geneid | 89839 |
---|---|
ensemblid | ENSG00000285077.4 |
hgncid | 15782 |
symbol | ARHGAP11B |
name | Rho GTPase activating protein 11B |
refseq_nuc | NM_001039841.3 |
refseq_prot | NP_001034930.1 |
ensembl_nuc | ENST00000697964.2 |
ensembl_prot | ENSP00000513489.1 |
mane_status | MANE Select |
chr | chr15 |
start | 30626128 |
end | 30638810 |
strand | + |
ver | v1.2 |
region | chr15:30626128-30638810 |
region5000 | chr15:30621128-30643810 |
regionname0 | ARHGAP11B_chr15_30626128_30638810 |
regionname5000 | ARHGAP11B_chr15_30621128_30643810 |
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 | 0/1 | 267 | 237 | 84 | 46 | 61 | 14 | 31 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0002 | 0/0 | 267 | 7 | 6 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0003 | 0/0 | 267 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0004 | 0/0 | 267 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0005 | 0/0 | 267 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | 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 | 0/1 | 804 | 237 | 84 | 46 | 61 | 14 | 31 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
c0002 | 0/0 | 804 | 7 | 6 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
c0003 | 0/0 | 804 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
c0004 | 0/0 | 804 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
c0005 | 0/0 | 804 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | 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 | 0/1 | 762 | 238 | 86 | 47 | 60 | 14 | 30 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
t0002 | 0/0 | 762 | 6 | 4 | 1 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
t0003 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
t0004 | 0/0 | 762 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
t0005 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | 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 | 0/0 | 46 | 3 | 14 | 17 | 4 | 8 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0002 | 0/0 | 15 | 1 | 4 | 3 | 5 | 2 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0003 | 0/0 | 14 | 13 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0004 | 0/0 | 13 | 3 | 2 | 4 | 1 | 3 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0005 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0006 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0007 | 0/0 | 7 | 0 | 2 | 0 | 1 | 4 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0008 | 0/0 | 6 | 2 | 1 | 0 | 2 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0010 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0017 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
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 | 0/1 | 237 | 84 | 46 | 61 | 14 | 31 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0002c0002 | a0002 | c0002 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0003c0005 | a0003 | c0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0004c0003 | a0004 | c0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0005c0004 | a0005 | c0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | 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 | 0/1 | 228 | 80 | 45 | 59 | 14 | 29 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 6 | 4 | 1 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0003c0005t0001 | a0003 | c0005 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0004c0003t0001 | a0004 | c0003 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | copy fasta |
a0005c0004t0001 | a0005 | c0004 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 45 | 3 | 14 | 16 | 4 | 8 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 15 | 1 | 4 | 3 | 5 | 2 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 14 | 13 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 12 | 3 | 1 | 4 | 1 | 3 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 6 | 0 | 2 | 0 | 1 | 3 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 6 | 2 | 1 | 0 | 2 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0002g0023 | a0001 | c0001 | t0002 | g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0002g0037 | a0001 | c0001 | t0002 | g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0002g0040 | a0001 | c0001 | t0002 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0002g0046 | a0001 | c0001 | t0002 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0002g0047 | a0001 | c0001 | t0002 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0002g0082 | a0001 | c0001 | t0002 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0003g0018 | a0001 | c0001 | t0003 | g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0004g0084 | a0001 | c0001 | t0004 | g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0001c0001t0005g0001 | a0001 | c0001 | t0005 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0002c0002t0001g0009 | a0002 | c0002 | t0001 | g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0002c0002t0001g0058 | a0002 | c0002 | t0001 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0002c0002t0001g0083 | a0002 | c0002 | t0001 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0002c0002t0001g0087 | a0002 | c0002 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0003c0005t0001g0004 | a0003 | c0005 | t0001 | g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0004c0003t0001g0018 | a0004 | c0003 | t0001 | g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
a0005c0004t0001g0007 | a0005 | c0004 | t0001 | g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00673 | hp2 | a0004 | c0003 | t0001 | g0018 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01952 | hp2 | a0003 | c0005 | t0001 | g0004 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0084 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG04204 | hp1 | a0005 | c0004 | t0001 | g0007 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | YRI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | YRI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19001 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ASW | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0083 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | USA | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | LWK | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0044 | REF | REF | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:30626947
|
G | C | 1 | a0002 | 7 | HG01081.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
missense_variant&splice_region_variant | MODERATE | c.127G>C | p.Gly43Arg | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/7 | 820/1565 | 127/804 | 43/267 | chr15 | 30626947 | ||
chr15:30633523
|
A | C | 1 | a0003 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.234A>C | p.Glu78Asp | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 3/7 | 927/1565 | 234/804 | 78/267 | chr15 | 30633523 | ||
chr15:30635148
|
G | A | 1 | a0004 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.620G>A | p.Ser207Asn | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 5/7 | 1313/1565 | 620/804 | 207/267 | chr15 | 30635148 | ||
chr15:30635624
|
C | A | 1 | a0005 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.798C>A | p.Asn266Lys | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/7 | 1491/1565 | 798/804 | 266/267 | chr15 | 30635624 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:30626400
|
G | T | 1 | a0001c0001t0005 | 1 | NA19001.hp2 | 5_prime_UTR_variant | MODIFIER | c.-421G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/7 | 421 | chr15 | 30626400 | |||||
chr15:30626570
|
C | G | 1 | a0001c0001t0002 | 6 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-251C>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/7 | 251 | chr15 | 30626570 | |||||
chr15:30626589
|
G | A | 1 | a0001c0001t0003 | 1 | NA18986.hp1 | 5_prime_UTR_variant | MODIFIER | c.-232G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/7 | 232 | chr15 | 30626589 | |||||
chr15:30626689
|
G | T | 1 | a0001c0001t0004 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/7 | 132 | chr15 | 30626689 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:30627116
|
G | GT | 4 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0101others(1): Show | 8 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.129+177dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 30627116 | |||||
chr15:30627134
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.129+185G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30627134 | ||||||
chr15:30627147
|
TGAGA | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 6 | HG01256.hp2 HG01258.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+201_129+204del others(4): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 30627147 | |||||
chr15:30627335
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.129+386A>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30627335 | ||||||
chr15:30627566
|
A | AT | 11 | a0001c0001t0001g0018a0001c0001t0001g0033a0001c0001t0001g0093others(8): Show | 11 | HG00423.hp1 HG00673.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.129+628dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 30627566 | |||||
chr15:30627758
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.129+809G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30627758 | ||||||
chr15:30627931
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.129+982G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30627931 | ||||||
chr15:30628079
|
C | CT | 18 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(15): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.129+1143dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 30628079 | |||||
chr15:30628195
|
C | G | 1 | a0001c0001t0001g0025 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.129+1246C>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30628195 | ||||||
chr15:30628275
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(40): Show | 77 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.129+1326G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30628275 | ||||||
chr15:30628282
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(40): Show | 77 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.129+1333T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30628282 | ||||||
chr15:30628515
|
C | A | 1 | a0001c0001t0001g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.129+1566C>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30628515 | ||||||
chr15:30628715
|
T | A | 1 | a0001c0001t0001g0092 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.129+1766T>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30628715 | ||||||
chr15:30628716
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.129+1767G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30628716 | ||||||
chr15:30629055
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.130-1648T>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629055 | ||||||
chr15:30629067
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130-1636G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629067 | ||||||
chr15:30629167
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.130-1536A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629167 | ||||||
chr15:30629310
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.130-1393G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629310 | ||||||
chr15:30629365
|
AC | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(58): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.130-1330delC | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 30629365 | |||||
chr15:30629375
|
C | G | 1 | a0001c0001t0004g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.130-1328C>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629375 | ||||||
chr15:30629426
|
C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0052others(2): Show | 13 | HG00280.hp1 HG01071.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.130-1277C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629426 | ||||||
chr15:30629508
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG00438.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.130-1195G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629508 | ||||||
chr15:30629602
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0101others(1): Show | 8 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-1101C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629602 | ||||||
chr15:30629765
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.130-938G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629765 | ||||||
chr15:30630143
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0090a0001c0001t0001g0091 | 4 | HG02572.hp1 HG02615.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-560A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30630143 | ||||||
chr15:30630181
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.130-522G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30630181 | ||||||
chr15:30630267
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.130-436C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30630267 | ||||||
chr15:30630295
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130-408G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30630295 | ||||||
chr15:30630401
|
TACTG | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0065 | 15 | HG01981.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.130-298_130-295del others(4): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 30630401 | |||||
chr15:30630673
|
G | A | 1 | a0001c0001t0001g0014 | 3 | HG00558.hp1 HG02132.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.130-30G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30630673 | ||||||
chr15:30630888
|
T | C | 1 | a0001c0001t0001g0015 | 3 | HG02622.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.200+115T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30630888 | ||||||
chr15:30630933
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.200+160T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30630933 | ||||||
chr15:30630970
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.200+197G>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30630970 | ||||||
chr15:30631131
|
A | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0101others(1): Show | 8 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.200+358A>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631131 | ||||||
chr15:30631151
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.200+378A>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631151 | ||||||
chr15:30631152
|
T | A | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.200+379T>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631152 | ||||||
chr15:30631153
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.200+380A>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631153 | ||||||
chr15:30631256
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.200+483T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631256 | ||||||
chr15:30631285
|
A | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 6 | HG00423.hp1 HG00673.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.200+512A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631285 | ||||||
chr15:30631352
|
C | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0039 | 3 | HG01975.hp2 HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.200+579C>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631352 | ||||||
chr15:30631353
|
C | CT | 1 | a0001c0001t0001g0005 | 9 | HG01884.hp2 HG01891.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.200+588dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30631353 | |||||
chr15:30631415
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0062 | 5 | HG02258.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.200+642A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631415 | ||||||
chr15:30631440
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.200+667C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631440 | ||||||
chr15:30631475
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.200+702A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631475 | ||||||
chr15:30631504
|
T | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(40): Show | 77 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.200+731T>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631504 | ||||||
chr15:30631537
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.200+764A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631537 | ||||||
chr15:30631626
|
C | A | 1 | a0001c0001t0001g0068 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.200+853C>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631626 | ||||||
chr15:30631784
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.200+1011G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631784 | ||||||
chr15:30631787
|
C | CT | 6 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0078others(3): Show | 6 | HG01261.hp1 HG01358.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.200+1030dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30631787 | |||||
chr15:30631803
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.200+1030T>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631803 | ||||||
chr15:30631816
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.200+1043C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631816 | ||||||
chr15:30631911
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.200+1138C>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631911 | ||||||
chr15:30632144
|
G | A | 1 | a0001c0001t0002g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.201-1346G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632144 | ||||||
chr15:30632166
|
A | AATCCCAG others(587): Show |
1 | a0001c0001t0001g0050 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.201-1312_201-1311i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(588): Show |
1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.201-1312_201-1311i others(597): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(586): Show |
1 | a0001c0001t0001g0092 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(586): Show |
1 | a0001c0001t0001g0069 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(589): Show |
2 | a0001c0001t0001g0020a0001c0001t0001g0081 | 3 | HG00544.hp2 HG02040.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.201-1312_201-1311i others(598): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(588): Show |
5 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG00741.hp1 HG01261.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.201-1312_201-1311i others(597): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(588): Show |
1 | a0002c0002t0001g0058 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.201-1312_201-1311i others(597): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(587): Show |
1 | a0001c0001t0001g0022 | 2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.201-1312_201-1311i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(587): Show |
44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(41): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.201-1312_201-1311i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(585): Show |
1 | a0001c0001t0001g0038 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.201-1312_201-1311i others(594): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(587): Show |
4 | a0001c0001t0001g0009a0001c0001t0001g0011a0002c0002t0001g0009others(1): Show | 10 | HG01081.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.201-1312_201-1311i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(586): Show |
2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02083.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(586): Show |
1 | a0002c0002t0001g0087 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(586): Show |
30 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(27): Show | 95 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(586): Show |
4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0101others(1): Show | 4 | HG01070.hp1 HG01496.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(585): Show |
1 | a0001c0001t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.201-1312_201-1311i others(594): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(585): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0098 | 4 | HG02735.hp1 HG03490.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.201-1312_201-1311i others(594): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(587): Show |
2 | a0001c0001t0001g0056a0001c0001t0001g0060 | 2 | HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.201-1312_201-1311i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(586): Show |
1 | a0001c0001t0001g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(588): Show |
1 | a0001c0001t0001g0052 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.201-1317_201-1316i others(597): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632166
|
A | AATCCCAG others(587): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0053 | 5 | HG00280.hp1 HG01258.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.201-1317_201-1316i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | |||||
chr15:30632169
|
C | CCCAGCAC others(587): Show |
1 | a0001c0001t0001g0068 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.201-1312_201-1311i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632169 | |||||
chr15:30632211
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.201-1279A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632211 | ||||||
chr15:30632220
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0057 | 10 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.201-1270A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632220 | ||||||
chr15:30632427
|
GA | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0076others(1): Show | 12 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.201-1052delA | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632427 | |||||
chr15:30632429
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.201-1061A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632429 | ||||||
chr15:30632451
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02630.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.201-1039C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632451 | ||||||
chr15:30632527
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.201-963T>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632527 | ||||||
chr15:30632558
|
C | A | 1 | a0001c0001t0001g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.201-932C>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632558 | ||||||
chr15:30632574
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.201-916C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632574 | ||||||
chr15:30632798
|
G | GA | 8 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0049others(5): Show | 8 | HG02109.hp2 HG02300.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-684dupA | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632798 | |||||
chr15:30632968
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.201-522G>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632968 | ||||||
chr15:30633076
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.201-414G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30633076 | ||||||
chr15:30633170
|
G | C | 1 | a0001c0001t0001g0067 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.201-320G>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30633170 | ||||||
chr15:30633246
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0102 | 5 | HG01070.hp1 HG01071.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.201-244G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30633246 | ||||||
chr15:30633331
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.201-159A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30633331 | ||||||
chr15:30633366
|
A | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0011a0002c0002t0001g0009others(3): Show | 12 | HG01081.hp2 HG02559.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.201-124A>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30633366 | ||||||
chr15:30633471
|
G | GA | 3 | a0001c0001t0001g0027a0001c0001t0001g0090a0001c0001t0001g0091 | 4 | HG02572.hp1 HG02615.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.201-13dupA | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30633471 | |||||
chr15:30633718
|
A | AT | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(68): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.297+143dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr15 | 30633718 | |||||
chr15:30633786
|
T | G | 1 | a0001c0001t0001g0044 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.297+200T>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 3/6 | chr15 | 30633786 | ||||||
chr15:30633807
|
T | C | 1 | a0001c0001t0001g0044 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.297+221T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 3/6 | chr15 | 30633807 | ||||||
chr15:30633877
|
T | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0062 | 5 | HG02258.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+291T>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 3/6 | chr15 | 30633877 | ||||||
chr15:30634106
|
G | C | 1 | a0001c0001t0001g0045 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.298-64G>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 3/6 | chr15 | 30634106 | ||||||
chr15:30634802
|
G | A | 1 | a0001c0001t0001g0003 | 14 | HG01981.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.552-278G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 4/6 | chr15 | 30634802 | ||||||
chr15:30634862
|
C | CTT | 1 | a0001c0001t0001g0015 | 3 | HG02622.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.552-217_552-216ins others(2): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 30634862 | |||||
chr15:30635007
|
A | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0057 | 10 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.552-73A>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 4/6 | chr15 | 30635007 | ||||||
chr15:30635211
|
TAC | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0101others(1): Show | 8 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.660+25_660+26delCA | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 30635211 | |||||
chr15:30635428
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0057 | 10 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.661-59T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 5/6 | chr15 | 30635428 | ||||||
chr15:30635642
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.*3+9T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30635642 | ||||||
chr15:30635664
|
A | G | 17 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(14): Show | 39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.*3+31A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30635664 | ||||||
chr15:30635776
|
G | T | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*3+143G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30635776 | ||||||
chr15:30635852
|
C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.*3+219C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30635852 | ||||||
chr15:30636249
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.*3+616G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30636249 | ||||||
chr15:30636373
|
T | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0057 | 10 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.*3+740T>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30636373 | ||||||
chr15:30636813
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*3+1180A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30636813 | ||||||
chr15:30636930
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.*3+1297C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30636930 | ||||||
chr15:30637121
|
A | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0034others(10): Show | 25 | HG01099.hp2 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.*3+1488A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30637121 | ||||||
chr15:30637542
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG02630.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.*4-1204G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30637542 | ||||||
chr15:30637666
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0101others(1): Show | 8 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.*4-1080G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30637666 | ||||||
chr15:30637722
|
A | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0038others(2): Show | 10 | HG01099.hp2 HG01243.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.*4-1024A>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30637722 | ||||||
chr15:30637781
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(20): Show | 47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.*4-965C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30637781 | ||||||
chr15:30637816
|
C | CT | 4 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0057others(1): Show | 13 | HG00544.hp1 HG01346.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.*4-909dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 30637816 | |||||
chr15:30637816
|
CT | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(47): Show | 103 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.*4-909delT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 30637816 | |||||
chr15:30637816
|
CTT | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0052others(8): Show | 14 | HG01081.hp2 HG01256.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.*4-910_*4-909delTT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 30637816 | |||||
chr15:30637902
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0062 | 5 | HG02258.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.*4-844C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30637902 | ||||||
chr15:30638046
|
C | T | 34 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0019others(31): Show | 52 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.*4-700C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30638046 | ||||||
chr15:30638109
|
TG | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.*4-635delG | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 30638109 | |||||
chr15:30638280
|
A | C | 1 | a0001c0001t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.*4-466A>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30638280 | ||||||
chr15:30638297
|
G | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.*4-449G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30638297 | ||||||
chr15:30638453
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0067others(1): Show | 7 | HG00438.hp1 HG00621.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.*4-293A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30638453 | ||||||
chr15:30638522
|
A | G | 1 | a0001c0001t0001g0025 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.*4-224A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30638522 |