C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902071 | ||||||
chr2:38902134
|
GA | G | 6 | a0001c0001t0002g0027a0001c0001t0002g0071a0001c0001t0004g0266others(3): Show | 6 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+6303delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38902134 | |||||
chr2:38902274
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-86+6425C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902274 | ||||||
chr2:38902381
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(126): Show | 132 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.-86+6532G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902381 | ||||||
chr2:38902409
|
A | C | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-86+6560A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902409 | ||||||
chr2:38902475
|
G | C | 3 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0009g0005 | 4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+6626G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902475 | ||||||
chr2:38902521
|
A | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+6672A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902521 | ||||||
chr2:38902539
|
C | G | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-86+6690C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902539 | ||||||
chr2:38902794
|
A | G | 59 | a0001c0001t0001g0066a0001c0001t0002g0006a0001c0001t0002g0007others(56): Show | 59 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.-86+6945A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902794 | ||||||
chr2:38902870
|
T | G | 2 | a0001c0001t0003g0209a0007c0011t0016g0210 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+7021T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902870 | ||||||
chr2:38903000
|
T | G | 1 | a0001c0001t0006g0239 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-86+7151T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903000 | ||||||
chr2:38903049
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-86+7200G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903049 | ||||||
chr2:38903057
|
A | G | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-86+7208A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903057 | ||||||
chr2:38903071
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-86+7222T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903071 | ||||||
chr2:38903192
|
A | C | 55 | a0001c0001t0001g0066a0001c0001t0002g0006a0001c0001t0002g0007others(52): Show | 55 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-86+7343A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903192 | ||||||
chr2:38903223
|
A | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+7374A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903223 | ||||||
chr2:38903239
|
TA | T | 9 | a0001c0001t0003g0209a0001c0001t0004g0208a0001c0001t0004g0263others(6): Show | 9 | HG02723.hp2 HG03471.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.-86+7398delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38903239 | |||||
chr2:38903286
|
A | G | 5 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0009g0005others(2): Show | 6 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-86+7437A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903286 | ||||||
chr2:38903310
|
A | G | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-86+7461A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903310 | ||||||
chr2:38903349
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-86+7500T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903349 | ||||||
chr2:38903417
|
A | AT | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(133): Show | 139 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.-86+7581dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38903417 | |||||
chr2:38903576
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-86+7727C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903576 | ||||||
chr2:38903957
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-86+8108A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903957 | ||||||
chr2:38904142
|
G | C | 54 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(51): Show | 54 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.-86+8293G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904142 | ||||||
chr2:38904231
|
T | C | 15 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(12): Show | 15 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-86+8382T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904231 | ||||||
chr2:38904264
|
C | T | 1 | a0002c0002t0004g0206 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-86+8415C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904264 | ||||||
chr2:38904280
|
A | G | 5 | a0001c0001t0002g0055a0001c0001t0002g0057a0001c0001t0002g0058others(2): Show | 5 | NA18960.hp2 NA18988.hp1 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86+8431A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904280 | ||||||
chr2:38904317
|
G | A | 1 | a0001c0003t0004g0204 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-86+8468G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904317 | ||||||
chr2:38904395
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-86+8546C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904395 | ||||||
chr2:38904415
|
GA | G | 54 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(51): Show | 54 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.-86+8572delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38904415 | |||||
chr2:38904471
|
T | C | 2 | a0001c0001t0002g0028a0001c0001t0002g0029 | 2 | HG02698.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-86+8622T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904471 | ||||||
chr2:38904639
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(151): Show | 157 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.-86+8790A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904639 | ||||||
chr2:38904690
|
G | A | 16 | a0001c0001t0003g0209a0001c0001t0004g0208a0001c0001t0004g0211others(13): Show | 16 | HG01361.hp2 HG02723.hp2 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.-86+8841G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904690 | ||||||
chr2:38904694
|
C | A | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-86+8845C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904694 | ||||||
chr2:38904694
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-86+8845C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904694 | ||||||
chr2:38904695
|
G | A | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-86+8846G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904695 | ||||||
chr2:38904707
|
C | CA | 9 | a0001c0001t0003g0209a0001c0001t0004g0266a0001c0001t0004g0267others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-86+8873dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38904707 | |||||
chr2:38904707
|
C | CAA | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(130): Show | 136 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.-86+8872_-86+8873d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38904707 | |||||
chr2:38904707
|
C | CAAA | 6 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | HG03942.hp2 NA18977.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.-86+8871_-86+8873d others(5): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38904707 | |||||
chr2:38904707
|
CA | C | 53 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(50): Show | 53 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.-86+8873delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38904707 | |||||
chr2:38904713
|
A | G | 3 | a0001c0001t0004g0211a0001c0001t0004g0212a0001c0001t0010g0213 | 3 | HG01361.hp2 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-86+8864A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904713 | ||||||
chr2:38904816
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(145): Show | 151 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.-86+8967G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904816 | ||||||
chr2:38904827
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-86+8978G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904827 | ||||||
chr2:38904989
|
G | A | 1 | a0002c0002t0001g0086 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-86+9140G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904989 | ||||||
chr2:38905057
|
G | A | 9 | a0001c0001t0001g0073a0001c0001t0001g0103a0001c0001t0001g0104others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-86+9208G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38905057 | ||||||
chr2:38905068
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-86+9219A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38905068 | ||||||
chr2:38905383
|
A | G | 2 | a0001c0001t0005g0065a0010c0010t0005g0063 | 2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-86+9534A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38905383 | ||||||
chr2:38905538
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-86+9689C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38905538 | ||||||
chr2:38905926
|
G | C | 20 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(17): Show | 20 | HG01106.hp2 HG01884.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.-86+10077G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38905926 | ||||||
chr2:38905986
|
G | A | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+10137G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38905986 | ||||||
chr2:38906109
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-86+10260T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906109 | ||||||
chr2:38906151
|
C | T | 5 | a0001c0001t0003g0209a0001c0001t0004g0266a0001c0001t0004g0267others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+10302C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906151 | ||||||
chr2:38906188
|
C | CA | 30 | a0001c0001t0001g0073a0001c0001t0001g0103a0001c0001t0001g0104others(27): Show | 30 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-86+10357dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38906188 | |||||
chr2:38906188
|
C | CAA | 8 | a0001c0001t0001g0083a0001c0001t0005g0010a0001c0001t0005g0012others(5): Show | 8 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-86+10356_-86+1035 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38906188 | |||||
chr2:38906262
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-86+10413T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906262 | ||||||
chr2:38906306
|
T | G | 1 | a0001c0001t0002g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-86+10457T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906306 | ||||||
chr2:38906543
|
G | A | 2 | a0001c0001t0003g0209a0007c0011t0016g0210 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+10694G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906543 | ||||||
chr2:38906683
|
C | T | 5 | a0001c0001t0003g0209a0001c0001t0004g0266a0001c0001t0004g0267others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+10834C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906683 | ||||||
chr2:38906713
|
A | T | 16 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(13): Show | 16 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-86+10864A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906713 | ||||||
chr2:38906749
|
G | A | 1 | a0001c0001t0003g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-86+10900G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906749 | ||||||
chr2:38906805
|
C | CA | 26 | a0001c0001t0001g0112a0001c0001t0002g0055a0001c0001t0002g0269others(23): Show | 27 | HG01361.hp2 HG01891.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.-86+10976dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38906805 | |||||
chr2:38906805
|
CA | C | 20 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(17): Show | 20 | HG00323.hp1 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.-86+10976delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38906805 | |||||
chr2:38906827
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-86+10978G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906827 | ||||||
chr2:38906880
|
C | A | 1 | a0001c0001t0018g0011 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-86+11031C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906880 | ||||||
chr2:38906986
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(204): Show | 211 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.-86+11137T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906986 | ||||||
chr2:38907224
|
A | G | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-86+11375A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907224 | ||||||
chr2:38907248
|
C | T | 16 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(13): Show | 16 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-86+11399C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907248 | ||||||
chr2:38907254
|
C | G | 1 | a0002c0002t0008g0197 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-86+11405C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907254 | ||||||
chr2:38907297
|
T | G | 34 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0003g0220others(31): Show | 34 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.-86+11448T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907297 | ||||||
chr2:38907860
|
A | AT | 11 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0002g0060others(8): Show | 11 | HG01981.hp2 HG02109.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-85-11486dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38907860 | |||||
chr2:38907861
|
T | TA | 7 | a0001c0001t0004g0208a0001c0001t0004g0263a0001c0001t0004g0264others(4): Show | 7 | NA18949.hp1 NA18961.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-11502_-85-1150 others(5): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907861 | ||||||
chr2:38907949
|
C | G | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-85-11414C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907949 | ||||||
chr2:38907981
|
C | T | 16 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(13): Show | 16 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-85-11382C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907981 | ||||||
chr2:38907986
|
C | T | 17 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0004g0208others(14): Show | 18 | HG01361.hp2 HG02280.hp1 HG02818.hp1 others(15): Show |
intron_variant | MODIFIER | c.-85-11377C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907986 | ||||||
chr2:38908079
|
G | A | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-11284G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908079 | ||||||
chr2:38908140
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-85-11223A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908140 | ||||||
chr2:38908208
|
G | T | 3 | a0001c0001t0001g0195a0002c0002t0001g0096a0002c0002t0001g0198 | 3 | NA18986.hp1 NA19068.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-85-11155G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908208 | ||||||
chr2:38908289
|
C | G | 2 | a0001c0001t0004g0264a0001c0001t0004g0265 | 2 | NA18963.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-85-11074C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908289 | ||||||
chr2:38908358
|
T | G | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-11005T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908358 | ||||||
chr2:38908367
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0167 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-85-10996A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908367 | ||||||
chr2:38908397
|
T | G | 3 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0009g0005 | 4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-10966T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908397 | ||||||
chr2:38908536
|
C | G | 12 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(9): Show | 12 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85-10827C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908536 | ||||||
chr2:38908569
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-85-10794T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908569 | ||||||
chr2:38908707
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-85-10656C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908707 | ||||||
chr2:38908781
|
G | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(9): Show | 12 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85-10582G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908781 | ||||||
chr2:38908786
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(151): Show | 157 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.-85-10577T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908786 | ||||||
chr2:38909184
|
T | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01074.hp2 HG01123.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-10179T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909184 | ||||||
chr2:38909465
|
T | C | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-85-9898T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909465 | ||||||
chr2:38909492
|
CT | C | 10 | a0001c0001t0001g0095a0001c0001t0001g0123a0001c0001t0001g0124others(7): Show | 10 | HG01168.hp2 HG01943.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-85-9853delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38909492 | |||||
chr2:38909494
|
T | C | 1 | a0001c0001t0004g0263 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-85-9869T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909494 | ||||||
chr2:38909560
|
A | C | 1 | a0001c0001t0001g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-85-9803A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909560 | ||||||
chr2:38909705
|
GAT | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0164others(3): Show | 7 | HG00738.hp2 HG01891.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-9657_-85-9656d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909705 | ||||||
chr2:38909706
|
A | AT | 5 | a0001c0001t0002g0021a0001c0001t0002g0236a0001c0001t0002g0269others(2): Show | 6 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-9638dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38909706 | |||||
chr2:38909706
|
AT | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(170): Show | 175 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.-85-9638delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38909706 | |||||
chr2:38909706
|
ATT | A | 19 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(16): Show | 19 | HG01070.hp2 HG01074.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.-85-9639_-85-9638d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38909706 | |||||
chr2:38909969
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-85-9394C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909969 | ||||||
chr2:38909975
|
G | GTTAT | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-85-9385_-85-9382d others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38909975 | |||||
chr2:38909982
|
T | A | 5 | a0001c0001t0003g0209a0001c0001t0004g0266a0001c0001t0004g0267others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-9381T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909982 | ||||||
chr2:38910129
|
C | G | 2 | a0001c0001t0003g0209a0007c0011t0016g0210 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-85-9234C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38910129 | ||||||
chr2:38910411
|
A | C | 1 | a0001c0001t0002g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-85-8952A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38910411 | ||||||
chr2:38910434
|
G | C | 16 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(13): Show | 16 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-85-8929G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38910434 | ||||||
chr2:38910830
|
C | G | 1 | a0001c0001t0005g0010 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-85-8533C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38910830 | ||||||
chr2:38911041
|
C | T | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-8322C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911041 | ||||||
chr2:38911051
|
A | C | 1 | a0001c0001t0001g0162 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-85-8312A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911051 | ||||||
chr2:38911341
|
A | C | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-85-8022A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911341 | ||||||
chr2:38911500
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(202): Show | 209 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.-85-7863A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911500 | ||||||
chr2:38911517
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-85-7846C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911517 | ||||||
chr2:38911566
|
A | G | 2 | a0001c0001t0003g0220a0001c0001t0003g0224 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-85-7797A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911566 | ||||||
chr2:38911753
|
G | A | 3 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0009g0005 | 4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-7610G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911753 | ||||||
chr2:38911806
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-85-7557G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911806 | ||||||
chr2:38911955
|
G | T | 6 | a0001c0001t0006g0239a0001c0001t0006g0254a0001c0001t0006g0255others(3): Show | 6 | NA18952.hp2 NA18956.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-7408G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911955 | ||||||
chr2:38911959
|
G | C | 1 | a0001c0001t0003g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-7404G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911959 | ||||||
chr2:38912068
|
C | T | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-85-7295C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912068 | ||||||
chr2:38912101
|
A | G | 8 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0009others(5): Show | 8 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-85-7262A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912101 | ||||||
chr2:38912135
|
C | T | 2 | a0001c0001t0003g0246a0001c0001t0003g0247 | 2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-85-7228C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912135 | ||||||
chr2:38912168
|
G | A | 1 | a0001c0001t0005g0012 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-85-7195G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912168 | ||||||
chr2:38912360
|
G | A | 1 | a0002c0002t0001g0179 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-85-7003G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912360 | ||||||
chr2:38912375
|
G | A | 4 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-6988G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912375 | ||||||
chr2:38912376
|
A | C | 7 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0009others(4): Show | 7 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-6987A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912376 | ||||||
chr2:38912403
|
C | G | 13 | a0001c0001t0002g0223a0001c0001t0003g0220a0001c0001t0003g0221others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-85-6960C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912403 | ||||||
chr2:38912640
|
G | A | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-85-6723G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912640 | ||||||
chr2:38912735
|
A | G | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-6628A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912735 | ||||||
chr2:38912775
|
C | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(124): Show | 130 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.-85-6588C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912775 | ||||||
chr2:38912784
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-85-6579A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912784 | ||||||
chr2:38912877
|
C | T | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-6486C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912877 | ||||||
chr2:38912967
|
G | C | 5 | a0001c0001t0003g0209a0001c0001t0004g0266a0001c0001t0004g0267others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-6396G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912967 | ||||||
chr2:38913038
|
G | GT | 11 | a0001c0001t0001g0127a0001c0001t0001g0161a0001c0001t0002g0052others(8): Show | 11 | HG02922.hp1 HG03471.hp2 HG03942.hp1 others(8): Show |
intron_variant | MODIFIER | c.-85-6309dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38913038 | |||||
chr2:38913038
|
G | GTT | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(14): Show | 17 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-85-6310_-85-6309d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38913038 | |||||
chr2:38913216
|
G | C | 10 | a0001c0001t0006g0239a0001c0001t0006g0250a0001c0001t0006g0251others(7): Show | 10 | HG01106.hp2 HG01993.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85-6147G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38913216 | ||||||
chr2:38913474
|
A | G | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-85-5889A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38913474 | ||||||
chr2:38913744
|
G | A | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-85-5619G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38913744 | ||||||
chr2:38913973
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(151): Show | 157 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.-85-5390C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38913973 | ||||||
chr2:38913984
|
A | G | 1 | a0001c0001t0005g0061 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-85-5379A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38913984 | ||||||
chr2:38913988
|
T | G | 1 | a0001c0001t0003g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-5375T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38913988 | ||||||
chr2:38914127
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-85-5236G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914127 | ||||||
chr2:38914165
|
T | G | 1 | a0001c0001t0001g0128 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-85-5198T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914165 | ||||||
chr2:38914226
|
A | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-85-5137A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914226 | ||||||
chr2:38914405
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-85-4958C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914405 | ||||||
chr2:38914431
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-85-4932G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914431 | ||||||
chr2:38914465
|
C | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-85-4898C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914465 | ||||||
chr2:38914530
|
G | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0159 | 2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-85-4833G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914530 | ||||||
chr2:38914599
|
G | A | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-85-4764G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914599 | ||||||
chr2:38914628
|
C | G | 1 | a0004c0006t0001g0102 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-85-4735C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914628 | ||||||
chr2:38914643
|
G | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG01074.hp2 HG01123.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-4720G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914643 | ||||||
chr2:38914664
|
CA | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(176): Show | 182 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.-85-4679delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38914664 | |||||
chr2:38914725
|
C | T | 1 | a0001c0001t0002g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-85-4638C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914725 | ||||||
chr2:38915188
|
C | G | 1 | a0001c0001t0001g0162 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-85-4175C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915188 | ||||||
chr2:38915318
|
G | A | 2 | a0001c0003t0002g0271a0001c0003t0002g0272 | 2 | NA18991.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-85-4045G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915318 | ||||||
chr2:38915371
|
T | C | 3 | a0002c0002t0001g0179a0002c0002t0001g0180a0002c0002t0001g0181 | 3 | HG02602.hp2 HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-85-3992T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915371 | ||||||
chr2:38915382
|
C | CT | 26 | a0001c0001t0002g0070a0001c0001t0002g0236a0001c0001t0003g0240others(23): Show | 26 | HG01106.hp2 HG01361.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.-85-3961dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38915382 | |||||
chr2:38915382
|
C | CTT | 29 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0003g0209others(26): Show | 29 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.-85-3962_-85-3961d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38915382 | |||||
chr2:38915382
|
CT | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(127): Show | 133 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.-85-3961delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38915382 | |||||
chr2:38915382
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-85-3970_-85-3961d others(12): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38915382 | |||||
chr2:38915459
|
A | G | 4 | a0001c0001t0004g0208a0001c0003t0004g0204a0001c0003t0004g0205others(1): Show | 4 | NA18949.hp1 NA18988.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-3904A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915459 | ||||||
chr2:38915518
|
G | A | 13 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0009others(10): Show | 13 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-85-3845G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915518 | ||||||
chr2:38915684
|
T | G | 5 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0009g0005others(2): Show | 6 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-3679T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915684 | ||||||
chr2:38915915
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0159 | 2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-85-3448G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915915 | ||||||
chr2:38915916
|
C | G | 15 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(12): Show | 15 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-85-3447C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915916 | ||||||
chr2:38916212
|
C | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(128): Show | 134 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.-85-3151C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916212 | ||||||
chr2:38916232
|
A | T | 16 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(13): Show | 16 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-85-3131A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916232 | ||||||
chr2:38916266
|
C | A | 18 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(15): Show | 18 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-85-3097C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916266 | ||||||
chr2:38916297
|
G | A | 18 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(15): Show | 18 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-85-3066G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916297 | ||||||
chr2:38916500
|
G | A | 1 | a0001c0001t0003g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-85-2863G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916500 | ||||||
chr2:38916533
|
G | T | 1 | a0001c0001t0003g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-85-2830G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916533 | ||||||
chr2:38916573
|
C | G | 13 | a0001c0001t0002g0223a0001c0001t0003g0220a0001c0001t0003g0221others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-85-2790C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916573 | ||||||
chr2:38916662
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(136): Show | 142 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-85-2701T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916662 | ||||||
chr2:38916801
|
C | CT | 27 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0003g0220others(24): Show | 27 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.-85-2546dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38916801 | |||||
chr2:38916801
|
C | CTT | 11 | a0001c0001t0003g0209a0001c0001t0004g0208a0001c0001t0004g0263others(8): Show | 11 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.-85-2547_-85-2546d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38916801 | |||||
chr2:38916875
|
ACTGCAAC others(2): Show |
A | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-85-2483_-85-2475d others(11): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38916875 | |||||
chr2:38916950
|
G | A | 4 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0004g0261others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-2413G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916950 | ||||||
chr2:38916957
|
C | T | 12 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0004g0211others(9): Show | 13 | HG01361.hp2 HG02280.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.-85-2406C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916957 | ||||||
chr2:38916958
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-85-2405G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916958 | ||||||
chr2:38916967
|
A | C | 22 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0003g0220others(19): Show | 22 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-85-2396A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916967 | ||||||
chr2:38917102
|
C | CTTTTTTT others(4): Show |
11 | a0001c0001t0003g0209a0001c0001t0004g0263a0001c0001t0004g0264others(8): Show | 11 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.-85-2254_-85-2253i others(13): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917102 | |||||
chr2:38917102
|
C | CTTTTTTT others(5): Show |
12 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0004g0208others(9): Show | 13 | HG01361.hp2 HG01993.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-85-2254_-85-2253i others(14): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917102 | |||||
chr2:38917102
|
C | CTTTTTTT others(6): Show |
37 | a0001c0001t0001g0112a0001c0001t0002g0222a0001c0001t0002g0223others(34): Show | 37 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.-85-2254_-85-2253i others(15): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917102 | |||||
chr2:38917102
|
C | CTTTTTTT others(7): Show |
146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(143): Show | 149 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.-85-2254_-85-2253i others(16): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917102 | |||||
chr2:38917102
|
C | CTTTTTTT others(8): Show |
6 | a0001c0001t0001g0101a0001c0001t0001g0114a0001c0001t0001g0202others(3): Show | 6 | HG01109.hp1 HG03209.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-2254_-85-2253i others(17): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917102 | |||||
chr2:38917102
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0005g0010 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-85-2254_-85-2253i others(18): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917102 | |||||
chr2:38917389
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0157 | 2 | HG01192.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-85-1974G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38917389 | ||||||
chr2:38917433
|
T | C | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-85-1930T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38917433 | ||||||
chr2:38917552
|
A | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0156a0001c0001t0005g0155 | 3 | HG03041.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-85-1811A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38917552 | ||||||
chr2:38917686
|
A | C | 2 | a0002c0002t0005g0067a0002c0002t0005g0068 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-85-1677A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38917686 | ||||||
chr2:38917828
|
C | CA | 8 | a0001c0001t0001g0123a0001c0001t0001g0130a0001c0001t0001g0157others(5): Show | 8 | HG01192.hp1 HG01978.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.-85-1516dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917828 | |||||
chr2:38917828
|
CA | C | 7 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0002g0223others(4): Show | 7 | HG01243.hp2 HG01361.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-1516delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917828 | |||||
chr2:38918065
|
G | A | 10 | a0001c0001t0004g0208a0001c0001t0004g0263a0001c0001t0004g0264others(7): Show | 10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85-1298G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918065 | ||||||
chr2:38918078
|
T | C | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-85-1285T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918078 | ||||||
chr2:38918145
|
T | C | 12 | a0001c0001t0003g0209a0001c0001t0004g0208a0001c0001t0004g0263others(9): Show | 12 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85-1218T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918145 | ||||||
chr2:38918193
|
C | T | 3 | a0001c0001t0004g0211a0001c0001t0004g0212a0001c0001t0010g0213 | 3 | HG01361.hp2 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-85-1170C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918193 | ||||||
chr2:38918372
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-85-991G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918372 | ||||||
chr2:38918643
|
C | T | 44 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0269others(41): Show | 45 | HG01106.hp2 HG01243.hp2 HG01361.hp2 others(42): Show |
intron_variant | MODIFIER | c.-85-720C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918643 | ||||||
chr2:38918877
|
C | CA | 48 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0137others(45): Show | 49 | HG00609.hp2 HG00741.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.-85-468dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38918877 | |||||
chr2:38918877
|
C | CAA | 9 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(6): Show | 9 | HG01361.hp2 HG01433.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-85-469_-85-468dup others(2): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38918877 | |||||
chr2:38918984
|
G | A | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-85-379G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918984 | ||||||
chr2:38919166
|
T | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0138 | 2 | HG01943.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-85-197T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38919166 | ||||||
chr2:38919167
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0138 | 2 | HG01943.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-85-196G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38919167 | ||||||
chr2:38919259
|
A | T | 1 | a0001c0001t0003g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-85-104A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38919259 | ||||||
chr2:38919309
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-85-54C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38919309 | ||||||
chr2:38919348
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-85-15G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38919348 | ||||||
chr2:38919349
|
A | C | 10 | a0001c0001t0014g0094a0002c0002t0001g0089a0002c0002t0001g0174others(7): Show | 10 | HG00597.hp2 HG02165.hp2 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85-14A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38919349 | ||||||
chr2:38919599
|
T | C | 8 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+127T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38919599 | ||||||
chr2:38919830
|
A | G | 40 | a0001c0001t0001g0079a0001c0001t0001g0178a0001c0001t0001g0183others(37): Show | 40 | HG00597.hp2 HG01123.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.25+358A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38919830 | ||||||
chr2:38920109
|
C | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(205): Show | 212 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.25+637C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920109 | ||||||
chr2:38920175
|
C | T | 2 | a0001c0001t0003g0209a0007c0011t0016g0210 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.25+703C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920175 | ||||||
chr2:38920199
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.25+727A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920199 | ||||||
chr2:38920398
|
C | CT | 9 | a0001c0001t0002g0007a0001c0001t0002g0020a0001c0001t0002g0023others(6): Show | 9 | HG00741.hp2 HG01106.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-950dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 38920398 | |||||
chr2:38920398
|
CT | C | 7 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0002g0053others(4): Show | 7 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-950delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 38920398 | |||||
chr2:38920398
|
CTT | C | 21 | a0001c0001t0001g0079a0001c0001t0001g0103a0001c0001t0001g0121others(18): Show | 21 | HG01123.hp1 HG01361.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+951_26-950delTT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 38920398 | |||||
chr2:38920398
|
CTTT | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(167): Show | 173 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.25+950_26-950delTT others(1): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 38920398 | |||||
chr2:38920398
|
CTTTT | C | 9 | a0001c0001t0001g0140a0001c0001t0001g0156a0001c0001t0002g0269others(6): Show | 10 | HG01257.hp1 HG01258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+949_26-950delTT others(2): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 38920398 | |||||
chr2:38920499
|
C | T | 3 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0062 | 3 | HG03654.hp1 HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.26-875C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920499 | ||||||
chr2:38920510
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18945.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.26-864C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920510 | ||||||
chr2:38920820
|
C | T | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.26-554C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920820 | ||||||
chr2:38920832
|
C | CT | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.26-538dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 38920832 | |||||
chr2:38920964
|
G | A | 2 | a0002c0002t0001g0175a0002c0002t0001g0177 | 2 | HG00597.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.26-410G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920964 | ||||||
chr2:38921143
|
G | A | 3 | a0001c0001t0002g0223a0001c0001t0003g0227a0001c0001t0003g0237 | 3 | HG01243.hp2 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.26-231G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38921143 | ||||||
chr2:38921252
|
G | A | 39 | a0001c0001t0001g0079a0001c0001t0001g0178a0001c0001t0001g0183others(36): Show | 39 | HG00597.hp2 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.26-122G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38921252 | ||||||
chr2:38922017
|
A | G | 1 | a0001c0001t0002g0016 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.75+594A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922017 | ||||||
chr2:38922075
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75+652A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922075 | ||||||
chr2:38922077
|
T | G | 1 | a0001c0001t0001g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.75+654T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922077 | ||||||
chr2:38922148
|
T | C | 12 | a0001c0001t0003g0209a0001c0001t0004g0208a0001c0001t0004g0263others(9): Show | 12 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+725T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922148 | ||||||
chr2:38922266
|
C | A | 34 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0003g0220others(31): Show | 34 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+843C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922266 | ||||||
chr2:38922342
|
G | T | 34 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0003g0220others(31): Show | 34 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+919G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922342 | ||||||
chr2:38922430
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.75+1007A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922430 | ||||||
chr2:38922637
|
T | G | 2 | a0001c0003t0002g0271a0001c0003t0002g0272 | 2 | NA18991.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.75+1214T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922637 | ||||||
chr2:38922642
|
C | T | 11 | a0001c0001t0003g0209a0001c0001t0004g0263a0001c0001t0004g0264others(8): Show | 11 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+1219C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922642 | ||||||
chr2:38922754
|
C | T | 8 | a0001c0001t0001g0178a0001c0001t0001g0195a0002c0002t0001g0096others(5): Show | 8 | NA18942.hp1 NA18953.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+1331C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922754 | ||||||
chr2:38922770
|
A | C | 12 | a0001c0001t0003g0209a0001c0001t0004g0208a0001c0001t0004g0263others(9): Show | 12 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+1347A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922770 | ||||||
chr2:38922918
|
T | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(202): Show | 209 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.75+1495T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922918 | ||||||
chr2:38922934
|
C | A | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.75+1511C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922934 | ||||||
chr2:38923150
|
A | G | 12 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(9): Show | 12 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+1727A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923150 | ||||||
chr2:38923180
|
A | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0156a0001c0001t0005g0155 | 3 | HG03041.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.75+1757A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923180 | ||||||
chr2:38923410
|
A | T | 1 | a0006c0009t0001g0129 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.75+1987A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923410 | ||||||
chr2:38923484
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(203): Show | 210 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.75+2061T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923484 | ||||||
chr2:38923518
|
T | C | 18 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(15): Show | 18 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+2095T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923518 | ||||||
chr2:38923713
|
A | G | 2 | a0001c0003t0002g0271a0001c0003t0002g0272 | 2 | NA18991.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.75+2290A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923713 | ||||||
chr2:38923760
|
T | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(141): Show | 147 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.75+2337T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923760 | ||||||
chr2:38924048
|
A | T | 1 | a0001c0001t0002g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.75+2625A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924048 | ||||||
chr2:38924053
|
A | C | 1 | a0001c0001t0002g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.75+2630A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924053 | ||||||
chr2:38924056
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.75+2633G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924056 | ||||||
chr2:38924166
|
A | C | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.75+2743A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924166 | ||||||
chr2:38924352
|
C | T | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.75+2929C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924352 | ||||||
chr2:38924691
|
G | C | 15 | a0001c0001t0003g0209a0001c0001t0004g0263a0001c0001t0004g0264others(12): Show | 15 | HG02572.hp2 HG02615.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+3268G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924691 | ||||||
chr2:38924720
|
T | G | 1 | a0002c0002t0001g0176 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.75+3297T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924720 | ||||||
chr2:38924942
|
A | C | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.75+3519A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924942 | ||||||
chr2:38925080
|
AAGAG | A | 6 | a0001c0001t0001g0195a0002c0002t0001g0096a0002c0002t0001g0187others(3): Show | 6 | NA18953.hp1 NA18955.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+3660_75+3663del others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 38925080 | |||||
chr2:38925124
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.75+3701T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925124 | ||||||
chr2:38925389
|
G | C | 33 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0003g0220others(30): Show | 33 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.76-3518G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925389 | ||||||
chr2:38925393
|
A | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(254): Show | 261 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(258): Show |
intron_variant | MODIFIER | c.76-3514A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925393 | ||||||
chr2:38925397
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.76-3510C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925397 | ||||||
chr2:38925518
|
A | G | 6 | a0001c0001t0003g0209a0001c0004t0004g0075a0001c0004t0004g0076others(3): Show | 6 | HG02615.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-3389A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925518 | ||||||
chr2:38925547
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.76-3360G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925547 | ||||||
chr2:38925561
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-3346T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925561 | ||||||
chr2:38925646
|
A | G | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.76-3261A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925646 | ||||||
chr2:38926011
|
C | A | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.76-2896C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38926011 | ||||||
chr2:38926491
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.76-2416G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38926491 | ||||||
chr2:38927101
|
T | C | 16 | a0001c0001t0003g0209a0001c0001t0004g0208a0001c0001t0004g0263others(13): Show | 16 | HG02572.hp2 HG02615.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.76-1806T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927101 | ||||||
chr2:38927124
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.76-1783C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927124 | ||||||
chr2:38927322
|
T | G | 132 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0001g0103others(129): Show | 134 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(131): Show |
intron_variant | MODIFIER | c.76-1585T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927322 | ||||||
chr2:38927418
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.76-1489G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927418 | ||||||
chr2:38927523
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.76-1384C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927523 | ||||||
chr2:38927525
|
G | A | 33 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0003g0220others(30): Show | 33 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.76-1382G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927525 | ||||||
chr2:38927644
|
C | T | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.76-1263C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927644 | ||||||
chr2:38927674
|
C | T | 3 | a0002c0002t0001g0174a0002c0002t0001g0199a0002c0002t0001g0200 | 3 | NA18977.hp1 NA19065.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.76-1233C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927674 | ||||||
chr2:38927791
|
C | T | 6 | a0001c0001t0002g0223a0001c0001t0003g0227a0001c0001t0003g0229others(3): Show | 6 | HG01243.hp2 HG02615.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-1116C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927791 | ||||||
chr2:38927911
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.76-996A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927911 | ||||||
chr2:38927952
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.76-955T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927952 | ||||||
chr2:38927953
|
T | C | 2 | a0001c0001t0002g0269a0001c0001t0009g0005 | 3 | HG02280.hp1 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.76-954T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927953 | ||||||
chr2:38927993
|
C | T | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.76-914C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927993 | ||||||
chr2:38928023
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.76-884C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928023 | ||||||
chr2:38928024
|
G | T | 1 | a0001c0001t0002g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.76-883G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928024 | ||||||
chr2:38928110
|
T | C | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.76-797T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928110 | ||||||
chr2:38928125
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-782A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928125 | ||||||
chr2:38928364
|
T | G | 1 | a0001c0001t0003g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.76-543T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928364 | ||||||
chr2:38928399
|
T | A | 6 | a0001c0001t0004g0208a0001c0004t0004g0075a0001c0004t0004g0076others(3): Show | 6 | HG02615.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-508T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928399 | ||||||
chr2:38928399
|
T | TA | 8 | a0001c0001t0004g0263a0001c0001t0004g0264a0001c0001t0004g0265others(5): Show | 8 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-500dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 38928399 | |||||
chr2:38928565
|
G | A | 9 | a0001c0001t0004g0208a0001c0001t0004g0263a0001c0001t0004g0264others(6): Show | 9 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-342G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928565 | ||||||
chr2:38928591
|
T | A | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.76-316T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928591 | ||||||
chr2:38928684
|
A | AT | 11 | a0001c0001t0003g0209a0001c0001t0004g0208a0001c0001t0004g0263others(8): Show | 11 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-220dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 38928684 | |||||
chr2:38928855
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.76-52C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928855 | ||||||
chr2:38929196
|
C | T | 9 | a0001c0001t0004g0263a0001c0001t0004g0264a0001c0001t0004g0265others(6): Show | 9 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+125C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | chr2 | 38929196 | ||||||
chr2:38929257
|
C | T | 1 | a0001c0001t0002g0016 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.240+186C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | chr2 | 38929257 | ||||||
chr2:38929283
|
G | T | 1 | a0001c0001t0003g0230 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.240+212G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | chr2 | 38929283 | ||||||
chr2:38929301
|
C | T | 1 | a0002c0002t0001g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.240+230C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | chr2 | 38929301 | ||||||
chr2:38929591
|
C | CTCAT | 10 | a0001c0001t0004g0208a0001c0001t0004g0263a0001c0001t0004g0264others(7): Show | 10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-98_241-95dupTT others(2): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 38929591 | |||||
chr2:38929665
|
T | C | 3 | a0001c0001t0001g0171a0001c0001t0002g0034a0001c0001t0002g0045 | 3 | HG01099.hp2 HG01516.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.241-44T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | chr2 | 38929665 | ||||||
chr2:38929680
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.241-29G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | chr2 | 38929680 | ||||||
chr2:38929920
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.362+90A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38929920 | ||||||
chr2:38930022
|
A | G | 4 | a0001c0001t0003g0241a0001c0001t0004g0211a0001c0001t0004g0212others(1): Show | 4 | HG01361.hp2 HG02886.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+192A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930022 | ||||||
chr2:38930189
|
T | C | 32 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0003g0220others(29): Show | 32 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.362+359T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930189 | ||||||
chr2:38930234
|
A | G | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.362+404A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930234 | ||||||
chr2:38930392
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.362+562C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930392 | ||||||
chr2:38930393
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.362+563A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930393 | ||||||
chr2:38930446
|
C | G | 3 | a0003c0005t0001g0002a0003c0005t0001g0139a0003c0005t0012g0002 | 3 | HG01257.hp1 HG01258.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.362+616C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930446 | ||||||
chr2:38930495
|
G | A | 1 | a0001c0001t0004g0261 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.363-614G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930495 | ||||||
chr2:38930588
|
C | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.363-521C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930588 | ||||||
chr2:38930951
|
T | C | 1 | a0002c0002t0001g0182 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.363-158T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930951 | ||||||
chr2:38931412
|
A | T | 6 | a0001c0001t0001g0195a0002c0002t0001g0096a0002c0002t0001g0187others(3): Show | 6 | NA18953.hp1 NA18955.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.505+161A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38931412 | ||||||
chr2:38931439
|
A | AT | 8 | a0001c0001t0001g0112a0001c0001t0001g0152a0001c0001t0001g0153others(5): Show | 8 | HG02723.hp2 HG03471.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.505+198dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38931439 | |||||
chr2:38931461
|
G | A | 7 | a0001c0001t0001g0134a0001c0001t0001g0142a0001c0001t0001g0143others(4): Show | 7 | HG00558.hp2 HG02165.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.505+210G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38931461 | ||||||
chr2:38931605
|
C | G | 13 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(10): Show | 13 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.505+354C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38931605 | ||||||
chr2:38931809
|
CTTTGTAT others(11): Show |
C | 1 | a0001c0001t0004g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.505+560_505+577del others(18): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38931809 | |||||
chr2:38932191
|
C | T | 1 | a0002c0002t0001g0082 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.505+940C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38932191 | ||||||
chr2:38932442
|
AT | A | 125 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0002g0004others(122): Show | 127 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(124): Show |
intron_variant | MODIFIER | c.505+1201delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38932442 | |||||
chr2:38932443
|
T | G | 2 | a0001c0001t0003g0209a0007c0011t0016g0210 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.505+1192T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38932443 | ||||||
chr2:38932444
|
T | G | 10 | a0001c0001t0004g0208a0001c0001t0004g0263a0001c0001t0004g0264others(7): Show | 10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.505+1193T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38932444 | ||||||
chr2:38932457
|
A | G | 1 | a0002c0002t0001g0192 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.505+1206A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38932457 | ||||||
chr2:38932475
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0133 | 2 | HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.505+1224G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38932475 | ||||||
chr2:38932626
|
T | G | 1 | a0001c0014t0002g0056 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.505+1375T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38932626 | ||||||
chr2:38933382
|
G | GT | 9 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0002g0055others(6): Show | 9 | HG02615.hp1 NA18949.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.505+2141dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38933382 | |||||
chr2:38933447
|
G | T | 12 | a0001c0001t0003g0209a0001c0001t0004g0208a0001c0001t0004g0263others(9): Show | 12 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.505+2196G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933447 | ||||||
chr2:38933453
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.505+2202G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933453 | ||||||
chr2:38933488
|
G | A | 124 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0002g0004others(121): Show | 126 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(123): Show |
intron_variant | MODIFIER | c.505+2237G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933488 | ||||||
chr2:38933709
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18945.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.506-2066A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933709 | ||||||
chr2:38933890
|
C | T | 13 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0003g0220others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.506-1885C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933890 | ||||||
chr2:38933944
|
A | T | 1 | a0006c0009t0001g0129 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.506-1831A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933944 | ||||||
chr2:38933996
|
T | C | 3 | a0001c0001t0003g0209a0005c0008t0004g0214a0007c0011t0016g0210 | 3 | HG02723.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.506-1779T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933996 | ||||||
chr2:38934047
|
T | C | 3 | a0001c0001t0002g0036a0001c0001t0003g0209a0007c0011t0016g0210 | 3 | HG01256.hp1 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.506-1728T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934047 | ||||||
chr2:38934063
|
T | C | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.506-1712T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934063 | ||||||
chr2:38934095
|
G | A | 1 | a0002c0002t0001g0176 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.506-1680G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934095 | ||||||
chr2:38934109
|
A | T | 10 | a0001c0001t0004g0208a0001c0001t0004g0263a0001c0001t0004g0264others(7): Show | 10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.506-1666A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934109 | ||||||
chr2:38934222
|
T | A | 2 | a0001c0001t0003g0209a0007c0011t0016g0210 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.506-1553T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934222 | ||||||
chr2:38934447
|
A | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(269): Show | 277 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(274): Show |
intron_variant | MODIFIER | c.506-1328A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934447 | ||||||
chr2:38934449
|
C | T | 1 | a0002c0002t0001g0192 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.506-1326C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934449 | ||||||
chr2:38934497
|
A | ATCCCTCC others(12): Show |
7 | a0001c0001t0004g0211a0001c0001t0004g0212a0001c0001t0004g0259others(4): Show | 7 | HG01361.hp2 HG02818.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.506-1246_506-1228d others(21): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934497 | |||||
chr2:38934497
|
ATCCCTCC others(12): Show |
A | 19 | a0001c0001t0003g0240a0001c0001t0003g0242a0001c0001t0003g0243others(16): Show | 19 | HG01106.hp2 HG01884.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.506-1246_506-1228d others(21): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934497 | |||||
chr2:38934515
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0133 | 2 | HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.506-1260C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934515 | ||||||
chr2:38934537
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0158 | 2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.506-1238C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934537 | ||||||
chr2:38934548
|
T | C | 10 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0003g0241others(7): Show | 11 | HG02280.hp1 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.506-1227T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934548 | ||||||
chr2:38934556
|
T | C | 10 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0003g0241others(7): Show | 11 | HG02280.hp1 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.506-1219T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934556 | ||||||
chr2:38934557
|
C | CCTCCCCC others(42): Show |
9 | a0001c0001t0002g0269a0001c0001t0003g0241a0001c0001t0009g0005others(6): Show | 10 | HG02280.hp1 HG02615.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.506-1213_506-1212i others(51): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934557 | |||||
chr2:38934557
|
C | CCTCCCCC others(102): Show |
1 | a0001c0001t0002g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.506-1213_506-1212i others(111): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934557 | |||||
chr2:38934557
|
C | CCTCCCGC others(24): Show |
7 | a0001c0001t0002g0023a0001c0001t0002g0062a0001c0001t0002g0223others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.506-1191_506-1190i others(33): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934557 | |||||
chr2:38934557
|
C | CCTCCCGC others(23): Show |
89 | a0001c0001t0001g0066a0001c0001t0001g0090a0001c0001t0001g0091others(86): Show | 90 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(87): Show |
intron_variant | MODIFIER | c.506-1122_506-1093d others(32): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934557 | |||||
chr2:38934557
|
CCTCCCGC others(23): Show |
C | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0003t0015g0173 | 3 | HG01069.hp1 HG01361.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.506-1122_506-1093d others(32): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934557 | |||||
chr2:38934578
|
T | TCCCCCCC others(25): Show |
1 | a0001c0001t0003g0246 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.506-1191_506-1190i others(34): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934578 | |||||
chr2:38934589
|
T | TCCCGCTT others(24): Show |
1 | a0001c0001t0002g0069 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.506-1183_506-1153d others(33): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934589 | |||||
chr2:38934608
|
T | TCCCCCCT others(24): Show |
3 | a0001c0001t0002g0007a0001c0001t0002g0232a0001c0014t0002g0056 | 3 | HG02055.hp2 HG02809.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.506-1161_506-1131d others(33): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934608 | |||||
chr2:38934638
|
T | TCCCCCCT others(24): Show |
1 | a0001c0001t0002g0006 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.506-1131_506-1101d others(33): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934638 | |||||
chr2:38934653
|
G | A | 7 | a0001c0001t0004g0208a0001c0001t0004g0263a0001c0001t0004g0264others(4): Show | 7 | NA18949.hp1 NA18961.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.506-1122G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934653 | ||||||
chr2:38934857
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.506-918T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934857 | ||||||
chr2:38934951
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.506-824A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934951 | ||||||
chr2:38934959
|
G | A | 2 | a0002c0002t0005g0067a0002c0002t0005g0068 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.506-816G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934959 | ||||||
chr2:38935003
|
C | T | 68 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0002g0004others(65): Show | 69 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.506-772C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935003 | ||||||
chr2:38935011
|
A | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.506-764A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935011 | ||||||
chr2:38935048
|
T | TA | 70 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0001g0101others(67): Show | 71 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.506-712dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38935048 | |||||
chr2:38935048
|
TA | T | 14 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(11): Show | 14 | HG01433.hp1 HG02572.hp2 HG03225.hp1 others(11): Show |
intron_variant | MODIFIER | c.506-712delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38935048 | |||||
chr2:38935076
|
A | C | 2 | a0001c0001t0003g0209a0007c0011t0016g0210 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.506-699A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935076 | ||||||
chr2:38935149
|
C | T | 68 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0002g0004others(65): Show | 69 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.506-626C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935149 | ||||||
chr2:38935245
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.506-530A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935245 | ||||||
chr2:38935296
|
T | C | 1 | a0001c0001t0002g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.506-479T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935296 | ||||||
chr2:38935342
|
G | A | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.506-433G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935342 | ||||||
chr2:38935644
|
CT | C | 69 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0002g0004others(66): Show | 70 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.506-123delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38935644 | |||||
chr2:38935676
|
C | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.506-99C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935676 | ||||||
chr2:38935691
|
C | G | 12 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(9): Show | 12 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.506-84C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935691 | ||||||
chr2:38936019
|
G | A | 3 | a0001c0001t0004g0211a0001c0001t0004g0212a0001c0001t0010g0213 | 3 | HG01361.hp2 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.565+185G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936019 | ||||||
chr2:38936036
|
G | A | 10 | a0001c0001t0004g0208a0001c0001t0004g0263a0001c0001t0004g0264others(7): Show | 10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+202G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936036 | ||||||
chr2:38936068
|
T | C | 141 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0083others(138): Show | 143 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(140): Show |
intron_variant | MODIFIER | c.565+234T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936068 | ||||||
chr2:38936069
|
T | C | 16 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(13): Show | 16 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+235T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936069 | ||||||
chr2:38936092
|
A | G | 1 | a0002c0002t0001g0191 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.565+258A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936092 | ||||||
chr2:38936184
|
C | G | 68 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0002g0004others(65): Show | 69 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.565+350C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936184 | ||||||
chr2:38936184
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.565+350C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936184 | ||||||
chr2:38936188
|
C | G | 1 | a0002c0002t0001g0190 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.565+354C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936188 | ||||||
chr2:38936199
|
G | A | 5 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0009g0005others(2): Show | 6 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+365G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936199 | ||||||
chr2:38936378
|
C | T | 10 | a0001c0001t0004g0208a0001c0001t0004g0263a0001c0001t0004g0264others(7): Show | 10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+544C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936378 | ||||||
chr2:38936489
|
A | G | 10 | a0001c0001t0004g0208a0001c0001t0004g0263a0001c0001t0004g0264others(7): Show | 10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+655A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936489 | ||||||
chr2:38936646
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.566-689G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936646 | ||||||
chr2:38936650
|
A | G | 3 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0062 | 3 | HG03654.hp1 HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.566-685A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936650 | ||||||
chr2:38936697
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0127 | 2 | NA19070.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.566-638C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936697 | ||||||
chr2:38936716
|
C | G | 15 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(12): Show | 15 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-619C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936716 | ||||||
chr2:38936860
|
C | G | 1 | a0001c0001t0002g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.566-475C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936860 | ||||||
chr2:38936875
|
C | G | 12 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0103others(9): Show | 12 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-460C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936875 | ||||||
chr2:38936989
|
G | A | 12 | a0001c0001t0002g0223a0001c0001t0003g0220a0001c0001t0003g0221others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-346G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936989 | ||||||
chr2:38936997
|
C | CT | 8 | a0001c0001t0001g0079a0001c0001t0002g0055a0001c0001t0003g0230others(5): Show | 8 | HG00741.hp2 HG02572.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-323dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 38936997 | |||||
chr2:38936997
|
CT | C | 6 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0009g0005others(3): Show | 7 | HG00738.hp1 HG02280.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-323delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 38936997 | |||||
chr2:38937051
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(219): Show | 226 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(223): Show |
intron_variant | MODIFIER | c.566-284A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937051 | ||||||
chr2:38937055
|
G | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(219): Show | 226 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(223): Show |
intron_variant | MODIFIER | c.566-280G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937055 | ||||||
chr2:38937056
|
G | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(219): Show | 226 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(223): Show |
intron_variant | MODIFIER | c.566-279G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937056 | ||||||
chr2:38937058
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(217): Show | 224 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(221): Show |
intron_variant | MODIFIER | c.566-277G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937058 | ||||||
chr2:38937074
|
A | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(213): Show | 220 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(217): Show |
intron_variant | MODIFIER | c.566-261A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937074 | ||||||
chr2:38937075
|
A | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(213): Show | 220 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(217): Show |
intron_variant | MODIFIER | c.566-260A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937075 | ||||||
chr2:38937087
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(221): Show | 228 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.566-248T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937087 | ||||||
chr2:38937089
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(221): Show | 228 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.566-246G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937089 | ||||||
chr2:38937098
|
G | C | 134 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0083others(131): Show | 136 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(133): Show |
intron_variant | MODIFIER | c.566-237G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937098 | ||||||
chr2:38937112
|
A | G | 2 | a0001c0001t0003g0229a0001c0001t0003g0248 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.566-223A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937112 | ||||||
chr2:38937151
|
C | T | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.566-184C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937151 | ||||||
chr2:38937187
|
G | C | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.566-148G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937187 | ||||||
chr2:38937208
|
A | G | 12 | a0001c0001t0003g0209a0001c0001t0003g0249a0001c0001t0006g0239others(9): Show | 12 | HG01106.hp2 HG01993.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-127A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937208 | ||||||
chr2:38937324
|
C | A | 43 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0092others(40): Show | 44 | HG01070.hp2 HG01106.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-11C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937324 | ||||||
chr2:38937643
|
C | A | 2 | a0001c0001t0003g0248a0007c0011t0016g0210 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.790+84C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38937643 | ||||||
chr2:38937694
|
A | C | 3 | a0002c0002t0001g0174a0002c0002t0001g0199a0002c0002t0001g0200 | 3 | NA18977.hp1 NA19065.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.790+135A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38937694 | ||||||
chr2:38937913
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(119): Show | 124 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.790+354C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38937913 | ||||||
chr2:38938028
|
G | T | 1 | a0001c0001t0001g0188 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.790+469G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938028 | ||||||
chr2:38938046
|
A | G | 52 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0123others(49): Show | 52 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(49): Show |
intron_variant | MODIFIER | c.790+487A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938046 | ||||||
chr2:38938070
|
A | G | 1 | a0001c0001t0001g0003 | 2 | HG00738.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.790+511A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938070 | ||||||
chr2:38938206
|
G | C | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.790+647G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938206 | ||||||
chr2:38938216
|
A | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(237): Show | 245 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(242): Show |
intron_variant | MODIFIER | c.790+657A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938216 | ||||||
chr2:38938332
|
G | T | 1 | a0001c0001t0004g0211 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.790+773G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938332 | ||||||
chr2:38938357
|
G | A | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.790+798G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938357 | ||||||
chr2:38938377
|
A | G | 9 | a0001c0001t0002g0222a0001c0001t0003g0209a0001c0001t0003g0240others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.790+818A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938377 | ||||||
chr2:38938425
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 8 | HG00738.hp2 HG01099.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.790+866G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938425 | ||||||
chr2:38938597
|
C | T | 2 | a0001c0003t0002g0271a0001c0003t0002g0272 | 2 | NA18991.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.790+1038C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938597 | ||||||
chr2:38938599
|
T | C | 1 | a0002c0002t0001g0194 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.790+1040T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938599 | ||||||
chr2:38938646
|
A | G | 1 | a0001c0001t0002g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.790+1087A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938646 | ||||||
chr2:38938676
|
A | T | 1 | a0002c0002t0001g0080 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.790+1117A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938676 | ||||||
chr2:38938878
|
A | T | 1 | a0001c0001t0001g0203 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.790+1319A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938878 | ||||||
chr2:38939032
|
T | G | 4 | a0001c0001t0002g0269a0001c0001t0009g0005a0005c0008t0004g0214others(1): Show | 5 | HG02280.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.790+1473T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939032 | ||||||
chr2:38939061
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.790+1502C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939061 | ||||||
chr2:38939071
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.790+1512C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939071 | ||||||
chr2:38939118
|
G | A | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.790+1559G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939118 | ||||||
chr2:38939134
|
G | T | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.790+1575G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939134 | ||||||
chr2:38939435
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(219): Show | 227 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(224): Show |
intron_variant | MODIFIER | c.790+1876T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939435 | ||||||
chr2:38939478
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.790+1919T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939478 | ||||||
chr2:38939606
|
C | G | 2 | a0001c0001t0001g0103a0001c0001t0010g0213 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.790+2047C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939606 | ||||||
chr2:38939612
|
A | G | 4 | a0001c0001t0002g0269a0001c0001t0009g0005a0005c0008t0004g0214others(1): Show | 5 | HG02280.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.790+2053A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939612 | ||||||
chr2:38939933
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.790+2374G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939933 | ||||||
chr2:38940067
|
C | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.790+2508C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38940067 | ||||||
chr2:38940190
|
A | G | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.790+2631A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38940190 | ||||||
chr2:38940195
|
G | A | 4 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0004g0261others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.790+2636G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38940195 | ||||||
chr2:38940391
|
G | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.790+2832G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38940391 | ||||||
chr2:38940431
|
CT | C | 6 | a0001c0001t0001g0115a0001c0001t0002g0008a0001c0001t0003g0224others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.790+2887delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38940431 | |||||
chr2:38940687
|
C | T | 2 | a0001c0001t0003g0220a0001c0001t0003g0224 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.790+3128C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38940687 | ||||||
chr2:38940868
|
A | G | 1 | a0002c0002t0004g0206 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.791-3033A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38940868 | ||||||
chr2:38941015
|
C | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 8 | HG00738.hp2 HG01099.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.791-2886C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941015 | ||||||
chr2:38941201
|
T | C | 5 | a0001c0001t0002g0037a0001c0001t0007g0032a0001c0001t0007g0038others(2): Show | 5 | HG00741.hp2 HG01081.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.791-2700T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941201 | ||||||
chr2:38941412
|
A | G | 4 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0004g0261others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.791-2489A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941412 | ||||||
chr2:38941552
|
C | CT | 7 | a0001c0001t0002g0028a0001c0001t0003g0241a0001c0001t0004g0266others(4): Show | 7 | HG01978.hp1 HG02572.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.791-2336dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38941552 | |||||
chr2:38941673
|
G | T | 2 | a0001c0001t0002g0021a0001c0001t0003g0238 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.791-2228G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941673 | ||||||
chr2:38941846
|
G | A | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.791-2055G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941846 | ||||||
chr2:38941894
|
G | A | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.791-2007G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941894 | ||||||
chr2:38941947
|
T | C | 11 | a0001c0001t0002g0004a0001c0001t0002g0084a0001c0001t0002g0215others(8): Show | 12 | HG01496.hp1 HG02109.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-1954T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941947 | ||||||
chr2:38942005
|
AT | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(8): Show | 12 | HG00738.hp2 HG01099.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.791-1882delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942005 | |||||
chr2:38942005
|
ATT | A | 6 | a0001c0001t0002g0270a0001c0001t0004g0208a0001c0001t0004g0259others(3): Show | 6 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.791-1883_791-1882d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942005 | |||||
chr2:38942005
|
ATTT | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(203): Show | 209 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.791-1884_791-1882d others(5): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942005 | |||||
chr2:38942131
|
C | G | 3 | a0001c0001t0002g0269a0001c0001t0009g0005a0005c0008t0004g0214 | 4 | HG02280.hp1 HG02818.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.791-1770C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942131 | ||||||
chr2:38942140
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.791-1761T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942140 | ||||||
chr2:38942164
|
CT | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0072others(115): Show | 120 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.791-1717delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942164 | |||||
chr2:38942164
|
CTT | C | 36 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0002g0024others(33): Show | 36 | HG01106.hp2 HG01243.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.791-1718_791-1717d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942164 | |||||
chr2:38942212
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.791-1689A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942212 | ||||||
chr2:38942304
|
C | T | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.791-1597C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942304 | ||||||
chr2:38942468
|
C | CT | 17 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0124others(14): Show | 17 | HG01167.hp1 HG01169.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.791-1416dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942468 | |||||
chr2:38942468
|
C | CTT | 102 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(99): Show | 104 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.791-1417_791-1416d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942468 | |||||
chr2:38942468
|
C | CTTT | 50 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(47): Show | 51 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.791-1418_791-1416d others(5): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942468 | |||||
chr2:38942468
|
CT | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0103a0001c0001t0001g0114others(48): Show | 52 | HG00738.hp2 HG01099.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.791-1416delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942468 | |||||
chr2:38942468
|
CTT | C | 11 | a0001c0001t0002g0269a0001c0001t0003g0224a0001c0001t0003g0241others(8): Show | 12 | HG01361.hp2 HG01993.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-1417_791-1416d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942468 | |||||
chr2:38942692
|
C | A | 2 | a0001c0001t0002g0269a0001c0001t0009g0005 | 3 | HG02280.hp1 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.791-1209C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942692 | ||||||
chr2:38942711
|
G | C | 1 | a0001c0001t0004g0266 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.791-1190G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942711 | ||||||
chr2:38942900
|
T | C | 5 | a0001c0001t0004g0264a0001c0001t0004g0265a0001c0003t0004g0204others(2): Show | 5 | NA18963.hp2 NA18988.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.791-1001T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942900 | ||||||
chr2:38943013
|
C | T | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.791-888C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943013 | ||||||
chr2:38943267
|
T | C | 3 | a0001c0001t0001g0103a0001c0003t0002g0271a0001c0003t0002g0272 | 3 | NA18991.hp2 NA19030.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.791-634T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943267 | ||||||
chr2:38943542
|
TG | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(207): Show | 213 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(210): Show |
intron_variant | MODIFIER | c.791-353delG | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38943542 | |||||
chr2:38943612
|
T | G | 4 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0004g0261others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.791-289T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943612 | ||||||
chr2:38943691
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.791-210C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943691 | ||||||
chr2:38943718
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.791-183T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943718 | ||||||
chr2:38943720
|
G | A | 33 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0002g0223others(30): Show | 33 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.791-181G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943720 | ||||||
chr2:38943720
|
G | T | 1 | a0001c0001t0002g0217 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.791-181G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943720 | ||||||
chr2:38943751
|
G | C | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.791-150G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943751 | ||||||
chr2:38943791
|
GT | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(157): Show | 163 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.791-100delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38943791 | |||||
chr2:38943817
|
C | A | 11 | a0001c0001t0002g0004a0001c0001t0002g0084a0001c0001t0002g0215others(8): Show | 12 | HG01496.hp1 HG02109.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-84C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943817 | ||||||
chr2:38944123
|
G | A | 2 | a0005c0008t0004g0214a0007c0011t0016g0210 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.920+93G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944123 | ||||||
chr2:38944155
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920+125A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944155 | ||||||
chr2:38944216
|
T | C | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.920+186T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944216 | ||||||
chr2:38944291
|
C | T | 2 | a0001c0001t0003g0209a0001c0001t0003g0240 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920+261C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944291 | ||||||
chr2:38944640
|
C | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(214): Show | 221 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(218): Show |
intron_variant | MODIFIER | c.920+610C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944640 | ||||||
chr2:38944649
|
T | A | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.920+619T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944649 | ||||||
chr2:38944655
|
C | G | 9 | a0001c0001t0004g0208a0001c0001t0004g0264a0001c0001t0004g0265others(6): Show | 9 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.920+625C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944655 | ||||||
chr2:38944876
|
G | GGT | 6 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0003g0230others(3): Show | 6 | HG01109.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.920+870_920+871dup others(2): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38944876 | |||||
chr2:38944876
|
G | GGTGT | 164 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(161): Show | 168 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.920+868_920+871dup others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38944876 | |||||
chr2:38944876
|
G | GGTGTGT | 13 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0002g0007others(10): Show | 13 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.920+866_920+871dup others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38944876 | |||||
chr2:38944876
|
G | GGTGTGTG others(1): Show |
33 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0114others(30): Show | 34 | HG00738.hp2 HG01099.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.920+864_920+871dup others(8): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38944876 | |||||
chr2:38944876
|
G | GGTGTGTG others(3): Show |
10 | a0001c0001t0001g0107a0001c0001t0002g0223a0001c0001t0003g0209others(7): Show | 10 | HG01069.hp1 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+862_920+871dup others(10): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38944876 | |||||
chr2:38944902
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(219): Show | 227 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(224): Show |
intron_variant | MODIFIER | c.920+872C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944902 | ||||||
chr2:38944922
|
C | A | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.920+892C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944922 | ||||||
chr2:38945323
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 10 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+1293A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945323 | ||||||
chr2:38945331
|
G | C | 1 | a0001c0001t0001g0124 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.920+1301G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945331 | ||||||
chr2:38945336
|
G | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(135): Show | 140 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.920+1306G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945336 | ||||||
chr2:38945402
|
A | G | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.920+1372A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945402 | ||||||
chr2:38945456
|
G | A | 1 | a0001c0001t0002g0016 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.920+1426G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945456 | ||||||
chr2:38945587
|
A | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.920+1557A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945587 | ||||||
chr2:38945706
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.920+1676G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945706 | ||||||
chr2:38945971
|
A | G | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.920+1941A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945971 | ||||||
chr2:38946064
|
A | G | 1 | a0001c0001t0002g0021 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.920+2034A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946064 | ||||||
chr2:38946165
|
A | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.920+2135A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946165 | ||||||
chr2:38946169
|
G | A | 2 | a0001c0001t0002g0222a0001c0001t0002g0270 | 2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.920+2139G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946169 | ||||||
chr2:38946253
|
A | G | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.920+2223A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946253 | ||||||
chr2:38946429
|
CCTT | C | 24 | a0001c0001t0001g0120a0001c0001t0002g0025a0001c0001t0002g0027others(21): Show | 24 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.920+2403_920+2405d others(5): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38946429 | |||||
chr2:38946433
|
CT | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0196a0001c0001t0007g0046 | 3 | HG00323.hp1 HG01081.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.920+2409delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38946433 | |||||
chr2:38946456
|
C | T | 1 | a0001c0001t0005g0013 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.920+2426C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946456 | ||||||
chr2:38946481
|
C | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 10 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+2451C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946481 | ||||||
chr2:38946756
|
G | T | 1 | a0001c0001t0001g0178 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.920+2726G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946756 | ||||||
chr2:38946982
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.920+2952T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946982 | ||||||
chr2:38947134
|
A | C | 1 | a0001c0001t0003g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.920+3104A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947134 | ||||||
chr2:38947191
|
A | T | 3 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | HG02717.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.920+3161A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947191 | ||||||
chr2:38947424
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.920+3394G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947424 | ||||||
chr2:38947553
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 10 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.921-3436T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947553 | ||||||
chr2:38947735
|
G | A | 1 | a0001c0001t0003g0243 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.921-3254G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947735 | ||||||
chr2:38947819
|
T | A | 4 | a0002c0002t0001g0176a0002c0002t0001g0180a0002c0002t0001g0185others(1): Show | 4 | HG02602.hp2 HG03710.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-3170T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947819 | ||||||
chr2:38947837
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.921-3152G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947837 | ||||||
chr2:38947841
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.921-3148G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947841 | ||||||
chr2:38948126
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.921-2863G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38948126 | ||||||
chr2:38948359
|
T | A | 2 | a0001c0001t0003g0230a0001c0001t0003g0248 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.921-2630T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38948359 | ||||||
chr2:38948393
|
T | C | 2 | a0001c0001t0002g0222a0001c0001t0002g0270 | 2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.921-2596T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38948393 | ||||||
chr2:38948778
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.921-2211A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38948778 | ||||||
chr2:38948876
|
G | A | 26 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0002g0223others(23): Show | 26 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.921-2113G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38948876 | ||||||
chr2:38949474
|
C | G | 1 | a0001c0001t0003g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.921-1515C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38949474 | ||||||
chr2:38949554
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(166): Show | 172 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.921-1435A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38949554 | ||||||
chr2:38949661
|
T | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 10 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.921-1328T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38949661 | ||||||
chr2:38950179
|
C | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(217): Show | 224 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(221): Show |
intron_variant | MODIFIER | c.921-810C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950179 | ||||||
chr2:38950193
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.921-796G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950193 | ||||||
chr2:38950387
|
C | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | NA18945.hp1 NA18952.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.921-602C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950387 | ||||||
chr2:38950512
|
C | T | 8 | a0001c0001t0004g0264a0001c0001t0004g0265a0001c0001t0004g0266others(5): Show | 8 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.921-477C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950512 | ||||||
chr2:38950631
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0002g0034 | 2 | HG01433.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.921-358G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950631 | ||||||
chr2:38950670
|
G | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0047 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.921-319G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950670 | ||||||
chr2:38950692
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.921-297C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950692 | ||||||
chr2:38950773
|
C | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0127 | 2 | NA19070.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.921-216C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950773 | ||||||
chr2:38950817
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.921-172G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950817 | ||||||
chr2:38950853
|
A | T | 1 | a0001c0001t0004g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.921-136A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950853 | ||||||
chr2:38950904
|
G | C | 1 | a0001c0001t0006g0251 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.921-85G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950904 | ||||||
chr2:38951272
|
T | C | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1053+151T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951272 | ||||||
chr2:38951352
|
G | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(228): Show | 236 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(233): Show |
intron_variant | MODIFIER | c.1053+231G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951352 | ||||||
chr2:38951377
|
A | T | 13 | a0001c0001t0002g0223a0001c0001t0003g0220a0001c0001t0003g0221others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1053+256A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951377 | ||||||
chr2:38951610
|
A | T | 1 | a0001c0001t0002g0021 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1053+489A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951610 | ||||||
chr2:38951640
|
TATATATA others(25): Show |
T | 1 | a0001c0001t0013g0144 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1053+538_1053+569d others(34): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 38951640 | |||||
chr2:38951659
|
A | G | 3 | a0001c0001t0003g0230a0001c0001t0003g0241a0001c0001t0010g0213 | 3 | HG02886.hp2 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1053+538A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951659 | ||||||
chr2:38951713
|
A | G | 34 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0002g0223others(31): Show | 34 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1053+592A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951713 | ||||||
chr2:38951718
|
C | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(165): Show | 171 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.1053+597C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951718 | ||||||
chr2:38951722
|
T | G | 1 | a0001c0001t0001g0178 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1053+601T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951722 | ||||||
chr2:38951743
|
C | CAT | 12 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(9): Show | 13 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1053+632_1053+633d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 38951743 | |||||
chr2:38951819
|
A | T | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1053+698A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951819 | ||||||
chr2:38951868
|
A | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0036 | 2 | HG01074.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1053+747A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951868 | ||||||
chr2:38952120
|
A | T | 1 | a0001c0001t0006g0257 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1053+999A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952120 | ||||||
chr2:38952366
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1054-796T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952366 | ||||||
chr2:38952399
|
A | T | 1 | a0001c0001t0002g0039 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1054-763A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952399 | ||||||
chr2:38952400
|
T | A | 1 | a0001c0001t0002g0039 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1054-762T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952400 | ||||||
chr2:38952408
|
G | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(7): Show | 11 | HG00738.hp2 HG01099.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1054-754G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952408 | ||||||
chr2:38952617
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1054-545C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952617 | ||||||
chr2:38952703
|
A | AT | 17 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(14): Show | 18 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.1054-446dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 38952703 | |||||
chr2:38952887
|
C | T | 37 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0270others(34): Show | 37 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1054-275C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952887 | ||||||
chr2:38952918
|
C | T | 4 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0004g0261others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054-244C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952918 | ||||||
chr2:38952988
|
C | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(165): Show | 171 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.1054-174C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952988 | ||||||
chr2:38953082
|
T | C | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1054-80T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38953082 | ||||||
chr2:38953120
|
G | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(9): Show | 13 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1054-42G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38953120 | ||||||
chr2:38953311
|
A | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0168 | 2 | HG01074.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1137+66A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953311 | ||||||
chr2:38953420
|
C | T | 1 | a0002c0002t0001g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1137+175C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953420 | ||||||
chr2:38953553
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1137+308G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953553 | ||||||
chr2:38953583
|
T | A | 1 | a0001c0001t0003g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1137+338T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953583 | ||||||
chr2:38953655
|
T | C | 14 | a0001c0001t0001g0003a0001c0001t0001g0097a0001c0001t0001g0114others(11): Show | 15 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1137+410T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953655 | ||||||
chr2:38953671
|
C | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01074.hp2 HG01123.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137+426C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953671 | ||||||
chr2:38953853
|
C | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0164others(11): Show | 15 | HG00738.hp2 HG01099.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1138-520C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953853 | ||||||
chr2:38953856
|
T | C | 19 | a0001c0001t0001g0103a0001c0001t0001g0172a0001c0001t0002g0009others(16): Show | 20 | HG01361.hp2 HG02258.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1138-517T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953856 | ||||||
chr2:38953942
|
G | C | 1 | a0001c0001t0006g0257 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1138-431G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953942 | ||||||
chr2:38953954
|
G | T | 3 | a0002c0002t0001g0174a0002c0002t0001g0199a0002c0002t0001g0200 | 3 | NA18977.hp1 NA19065.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1138-419G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953954 | ||||||
chr2:38954223
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1138-150C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38954223 | ||||||
chr2:38954231
|
T | A | 1 | a0001c0001t0014g0094 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1138-142T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38954231 | ||||||
chr2:38954558
|
T | C | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1221+102T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954558 | ||||||
chr2:38954633
|
CT | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(213): Show | 220 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(217): Show |
intron_variant | MODIFIER | c.1221+195delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38954633 | |||||
chr2:38954633
|
CTT | C | 5 | a0001c0001t0002g0217a0001c0001t0003g0231a0001c0001t0005g0014others(2): Show | 5 | HG01167.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221+194_1221+195d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38954633 | |||||
chr2:38954651
|
T | G | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1221+195T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954651 | ||||||
chr2:38954693
|
G | T | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1221+237G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954693 | ||||||
chr2:38954722
|
C | G | 1 | a0001c0001t0002g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1221+266C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954722 | ||||||
chr2:38954726
|
T | C | 3 | a0001c0001t0004g0208a0001c0003t0004g0204a0001c0003t0004g0205 | 3 | NA18949.hp1 NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1221+270T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954726 | ||||||
chr2:38954789
|
A | G | 8 | a0001c0001t0002g0008a0001c0001t0002g0222a0001c0001t0002g0270others(5): Show | 8 | HG01361.hp2 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1221+333A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954789 | ||||||
chr2:38954806
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1221+350G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954806 | ||||||
chr2:38954840
|
G | T | 3 | a0001c0001t0002g0009a0001c0001t0002g0018a0001c0001t0002g0269 | 3 | HG02258.hp1 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1221+384G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954840 | ||||||
chr2:38954880
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(220): Show | 227 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(224): Show |
intron_variant | MODIFIER | c.1221+424C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954880 | ||||||
chr2:38954921
|
G | A | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1221+465G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954921 | ||||||
chr2:38954921
|
G | T | 2 | a0001c0001t0004g0211a0001c0001t0004g0212 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1221+465G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954921 | ||||||
chr2:38955481
|
C | CT | 42 | a0001c0001t0001g0156a0001c0001t0002g0008a0001c0001t0002g0222others(39): Show | 42 | HG01106.hp2 HG01243.hp2 HG01361.hp2 others(39): Show |
intron_variant | MODIFIER | c.1221+1050dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38955481 | |||||
chr2:38955481
|
C | CTT | 22 | a0001c0001t0001g0072a0001c0001t0001g0097a0001c0001t0001g0104others(19): Show | 23 | HG00323.hp2 HG01167.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.1221+1049_1221+105 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38955481 | |||||
chr2:38955481
|
C | CTTT | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(138): Show | 145 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.1221+1048_1221+105 others(7): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38955481 | |||||
chr2:38955481
|
C | CTTTT | 20 | a0001c0001t0001g0098a0001c0001t0001g0119a0001c0001t0001g0121others(17): Show | 20 | HG01074.hp2 HG01099.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1221+1047_1221+105 others(8): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38955481 | |||||
chr2:38955530
|
T | C | 1 | a0001c0001t0002g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1221+1074T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955530 | ||||||
chr2:38955625
|
G | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(160): Show | 166 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.1221+1169G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955625 | ||||||
chr2:38955645
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(231): Show | 239 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(236): Show |
intron_variant | MODIFIER | c.1221+1189A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955645 | ||||||
chr2:38955716
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0156a0001c0001t0002g0084others(2): Show | 5 | HG02109.hp1 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222-1183G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955716 | ||||||
chr2:38955749
|
T | G | 2 | a0001c0003t0004g0204a0001c0003t0004g0205 | 2 | NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1222-1150T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955749 | ||||||
chr2:38955830
|
C | T | 1 | a0001c0001t0003g0249 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1222-1069C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955830 | ||||||
chr2:38955942
|
G | T | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1222-957G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955942 | ||||||
chr2:38956131
|
AAC | A | 4 | a0001c0001t0002g0025a0001c0001t0002g0031a0001c0001t0002g0048others(1): Show | 4 | HG00735.hp1 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222-763_1222-762d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38956131 | |||||
chr2:38956141
|
G | A | 2 | a0001c0003t0004g0204a0001c0003t0004g0205 | 2 | NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1222-758G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38956141 | ||||||
chr2:38956272
|
A | G | 1 | a0002c0002t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1222-627A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38956272 | ||||||
chr2:38956488
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1222-411C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38956488 | ||||||
chr2:38956877
|
C | T | 1 | a0002c0002t0001g0194 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1222-22C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38956877 | ||||||
chr2:38956886
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1222-13C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38956886 | ||||||
chr2:38957147
|
G | A | 1 | a0002c0002t0001g0181 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1370+100G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957147 | ||||||
chr2:38957215
|
C | T | 7 | a0001c0003t0004g0204a0001c0003t0004g0205a0001c0003t0015g0173others(4): Show | 7 | HG02615.hp2 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1370+168C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957215 | ||||||
chr2:38957225
|
A | G | 6 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0116others(3): Show | 6 | HG00597.hp1 HG03834.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1370+178A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957225 | ||||||
chr2:38957368
|
T | C | 1 | a0011c0007t0001g0170 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1370+321T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957368 | ||||||
chr2:38957406
|
C | G | 11 | a0001c0001t0006g0239a0001c0001t0006g0250a0001c0001t0006g0251others(8): Show | 11 | HG01106.hp2 HG01993.hp2 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1370+359C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957406 | ||||||
chr2:38957443
|
T | C | 2 | a0001c0001t0009g0005a0005c0008t0004g0214 | 3 | HG02280.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1370+396T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957443 | ||||||
chr2:38957451
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1370+404G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957451 | ||||||
chr2:38957610
|
A | C | 9 | a0001c0001t0001g0103a0001c0001t0002g0008a0001c0001t0002g0222others(6): Show | 9 | HG01361.hp2 HG02572.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1371-424A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957610 | ||||||
chr2:38957773
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1371-261A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957773 | ||||||
chr2:38957808
|
C | G | 1 | a0001c0001t0002g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1371-226C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957808 | ||||||
chr2:38957823
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0072a0001c0001t0001g0074others(90): Show | 95 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1371-211A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957823 | ||||||
chr2:38957838
|
A | G | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1371-196A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957838 | ||||||
chr2:38957907
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(222): Show | 229 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(226): Show |
intron_variant | MODIFIER | c.1371-127C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957907 | ||||||
chr2:38957973
|
T | C | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1371-61T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957973 | ||||||
chr2:38957987
|
C | T | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1371-47C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957987 | ||||||
chr2:38958215
|
G | T | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1535+17G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38958215 | ||||||
chr2:38958248
|
A | G | 33 | a0001c0001t0002g0223a0001c0001t0002g0234a0001c0001t0003g0209others(30): Show | 33 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1535+50A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38958248 | ||||||
chr2:38958672
|
G | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(162): Show | 168 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.1535+474G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38958672 | ||||||
chr2:38958714
|
AT | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(222): Show | 229 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(226): Show |
intron_variant | MODIFIER | c.1535+525delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 38958714 | |||||
chr2:38958905
|
C | T | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1535+707C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38958905 | ||||||
chr2:38958910
|
A | C | 3 | a0001c0001t0004g0208a0001c0003t0004g0204a0001c0003t0004g0205 | 3 | NA18949.hp1 NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1535+712A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38958910 | ||||||
chr2:38959198
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(222): Show | 229 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(226): Show |
intron_variant | MODIFIER | c.1536-643C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38959198 | ||||||
chr2:38959392
|
C | T | 2 | a0001c0001t0003g0209a0001c0001t0003g0240 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1536-449C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38959392 | ||||||
chr2:38959435
|
T | G | 4 | a0001c0003t0015g0173a0001c0004t0004g0075a0001c0004t0004g0076others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536-406T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38959435 | ||||||
chr2:38959550
|
A | G | 1 | a0010c0010t0005g0063 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1536-291A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38959550 | ||||||
chr2:38959755
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG01069.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1536-86G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38959755 | ||||||
chr2:38960883
|
A | G | 1 | a0001c0001t0017g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2343+235A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38960883 | ||||||
chr2:38960884
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2343+236G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38960884 | ||||||
chr2:38960887
|
C | G | 1 | a0008c0012t0002g0033 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2343+239C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38960887 | ||||||
chr2:38961036
|
C | G | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2343+388C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961036 | ||||||
chr2:38961158
|
G | T | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2343+510G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961158 | ||||||
chr2:38961369
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(225): Show | 233 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(230): Show |
intron_variant | MODIFIER | c.2343+721A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961369 | ||||||
chr2:38961540
|
G | A | 2 | a0001c0003t0004g0204a0001c0003t0004g0205 | 2 | NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2343+892G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961540 | ||||||
chr2:38961543
|
C | T | 1 | a0002c0002t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2343+895C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961543 | ||||||
chr2:38961551
|
C | T | 10 | a0001c0001t0001g0112a0001c0001t0001g0152a0001c0001t0001g0153others(7): Show | 10 | NA18948.hp2 NA18949.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.2343+903C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961551 | ||||||
chr2:38961579
|
A | C | 3 | a0002c0002t0001g0085a0002c0002t0001g0086a0002c0002t0001g0087 | 3 | NA18945.hp2 NA18980.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2343+931A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961579 | ||||||
chr2:38961581
|
A | T | 4 | a0001c0003t0015g0173a0001c0004t0004g0075a0001c0004t0004g0076others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2343+933A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961581 | ||||||
chr2:38961774
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(225): Show | 233 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(230): Show |
intron_variant | MODIFIER | c.2343+1126A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961774 | ||||||
chr2:38961836
|
C | T | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2343+1188C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961836 | ||||||
chr2:38961997
|
C | G | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2343+1349C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961997 | ||||||
chr2:38962176
|
T | G | 1 | a0005c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2343+1528T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962176 | ||||||
chr2:38962421
|
G | C | 1 | a0001c0001t0002g0233 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2343+1773G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962421 | ||||||
chr2:38962495
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(228): Show | 236 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(233): Show |
intron_variant | MODIFIER | c.2343+1847G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962495 | ||||||
chr2:38962637
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2343+1989A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962637 | ||||||
chr2:38962657
|
C | T | 7 | a0002c0002t0001g0096a0002c0002t0001g0182a0002c0002t0001g0187others(4): Show | 7 | NA18942.hp1 NA18953.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.2343+2009C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962657 | ||||||
chr2:38962690
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(225): Show | 233 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(230): Show |
intron_variant | MODIFIER | c.2343+2042A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962690 | ||||||
chr2:38962757
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2343+2109G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962757 | ||||||
chr2:38962825
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(232): Show | 240 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(237): Show |
intron_variant | MODIFIER | c.2343+2177C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962825 | ||||||
chr2:38962849
|
C | CA | 46 | a0001c0001t0001g0123a0001c0001t0002g0021a0001c0001t0002g0222others(43): Show | 47 | HG01071.hp1 HG01243.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.2343+2226dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 38962849 | |||||
chr2:38962849
|
C | CAA | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(148): Show | 155 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.2343+2225_2343+222 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 38962849 | |||||
chr2:38962849
|
C | CAAA | 33 | a0001c0001t0001g0073a0001c0001t0001g0093a0001c0001t0001g0099others(30): Show | 33 | HG00597.hp1 HG00735.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.2343+2224_2343+222 others(7): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 38962849 | |||||
chr2:38962934
|
G | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(222): Show | 229 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(226): Show |
intron_variant | MODIFIER | c.2343+2286G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962934 | ||||||
chr2:38963023
|
CA | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(211): Show | 218 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.2343+2392delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 38963023 | |||||
chr2:38963288
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2343+2640T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963288 | ||||||
chr2:38963355
|
T | C | 1 | a0001c0001t0003g0243 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2344-2651T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963355 | ||||||
chr2:38963569
|
A | G | 9 | a0001c0001t0002g0234a0001c0001t0003g0209a0001c0001t0003g0240others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2344-2437A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963569 | ||||||
chr2:38963712
|
A | G | 3 | a0001c0001t0001g0160a0001c0001t0002g0069a0001c0001t0002g0070 | 3 | NA18948.hp2 NA18964.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.2344-2294A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963712 | ||||||
chr2:38963823
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(207): Show | 214 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.2344-2183C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963823 | ||||||
chr2:38963844
|
C | T | 25 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0224others(22): Show | 25 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.2344-2162C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963844 | ||||||
chr2:38963846
|
G | A | 8 | a0001c0001t0003g0209a0001c0001t0003g0240a0001c0001t0003g0242others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2344-2160G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963846 | ||||||
chr2:38964059
|
G | A | 4 | a0001c0001t0001g0107a0001c0001t0004g0266a0001c0001t0004g0267others(1): Show | 4 | HG01069.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2344-1947G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38964059 | ||||||
chr2:38964144
|
T | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(12): Show | 16 | HG00738.hp2 HG01099.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2344-1862T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38964144 | ||||||
chr2:38964697
|
G | A | 3 | a0001c0001t0002g0029a0001c0001t0002g0035a0001c0001t0002g0036 | 3 | HG01074.hp1 HG01256.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2344-1309G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38964697 | ||||||
chr2:38964837
|
T | C | 3 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0001t0004g0268 | 3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2344-1169T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38964837 | ||||||
chr2:38964849
|
T | A | 2 | a0001c0003t0004g0204a0001c0003t0004g0205 | 2 | NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2344-1157T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38964849 | ||||||
chr2:38965097
|
A | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2344-909A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38965097 | ||||||
chr2:38965241
|
T | G | 1 | a0002c0002t0001g0192 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2344-765T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38965241 | ||||||
chr2:38965590
|
G | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2344-416G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38965590 | ||||||
chr2:38965681
|
A | T | 13 | a0001c0001t0001g0120a0001c0001t0002g0025a0001c0001t0002g0030others(10): Show | 13 | HG00735.hp1 HG00741.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2344-325A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38965681 | ||||||
chr2:38965836
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2344-170C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38965836 | ||||||
chr2:38965964
|
T | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0222a0001c0001t0002g0270others(2): Show | 5 | HG01361.hp2 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2344-42T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38965964 | ||||||
chr2:38966189
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2483+44T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966189 | ||||||
chr2:38966195
|
T | A | 8 | a0001c0001t0002g0008a0001c0001t0002g0222a0001c0001t0002g0270others(5): Show | 8 | HG01361.hp2 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.2483+50T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966195 | ||||||
chr2:38966289
|
G | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0167a0001c0001t0005g0012others(2): Show | 5 | HG01192.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2483+144G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966289 | ||||||
chr2:38966311
|
T | C | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2483+166T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966311 | ||||||
chr2:38966384
|
T | C | 1 | a0001c0001t0002g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2483+239T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966384 | ||||||
chr2:38966540
|
G | A | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2483+395G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966540 | ||||||
chr2:38966596
|
C | A | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2483+451C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966596 | ||||||
chr2:38966606
|
T | A | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2483+461T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966606 | ||||||
chr2:38966613
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2483+468G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966613 | ||||||
chr2:38966690
|
T | C | 1 | a0001c0001t0003g0249 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2483+545T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966690 | ||||||
chr2:38966772
|
C | G | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2483+627C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966772 | ||||||
chr2:38966813
|
A | G | 1 | a0010c0010t0005g0063 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2483+668A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966813 | ||||||
chr2:38967215
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2483+1070G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967215 | ||||||
chr2:38967243
|
G | A | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2483+1098G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967243 | ||||||
chr2:38967444
|
G | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0060 | 2 | NA19001.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2483+1299G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967444 | ||||||
chr2:38967453
|
A | C | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2483+1308A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967453 | ||||||
chr2:38967606
|
G | C | 1 | a0001c0001t0009g0005 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2483+1461G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967606 | ||||||
chr2:38967637
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2483+1492G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967637 | ||||||
chr2:38967742
|
A | AT | 10 | a0001c0001t0001g0091a0001c0001t0001g0134a0001c0001t0002g0016others(7): Show | 10 | HG00597.hp2 HG02055.hp1 HG04199.hp1 others(7): Show |
intron_variant | MODIFIER | c.2483+1615dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 38967742 | |||||
chr2:38967772
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2483+1627A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967772 | ||||||
chr2:38967906
|
C | T | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2483+1761C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967906 | ||||||
chr2:38967936
|
C | CT | 8 | a0001c0001t0001g0140a0001c0001t0001g0158a0001c0001t0004g0262others(5): Show | 8 | HG02818.hp2 HG03710.hp2 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.2483+1819dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 38967936 | |||||
chr2:38967936
|
CT | C | 55 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0103others(52): Show | 56 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.2483+1819delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 38967936 | |||||
chr2:38967936
|
CTT | C | 5 | a0001c0001t0003g0229a0001c0001t0003g0240a0001c0004t0004g0075others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2483+1818_2483+181 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 38967936 | |||||
chr2:38967936
|
CTTTTTTT others(4): Show |
C | 17 | a0001c0001t0001g0099a0001c0001t0002g0006a0001c0001t0002g0007others(14): Show | 17 | HG01106.hp1 HG01109.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.2483+1809_2483+181 others(15): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 38967936 | |||||
chr2:38967986
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2483+1841A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967986 | ||||||
chr2:38968172
|
A | T | 4 | a0001c0001t0001g0160a0001c0001t0002g0069a0001c0001t0002g0070others(1): Show | 4 | NA18948.hp2 NA18964.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.2483+2027A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38968172 | ||||||
chr2:38968225
|
C | G | 1 | a0001c0001t0009g0005 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2483+2080C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38968225 | ||||||
chr2:38968490
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2483+2345T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38968490 | ||||||
chr2:38968587
|
G | T | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2483+2442G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38968587 | ||||||
chr2:38968688
|
A | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2483+2543A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38968688 | ||||||
chr2:38968874
|
G | A | 1 | a0001c0001t0003g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2483+2729G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38968874 | ||||||
chr2:38969255
|
C | G | 1 | a0001c0001t0013g0144 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2483+3110C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38969255 | ||||||
chr2:38969315
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2483+3170T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38969315 | ||||||
chr2:38969585
|
T | C | 3 | a0001c0001t0002g0008a0001c0001t0002g0222a0001c0001t0002g0270 | 3 | HG02895.hp2 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2483+3440T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38969585 | ||||||
chr2:38969783
|
A | G | 7 | a0001c0001t0002g0027a0001c0001t0002g0055a0001c0001t0002g0057others(4): Show | 7 | NA18960.hp2 NA18988.hp1 NA18997.hp2 others(4): Show |
intron_variant | MODIFIER | c.2483+3638A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38969783 | ||||||
chr2:38969836
|
C | T | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2483+3691C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38969836 | ||||||
chr2:38969881
|
A | G | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2483+3736A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38969881 | ||||||
chr2:38970181
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2484-3533A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38970181 | ||||||
chr2:38970402
|
G | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(231): Show | 239 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(236): Show |
intron_variant | MODIFIER | c.2484-3312G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38970402 | ||||||
chr2:38970513
|
A | G | 2 | a0001c0001t0006g0250a0001c0001t0006g0251 | 2 | HG01106.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.2484-3201A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38970513 | ||||||
chr2:38970605
|
A | G | 1 | a0002c0002t0001g0192 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2484-3109A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38970605 | ||||||
chr2:38970895
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(191): Show | 199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.2484-2819A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38970895 | ||||||
chr2:38971825
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(224): Show | 232 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(229): Show |
intron_variant | MODIFIER | c.2484-1889A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38971825 | ||||||
chr2:38972074
|
G | A | 1 | a0001c0001t0005g0013 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2484-1640G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972074 | ||||||
chr2:38972130
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(230): Show | 238 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(235): Show |
intron_variant | MODIFIER | c.2484-1584T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972130 | ||||||
chr2:38972268
|
G | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0135a0001c0001t0001g0138 | 3 | HG00609.hp2 HG01943.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2484-1446G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972268 | ||||||
chr2:38972302
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2484-1412G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972302 | ||||||
chr2:38972395
|
T | C | 1 | a0001c0001t0009g0005 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2484-1319T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972395 | ||||||
chr2:38972511
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2484-1203G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972511 | ||||||
chr2:38972542
|
A | G | 14 | a0001c0001t0002g0223a0001c0001t0003g0220a0001c0001t0003g0221others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2484-1172A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972542 | ||||||
chr2:38972561
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(232): Show | 240 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(237): Show |
intron_variant | MODIFIER | c.2484-1153C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972561 | ||||||
chr2:38972615
|
A | G | 1 | a0001c0001t0003g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2484-1099A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972615 | ||||||
chr2:38972739
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(225): Show | 233 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(230): Show |
intron_variant | MODIFIER | c.2484-975A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972739 | ||||||
chr2:38972804
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2484-910A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972804 | ||||||
chr2:38972814
|
C | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0072others(164): Show | 170 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.2484-900C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972814 | ||||||
chr2:38972908
|
T | C | 3 | a0001c0004t0004g0075a0001c0004t0004g0076a0001c0004t0011g0077 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2484-806T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972908 | ||||||
chr2:38973057
|
T | G | 10 | a0001c0001t0001g0083a0001c0001t0001g0117a0001c0001t0001g0167others(7): Show | 10 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2484-657T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38973057 | ||||||
chr2:38973220
|
AC | A | 6 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0017others(3): Show | 6 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2484-492delC | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 38973220 | |||||
chr2:38973531
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2484-183C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38973531 |