geneid | 115703 |
---|---|
ensemblid | ENSG00000004777.19 |
hgncid | 23085 |
symbol | ARHGAP33 |
name | Rho GTPase activating protein 33 |
refseq_nuc | NM_001366178.1 |
refseq_prot | NP_001353107.1 |
ensembl_nuc | ENST00000007510.9 |
ensembl_prot | ENSP00000007510.6 |
mane_status | MANE Select |
chr | chr19 |
start | 35775564 |
end | 35788822 |
strand | + |
ver | v1.2 |
region | chr19:35775564-35788822 |
region5000 | chr19:35770564-35793822 |
regionname0 | ARHGAP33_chr19_35775564_35788822 |
regionname5000 | ARHGAP33_chr19_35770564_35793822 |
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 | regionname | genename | aa |
---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1287 | 385 | 89 | 70 | 167 | 12 | 45 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0002 | 0/0 | 893 | 8 | 1 | 0 | 6 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0003 | 0/0 | 1287 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0004 | 0/0 | 1287 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0005 | 0/0 | 1287 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0006 | 0/0 | 1287 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0007 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0008 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0009 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0010 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0011 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0012 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0013 | 0/0 | 1287 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0014 | 0/0 | 1287 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0015 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0016 | 0/0 | 1271 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0017 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0018 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0019 | 0/0 | 893 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3864 | 97 | 26 | 12 | 50 | 3 | 6 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0002 | 1/0 | 3864 | 88 | 7 | 19 | 42 | 5 | 14 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0003 | 0/1 | 3864 | 69 | 9 | 16 | 26 | 1 | 16 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0004 | 0/0 | 3864 | 57 | 22 | 10 | 22 | 1 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0005 | 0/0 | 3864 | 43 | 7 | 13 | 19 | 2 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0006 | 0/0 | 3864 | 10 | 9 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0007 | 0/0 | 3864 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0008 | 0/0 | 3864 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0009 | 0/0 | 3864 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0010 | 0/0 | 3864 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0011 | 0/0 | 3865 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0012 | 0/0 | 3864 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0013 | 0/0 | 3865 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0014 | 0/0 | 3865 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0015 | 0/0 | 3864 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0016 | 0/0 | 3864 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0017 | 0/0 | 3864 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0018 | 0/0 | 3864 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0019 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0020 | 0/0 | 3865 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0021 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0022 | 0/0 | 3864 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0023 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0024 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0025 | 0/0 | 3864 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0026 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0027 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0028 | 0/0 | 3864 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0029 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0030 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0031 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0032 | 0/0 | 3864 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0033 | 0/0 | 3816 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0034 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0035 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0036 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0037 | 0/0 | 3865 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0038 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
c0039 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 489 | 420 | 96 | 72 | 190 | 12 | 48 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
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 |
---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 52 | 6 | 17 | 14 | 4 | 10 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0002 | 0/0 | 33 | 2 | 6 | 25 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0003 | 0/0 | 25 | 6 | 8 | 5 | 2 | 4 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0004 | 0/0 | 24 | 0 | 2 | 17 | 0 | 5 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0005 | 0/0 | 24 | 0 | 0 | 24 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0006 | 0/1 | 23 | 3 | 15 | 0 | 1 | 3 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0007 | 0/0 | 21 | 6 | 4 | 7 | 3 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0008 | 0/0 | 20 | 7 | 5 | 5 | 1 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0009 | 0/0 | 17 | 0 | 0 | 15 | 0 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0010 | 0/0 | 14 | 0 | 1 | 13 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0011 | 0/0 | 14 | 0 | 0 | 12 | 0 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0012 | 0/0 | 13 | 0 | 4 | 9 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0013 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0014 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0015 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0016 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0017 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | a0001 | c0001 | 0/0 | 97 | 26 | 12 | 50 | 3 | 6 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0002 | a0001 | c0002 | 1/0 | 88 | 7 | 19 | 42 | 5 | 14 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0003 | a0001 | c0003 | 0/1 | 69 | 9 | 16 | 26 | 1 | 16 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0004 | a0001 | c0004 | 0/0 | 57 | 22 | 10 | 22 | 1 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0005 | a0001 | c0005 | 0/0 | 43 | 7 | 13 | 19 | 2 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0006 | a0001 | c0006 | 0/0 | 10 | 9 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0007 | a0001 | c0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0010 | a0001 | c0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0012 | a0001 | c0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0017 | a0001 | c0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0018 | a0001 | c0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0021 | a0001 | c0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0022 | a0001 | c0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0023 | a0001 | c0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0025 | a0001 | c0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0031 | a0001 | c0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0035 | a0001 | c0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0038 | a0001 | c0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0002c0011 | a0002 | c0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0002c0013 | a0002 | c0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0002c0014 | a0002 | c0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0002c0037 | a0002 | c0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0003c0009 | a0003 | c0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0004c0008 | a0004 | c0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0005c0015 | a0005 | c0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0006c0016 | a0006 | c0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0007c0019 | a0007 | c0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0008c0030 | a0008 | c0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0009c0024 | a0009 | c0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0010c0028 | a0010 | c0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0011c0027 | a0011 | c0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0012c0036 | a0012 | c0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0013c0026 | a0013 | c0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0014c0034 | a0014 | c0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0015c0029 | a0015 | c0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0016c0033 | a0016 | c0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0017c0039 | a0017 | c0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0018c0032 | a0018 | c0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0019c0020 | a0019 | c0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
acthapid | ahapid | chapid | thapid | 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 | actseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 97 | 26 | 12 | 50 | 3 | 6 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0002t0001 | a0001 | c0002 | t0001 | 1/0 | 88 | 7 | 19 | 42 | 5 | 14 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0003t0001 | a0001 | c0003 | t0001 | 0/1 | 69 | 9 | 16 | 26 | 1 | 16 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 57 | 22 | 10 | 22 | 1 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 43 | 7 | 13 | 19 | 2 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 10 | 9 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0007t0001 | a0001 | c0007 | t0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0010t0001 | a0001 | c0010 | t0001 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0012t0001 | a0001 | c0012 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0017t0001 | a0001 | c0017 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0018t0001 | a0001 | c0018 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0021t0001 | a0001 | c0021 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0022t0001 | a0001 | c0022 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0023t0001 | a0001 | c0023 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0025t0001 | a0001 | c0025 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0031t0001 | a0001 | c0031 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0035t0001 | a0001 | c0035 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0001c0038t0001 | a0001 | c0038 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0002c0011t0001 | a0002 | c0011 | t0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0002c0013t0001 | a0002 | c0013 | t0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0002c0014t0001 | a0002 | c0014 | t0001 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0002c0037t0001 | a0002 | c0037 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0003c0009t0001 | a0003 | c0009 | t0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0004c0008t0001 | a0004 | c0008 | t0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0005c0015t0001 | a0005 | c0015 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0006c0016t0001 | a0006 | c0016 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0007c0019t0001 | a0007 | c0019 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0008c0030t0001 | a0008 | c0030 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0009c0024t0001 | a0009 | c0024 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0010c0028t0001 | a0010 | c0028 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0011c0027t0001 | a0011 | c0027 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0012c0036t0001 | a0012 | c0036 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0013c0026t0001 | a0013 | c0026 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0014c0034t0001 | a0014 | c0034 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0015c0029t0001 | a0015 | c0029 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0016c0033t0001 | a0016 | c0033 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0017c0039t0001 | a0017 | c0039 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0018c0032t0001 | a0018 | c0032 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
a0019c0020t0001 | a0019 | c0020 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 | copy fasta |
actghapid | ahapid | chapid | thapid | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 31 | 2 | 5 | 24 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 17 | 0 | 2 | 11 | 0 | 4 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 21 | 6 | 4 | 7 | 3 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0002t0001g0001 | a0001 | c0002 | t0001 | g0001 | 1/0 | 46 | 2 | 17 | 13 | 4 | 9 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0002t0001g0005 | a0001 | c0002 | t0001 | g0005 | 0/0 | 22 | 0 | 0 | 22 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0002t0001g0017 | a0001 | c0002 | t0001 | g0017 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0002t0001g0018 | a0001 | c0002 | t0001 | g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0002t0001g0020 | a0001 | c0002 | t0001 | g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0002t0001g0028 | a0001 | c0002 | t0001 | g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0002t0001g0030 | a0001 | c0002 | t0001 | g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0002t0001g0044 | a0001 | c0002 | t0001 | g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0002t0001g0045 | a0001 | c0002 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0002t0001g0048 | a0001 | c0002 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0002t0001g0050 | a0001 | c0002 | t0001 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0002t0001g0080 | a0001 | c0002 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0006 | a0001 | c0003 | t0001 | g0006 | 0/1 | 23 | 3 | 15 | 0 | 1 | 3 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0009 | a0001 | c0003 | t0001 | g0009 | 0/0 | 12 | 0 | 0 | 10 | 0 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0011 | a0001 | c0003 | t0001 | g0011 | 0/0 | 14 | 0 | 0 | 12 | 0 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0021 | a0001 | c0003 | t0001 | g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0022 | a0001 | c0003 | t0001 | g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0024 | a0001 | c0003 | t0001 | g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0026 | a0001 | c0003 | t0001 | g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0038 | a0001 | c0003 | t0001 | g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0039 | a0001 | c0003 | t0001 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0041 | a0001 | c0003 | t0001 | g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0043 | a0001 | c0003 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0046 | a0001 | c0003 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0047 | a0001 | c0003 | t0001 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0089 | a0001 | c0003 | t0001 | g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0090 | a0001 | c0003 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0003t0001g0091 | a0001 | c0003 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0008 | a0001 | c0004 | t0001 | g0008 | 0/0 | 18 | 6 | 5 | 4 | 1 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0010 | a0001 | c0004 | t0001 | g0010 | 0/0 | 14 | 0 | 1 | 13 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0013 | a0001 | c0004 | t0001 | g0013 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0016 | a0001 | c0004 | t0001 | g0016 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0032 | a0001 | c0004 | t0001 | g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0033 | a0001 | c0004 | t0001 | g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0051 | a0001 | c0004 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0052 | a0001 | c0004 | t0001 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0053 | a0001 | c0004 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0054 | a0001 | c0004 | t0001 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0055 | a0001 | c0004 | t0001 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0058 | a0001 | c0004 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0004t0001g0066 | a0001 | c0004 | t0001 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0003 | a0001 | c0005 | t0001 | g0003 | 0/0 | 20 | 5 | 7 | 4 | 2 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0012 | a0001 | c0005 | t0001 | g0012 | 0/0 | 11 | 0 | 4 | 7 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0037 | a0001 | c0005 | t0001 | g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0059 | a0001 | c0005 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0060 | a0001 | c0005 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0061 | a0001 | c0005 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0062 | a0001 | c0005 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0063 | a0001 | c0005 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0064 | a0001 | c0005 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0084 | a0001 | c0005 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0085 | a0001 | c0005 | t0001 | g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0087 | a0001 | c0005 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0005t0001g0088 | a0001 | c0005 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0006t0001g0001 | a0001 | c0006 | t0001 | g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0006t0001g0019 | a0001 | c0006 | t0001 | g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0006t0001g0031 | a0001 | c0006 | t0001 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0006t0001g0057 | a0001 | c0006 | t0001 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0007t0001g0009 | a0001 | c0007 | t0001 | g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0010t0001g0036 | a0001 | c0010 | t0001 | g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0010t0001g0078 | a0001 | c0010 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0012t0001g0027 | a0001 | c0012 | t0001 | g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0017t0001g0013 | a0001 | c0017 | t0001 | g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0018t0001g0034 | a0001 | c0018 | t0001 | g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0021t0001g0022 | a0001 | c0021 | t0001 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0022t0001g0042 | a0001 | c0022 | t0001 | g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0023t0001g0056 | a0001 | c0023 | t0001 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0025t0001g0001 | a0001 | c0025 | t0001 | g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0031t0001g0081 | a0001 | c0031 | t0001 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0035t0001g0086 | a0001 | c0035 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0001c0038t0001g0008 | a0001 | c0038 | t0001 | g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0002c0011t0001g0003 | a0002 | c0011 | t0001 | g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0002c0011t0001g0065 | a0002 | c0011 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0002c0013t0001g0005 | a0002 | c0013 | t0001 | g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0002c0014t0001g0002 | a0002 | c0014 | t0001 | g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0002c0014t0001g0015 | a0002 | c0014 | t0001 | g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0002c0037t0001g0012 | a0002 | c0037 | t0001 | g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0003c0009t0001g0023 | a0003 | c0009 | t0001 | g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0003c0009t0001g0082 | a0003 | c0009 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0003c0009t0001g0083 | a0003 | c0009 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0004c0008t0001g0004 | a0004 | c0008 | t0001 | g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0005c0015t0001g0025 | a0005 | c0015 | t0001 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0005c0015t0001g0040 | a0005 | c0015 | t0001 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0006c0016t0001g0029 | a0006 | c0016 | t0001 | g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0007c0019t0001g0004 | a0007 | c0019 | t0001 | g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0008c0030t0001g0020 | a0008 | c0030 | t0001 | g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0009c0024t0001g0049 | a0009 | c0024 | t0001 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0010c0028t0001g0004 | a0010 | c0028 | t0001 | g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0011c0027t0001g0001 | a0011 | c0027 | t0001 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0012c0036t0001g0003 | a0012 | c0036 | t0001 | g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0013c0026t0001g0002 | a0013 | c0026 | t0001 | g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0014c0034t0001g0003 | a0014 | c0034 | t0001 | g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0015c0029t0001g0031 | a0015 | c0029 | t0001 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0016c0033t0001g0012 | a0016 | c0033 | t0001 | g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0017c0039t0001g0008 | a0017 | c0039 | t0001 | g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0018c0032t0001g0003 | a0018 | c0032 | t0001 | g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
a0019c0020t0001g0075 | a0019 | c0020 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0030 | EUR | GBR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00140 | hp2 | a0001 | c0004 | t0001 | g0008 | EUR | GBR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00408 | hp1 | a0016 | c0033 | t0001 | g0012 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00408 | hp2 | a0001 | c0007 | t0001 | g0009 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00423 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00544 | hp2 | a0004 | c0008 | t0001 | g0004 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00558 | hp1 | a0004 | c0008 | t0001 | g0004 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00558 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00597 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00597 | hp2 | a0017 | c0039 | t0001 | g0008 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00609 | hp2 | a0001 | c0005 | t0001 | g0060 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00621 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00621 | hp2 | a0002 | c0037 | t0001 | g0012 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00673 | hp1 | a0001 | c0004 | t0001 | g0016 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00673 | hp2 | a0008 | c0030 | t0001 | g0020 | EAS | CHS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00733 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00738 | hp1 | a0001 | c0004 | t0001 | g0008 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00741 | hp1 | a0001 | c0004 | t0001 | g0008 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01070 | hp1 | a0001 | c0004 | t0001 | g0008 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01070 | hp2 | a0001 | c0005 | t0001 | g0003 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01071 | hp2 | a0001 | c0005 | t0001 | g0003 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01106 | hp2 | a0001 | c0004 | t0001 | g0008 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01109 | hp1 | a0001 | c0004 | t0001 | g0013 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01255 | hp2 | a0001 | c0004 | t0001 | g0016 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01256 | hp1 | a0001 | c0005 | t0001 | g0037 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01261 | hp1 | a0001 | c0005 | t0001 | g0012 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01261 | hp2 | a0014 | c0034 | t0001 | g0003 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01346 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01358 | hp1 | a0001 | c0004 | t0001 | g0008 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01361 | hp2 | a0001 | c0005 | t0001 | g0085 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01433 | hp2 | a0001 | c0005 | t0001 | g0012 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01517 | hp1 | a0001 | c0005 | t0001 | g0003 | EUR | IBS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01891 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0021 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01928 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01934 | hp1 | a0001 | c0005 | t0001 | g0003 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01943 | hp1 | a0013 | c0026 | t0001 | g0002 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01952 | hp2 | a0001 | c0005 | t0001 | g0003 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01975 | hp2 | a0001 | c0005 | t0001 | g0012 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01993 | hp1 | a0001 | c0004 | t0001 | g0016 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01993 | hp2 | a0001 | c0005 | t0001 | g0003 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02027 | hp2 | a0001 | c0031 | t0001 | g0081 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02040 | hp2 | a0001 | c0005 | t0001 | g0084 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02055 | hp2 | a0001 | c0012 | t0001 | g0027 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02056 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02074 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02132 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02135 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0021 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02148 | hp1 | a0001 | c0004 | t0001 | g0016 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02148 | hp2 | a0001 | c0005 | t0001 | g0012 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02155 | hp1 | a0001 | c0005 | t0001 | g0012 | EAS | CDX | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02155 | hp2 | a0001 | c0004 | t0001 | g0053 | EAS | CDX | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02165 | hp1 | a0001 | c0005 | t0001 | g0012 | EAS | CDX | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02165 | hp2 | a0001 | c0007 | t0001 | g0009 | EAS | CDX | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02257 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02273 | hp1 | a0001 | c0005 | t0001 | g0003 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02273 | hp2 | a0001 | c0003 | t0001 | g0047 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02280 | hp1 | a0001 | c0005 | t0001 | g0003 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02293 | hp1 | a0001 | c0005 | t0001 | g0003 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02523 | hp1 | a0003 | c0009 | t0001 | g0023 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02523 | hp2 | a0001 | c0005 | t0001 | g0062 | EAS | KHV | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02572 | hp1 | a0001 | c0023 | t0001 | g0056 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02572 | hp2 | a0001 | c0004 | t0001 | g0033 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02602 | hp2 | a0001 | c0003 | t0001 | g0006 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02615 | hp2 | a0001 | c0006 | t0001 | g0001 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02622 | hp1 | a0001 | c0005 | t0001 | g0003 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02630 | hp1 | a0005 | c0015 | t0001 | g0025 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02630 | hp2 | a0001 | c0006 | t0001 | g0019 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02647 | hp1 | a0012 | c0036 | t0001 | g0003 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02647 | hp2 | a0001 | c0004 | t0001 | g0055 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02683 | hp1 | a0001 | c0005 | t0001 | g0003 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02717 | hp1 | a0001 | c0006 | t0001 | g0019 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02723 | hp1 | a0009 | c0024 | t0001 | g0049 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02723 | hp2 | a0001 | c0005 | t0001 | g0037 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02735 | hp2 | a0001 | c0003 | t0001 | g0041 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02809 | hp1 | a0001 | c0021 | t0001 | g0022 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02809 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02818 | hp2 | a0001 | c0005 | t0001 | g0003 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0052 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02886 | hp2 | a0001 | c0004 | t0001 | g0066 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02896 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02896 | hp2 | a0001 | c0006 | t0001 | g0057 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02897 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02922 | hp1 | a0001 | c0004 | t0001 | g0032 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02922 | hp2 | a0001 | c0005 | t0001 | g0003 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02976 | hp1 | a0001 | c0006 | t0001 | g0019 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0089 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03017 | hp2 | a0001 | c0003 | t0001 | g0026 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03098 | hp1 | a0002 | c0014 | t0001 | g0015 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03098 | hp2 | a0001 | c0006 | t0001 | g0001 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03130 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03139 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03139 | hp2 | a0001 | c0006 | t0001 | g0001 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03209 | hp1 | a0001 | c0017 | t0001 | g0013 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03225 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03225 | hp2 | a0001 | c0012 | t0001 | g0027 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03239 | hp1 | a0001 | c0010 | t0001 | g0078 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03239 | hp2 | a0001 | c0022 | t0001 | g0042 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03453 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03486 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03486 | hp2 | a0001 | c0038 | t0001 | g0008 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03490 | hp2 | a0001 | c0010 | t0001 | g0036 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03491 | hp1 | a0001 | c0003 | t0001 | g0011 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03492 | hp1 | a0001 | c0010 | t0001 | g0036 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03516 | hp1 | a0001 | c0018 | t0001 | g0034 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03579 | hp2 | a0001 | c0018 | t0001 | g0034 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0011 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0024 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03669 | hp2 | a0001 | c0004 | t0001 | g0008 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0006 | SAS | STU | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0009 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03704 | hp2 | a0001 | c0003 | t0001 | g0024 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0026 | SAS | PJL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03831 | hp1 | a0001 | c0003 | t0001 | g0038 | SAS | BEB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03834 | hp1 | a0001 | c0005 | t0001 | g0003 | SAS | BEB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | BEB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0017 | SAS | BEB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03927 | hp2 | a0002 | c0011 | t0001 | g0003 | SAS | BEB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03942 | hp2 | a0001 | c0025 | t0001 | g0001 | SAS | BEB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG04115 | hp1 | a0010 | c0028 | t0001 | g0004 | SAS | STU | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | STU | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0090 | SAS | BEB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG04199 | hp1 | a0001 | c0004 | t0001 | g0008 | SAS | STU | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG04199 | hp2 | a0001 | c0003 | t0001 | g0038 | SAS | STU | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0006 | SAS | STU | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG04228 | hp1 | a0018 | c0032 | t0001 | g0003 | SAS | STU | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0024 | SAS | STU | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18522 | hp2 | a0001 | c0005 | t0001 | g0003 | AFR | YRI | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18612 | hp2 | a0001 | c0005 | t0001 | g0064 | EAS | CHB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | CHB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | CHB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18906 | hp1 | a0006 | c0016 | t0001 | g0029 | AFR | YRI | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18939 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18940 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18940 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18943 | hp1 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18946 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18947 | hp1 | a0015 | c0029 | t0001 | g0031 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0091 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18949 | hp1 | a0002 | c0013 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18949 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18950 | hp2 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18951 | hp1 | a0019 | c0020 | t0001 | g0075 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18951 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18952 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18959 | hp2 | a0001 | c0005 | t0001 | g0012 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18960 | hp2 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18961 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18961 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18964 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18966 | hp1 | a0001 | c0005 | t0001 | g0012 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18966 | hp2 | a0011 | c0027 | t0001 | g0001 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18970 | hp1 | a0001 | c0007 | t0001 | g0009 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18970 | hp2 | a0001 | c0005 | t0001 | g0059 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18973 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18979 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18980 | hp1 | a0001 | c0007 | t0001 | g0009 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18981 | hp2 | a0004 | c0008 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18982 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18983 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18986 | hp2 | a0001 | c0005 | t0001 | g0012 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18988 | hp1 | a0001 | c0004 | t0001 | g0051 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18991 | hp2 | a0001 | c0035 | t0001 | g0086 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18995 | hp1 | a0003 | c0009 | t0001 | g0023 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18997 | hp2 | a0001 | c0006 | t0001 | g0031 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18998 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18999 | hp1 | a0001 | c0005 | t0001 | g0088 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19000 | hp1 | a0002 | c0011 | t0001 | g0003 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19003 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19003 | hp2 | a0003 | c0009 | t0001 | g0082 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19004 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19004 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19005 | hp1 | a0001 | c0004 | t0001 | g0058 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19007 | hp2 | a0001 | c0005 | t0001 | g0061 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19010 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19011 | hp1 | a0001 | c0007 | t0001 | g0009 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19012 | hp2 | a0004 | c0008 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0054 | AFR | LWK | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19030 | hp2 | a0001 | c0004 | t0001 | g0032 | AFR | LWK | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19043 | hp1 | a0001 | c0004 | t0001 | g0033 | AFR | LWK | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | LWK | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19062 | hp2 | a0001 | c0005 | t0001 | g0012 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19063 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19064 | hp1 | a0003 | c0009 | t0001 | g0023 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19065 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19067 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19067 | hp2 | a0002 | c0014 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19068 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19068 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19072 | hp1 | a0001 | c0005 | t0001 | g0063 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19074 | hp1 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19074 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19077 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19077 | hp2 | a0001 | c0005 | t0001 | g0012 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19082 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19084 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19085 | hp2 | a0004 | c0008 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19086 | hp1 | a0002 | c0011 | t0001 | g0065 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19086 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19089 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19089 | hp2 | a0007 | c0019 | t0001 | g0004 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19090 | hp2 | a0002 | c0013 | t0001 | g0005 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19240 | hp1 | a0001 | c0005 | t0001 | g0087 | AFR | YRI | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0021 | AFR | YRI | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA20129 | hp1 | a0005 | c0015 | t0001 | g0040 | AFR | ASW | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ASW | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0006 | EUR | TSI | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA20805 | hp1 | a0001 | c0005 | t0001 | g0003 | EUR | TSI | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | GIH | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA20905 | hp2 | a0001 | c0003 | t0001 | g0009 | SAS | GIH | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02109 | hp1 | a0001 | c0006 | t0001 | g0001 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02486 | hp2 | a0001 | c0006 | t0001 | g0019 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02559 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ACB | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03471 | hp1 | a0001 | c0017 | t0001 | g0013 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | MSL | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | USA | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | USA | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18955 | hp1 | a0001 | c0004 | t0001 | g0016 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA18955 | hp2 | a0003 | c0009 | t0001 | g0083 | EAS | JPT | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA20300 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | USA | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA20300 | hp2 | a0006 | c0016 | t0001 | g0029 | AFR | USA | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | LWK | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0006 | REF | REF | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0001 | REF | REF | ARHGAP33_chr19_35770564_35793822 | ARHGAP33 |
chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:35780977
|
G | A | 1 | a0007 | 1 | NA19089.hp2 | missense_variant | MODERATE | c.887G>A | p.Arg296His | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 11/21 | 982/4352 | 887/3864 | 296/1287 | chr19 | 35780977 | ||
chr19:35782380
|
T | A | 1 | a0019 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.1093T>A | p.Phe365Ile | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 13/21 | 1188/4352 | 1093/3864 | 365/1287 | chr19 | 35782380 | ||
chr19:35782830
|
C | A | 1 | a0018 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1382C>A | p.Ala461Asp | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 15/21 | 1477/4352 | 1382/3864 | 461/1287 | chr19 | 35782830 | ||
chr19:35784176
|
A | G | 1 | a0017 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1426A>G | p.Met476Val | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 16/21 | 1521/4352 | 1426/3864 | 476/1287 | chr19 | 35784176 | ||
chr19:35784970
|
A | G | 1 | a0019 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.1585A>G | p.Arg529Gly | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 17/21 | 1680/4352 | 1585/3864 | 529/1287 | chr19 | 35784970 | ||
chr19:35785271
|
A | T | 1 | a0008 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.1804A>T | p.Ser602Cys | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 18/21 | 1899/4352 | 1804/3864 | 602/1287 | chr19 | 35785271 | ||
chr19:35786630
|
TGGTGATG others(41): Show |
T | 1 | a0016 | 1 | HG00408.hp1 | disruptive_inframe_deletion | MODERATE | c.2163_2210delTGATGA others(42): Show |
p.Asp722_Gly737del | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2258/4352 | 2163/3864 | 721/1287 | INFO_REALIGN_3_PRIME | chr19 | 35786630 | |
chr19:35786677
|
G | C | 1 | a0009 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.2207G>C | p.Arg736Pro | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2302/4352 | 2207/3864 | 736/1287 | chr19 | 35786677 | ||
chr19:35786907
|
G | A | 1 | a0006 | 2 | NA18906.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.2437G>A | p.Ala813Thr | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2532/4352 | 2437/3864 | 813/1287 | chr19 | 35786907 | ||
chr19:35786953
|
C | G | 1 | a0015 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.2483C>G | p.Pro828Arg | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2578/4352 | 2483/3864 | 828/1287 | chr19 | 35786953 | ||
chr19:35786955
|
G | A | 1 | a0014 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.2485G>A | p.Gly829Ser | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2580/4352 | 2485/3864 | 829/1287 | chr19 | 35786955 | ||
chr19:35787042
|
A | G | 1 | a0007 | 1 | NA19089.hp2 | missense_variant | MODERATE | c.2572A>G | p.Ser858Gly | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2667/4352 | 2572/3864 | 858/1287 | chr19 | 35787042 | ||
chr19:35787193
|
A | AC | 2 | a0002a0019 | 9 | HG00621.hp2 HG03098.hp1 HG03927.hp2 others(6): Show |
frameshift_variant | HIGH | c.2633dupC | p.Pro879fs | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 2729/4352 | 2634/3864 | 878/1287 | INFO_REALIGN_3_PRIME | chr19 | 35787193 | |
chr19:35787209
|
C | A | 1 | a0003 | 5 | HG02523.hp1 NA18955.hp2 NA18995.hp1 others(2): Show |
missense_variant | MODERATE | c.2644C>A | p.Leu882Ile | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 2739/4352 | 2644/3864 | 882/1287 | chr19 | 35787209 | ||
chr19:35787362
|
C | T | 1 | a0010 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.2797C>T | p.Arg933Cys | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 2892/4352 | 2797/3864 | 933/1287 | chr19 | 35787362 | ||
chr19:35787383
|
G | C | 1 | a0013 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.2818G>C | p.Gly940Arg | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 2913/4352 | 2818/3864 | 940/1287 | chr19 | 35787383 | ||
chr19:35787444
|
G | C | 1 | a0004 | 5 | HG00544.hp2 HG00558.hp1 NA18981.hp2 others(2): Show |
missense_variant | MODERATE | c.2879G>C | p.Gly960Ala | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 2974/4352 | 2879/3864 | 960/1287 | chr19 | 35787444 | ||
chr19:35787567
|
C | T | 1 | a0005 | 2 | HG02630.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.3002C>T | p.Ala1001Val | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 3097/4352 | 3002/3864 | 1001/1287 | chr19 | 35787567 | ||
chr19:35787893
|
A | C | 1 | a0011 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.3328A>C | p.Met1110Leu | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 3423/4352 | 3328/3864 | 1110/1287 | chr19 | 35787893 | ||
chr19:35787912
|
A | G | 1 | a0012 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.3347A>G | p.Asn1116Ser | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 3442/4352 | 3347/3864 | 1116/1287 | chr19 | 35787912 |
chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:35777869
|
C | T | 14 | a0001c0004a0001c0005a0001c0017others(11): Show | 120 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
synonymous_variant | LOW | c.150C>T | p.Ala50Ala | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3/21 | 245/4352 | 150/3864 | 50/1287 | chr19 | 35777869 | ||
chr19:35780237
|
C | T | 5 | a0001c0004a0001c0017a0001c0018others(2): Show | 63 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(60): Show |
synonymous_variant | LOW | c.528C>T | p.Leu176Leu | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 7/21 | 623/4352 | 528/3864 | 176/1287 | chr19 | 35780237 | ||
chr19:35781175
|
C | T | 1 | a0001c0031 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.1008C>T | p.Ser336Ser | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/21 | 1103/4352 | 1008/3864 | 336/1287 | chr19 | 35781175 | ||
chr19:35782406
|
G | A | 9 | a0001c0005a0001c0035a0002c0011others(6): Show | 57 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(54): Show |
synonymous_variant | LOW | c.1119G>A | p.Leu373Leu | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 13/21 | 1214/4352 | 1119/3864 | 373/1287 | chr19 | 35782406 | ||
chr19:35782632
|
G | A | 4 | a0001c0003a0001c0012a0001c0021others(1): Show | 73 | HG00621.hp1 HG00733.hp1 HG00738.hp2 others(70): Show |
synonymous_variant | LOW | c.1266G>A | p.Leu422Leu | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 14/21 | 1361/4352 | 1266/3864 | 422/1287 | chr19 | 35782632 | ||
chr19:35782807
|
C | T | 1 | a0002c0037 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.1359C>T | p.His453His | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 15/21 | 1454/4352 | 1359/3864 | 453/1287 | chr19 | 35782807 | ||
chr19:35784172
|
G | A | 4 | a0001c0003a0001c0007a0001c0021others(1): Show | 76 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(73): Show |
splice_region_variant&synonymous_variant | LOW | c.1422G>A | p.Arg474Arg | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 16/21 | 1517/4352 | 1422/3864 | 474/1287 | chr19 | 35784172 | ||
chr19:35785017
|
G | A | 1 | a0001c0023 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1632G>A | p.Thr544Thr | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 17/21 | 1727/4352 | 1632/3864 | 544/1287 | chr19 | 35785017 | ||
chr19:35785243
|
G | A | 1 | a0001c0017 | 2 | HG03209.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.1776G>A | p.Lys592Lys | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 18/21 | 1871/4352 | 1776/3864 | 592/1287 | chr19 | 35785243 | ||
chr19:35785425
|
C | T | 1 | a0006c0016 | 2 | NA18906.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.1884C>T | p.Thr628Thr | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 19/21 | 1979/4352 | 1884/3864 | 628/1287 | chr19 | 35785425 | ||
chr19:35786735
|
C | T | 3 | a0001c0006a0001c0023a0015c0029 | 12 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(9): Show |
synonymous_variant | LOW | c.2265C>T | p.Pro755Pro | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2360/4352 | 2265/3864 | 755/1287 | chr19 | 35786735 | ||
chr19:35786855
|
C | A | 1 | a0001c0017 | 2 | HG03209.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.2385C>A | p.Ile795Ile | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2480/4352 | 2385/3864 | 795/1287 | chr19 | 35786855 | ||
chr19:35786867
|
G | C | 1 | a0001c0038 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.2397G>C | p.Leu799Leu | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2492/4352 | 2397/3864 | 799/1287 | chr19 | 35786867 | ||
chr19:35786966
|
G | A | 1 | a0001c0035 | 1 | NA18991.hp2 | synonymous_variant | LOW | c.2496G>A | p.Leu832Leu | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2591/4352 | 2496/3864 | 832/1287 | chr19 | 35786966 | ||
chr19:35787217
|
C | A | 1 | a0001c0025 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.2652C>A | p.Arg884Arg | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 2747/4352 | 2652/3864 | 884/1287 | chr19 | 35787217 | ||
chr19:35787568
|
C | G | 22 | a0001c0001a0001c0004a0001c0005others(19): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
synonymous_variant | LOW | c.3003C>G | p.Ala1001Ala | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 3098/4352 | 3003/3864 | 1001/1287 | chr19 | 35787568 | ||
chr19:35787721
|
G | A | 1 | a0001c0010 | 3 | HG03239.hp1 HG03490.hp2 HG03492.hp1 |
synonymous_variant | LOW | c.3156G>A | p.Leu1052Leu | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 3251/4352 | 3156/3864 | 1052/1287 | chr19 | 35787721 | ||
chr19:35788282
|
G | A | 1 | a0001c0021 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.3717G>A | p.Pro1239Pro | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 3812/4352 | 3717/3864 | 1239/1287 | chr19 | 35788282 | ||
chr19:35788322
|
T | C | 1 | a0001c0022 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.3757T>C | p.Leu1253Leu | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 3852/4352 | 3757/3864 | 1253/1287 | chr19 | 35788322 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:35775680
|
G | T | 1 | a0001c0003t0001g0038 | 2 | HG03831.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.6+16G>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35775680 | ||||||
chr19:35775689
|
C | G | 4 | a0001c0003t0001g0011a0001c0003t0001g0024a0001c0003t0001g0090others(1): Show | 19 | HG03491.hp1 HG03654.hp2 HG03669.hp1 others(16): Show |
intron_variant | MODIFIER | c.6+25C>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35775689 | ||||||
chr19:35775743
|
C | T | 1 | a0001c0003t0001g0091 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.6+79C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35775743 | ||||||
chr19:35775757
|
C | T | 1 | a0001c0003t0001g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6+93C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35775757 | ||||||
chr19:35775874
|
A | G | 14 | a0001c0005t0001g0003a0001c0005t0001g0037a0001c0005t0001g0084others(11): Show | 37 | HG01070.hp2 HG01071.hp2 HG01256.hp1 others(34): Show |
intron_variant | MODIFIER | c.6+210A>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35775874 | ||||||
chr19:35775920
|
A | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(73): Show | 266 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.6+256A>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35775920 | ||||||
chr19:35776044
|
C | T | 6 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0080others(3): Show | 30 | HG00673.hp2 HG02027.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.6+380C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776044 | ||||||
chr19:35776102
|
C | A | 1 | a0001c0004t0001g0051 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6+438C>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776102 | ||||||
chr19:35776102
|
C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(34): Show | 131 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.6+438C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776102 | ||||||
chr19:35776103
|
A | C | 1 | a0001c0004t0001g0051 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6+439A>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776103 | ||||||
chr19:35776182
|
C | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(36): Show | 133 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.6+518C>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776182 | ||||||
chr19:35776210
|
T | A | 1 | a0001c0003t0001g0039 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6+546T>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776210 | ||||||
chr19:35776317
|
C | G | 2 | a0001c0002t0001g0018a0001c0002t0001g0050 | 5 | HG02055.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+653C>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776317 | ||||||
chr19:35776389
|
G | T | 1 | a0001c0001t0001g0079 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.6+725G>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776389 | ||||||
chr19:35776616
|
G | C | 16 | a0001c0004t0001g0008a0001c0004t0001g0010a0001c0004t0001g0013others(13): Show | 62 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.6+952G>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776616 | ||||||
chr19:35776640
|
G | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(21): Show | 108 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.6+976G>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776640 | ||||||
chr19:35776844
|
G | A | 1 | a0001c0004t0001g0052 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7-801G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776844 | ||||||
chr19:35776875
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(73): Show | 263 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.7-770T>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776875 | ||||||
chr19:35776936
|
G | T | 2 | a0001c0010t0001g0036a0001c0010t0001g0078 | 3 | HG03239.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.7-709G>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776936 | ||||||
chr19:35776977
|
G | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(26): Show | 113 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.7-668G>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776977 | ||||||
chr19:35776978
|
A | G | 1 | a0009c0024t0001g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.7-667A>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776978 | ||||||
chr19:35776994
|
G | A | 3 | a0003c0009t0001g0023a0003c0009t0001g0082a0003c0009t0001g0083 | 5 | HG02523.hp1 NA18955.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-651G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35776994 | ||||||
chr19:35777081
|
G | T | 1 | a0001c0005t0001g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.7-564G>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35777081 | ||||||
chr19:35777165
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(73): Show | 263 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.7-480G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35777165 | ||||||
chr19:35777256
|
C | T | 1 | a0001c0004t0001g0066 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.7-389C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35777256 | ||||||
chr19:35777259
|
A | T | 1 | a0001c0002t0001g0048 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.7-386A>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35777259 | ||||||
chr19:35777368
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7-277G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35777368 | ||||||
chr19:35777409
|
C | G | 6 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0080others(3): Show | 30 | HG00673.hp2 HG02027.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.7-236C>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35777409 | ||||||
chr19:35777419
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0069others(1): Show | 9 | HG01123.hp2 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-226G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35777419 | ||||||
chr19:35777569
|
G | A | 8 | a0001c0004t0001g0008a0001c0004t0001g0010a0001c0004t0001g0016others(5): Show | 42 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.7-76G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1/20 | chr19 | 35777569 | ||||||
chr19:35777914
|
G | A | 1 | a0001c0002t0001g0080 | 1 | NA19060.hp1 | splice_region_variant&intron_variant | LOW | c.189+6G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3/20 | chr19 | 35777914 | ||||||
chr19:35777929
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.189+21C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3/20 | chr19 | 35777929 | ||||||
chr19:35778021
|
C | T | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(67): Show | 233 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.189+113C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3/20 | chr19 | 35778021 | ||||||
chr19:35778071
|
A | G | 1 | a0002c0011t0001g0065 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.189+163A>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3/20 | chr19 | 35778071 | ||||||
chr19:35778131
|
A | G | 1 | a0001c0005t0001g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.190-149A>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3/20 | chr19 | 35778131 | ||||||
chr19:35778176
|
G | A | 6 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0080others(3): Show | 30 | HG00673.hp2 HG02027.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.190-104G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3/20 | chr19 | 35778176 | ||||||
chr19:35778214
|
T | C | 1 | a0001c0004t0001g0052 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.190-66T>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3/20 | chr19 | 35778214 | ||||||
chr19:35778261
|
C | T | 2 | a0001c0003t0001g0022a0001c0021t0001g0022 | 3 | HG02622.hp2 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.190-19C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3/20 | chr19 | 35778261 | ||||||
chr19:35778668
|
A | T | 1 | a0001c0010t0001g0036 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.408+67A>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 5/20 | chr19 | 35778668 | ||||||
chr19:35778700
|
G | C | 2 | a0001c0003t0001g0026a0001c0003t0001g0038 | 4 | HG03017.hp2 HG03710.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+99G>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 5/20 | chr19 | 35778700 | ||||||
chr19:35778750
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0070a0004c0008t0001g0004others(2): Show | 25 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.408+149G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 5/20 | chr19 | 35778750 | ||||||
chr19:35778838
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(73): Show | 263 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.409-194G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 5/20 | chr19 | 35778838 | ||||||
chr19:35778876
|
A | C | 1 | a0005c0015t0001g0040 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.409-156A>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 5/20 | chr19 | 35778876 | ||||||
chr19:35778992
|
C | T | 1 | a0001c0031t0001g0081 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.409-40C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 5/20 | chr19 | 35778992 | ||||||
chr19:35779013
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(73): Show | 263 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.409-19T>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 5/20 | chr19 | 35779013 | ||||||
chr19:35779150
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(74): Show | 266 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.501+26A>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 6/20 | chr19 | 35779150 | ||||||
chr19:35779206
|
G | A | 4 | a0001c0001t0001g0070a0001c0002t0001g0005a0001c0002t0001g0080others(1): Show | 26 | HG00609.hp1 HG02056.hp2 NA18939.hp1 others(23): Show |
intron_variant | MODIFIER | c.501+82G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 6/20 | chr19 | 35779206 | ||||||
chr19:35779282
|
G | C | 8 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0080others(5): Show | 32 | HG00609.hp2 HG00673.hp2 HG02027.hp2 others(29): Show |
intron_variant | MODIFIER | c.501+158G>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 6/20 | chr19 | 35779282 | ||||||
chr19:35779350
|
G | C | 1 | a0001c0023t0001g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.501+226G>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 6/20 | chr19 | 35779350 | ||||||
chr19:35779428
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.501+304G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 6/20 | chr19 | 35779428 | ||||||
chr19:35779445
|
C | T | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(67): Show | 233 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.501+321C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 6/20 | chr19 | 35779445 | ||||||
chr19:35779510
|
A | C | 1 | a0001c0001t0001g0076 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.501+386A>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 6/20 | chr19 | 35779510 | ||||||
chr19:35779516
|
G | T | 1 | a0001c0035t0001g0086 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.501+392G>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 6/20 | chr19 | 35779516 | ||||||
chr19:35779739
|
T | TA | 23 | a0001c0005t0001g0003a0001c0005t0001g0012a0001c0005t0001g0037others(20): Show | 56 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.502-463dupA | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 35779739 | |||||
chr19:35779822
|
G | A | 1 | a0001c0005t0001g0084 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.502-389G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 6/20 | chr19 | 35779822 | ||||||
chr19:35780102
|
G | A | 1 | a0001c0012t0001g0027 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.502-109G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 6/20 | chr19 | 35780102 | ||||||
chr19:35780200
|
C | G | 2 | a0001c0006t0001g0031a0015c0029t0001g0031 | 2 | NA18947.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.502-11C>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 6/20 | chr19 | 35780200 | ||||||
chr19:35780516
|
C | T | 2 | a0001c0004t0001g0053a0001c0005t0001g0060 | 2 | HG00609.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.702+18C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 8/20 | chr19 | 35780516 | ||||||
chr19:35780517
|
G | A | 2 | a0001c0005t0001g0061a0001c0005t0001g0085 | 2 | HG01361.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.702+19G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 8/20 | chr19 | 35780517 | ||||||
chr19:35780533
|
G | T | 1 | a0001c0005t0001g0064 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.702+35G>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 8/20 | chr19 | 35780533 | ||||||
chr19:35780685
|
G | T | 1 | a0019c0020t0001g0075 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.769+37G>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 9/20 | chr19 | 35780685 | ||||||
chr19:35780686
|
T | G | 1 | a0019c0020t0001g0075 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.769+38T>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 9/20 | chr19 | 35780686 | ||||||
chr19:35780709
|
G | A | 3 | a0001c0004t0001g0032a0001c0004t0001g0033a0001c0004t0001g0054 | 5 | HG02572.hp2 HG02922.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-48G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 9/20 | chr19 | 35780709 | ||||||
chr19:35781094
|
C | G | 1 | a0001c0004t0001g0052 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.982+22C>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 11/20 | chr19 | 35781094 | ||||||
chr19:35781132
|
G | C | 1 | a0001c0001t0001g0072 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.983-18G>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 11/20 | chr19 | 35781132 | ||||||
chr19:35781422
|
C | T | 1 | a0001c0004t0001g0066 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1085+170C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35781422 | ||||||
chr19:35781512
|
C | G | 3 | a0001c0004t0001g0032a0001c0004t0001g0033a0001c0004t0001g0054 | 5 | HG02572.hp2 HG02922.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1085+260C>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35781512 | ||||||
chr19:35781866
|
C | T | 1 | a0001c0004t0001g0055 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1086-507C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35781866 | ||||||
chr19:35781867
|
G | A | 1 | a0001c0005t0001g0062 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1086-506G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35781867 | ||||||
chr19:35781881
|
C | T | 1 | a0001c0003t0001g0047 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1086-492C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35781881 | ||||||
chr19:35781902
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1086-471G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35781902 | ||||||
chr19:35781931
|
G | A | 1 | a0001c0004t0001g0032 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1086-442G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35781931 | ||||||
chr19:35782040
|
C | A | 1 | a0001c0004t0001g0051 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1086-333C>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35782040 | ||||||
chr19:35782041
|
A | T | 1 | a0001c0004t0001g0051 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1086-332A>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35782041 | ||||||
chr19:35782042
|
T | G | 1 | a0001c0004t0001g0051 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1086-331T>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35782042 | ||||||
chr19:35782069
|
G | T | 2 | a0001c0003t0001g0039a0001c0003t0001g0046 | 2 | NA19082.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1086-304G>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35782069 | ||||||
chr19:35782120
|
T | C | 6 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0080others(3): Show | 30 | HG00673.hp2 HG02027.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.1086-253T>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35782120 | ||||||
chr19:35782178
|
C | T | 2 | a0001c0003t0001g0024a0001c0003t0001g0090 | 4 | HG03669.hp1 HG03704.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1086-195C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35782178 | ||||||
chr19:35782308
|
A | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0072others(5): Show | 39 | HG00423.hp2 HG00639.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.1086-65A>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35782308 | ||||||
chr19:35782319
|
G | A | 2 | a0001c0003t0001g0041a0001c0022t0001g0042 | 2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1086-54G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35782319 | ||||||
chr19:35782328
|
C | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(68): Show | 234 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1086-45C>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 12/20 | chr19 | 35782328 | ||||||
chr19:35782753
|
C | A | 1 | a0019c0020t0001g0075 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1314-9C>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 14/20 | chr19 | 35782753 | ||||||
chr19:35783586
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(72): Show | 261 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1422-586T>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 15/20 | chr19 | 35783586 | ||||||
chr19:35783598
|
G | A | 1 | a0001c0002t0001g0017 | 4 | HG02602.hp1 HG03834.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1422-574G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 15/20 | chr19 | 35783598 | ||||||
chr19:35783608
|
G | A | 6 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0080others(3): Show | 30 | HG00673.hp2 HG02027.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.1422-564G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 15/20 | chr19 | 35783608 | ||||||
chr19:35783640
|
G | C | 1 | a0001c0003t0001g0043 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1422-532G>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 15/20 | chr19 | 35783640 | ||||||
chr19:35783891
|
G | C | 6 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0080others(3): Show | 30 | HG00673.hp2 HG02027.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.1422-281G>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 15/20 | chr19 | 35783891 | ||||||
chr19:35783959
|
T | C | 23 | a0001c0005t0001g0003a0001c0005t0001g0012a0001c0005t0001g0059others(20): Show | 55 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1422-213T>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 15/20 | chr19 | 35783959 | ||||||
chr19:35784027
|
T | C | 2 | a0001c0001t0001g0035a0001c0003t0001g0041 | 3 | HG02735.hp2 NA18986.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1422-145T>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 15/20 | chr19 | 35784027 | ||||||
chr19:35784428
|
C | T | 1 | a0001c0003t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1567+111C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 16/20 | chr19 | 35784428 | ||||||
chr19:35784455
|
C | T | 1 | a0001c0001t0001g0014 | 8 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1567+138C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 16/20 | chr19 | 35784455 | ||||||
chr19:35784466
|
T | C | 1 | a0019c0020t0001g0075 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1567+149T>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 16/20 | chr19 | 35784466 | ||||||
chr19:35784477
|
C | G | 2 | a0001c0003t0001g0041a0001c0022t0001g0042 | 2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1567+160C>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 16/20 | chr19 | 35784477 | ||||||
chr19:35784810
|
C | T | 1 | a0001c0002t0001g0030 | 2 | HG00140.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1568-143C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 16/20 | chr19 | 35784810 | ||||||
chr19:35785125
|
G | A | 6 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0080others(3): Show | 30 | HG00673.hp2 HG02027.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.1721+19G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 17/20 | chr19 | 35785125 | ||||||
chr19:35785184
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(38): Show | 177 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(174): Show |
splice_region_variant&intron_variant | LOW | c.1722-5C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 17/20 | chr19 | 35785184 | ||||||
chr19:35785358
|
G | C | 1 | a0003c0009t0001g0082 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1867+24G>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 18/20 | chr19 | 35785358 | ||||||
chr19:35785366
|
C | T | 1 | a0001c0004t0001g0016 | 5 | HG00673.hp1 HG01255.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1867+32C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 18/20 | chr19 | 35785366 | ||||||
chr19:35785400
|
C | T | 1 | a0001c0005t0001g0063 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1868-9C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 18/20 | chr19 | 35785400 | ||||||
chr19:35785501
|
T | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(73): Show | 263 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1942+18T>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 19/20 | chr19 | 35785501 | ||||||
chr19:35785641
|
C | CA | 6 | a0001c0001t0001g0004a0001c0001t0001g0070a0001c0001t0001g0074others(3): Show | 26 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.1942+159dupA | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 35785641 | |||||
chr19:35785806
|
G | A | 9 | a0001c0003t0001g0009a0001c0003t0001g0011a0001c0003t0001g0024others(6): Show | 39 | HG00408.hp2 HG00621.hp1 HG02165.hp2 others(36): Show |
intron_variant | MODIFIER | c.1942+323G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 19/20 | chr19 | 35785806 | ||||||
chr19:35785865
|
A | C | 2 | a0001c0005t0001g0062a0001c0005t0001g0064 | 2 | HG02523.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1942+382A>C | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 19/20 | chr19 | 35785865 | ||||||
chr19:35785865
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(96): Show | 348 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(345): Show |
intron_variant | MODIFIER | c.1942+382A>G | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 19/20 | chr19 | 35785865 | ||||||
chr19:35785996
|
G | A | 5 | a0001c0004t0001g0010a0001c0004t0001g0016a0001c0004t0001g0051others(2): Show | 22 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.1943-417G>A | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 19/20 | chr19 | 35785996 | ||||||
chr19:35786010
|
C | T | 1 | a0001c0005t0001g0085 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1943-403C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 19/20 | chr19 | 35786010 | ||||||
chr19:35786057
|
A | T | 1 | a0001c0004t0001g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1943-356A>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 19/20 | chr19 | 35786057 | ||||||
chr19:35786103
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1943-310C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 19/20 | chr19 | 35786103 | ||||||
chr19:35786406
|
C | T | 2 | a0001c0002t0001g0028a0001c0002t0001g0045 | 3 | HG00544.hp1 NA18747.hp2 NA19063.hp1 |
splice_region_variant&intron_variant | LOW | c.1943-7C>T | ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 19/20 | chr19 | 35786406 |