geneid | 57636 |
---|---|
ensemblid | ENSG00000275832.5 |
hgncid | 29293 |
symbol | ARHGAP23 |
name | Rho GTPase activating protein 23 |
refseq_nuc | NM_001199417.2 |
refseq_prot | NP_001186346.1 |
ensembl_nuc | ENST00000622683.5 |
ensembl_prot | ENSP00000481862.1 |
mane_status | MANE Select |
chr | chr17 |
start | 38428464 |
end | 38512385 |
strand | + |
ver | v1.2 |
region | chr17:38428464-38512385 |
region5000 | chr17:38423464-38517385 |
regionname0 | ARHGAP23_chr17_38428464_38512385 |
regionname5000 | ARHGAP23_chr17_38423464_38517385 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1491 | 267 | 68 | 58 | 91 | 14 | 35 | 63 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0002 | 0/0 | 352 | 8 | 1 | 2 | 4 | 0 | 1 | 4 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0003 | 0/0 | 1491 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0004 | 0/0 | 1491 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0005 | 0/0 | 1491 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0006 | 0/0 | 1491 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0007 | 0/0 | 1491 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0008 | 0/0 | 1491 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0009 | 0/0 | 1491 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0010 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0011 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0012 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0013 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0014 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0015 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0016 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0017 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0018 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0019 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 4476 | 128 | 17 | 32 | 53 | 10 | 15 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0002 | 0/0 | 4476 | 24 | 1 | 4 | 10 | 0 | 9 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0003 | 0/0 | 4476 | 21 | 0 | 6 | 10 | 1 | 4 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0004 | 0/0 | 4476 | 20 | 10 | 6 | 1 | 2 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0005 | 0/0 | 4476 | 17 | 16 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0006 | 0/0 | 4476 | 7 | 0 | 0 | 7 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0007 | 0/0 | 4476 | 6 | 2 | 2 | 1 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0008 | 0/0 | 4476 | 5 | 0 | 1 | 2 | 1 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0009 | 0/0 | 4476 | 5 | 4 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0010 | 0/0 | 4476 | 5 | 3 | 2 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0011 | 0/0 | 4476 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0012 | 0/0 | 4476 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0013 | 0/0 | 4476 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0014 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0015 | 0/0 | 4477 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0016 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0017 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0018 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0019 | 0/0 | 4476 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0020 | 0/0 | 4476 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0021 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0022 | 0/0 | 4477 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0023 | 0/0 | 4477 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0024 | 0/0 | 4476 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0025 | 0/0 | 4476 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0026 | 0/0 | 4476 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0027 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0028 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0029 | 0/0 | 4476 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0030 | 0/0 | 4476 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0031 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0032 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0033 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0034 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0035 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0036 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0037 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0038 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0039 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0040 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0041 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0042 | 0/0 | 4476 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0043 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0044 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0045 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0046 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0047 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0048 | 0/0 | 4476 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0049 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0050 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0051 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0052 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0053 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0054 | 0/0 | 4476 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0055 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0056 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0057 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0058 | 0/0 | 4476 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
c0059 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1436 | 227 | 60 | 52 | 78 | 13 | 23 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0002 | 0/0 | 1436 | 36 | 1 | 5 | 19 | 0 | 11 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0003 | 0/0 | 1436 | 23 | 16 | 4 | 1 | 1 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0004 | 0/0 | 1433 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0005 | 0/0 | 1436 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0006 | 0/0 | 1432 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0007 | 0/0 | 1436 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0008 | 0/0 | 1436 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0009 | 0/0 | 1436 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0010 | 0/0 | 1436 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0011 | 0/0 | 1436 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0012 | 0/0 | 1436 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0013 | 0/0 | 1436 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0014 | 0/0 | 1436 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
t0015 | 0/0 | 1436 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0248 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4476 | 128 | 17 | 32 | 53 | 10 | 15 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0002 | 0/0 | 4476 | 24 | 1 | 4 | 10 | 0 | 9 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0003 | 0/0 | 4476 | 21 | 0 | 6 | 10 | 1 | 4 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0004 | 0/0 | 4476 | 20 | 10 | 6 | 1 | 2 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0005 | 0/0 | 4476 | 17 | 16 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0006 | 0/0 | 4476 | 7 | 0 | 0 | 7 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0007 | 0/0 | 4476 | 6 | 2 | 2 | 1 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0008 | 0/0 | 4476 | 5 | 0 | 1 | 2 | 1 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0009 | 0/0 | 4476 | 5 | 4 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0010 | 0/0 | 4476 | 5 | 3 | 2 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0011 | 0/0 | 4476 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0012 | 0/0 | 4476 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0016 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0018 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0020 | 0/0 | 4476 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0024 | 0/0 | 4476 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0025 | 0/0 | 4476 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0027 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0031 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0032 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0037 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0040 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0042 | 0/0 | 4476 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0043 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0045 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0048 | 0/0 | 4476 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0051 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0052 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0054 | 0/0 | 4476 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0002c0015 | 0/0 | 4477 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0002c0022 | 0/0 | 4477 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0002c0023 | 0/0 | 4477 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0002c0035 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0002c0036 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0003c0013 | 0/0 | 4476 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0003c0014 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0003c0028 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0003c0038 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0004c0017 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0004c0019 | 0/0 | 4476 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0004c0055 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0005c0033 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0005c0041 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0005c0053 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0006c0021 | 0/0 | 4476 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0007c0029 | 0/0 | 4476 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0008c0049 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0008c0050 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0009c0026 | 0/0 | 4476 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0010c0059 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0011c0030 | 0/0 | 4476 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0012c0034 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0013c0044 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0014c0046 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0015c0039 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0016c0056 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0017c0057 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0018c0047 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0019c0058 | 0/0 | 4476 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5911 | 122 | 16 | 31 | 51 | 9 | 14 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0001t0003 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0001t0007 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0001t0008 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0001t0009 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0001t0011 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0001t0014 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0002t0002 | 0/0 | 5911 | 23 | 1 | 4 | 10 | 0 | 8 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0002t0012 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0003t0001 | 0/0 | 5911 | 20 | 0 | 6 | 9 | 1 | 4 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0003t0007 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0004t0001 | 0/0 | 5911 | 19 | 9 | 6 | 1 | 2 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0004t0006 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0005t0001 | 0/0 | 5911 | 16 | 15 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0005t0006 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0006t0002 | 0/0 | 5911 | 7 | 0 | 0 | 7 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0007t0003 | 0/0 | 5911 | 4 | 1 | 2 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0007t0013 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0007t0015 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0008t0001 | 0/0 | 5911 | 5 | 0 | 1 | 2 | 1 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0009t0003 | 0/0 | 5911 | 5 | 4 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0010t0001 | 0/0 | 5911 | 5 | 3 | 2 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0011t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0011t0006 | 0/0 | 5907 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0012t0003 | 0/0 | 5911 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0016t0003 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0018t0001 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0020t0005 | 0/0 | 5911 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0024t0001 | 0/0 | 5911 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0025t0002 | 0/0 | 5911 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0027t0005 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0031t0003 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0032t0001 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0037t0003 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0040t0002 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0042t0001 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0043t0001 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0045t0001 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0048t0002 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0051t0003 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0052t0001 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0001c0054t0002 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0002c0015t0001 | 0/0 | 5912 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0002c0022t0001 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0002c0022t0010 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0002c0023t0001 | 0/0 | 5912 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0002c0035t0001 | 0/0 | 5912 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0002c0036t0003 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0003c0013t0001 | 0/0 | 5911 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0003c0014t0001 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0003c0028t0001 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0003c0038t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0004c0017t0004 | 0/0 | 5908 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0004c0019t0004 | 0/0 | 5908 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0004c0055t0004 | 0/0 | 5908 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0005c0033t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0005c0041t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0005c0053t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0006c0021t0003 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0007c0029t0001 | 0/0 | 5911 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0008c0049t0001 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0008c0050t0003 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0009c0026t0001 | 0/0 | 5911 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0010c0059t0001 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0011c0030t0001 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0012c0034t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0013c0044t0001 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0014c0046t0003 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0015c0039t0001 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0016c0056t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0017c0057t0001 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0018c0047t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
a0019c0058t0002 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | copy fasta | chr17 | 38423464 | 38517385 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0248 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0001t0014g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0002t0012g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0003t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0004t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0005t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0006t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0006t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0006t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0006t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0006t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0006t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0006t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0007t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0007t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0007t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0007t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0007t0013g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0007t0015g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0008t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0008t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0008t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0008t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0008t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0009t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0009t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0009t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0009t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0009t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0010t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0010t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0010t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0010t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0010t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0011t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0011t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0011t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0012t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0012t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0012t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0016t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0016t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0018t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0018t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0020t0005g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0020t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0024t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0024t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0025t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0025t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0027t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0027t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0031t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0032t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0037t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0040t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0042t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0043t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0045t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0048t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0051t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0052t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0001c0054t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0002c0015t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0002c0015t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0002c0022t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0002c0022t0010g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0002c0023t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0002c0023t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0002c0035t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0002c0036t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0003c0013t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0003c0013t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0003c0013t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0003c0014t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0003c0014t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0003c0028t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0003c0028t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0003c0038t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0004c0017t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0004c0017t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0004c0019t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0004c0019t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0004c0055t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0005c0033t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0005c0041t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0005c0053t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0006c0021t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0006c0021t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0007c0029t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0007c0029t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0008c0049t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0008c0050t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0009c0026t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0009c0026t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0010c0059t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0011c0030t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0012c0034t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0013c0044t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0014c0046t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0015c0039t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0016c0056t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0017c0057t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0018c0047t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
a0019c0058t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0008 | t0001 | g0198 | EUR | GBR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | GBR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | GBR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | FIN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | FIN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | FIN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00323 | hp2 | a0001 | c0004 | t0001 | g0069 | EUR | FIN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00544 | hp1 | a0001 | c0007 | t0003 | g0110 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00558 | hp1 | a0001 | c0006 | t0002 | g0176 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00597 | hp2 | a0001 | c0003 | t0007 | g0076 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00609 | hp1 | a0001 | c0025 | t0002 | g0183 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00621 | hp1 | a0001 | c0006 | t0002 | g0175 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00733 | hp1 | a0001 | c0005 | t0001 | g0034 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00733 | hp2 | a0014 | c0046 | t0003 | g0027 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00735 | hp2 | a0001 | c0040 | t0002 | g0135 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG00741 | hp2 | a0002 | c0015 | t0001 | g0243 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01070 | hp1 | a0001 | c0004 | t0001 | g0171 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01071 | hp1 | a0001 | c0004 | t0001 | g0170 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01071 | hp2 | a0001 | c0004 | t0001 | g0194 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01074 | hp2 | a0001 | c0010 | t0001 | g0169 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01081 | hp1 | a0001 | c0020 | t0005 | g0009 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01099 | hp2 | a0010 | c0059 | t0001 | g0021 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0063 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01109 | hp2 | a0001 | c0051 | t0003 | g0270 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01175 | hp1 | a0001 | c0004 | t0001 | g0182 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01243 | hp1 | a0001 | c0007 | t0003 | g0281 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01243 | hp2 | a0004 | c0019 | t0004 | g0058 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01255 | hp2 | a0015 | c0039 | t0001 | g0186 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0024 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01261 | hp2 | a0001 | c0001 | t0008 | g0260 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01346 | hp2 | a0001 | c0003 | t0001 | g0020 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01358 | hp1 | a0001 | c0032 | t0001 | g0201 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01361 | hp1 | a0002 | c0035 | t0001 | g0237 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0255 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01433 | hp2 | a0001 | c0004 | t0001 | g0131 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | IBS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01884 | hp1 | a0001 | c0005 | t0001 | g0050 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01884 | hp2 | a0003 | c0014 | t0001 | g0072 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01891 | hp1 | a0001 | c0004 | t0001 | g0052 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01891 | hp2 | a0018 | c0047 | t0001 | g0016 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01952 | hp1 | a0001 | c0008 | t0001 | g0197 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01952 | hp2 | a0001 | c0003 | t0001 | g0113 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01981 | hp2 | a0001 | c0003 | t0001 | g0263 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01993 | hp1 | a0001 | c0010 | t0001 | g0168 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02055 | hp1 | a0001 | c0004 | t0001 | g0029 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02055 | hp2 | a0001 | c0005 | t0001 | g0031 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02071 | hp1 | a0001 | c0006 | t0002 | g0177 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02071 | hp2 | a0001 | c0024 | t0001 | g0096 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02135 | hp1 | a0013 | c0044 | t0001 | g0192 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02145 | hp1 | a0006 | c0021 | t0003 | g0068 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02145 | hp2 | a0003 | c0028 | t0001 | g0015 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02148 | hp1 | a0001 | c0004 | t0001 | g0199 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02148 | hp2 | a0001 | c0007 | t0003 | g0018 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | CDX | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02165 | hp2 | a0017 | c0057 | t0001 | g0282 | EAS | CDX | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02257 | hp2 | a0001 | c0005 | t0001 | g0156 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02258 | hp1 | a0001 | c0005 | t0001 | g0048 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02258 | hp2 | a0001 | c0011 | t0006 | g0071 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02280 | hp1 | a0005 | c0053 | t0001 | g0126 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02280 | hp2 | a0006 | c0021 | t0003 | g0070 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0193 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02451 | hp2 | a0001 | c0010 | t0001 | g0161 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02572 | hp1 | a0001 | c0005 | t0006 | g0033 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0120 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02602 | hp2 | a0001 | c0054 | t0002 | g0230 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02622 | hp1 | a0001 | c0004 | t0001 | g0162 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02622 | hp2 | a0001 | c0009 | t0003 | g0173 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02630 | hp2 | a0012 | c0034 | t0001 | g0037 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02647 | hp1 | a0001 | c0012 | t0003 | g0043 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02647 | hp2 | a0001 | c0004 | t0001 | g0053 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02723 | hp1 | a0001 | c0005 | t0001 | g0036 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02723 | hp2 | a0001 | c0031 | t0003 | g0065 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02735 | hp1 | a0001 | c0007 | t0015 | g0273 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0025 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0229 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02738 | hp2 | a0002 | c0023 | t0001 | g0239 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02809 | hp2 | a0001 | c0009 | t0003 | g0172 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02818 | hp1 | a0001 | c0004 | t0006 | g0008 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02818 | hp2 | a0001 | c0005 | t0001 | g0042 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02886 | hp1 | a0001 | c0005 | t0001 | g0038 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02886 | hp2 | a0001 | c0016 | t0003 | g0045 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02895 | hp2 | a0003 | c0013 | t0001 | g0127 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02896 | hp1 | a0003 | c0014 | t0001 | g0066 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02896 | hp2 | a0003 | c0013 | t0001 | g0130 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02922 | hp1 | a0003 | c0038 | t0001 | g0158 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02922 | hp2 | a0001 | c0027 | t0005 | g0144 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02965 | hp1 | a0001 | c0004 | t0001 | g0129 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02970 | hp1 | a0004 | c0019 | t0004 | g0061 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02970 | hp2 | a0001 | c0018 | t0001 | g0039 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03017 | hp1 | a0001 | c0008 | t0001 | g0028 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0121 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03041 | hp1 | a0001 | c0004 | t0001 | g0057 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03098 | hp2 | a0001 | c0005 | t0001 | g0035 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03130 | hp1 | a0001 | c0001 | t0011 | g0062 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03139 | hp2 | a0004 | c0017 | t0004 | g0138 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03195 | hp1 | a0001 | c0007 | t0003 | g0051 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03195 | hp2 | a0001 | c0011 | t0006 | g0074 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03209 | hp1 | a0004 | c0017 | t0004 | g0139 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03209 | hp2 | a0001 | c0012 | t0003 | g0049 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03225 | hp1 | a0001 | c0018 | t0001 | g0044 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03225 | hp2 | a0001 | c0009 | t0003 | g0159 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03453 | hp1 | a0001 | c0005 | t0001 | g0047 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03453 | hp2 | a0001 | c0037 | t0003 | g0137 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03486 | hp1 | a0003 | c0013 | t0001 | g0128 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03486 | hp2 | a0001 | c0004 | t0001 | g0059 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0123 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03516 | hp1 | a0001 | c0012 | t0003 | g0046 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03516 | hp2 | a0001 | c0004 | t0001 | g0060 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03540 | hp2 | a0001 | c0010 | t0001 | g0160 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03579 | hp1 | a0001 | c0009 | t0003 | g0055 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03579 | hp2 | a0001 | c0005 | t0001 | g0157 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0258 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0242 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03688 | hp1 | a0019 | c0058 | t0002 | g0202 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03688 | hp2 | a0001 | c0009 | t0003 | g0190 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03710 | hp1 | a0001 | c0004 | t0001 | g0287 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03710 | hp2 | a0001 | c0002 | t0012 | g0106 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03927 | hp1 | a0001 | c0048 | t0002 | g0111 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0022 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0114 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG04115 | hp2 | a0001 | c0042 | t0001 | g0261 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0099 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG04199 | hp1 | a0011 | c0030 | t0001 | g0167 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG04199 | hp2 | a0001 | c0003 | t0001 | g0232 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0185 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18522 | hp1 | a0001 | c0010 | t0001 | g0014 | AFR | YRI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18522 | hp2 | a0001 | c0005 | t0001 | g0040 | AFR | YRI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18747 | hp1 | a0001 | c0025 | t0002 | g0212 | EAS | CHB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18906 | hp1 | a0003 | c0028 | t0001 | g0303 | AFR | YRI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18906 | hp2 | a0001 | c0005 | t0001 | g0041 | AFR | YRI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18940 | hp1 | a0007 | c0029 | t0001 | g0289 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18940 | hp2 | a0007 | c0029 | t0001 | g0181 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18948 | hp2 | a0001 | c0006 | t0002 | g0084 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18957 | hp1 | a0001 | c0006 | t0002 | g0204 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18960 | hp1 | a0001 | c0052 | t0001 | g0291 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18963 | hp1 | a0008 | c0049 | t0001 | g0266 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18963 | hp2 | a0001 | c0006 | t0002 | g0209 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18966 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18970 | hp1 | a0009 | c0026 | t0001 | g0097 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18975 | hp1 | a0001 | c0024 | t0001 | g0103 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18979 | hp1 | a0001 | c0001 | t0007 | g0104 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18979 | hp2 | a0001 | c0003 | t0001 | g0293 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18983 | hp1 | a0001 | c0008 | t0001 | g0195 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18985 | hp1 | a0002 | c0015 | t0001 | g0189 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18985 | hp2 | a0001 | c0043 | t0001 | g0178 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18995 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18998 | hp2 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19004 | hp1 | a0001 | c0003 | t0001 | g0191 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19030 | hp1 | a0001 | c0011 | t0001 | g0067 | AFR | LWK | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19030 | hp2 | a0005 | c0041 | t0001 | g0030 | AFR | LWK | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19043 | hp1 | a0002 | c0036 | t0003 | g0179 | AFR | LWK | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19043 | hp2 | a0001 | c0007 | t0013 | g0146 | AFR | LWK | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19054 | hp1 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19062 | hp1 | a0002 | c0022 | t0010 | g0257 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19062 | hp2 | a0002 | c0022 | t0001 | g0095 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19065 | hp1 | a0009 | c0026 | t0001 | g0284 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19067 | hp2 | a0001 | c0045 | t0001 | g0094 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19077 | hp2 | a0001 | c0006 | t0002 | g0210 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19087 | hp1 | a0001 | c0008 | t0001 | g0188 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19090 | hp1 | a0002 | c0023 | t0001 | g0180 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19091 | hp1 | a0001 | c0004 | t0001 | g0304 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0155 | AFR | YRI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA19240 | hp2 | a0001 | c0005 | t0001 | g0145 | AFR | YRI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ASW | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA20129 | hp2 | a0001 | c0004 | t0001 | g0054 | AFR | ASW | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | TSI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0174 | EUR | TSI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA20805 | hp1 | a0001 | c0004 | t0001 | g0280 | EUR | TSI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0279 | EUR | TSI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA20905 | hp1 | a0001 | c0001 | t0014 | g0274 | SAS | GIH | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02109 | hp1 | a0008 | c0050 | t0003 | g0136 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02109 | hp2 | a0016 | c0056 | t0001 | g0011 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02486 | hp1 | a0004 | c0055 | t0004 | g0302 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG02486 | hp2 | a0001 | c0005 | t0001 | g0142 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG03471 | hp2 | a0001 | c0020 | t0005 | g0141 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | USA | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
HG06807 | hp2 | a0005 | c0033 | t0001 | g0073 | AFR | USA | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA20300 | hp2 | a0001 | c0016 | t0003 | g0301 | AFR | USA | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA21309 | hp1 | a0001 | c0005 | t0001 | g0140 | AFR | LWK | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
NA21309 | hp2 | a0001 | c0027 | t0005 | g0153 | AFR | LWK | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0248 | REF | REF | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:38458241
|
C | T | 1 | a0010 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.203C>T | p.Ser68Leu | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/24 | 225/5911 | 203/4476 | 68/1491 | chr17 | 38458241 | ||
chr17:38462857
|
C | T | 1 | a0019 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.265C>T | p.Arg89Trp | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4/24 | 287/5911 | 265/4476 | 89/1491 | chr17 | 38462857 | ||
chr17:38462864
|
G | A | 1 | a0011 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.272G>A | p.Arg91His | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4/24 | 294/5911 | 272/4476 | 91/1491 | chr17 | 38462864 | ||
chr17:38466282
|
G | A | 1 | a0012 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.599G>A | p.Arg200Gln | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 621/5911 | 599/4476 | 200/1491 | chr17 | 38466282 | ||
chr17:38466480
|
C | T | 1 | a0006 | 2 | HG02145.hp1 HG02280.hp2 |
missense_variant | MODERATE | c.797C>T | p.Thr266Met | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 819/5911 | 797/4476 | 266/1491 | chr17 | 38466480 | ||
chr17:38466571
|
A | AC | 1 | a0002 | 8 | HG00741.hp2 HG01361.hp1 HG02738.hp2 others(5): Show |
frameshift_variant | HIGH | c.892dupC | p.Arg298fs | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 915/5911 | 893/4476 | 298/1491 | INFO_REALIGN_3_PRIME | chr17 | 38466571 | |
chr17:38466804
|
G | T | 1 | a0007 | 2 | NA18940.hp1 NA18940.hp2 |
missense_variant | MODERATE | c.1121G>T | p.Arg374Leu | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1143/5911 | 1121/4476 | 374/1491 | chr17 | 38466804 | ||
chr17:38466879
|
G | A | 1 | a0013 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.1196G>A | p.Gly399Glu | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1218/5911 | 1196/4476 | 399/1491 | chr17 | 38466879 | ||
chr17:38466942
|
G | A | 1 | a0014 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.1259G>A | p.Arg420Gln | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1281/5911 | 1259/4476 | 420/1491 | chr17 | 38466942 | ||
chr17:38467128
|
C | T | 1 | a0006 | 2 | HG02145.hp1 HG02280.hp2 |
missense_variant | MODERATE | c.1445C>T | p.Ala482Val | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1467/5911 | 1445/4476 | 482/1491 | chr17 | 38467128 | ||
chr17:38467266
|
G | A | 1 | a0015 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1583G>A | p.Arg528His | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1605/5911 | 1583/4476 | 528/1491 | chr17 | 38467266 | ||
chr17:38471937
|
T | G | 1 | a0018 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2049T>G | p.Asp683Glu | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/24 | 2071/5911 | 2049/4476 | 683/1491 | chr17 | 38471937 | ||
chr17:38477679
|
C | T | 1 | a0017 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.2219C>T | p.Ala740Val | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/24 | 2241/5911 | 2219/4476 | 740/1491 | chr17 | 38477679 | ||
chr17:38477718
|
C | T | 1 | a0016 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2258C>T | p.Ala753Val | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/24 | 2280/5911 | 2258/4476 | 753/1491 | chr17 | 38477718 | ||
chr17:38491417
|
G | A | 1 | a0008 | 2 | HG02109.hp1 NA18963.hp1 |
missense_variant | MODERATE | c.3161G>A | p.Arg1054Gln | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/24 | 3183/5911 | 3161/4476 | 1054/1491 | chr17 | 38491417 | ||
chr17:38510370
|
G | C | 1 | a0005 | 3 | HG02280.hp1 HG06807.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.3874G>C | p.Ala1292Pro | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3896/5911 | 3874/4476 | 1292/1491 | chr17 | 38510370 | ||
chr17:38510613
|
C | T | 1 | a0009 | 2 | NA18970.hp1 NA19065.hp1 |
missense_variant | MODERATE | c.4117C>T | p.Arg1373Cys | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4139/5911 | 4117/4476 | 1373/1491 | chr17 | 38510613 | ||
chr17:38510616
|
C | G | 1 | a0003 | 8 | HG01884.hp2 HG02145.hp2 HG02895.hp2 others(5): Show |
missense_variant | MODERATE | c.4120C>G | p.Leu1374Val | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4142/5911 | 4120/4476 | 1374/1491 | chr17 | 38510616 | ||
chr17:38510947
|
C | T | 1 | a0004 | 5 | HG01243.hp2 HG02486.hp1 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.4451C>T | p.Ala1484Val | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4473/5911 | 4451/4476 | 1484/1491 | chr17 | 38510947 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:38462898
|
T | C | 1 | a0001c0031 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.306T>C | p.Asn102Asn | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4/24 | 328/5911 | 306/4476 | 102/1491 | chr17 | 38462898 | ||
chr17:38466205
|
G | A | 4 | a0001c0011a0001c0032a0003c0014others(1): Show | 7 | HG01358.hp1 HG01884.hp2 HG02258.hp2 others(4): Show |
synonymous_variant | LOW | c.522G>A | p.Pro174Pro | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 544/5911 | 522/4476 | 174/1491 | chr17 | 38466205 | ||
chr17:38466241
|
C | G | 31 | a0001c0001a0001c0002a0001c0003others(28): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
synonymous_variant | LOW | c.558C>G | p.Pro186Pro | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 580/5911 | 558/4476 | 186/1491 | chr17 | 38466241 | ||
chr17:38466469
|
G | A | 1 | a0001c0043 | 1 | NA18985.hp2 | synonymous_variant | LOW | c.786G>A | p.Ser262Ser | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 808/5911 | 786/4476 | 262/1491 | chr17 | 38466469 | ||
chr17:38466661
|
C | T | 1 | a0006c0021 | 2 | HG02145.hp1 HG02280.hp2 |
synonymous_variant | LOW | c.978C>T | p.Pro326Pro | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1000/5911 | 978/4476 | 326/1491 | chr17 | 38466661 | ||
chr17:38466898
|
G | A | 6 | a0001c0016a0001c0024a0001c0037others(3): Show | 10 | HG02071.hp2 HG02886.hp2 HG03139.hp2 others(7): Show |
synonymous_variant | LOW | c.1215G>A | p.Pro405Pro | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1237/5911 | 1215/4476 | 405/1491 | chr17 | 38466898 | ||
chr17:38466916
|
G | A | 5 | a0001c0005a0001c0012a0001c0018others(2): Show | 24 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
synonymous_variant | LOW | c.1233G>A | p.Leu411Leu | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1255/5911 | 1233/4476 | 411/1491 | chr17 | 38466916 | ||
chr17:38469295
|
C | T | 3 | a0001c0016a0001c0037a0004c0017 | 5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
synonymous_variant | LOW | c.1800C>T | p.Asp600Asp | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 8/24 | 1822/5911 | 1800/4476 | 600/1491 | chr17 | 38469295 | ||
chr17:38479480
|
C | T | 50 | a0001c0001a0001c0002a0001c0003others(47): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
synonymous_variant | LOW | c.2481C>T | p.Asn827Asn | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/24 | 2503/5911 | 2481/4476 | 827/1491 | chr17 | 38479480 | ||
chr17:38482624
|
C | T | 1 | a0001c0042 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.2853C>T | p.Ser951Ser | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/24 | 2875/5911 | 2853/4476 | 951/1491 | chr17 | 38482624 | ||
chr17:38490133
|
C | T | 1 | a0004c0055 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.3018C>T | p.Arg1006Arg | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 18/24 | 3040/5911 | 3018/4476 | 1006/1491 | chr17 | 38490133 | ||
chr17:38490145
|
G | A | 4 | a0001c0032a0001c0040a0001c0048others(1): Show | 4 | HG00735.hp2 HG01358.hp1 HG01361.hp1 others(1): Show |
synonymous_variant | LOW | c.3030G>A | p.Ala1010Ala | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 18/24 | 3052/5911 | 3030/4476 | 1010/1491 | chr17 | 38490145 | ||
chr17:38510093
|
G | A | 1 | a0001c0051 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.3597G>A | p.Lys1199Lys | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3619/5911 | 3597/4476 | 1199/1491 | chr17 | 38510093 | ||
chr17:38510126
|
G | A | 1 | a0001c0052 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.3630G>A | p.Gln1210Gln | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3652/5911 | 3630/4476 | 1210/1491 | chr17 | 38510126 | ||
chr17:38510222
|
C | T | 1 | a0001c0054 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.3726C>T | p.Asp1242Asp | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3748/5911 | 3726/4476 | 1242/1491 | chr17 | 38510222 | ||
chr17:38510315
|
T | C | 47 | a0001c0001a0001c0002a0001c0004others(44): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
synonymous_variant | LOW | c.3819T>C | p.Asp1273Asp | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3841/5911 | 3819/4476 | 1273/1491 | chr17 | 38510315 | ||
chr17:38510375
|
G | A | 7 | a0001c0002a0001c0006a0001c0025others(4): Show | 37 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(34): Show |
synonymous_variant | LOW | c.3879G>A | p.Ala1293Ala | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3901/5911 | 3879/4476 | 1293/1491 | chr17 | 38510375 | ||
chr17:38510504
|
C | T | 2 | a0001c0020a0001c0027 | 4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
synonymous_variant | LOW | c.4008C>T | p.Gly1336Gly | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4030/5911 | 4008/4476 | 1336/1491 | chr17 | 38510504 | ||
chr17:38510783
|
C | A | 1 | a0001c0025 | 2 | HG00609.hp1 NA18747.hp1 |
synonymous_variant | LOW | c.4287C>A | p.Gly1429Gly | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4309/5911 | 4287/4476 | 1429/1491 | chr17 | 38510783 | ||
chr17:38510786
|
C | T | 10 | a0001c0007a0001c0009a0001c0012others(7): Show | 22 | HG00544.hp1 HG00733.hp2 HG01109.hp2 others(19): Show |
synonymous_variant | LOW | c.4290C>T | p.Pro1430Pro | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4312/5911 | 4290/4476 | 1430/1491 | chr17 | 38510786 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:38428471
|
C | G | 1 | a0001c0007t0015 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/24 | 15 | chr17 | 38428471 | |||||
chr17:38511244
|
C | T | 1 | a0001c0001t0014 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 272 | chr17 | 38511244 | |||||
chr17:38511384
|
C | A | 1 | a0001c0001t0008 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*412C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 412 | chr17 | 38511384 | |||||
chr17:38511428
|
AGAG | A | 6 | a0001c0004t0006a0001c0005t0006a0001c0011t0006others(3): Show | 9 | HG01243.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*461_*463delAGG | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 461 | INFO_REALIGN_3_PRIME | chr17 | 38511428 | ||||
chr17:38511523
|
T | C | 6 | a0001c0004t0006a0001c0005t0006a0001c0011t0006others(3): Show | 9 | HG01243.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*551T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 551 | chr17 | 38511523 | |||||
chr17:38511671
|
A | C | 1 | a0001c0007t0013 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*699A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 699 | chr17 | 38511671 | |||||
chr17:38511690
|
A | G | 1 | a0001c0002t0012 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*718A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 718 | chr17 | 38511690 | |||||
chr17:38511743
|
GT | G | 3 | a0001c0004t0006a0001c0005t0006a0001c0011t0006 | 4 | HG02258.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*772delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 772 | chr17 | 38511743 | |||||
chr17:38511744
|
T | G | 3 | a0004c0017t0004a0004c0019t0004a0004c0055t0004 | 5 | HG01243.hp2 HG02486.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*772T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 772 | chr17 | 38511744 | |||||
chr17:38511846
|
C | T | 1 | a0001c0001t0008 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*874C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 874 | chr17 | 38511846 | |||||
chr17:38511861
|
G | A | 1 | a0001c0001t0009 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*889G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 889 | chr17 | 38511861 | |||||
chr17:38511867
|
G | A | 8 | a0001c0002t0002a0001c0002t0012a0001c0006t0002others(5): Show | 37 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*895G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 895 | chr17 | 38511867 | |||||
chr17:38511960
|
G | A | 1 | a0002c0022t0010 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*988G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 988 | chr17 | 38511960 | |||||
chr17:38512057
|
C | G | 1 | a0001c0001t0011 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1085C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 1085 | chr17 | 38512057 | |||||
chr17:38512060
|
G | A | 22 | a0001c0001t0003a0001c0002t0002a0001c0002t0012others(19): Show | 62 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1088G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 1088 | chr17 | 38512060 | |||||
chr17:38512117
|
C | A | 2 | a0001c0020t0005a0001c0027t0005 | 4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1145C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 1145 | chr17 | 38512117 | |||||
chr17:38512182
|
A | T | 2 | a0001c0001t0007a0001c0003t0007 | 2 | HG00597.hp2 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1210A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 1210 | chr17 | 38512182 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:38428861
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+313G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38428861 | ||||||
chr17:38428900
|
C | A | 1 | a0001c0001t0001g0005 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.63+352C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38428900 | ||||||
chr17:38429027
|
C | A | 1 | a0001c0001t0001g0006 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.63+479C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429027 | ||||||
chr17:38429080
|
G | A | 1 | a0001c0001t0001g0007 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.63+532G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429080 | ||||||
chr17:38429209
|
C | T | 1 | a0001c0002t0002g0306 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.63+661C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429209 | ||||||
chr17:38429370
|
C | A | 167 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(164): Show | 167 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.63+822C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429370 | ||||||
chr17:38429402
|
G | T | 6 | a0001c0004t0001g0170a0001c0004t0001g0171a0001c0009t0003g0172others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+854G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429402 | ||||||
chr17:38429545
|
C | T | 6 | a0001c0004t0001g0170a0001c0004t0001g0171a0001c0009t0003g0172others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+997C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429545 | ||||||
chr17:38429586
|
T | C | 60 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(57): Show | 60 | HG00733.hp1 HG00733.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+1038T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429586 | ||||||
chr17:38429717
|
G | C | 1 | a0001c0001t0011g0062 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.63+1169G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429717 | ||||||
chr17:38429827
|
C | T | 1 | a0011c0030t0001g0167 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.63+1279C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429827 | ||||||
chr17:38429997
|
C | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | NA18945.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.63+1449C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429997 | ||||||
chr17:38430151
|
C | T | 6 | a0001c0001t0001g0056a0001c0004t0001g0057a0001c0004t0001g0059others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+1603C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430151 | ||||||
chr17:38430232
|
T | C | 61 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(58): Show | 61 | HG00733.hp1 HG00733.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+1684T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430232 | ||||||
chr17:38430280
|
G | A | 2 | a0001c0004t0006g0008a0001c0020t0005g0009 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+1732G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430280 | ||||||
chr17:38430339
|
G | T | 3 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054 | 3 | HG01891.hp1 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+1791G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430339 | ||||||
chr17:38430354
|
G | A | 4 | a0001c0006t0002g0175a0001c0006t0002g0176a0001c0006t0002g0177others(1): Show | 4 | HG00558.hp1 HG00621.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1806G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430354 | ||||||
chr17:38430476
|
G | C | 2 | a0001c0001t0001g0064a0001c0031t0003g0065 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.63+1928G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430476 | ||||||
chr17:38430522
|
G | A | 1 | a0002c0036t0003g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.63+1974G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430522 | ||||||
chr17:38430610
|
A | G | 235 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(232): Show | 235 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.63+2062A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430610 | ||||||
chr17:38430755
|
A | T | 1 | a0001c0002t0002g0164 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.63+2207A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430755 | ||||||
chr17:38430859
|
A | G | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.63+2311A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430859 | ||||||
chr17:38430920
|
C | T | 1 | a0002c0015t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.63+2372C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430920 | ||||||
chr17:38430940
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.63+2392C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430940 | ||||||
chr17:38431274
|
G | T | 6 | a0001c0004t0001g0170a0001c0004t0001g0171a0001c0009t0003g0172others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+2726G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38431274 | ||||||
chr17:38431295
|
C | G | 1 | a0001c0007t0003g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+2747C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38431295 | ||||||
chr17:38431394
|
A | G | 3 | a0001c0005t0001g0048a0001c0005t0001g0050a0001c0012t0003g0049 | 3 | HG01884.hp1 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.63+2846A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38431394 | ||||||
chr17:38431455
|
G | C | 2 | a0001c0004t0006g0008a0001c0020t0005g0009 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+2907G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38431455 | ||||||
chr17:38431489
|
C | T | 1 | a0001c0004t0001g0304 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.63+2941C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38431489 | ||||||
chr17:38432070
|
C | T | 75 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0064others(72): Show | 75 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.63+3522C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432070 | ||||||
chr17:38432140
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+3592C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432140 | ||||||
chr17:38432258
|
C | T | 1 | a0001c0008t0001g0028 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.63+3710C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432258 | ||||||
chr17:38432259
|
G | A | 2 | a0001c0001t0001g0056a0001c0004t0001g0029 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.63+3711G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432259 | ||||||
chr17:38432419
|
C | T | 2 | a0001c0005t0001g0047a0001c0012t0003g0046 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.63+3871C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432419 | ||||||
chr17:38432517
|
T | G | 1 | a0001c0002t0002g0244 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.63+3969T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432517 | ||||||
chr17:38432591
|
A | T | 1 | a0008c0050t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.63+4043A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432591 | ||||||
chr17:38432631
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.63+4083A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432631 | ||||||
chr17:38432635
|
C | T | 3 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054 | 3 | HG01891.hp1 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+4087C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432635 | ||||||
chr17:38432651
|
T | C | 75 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0064others(72): Show | 75 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.63+4103T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432651 | ||||||
chr17:38432851
|
A | T | 4 | a0001c0004t0001g0162a0001c0009t0003g0055a0001c0010t0001g0160others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+4303A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432851 | ||||||
chr17:38432931
|
T | A | 69 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0064others(66): Show | 69 | HG00733.hp1 HG01081.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.63+4383T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432931 | ||||||
chr17:38432954
|
C | T | 69 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0064others(66): Show | 69 | HG00733.hp1 HG01081.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.63+4406C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432954 | ||||||
chr17:38433509
|
G | A | 75 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0064others(72): Show | 75 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.63+4961G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433509 | ||||||
chr17:38433627
|
T | C | 6 | a0001c0005t0001g0140a0001c0016t0003g0301a0001c0020t0005g0141others(3): Show | 6 | HG03139.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+5079T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433627 | ||||||
chr17:38433633
|
A | G | 1 | a0001c0040t0002g0135 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.63+5085A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433633 | ||||||
chr17:38433857
|
G | T | 1 | a0001c0002t0002g0242 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.63+5309G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433857 | ||||||
chr17:38433860
|
G | A | 2 | a0001c0011t0001g0067a0003c0014t0001g0066 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.63+5312G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433860 | ||||||
chr17:38433872
|
G | A | 4 | a0001c0001t0003g0174a0001c0003t0001g0010a0001c0003t0001g0012others(1): Show | 4 | HG01261.hp1 HG02109.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+5324G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433872 | ||||||
chr17:38433981
|
T | G | 6 | a0001c0004t0001g0170a0001c0004t0001g0171a0001c0009t0003g0172others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+5433T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433981 | ||||||
chr17:38434204
|
C | T | 4 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG00639.hp2 HG02004.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+5656C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434204 | ||||||
chr17:38434265
|
G | T | 1 | a0001c0009t0003g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63+5717G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434265 | ||||||
chr17:38434492
|
G | A | 71 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0064others(68): Show | 71 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.63+5944G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434492 | ||||||
chr17:38434591
|
G | A | 10 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(7): Show | 10 | HG00280.hp2 HG01106.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+6043G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434591 | ||||||
chr17:38434825
|
C | T | 1 | a0002c0035t0001g0237 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.63+6277C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434825 | ||||||
chr17:38434947
|
G | C | 65 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0064others(62): Show | 65 | HG00733.hp1 HG01081.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.63+6399G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434947 | ||||||
chr17:38434985
|
G | A | 2 | a0001c0004t0006g0008a0001c0020t0005g0009 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+6437G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434985 | ||||||
chr17:38434990
|
G | C | 2 | a0001c0004t0006g0008a0001c0020t0005g0009 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+6442G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434990 | ||||||
chr17:38435060
|
A | C | 1 | a0001c0001t0001g0299 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.63+6512A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435060 | ||||||
chr17:38435145
|
G | C | 6 | a0001c0005t0001g0140a0001c0016t0003g0301a0001c0020t0005g0141others(3): Show | 6 | HG03139.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+6597G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435145 | ||||||
chr17:38435302
|
G | A | 1 | a0001c0004t0001g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.63+6754G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435302 | ||||||
chr17:38435302
|
G | GGAGA | 63 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0064others(60): Show | 63 | HG00733.hp1 HG01081.hp1 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.63+6754_63+6755ins others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435302 | ||||||
chr17:38435354
|
A | G | 4 | a0001c0004t0001g0059a0001c0004t0001g0060a0004c0019t0004g0058others(1): Show | 4 | HG01243.hp2 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6806A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435354 | ||||||
chr17:38435620
|
C | T | 2 | a0001c0009t0003g0172a0001c0009t0003g0173 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.63+7072C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435620 | ||||||
chr17:38435748
|
T | C | 2 | a0001c0004t0006g0008a0001c0020t0005g0009 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+7200T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435748 | ||||||
chr17:38435791
|
G | A | 160 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(157): Show | 160 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.63+7243G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435791 | ||||||
chr17:38435802
|
T | C | 2 | a0001c0004t0006g0008a0001c0020t0005g0009 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+7254T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435802 | ||||||
chr17:38435872
|
A | G | 1 | a0001c0003t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.63+7324A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435872 | ||||||
chr17:38435881
|
G | A | 7 | a0001c0002t0002g0244a0001c0005t0001g0140a0001c0016t0003g0301others(4): Show | 7 | HG02074.hp1 HG03139.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+7333G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435881 | ||||||
chr17:38435890
|
C | T | 150 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(147): Show | 150 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.63+7342C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435890 | ||||||
chr17:38436075
|
G | A | 1 | a0001c0004t0006g0008 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.63+7527G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436075 | ||||||
chr17:38436084
|
C | T | 161 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(158): Show | 161 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.63+7536C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436084 | ||||||
chr17:38436110
|
C | T | 161 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(158): Show | 161 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.63+7562C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436110 | ||||||
chr17:38436162
|
C | T | 80 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(77): Show | 80 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.63+7614C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436162 | ||||||
chr17:38436396
|
C | CA | 106 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0019others(103): Show | 106 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.63+7856dupA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38436396 | |||||
chr17:38436396
|
C | CAA | 7 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+7855_63+7856dup others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38436396 | |||||
chr17:38436397
|
A | C | 3 | a0001c0004t0006g0008a0001c0020t0005g0009a0001c0020t0005g0141 | 3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.63+7849A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436397 | ||||||
chr17:38436559
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.63+8011G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436559 | ||||||
chr17:38436774
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.63+8226C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436774 | ||||||
chr17:38436873
|
C | T | 1 | a0019c0058t0002g0202 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.63+8325C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436873 | ||||||
chr17:38437036
|
C | T | 3 | a0001c0010t0001g0014a0001c0011t0001g0067a0003c0014t0001g0066 | 3 | HG02896.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.63+8488C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437036 | ||||||
chr17:38437121
|
A | G | 1 | a0001c0010t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.63+8573A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437121 | ||||||
chr17:38437208
|
A | AT | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(172): Show | 177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.63+8675dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38437208 | |||||
chr17:38437208
|
A | ATT | 25 | a0001c0001t0001g0254a0001c0005t0001g0034a0001c0005t0001g0035others(22): Show | 25 | HG00733.hp1 HG01884.hp1 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+8674_63+8675dup others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38437208 | |||||
chr17:38437247
|
C | T | 14 | a0001c0001t0001g0305a0001c0003t0001g0263a0001c0004t0001g0069others(11): Show | 14 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.63+8699C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437247 | ||||||
chr17:38437270
|
A | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0163a0001c0010t0001g0014others(6): Show | 9 | HG02451.hp1 HG02572.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+8722A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437270 | ||||||
chr17:38437411
|
C | T | 1 | a0001c0004t0001g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.63+8863C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437411 | ||||||
chr17:38437486
|
G | A | 3 | a0001c0010t0001g0014a0001c0011t0001g0067a0003c0014t0001g0066 | 3 | HG02896.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.63+8938G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437486 | ||||||
chr17:38437559
|
G | C | 1 | a0004c0019t0004g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.63+9011G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437559 | ||||||
chr17:38437622
|
AC | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(121): Show | 126 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.63+9082delC | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38437622 | |||||
chr17:38437631
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+9083A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437631 | ||||||
chr17:38437738
|
T | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(121): Show | 126 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.63+9190T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437738 | ||||||
chr17:38437795
|
A | AG | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.63+9255dupG | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38437795 | |||||
chr17:38437799
|
G | GA | 31 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(28): Show | 31 | HG00733.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+9251_63+9252ins others(1): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437799 | ||||||
chr17:38437831
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+9283A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437831 | ||||||
chr17:38437866
|
T | C | 77 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0019others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.63+9318T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437866 | ||||||
chr17:38437913
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+9365G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437913 | ||||||
chr17:38437968
|
G | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(140): Show | 145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.63+9420G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437968 | ||||||
chr17:38437987
|
A | AAGGCTTC | 11 | a0001c0001t0001g0305a0001c0003t0001g0263a0001c0004t0001g0069others(8): Show | 11 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+9441_63+9447dup others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38437987 | |||||
chr17:38438212
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+9664T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438212 | ||||||
chr17:38438213
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.63+9665T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438213 | ||||||
chr17:38438215
|
G | A | 1 | a0001c0010t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.63+9667G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438215 | ||||||
chr17:38438244
|
C | T | 1 | a0001c0004t0001g0162 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.63+9696C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438244 | ||||||
chr17:38438321
|
C | CA | 122 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(119): Show | 122 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+9793dupA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38438321 | |||||
chr17:38438321
|
C | CAA | 55 | a0001c0001t0001g0003a0001c0001t0001g0056a0001c0001t0001g0075others(52): Show | 55 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.63+9792_63+9793dup others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38438321 | |||||
chr17:38438321
|
CAAAAAAA others(2): Show |
C | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(97): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.63+9785_63+9793del others(9): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38438321 | |||||
chr17:38438402
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(96): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.63+9854G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438402 | ||||||
chr17:38438522
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.63+9974C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438522 | ||||||
chr17:38438655
|
G | GA | 70 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(67): Show | 70 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+10110dupA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38438655 | |||||
chr17:38438710
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+10162G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438710 | ||||||
chr17:38438771
|
G | T | 1 | a0008c0050t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.63+10223G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438771 | ||||||
chr17:38438966
|
T | C | 1 | a0001c0009t0003g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.63+10418T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438966 | ||||||
chr17:38439125
|
C | T | 41 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0093others(38): Show | 41 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.63+10577C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439125 | ||||||
chr17:38439190
|
A | G | 1 | a0001c0004t0001g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.63+10642A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439190 | ||||||
chr17:38439415
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.63+10867C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439415 | ||||||
chr17:38439465
|
C | T | 1 | a0001c0042t0001g0261 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.63+10917C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439465 | ||||||
chr17:38439535
|
T | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(112): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.63+10987T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439535 | ||||||
chr17:38439570
|
C | T | 1 | a0001c0004t0001g0199 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.63+11022C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439570 | ||||||
chr17:38439633
|
A | C | 2 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.63+11085A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439633 | ||||||
chr17:38439644
|
C | T | 4 | a0001c0016t0003g0301a0001c0037t0003g0137a0004c0017t0004g0138others(1): Show | 4 | HG03139.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+11096C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439644 | ||||||
chr17:38439659
|
A | G | 11 | a0001c0001t0001g0124a0001c0001t0001g0305a0001c0003t0001g0263others(8): Show | 11 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+11111A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439659 | ||||||
chr17:38439684
|
T | G | 3 | a0001c0004t0001g0060a0004c0019t0004g0058a0004c0019t0004g0061 | 3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.63+11136T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439684 | ||||||
chr17:38439777
|
CT | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(96): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.63+11244delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38439777 | |||||
chr17:38439866
|
A | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(226): Show | 231 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.63+11318A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439866 | ||||||
chr17:38439889
|
C | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG01256.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.63+11341C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439889 | ||||||
chr17:38439916
|
G | T | 67 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(64): Show | 67 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.63+11368G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439916 | ||||||
chr17:38440264
|
C | T | 1 | a0001c0012t0003g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.63+11716C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38440264 | ||||||
chr17:38440324
|
T | C | 3 | a0001c0010t0001g0014a0001c0011t0001g0067a0003c0014t0001g0066 | 3 | HG02896.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.63+11776T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38440324 | ||||||
chr17:38440587
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.63+12039C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38440587 | ||||||
chr17:38440590
|
G | A | 7 | a0001c0004t0006g0008a0001c0010t0001g0014a0001c0011t0001g0067others(4): Show | 7 | HG01081.hp1 HG02071.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+12042G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38440590 | ||||||
chr17:38440824
|
C | T | 3 | a0001c0004t0006g0008a0001c0020t0005g0009a0001c0020t0005g0141 | 3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.63+12276C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38440824 | ||||||
chr17:38440926
|
C | T | 10 | a0001c0001t0001g0305a0001c0003t0001g0263a0001c0004t0001g0069others(7): Show | 10 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+12378C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38440926 | ||||||
chr17:38441001
|
C | A | 1 | a0001c0009t0003g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.63+12453C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441001 | ||||||
chr17:38441103
|
C | T | 4 | a0001c0016t0003g0301a0001c0037t0003g0137a0004c0017t0004g0138others(1): Show | 4 | HG03139.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+12555C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441103 | ||||||
chr17:38441128
|
G | A | 2 | a0001c0024t0001g0103a0002c0022t0001g0095 | 2 | NA18975.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.63+12580G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441128 | ||||||
chr17:38441244
|
C | T | 1 | a0001c0003t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.63+12696C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441244 | ||||||
chr17:38441347
|
G | A | 2 | a0001c0001t0007g0104a0001c0002t0002g0306 | 2 | NA18943.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.63+12799G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441347 | ||||||
chr17:38441355
|
T | C | 1 | a0001c0009t0003g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.63+12807T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441355 | ||||||
chr17:38441432
|
C | G | 10 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0124others(7): Show | 10 | HG00733.hp2 HG01081.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+12884C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441432 | ||||||
chr17:38441484
|
C | T | 1 | a0001c0031t0003g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.63+12936C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441484 | ||||||
chr17:38441489
|
G | C | 9 | a0001c0001t0001g0093a0001c0001t0001g0265a0001c0001t0007g0104others(6): Show | 9 | HG00597.hp2 NA18943.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+12941G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441489 | ||||||
chr17:38441496
|
A | C | 1 | a0001c0007t0003g0018 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.63+12948A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441496 | ||||||
chr17:38441537
|
C | T | 68 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(65): Show | 68 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.63+12989C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441537 | ||||||
chr17:38441554
|
A | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(238): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.63+13006A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441554 | ||||||
chr17:38441662
|
G | T | 1 | a0005c0033t0001g0073 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.63+13114G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441662 | ||||||
chr17:38441738
|
G | A | 5 | a0001c0016t0003g0045a0001c0016t0003g0301a0001c0037t0003g0137others(2): Show | 5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+13190G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441738 | ||||||
chr17:38441846
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.63+13298G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441846 | ||||||
chr17:38441936
|
C | G | 1 | a0001c0001t0001g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.63+13388C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441936 | ||||||
chr17:38441946
|
C | T | 2 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.63+13398C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441946 | ||||||
chr17:38441951
|
C | T | 2 | a0001c0001t0001g0122a0001c0002t0002g0123 | 2 | HG01175.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.63+13403C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441951 | ||||||
chr17:38441966
|
C | CT | 9 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(6): Show | 9 | HG01891.hp1 HG02647.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+13426dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38441966 | |||||
chr17:38442031
|
A | G | 25 | a0001c0005t0001g0031a0001c0005t0001g0034a0001c0005t0001g0035others(22): Show | 25 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.63+13483A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442031 | ||||||
chr17:38442250
|
T | C | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.63+13702T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442250 | ||||||
chr17:38442254
|
C | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0124others(7): Show | 10 | HG00733.hp2 HG01081.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+13706C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442254 | ||||||
chr17:38442381
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(159): Show | 164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.63+13833T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442381 | ||||||
chr17:38442559
|
A | G | 8 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(5): Show | 8 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+14011A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442559 | ||||||
chr17:38442726
|
C | T | 1 | a0001c0005t0001g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.63+14178C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442726 | ||||||
chr17:38442957
|
G | A | 1 | a0001c0004t0001g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+14409G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442957 | ||||||
chr17:38443004
|
A | G | 1 | a0001c0031t0003g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.63+14456A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443004 | ||||||
chr17:38443024
|
C | A | 1 | a0002c0022t0001g0095 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.63+14476C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443024 | ||||||
chr17:38443150
|
A | G | 4 | a0001c0004t0001g0057a0001c0031t0003g0065a0006c0021t0003g0068others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+14602A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443150 | ||||||
chr17:38443189
|
T | G | 54 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(51): Show | 54 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.63+14641T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443189 | ||||||
chr17:38443767
|
C | T | 1 | a0009c0026t0001g0284 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.64-14335C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443767 | ||||||
chr17:38443768
|
G | A | 1 | a0001c0004t0001g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-14334G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443768 | ||||||
chr17:38443918
|
G | A | 52 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(49): Show | 52 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-14184G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443918 | ||||||
chr17:38443935
|
T | C | 52 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(49): Show | 52 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-14167T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443935 | ||||||
chr17:38443938
|
C | T | 52 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(49): Show | 52 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-14164C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443938 | ||||||
chr17:38443962
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.64-14140G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443962 | ||||||
chr17:38444100
|
C | T | 1 | a0001c0003t0001g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.64-14002C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444100 | ||||||
chr17:38444201
|
G | A | 8 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(5): Show | 8 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-13901G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444201 | ||||||
chr17:38444256
|
C | T | 30 | a0001c0001t0001g0163a0001c0005t0001g0031a0001c0005t0001g0034others(27): Show | 30 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.64-13846C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444256 | ||||||
chr17:38444257
|
G | A | 1 | a0016c0056t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.64-13845G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444257 | ||||||
chr17:38444321
|
C | A | 2 | a0001c0001t0001g0285a0002c0022t0010g0257 | 2 | NA19062.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.64-13781C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444321 | ||||||
chr17:38444333
|
C | T | 3 | a0001c0004t0006g0008a0001c0020t0005g0009a0001c0020t0005g0141 | 3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.64-13769C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444333 | ||||||
chr17:38444430
|
G | A | 52 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(49): Show | 52 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-13672G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444430 | ||||||
chr17:38444486
|
T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(109): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.64-13616T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444486 | ||||||
chr17:38444625
|
G | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(100): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.64-13477G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444625 | ||||||
chr17:38444820
|
AT | A | 49 | a0001c0001t0001g0163a0001c0001t0001g0203a0001c0001t0001g0246others(46): Show | 49 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.64-13268delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38444820 | |||||
chr17:38444860
|
C | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0205 | 2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.64-13242C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444860 | ||||||
chr17:38444880
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(238): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.64-13222T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444880 | ||||||
chr17:38445209
|
G | A | 52 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(49): Show | 52 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-12893G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445209 | ||||||
chr17:38445303
|
TA | T | 75 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.64-12776delA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38445303 | |||||
chr17:38445303
|
TAA | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(104): Show | 109 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.64-12777_64-12776d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38445303 | |||||
chr17:38445303
|
TAAA | T | 12 | a0001c0001t0001g0163a0001c0001t0001g0253a0001c0002t0002g0155others(9): Show | 12 | HG01167.hp2 HG01891.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-12778_64-12776d others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38445303 | |||||
chr17:38445303
|
TAAAA | T | 41 | a0001c0004t0001g0057a0001c0004t0001g0069a0001c0004t0001g0170others(38): Show | 41 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.64-12779_64-12776d others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38445303 | |||||
chr17:38445432
|
A | G | 52 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(49): Show | 52 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-12670A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445432 | ||||||
chr17:38445491
|
T | A | 8 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(5): Show | 8 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-12611T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445491 | ||||||
chr17:38445639
|
CT | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.64-12450delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38445639 | |||||
chr17:38445751
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.64-12351C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445751 | ||||||
chr17:38445757
|
C | T | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-12345C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445757 | ||||||
chr17:38445820
|
G | T | 1 | a0008c0050t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.64-12282G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445820 | ||||||
chr17:38445885
|
C | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(103): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.64-12217C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445885 | ||||||
chr17:38446020
|
CT | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(139): Show | 142 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.64-12066delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446020 | |||||
chr17:38446020
|
CTT | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(89): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.64-12067_64-12066d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446020 | |||||
chr17:38446020
|
CTTT | C | 50 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(47): Show | 50 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.64-12068_64-12066d others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446020 | |||||
chr17:38446061
|
C | G | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-12041C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446061 | ||||||
chr17:38446181
|
AT | A | 72 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(69): Show | 72 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.64-11898delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446181 | |||||
chr17:38446181
|
ATT | A | 14 | a0001c0001t0001g0100a0001c0001t0001g0163a0001c0002t0002g0090others(11): Show | 14 | HG01243.hp2 HG01256.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-11899_64-11898d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446181 | |||||
chr17:38446181
|
ATTT | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.64-11900_64-11898d others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446181 | |||||
chr17:38446181
|
ATTTT | A | 16 | a0001c0001t0001g0001a0001c0001t0001g0211a0001c0001t0001g0288others(13): Show | 17 | HG00609.hp1 HG01891.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-11901_64-11898d others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446181 | |||||
chr17:38446181
|
ATTTTT | A | 11 | a0001c0004t0001g0057a0001c0004t0001g0069a0001c0004t0001g0170others(8): Show | 11 | HG00323.hp2 HG00735.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-11902_64-11898d others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446181 | |||||
chr17:38446244
|
A | G | 10 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(7): Show | 10 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-11858A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446244 | ||||||
chr17:38446273
|
C | A | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-11829C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446273 | ||||||
chr17:38446280
|
C | T | 1 | a0001c0031t0003g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-11822C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446280 | ||||||
chr17:38446316
|
C | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-11786C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446316 | ||||||
chr17:38446609
|
A | AT | 7 | a0001c0001t0001g0125a0001c0001t0001g0267a0001c0002t0002g0026others(4): Show | 7 | HG00438.hp1 HG01258.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-11474dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446609 | |||||
chr17:38446609
|
AT | A | 8 | a0001c0001t0011g0062a0001c0002t0002g0108a0001c0002t0012g0106others(5): Show | 8 | HG00544.hp1 HG03130.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-11474delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446609 | |||||
chr17:38446609
|
ATTT | A | 48 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(45): Show | 48 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.64-11476_64-11474d others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446609 | |||||
chr17:38446672
|
C | T | 3 | a0001c0004t0001g0060a0004c0019t0004g0058a0004c0019t0004g0061 | 3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-11430C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446672 | ||||||
chr17:38446673
|
G | A | 1 | a0004c0055t0004g0302 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-11429G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446673 | ||||||
chr17:38446675
|
G | A | 30 | a0001c0005t0001g0031a0001c0005t0001g0034a0001c0005t0001g0035others(27): Show | 30 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.64-11427G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446675 | ||||||
chr17:38446782
|
C | A | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.64-11320C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446782 | ||||||
chr17:38446833
|
T | C | 39 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(36): Show | 39 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.64-11269T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446833 | ||||||
chr17:38447040
|
T | G | 1 | a0001c0004t0001g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-11062T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447040 | ||||||
chr17:38447271
|
A | G | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-10831A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447271 | ||||||
chr17:38447276
|
C | T | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-10826C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447276 | ||||||
chr17:38447303
|
G | A | 2 | a0001c0011t0001g0067a0003c0014t0001g0066 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.64-10799G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447303 | ||||||
chr17:38447334
|
C | T | 9 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(6): Show | 9 | HG01891.hp1 HG02647.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-10768C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447334 | ||||||
chr17:38447398
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.64-10704C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447398 | ||||||
chr17:38447437
|
G | GA | 37 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0133others(34): Show | 37 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.64-10637dupA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | |||||
chr17:38447437
|
G | GAA | 20 | a0001c0004t0001g0131a0001c0005t0001g0036a0001c0005t0001g0038others(17): Show | 20 | HG01358.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-10638_64-10637d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | |||||
chr17:38447437
|
G | GAAA | 7 | a0001c0001t0003g0174a0001c0005t0001g0031a0001c0005t0001g0034others(4): Show | 7 | HG00733.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-10639_64-10637d others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | |||||
chr17:38447437
|
G | GAAAAAAA others(3): Show |
1 | a0001c0001t0011g0062 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.64-10646_64-10637d others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | |||||
chr17:38447437
|
G | GAAAAAAA others(4): Show |
10 | a0001c0001t0001g0093a0001c0002t0002g0013a0001c0002t0002g0108others(7): Show | 10 | HG01169.hp1 HG03017.hp2 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-10647_64-10637d others(13): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | |||||
chr17:38447437
|
G | GAAAAAAA others(5): Show |
24 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0077others(21): Show | 24 | HG00597.hp2 HG01106.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.64-10648_64-10637d others(14): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | |||||
chr17:38447437
|
G | GAAAAAAA others(6): Show |
14 | a0001c0001t0001g0056a0001c0001t0001g0078a0001c0001t0001g0098others(11): Show | 14 | HG00621.hp2 HG00733.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-10649_64-10637d others(15): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | |||||
chr17:38447437
|
G | GAAAAAAA others(7): Show |
4 | a0001c0001t0001g0019a0001c0002t0002g0256a0001c0048t0002g0111others(1): Show | 4 | HG01081.hp2 HG02109.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-10650_64-10637d others(16): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | |||||
chr17:38447437
|
GA | G | 10 | a0001c0001t0001g0147a0001c0001t0001g0163a0001c0001t0001g0265others(7): Show | 10 | HG02055.hp1 HG02572.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-10637delA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | |||||
chr17:38447437
|
GAAAAAAA others(3): Show |
G | 1 | a0001c0003t0001g0263 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.64-10646_64-10637d others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | |||||
chr17:38447437
|
GAAAAAAA others(7): Show |
G | 2 | a0001c0003t0001g0109a0001c0007t0003g0110 | 2 | HG00544.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.64-10650_64-10637d others(16): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | |||||
chr17:38447439
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.64-10663A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447439 | ||||||
chr17:38447453
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0119 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.64-10645_64-10633d others(15): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447453 | |||||
chr17:38447574
|
C | A | 5 | a0001c0016t0003g0045a0001c0016t0003g0301a0001c0037t0003g0137others(2): Show | 5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-10528C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447574 | ||||||
chr17:38447740
|
T | C | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-10362T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447740 | ||||||
chr17:38447795
|
A | AG | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-10303dupG | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447795 | |||||
chr17:38447876
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.64-10226T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447876 | ||||||
chr17:38448083
|
C | T | 5 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(2): Show | 5 | HG01891.hp1 HG02647.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-10019C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448083 | ||||||
chr17:38448212
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(169): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.64-9890A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448212 | ||||||
chr17:38448229
|
T | C | 4 | a0001c0001t0003g0174a0001c0003t0001g0012a0001c0007t0003g0018others(1): Show | 4 | HG01261.hp1 HG02109.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-9873T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448229 | ||||||
chr17:38448242
|
G | A | 1 | a0001c0002t0002g0123 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.64-9860G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448242 | ||||||
chr17:38448364
|
G | A | 1 | a0001c0031t0003g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-9738G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448364 | ||||||
chr17:38448366
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(110): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.64-9736C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448366 | ||||||
chr17:38448538
|
T | C | 30 | a0001c0005t0001g0031a0001c0005t0001g0034a0001c0005t0001g0035others(27): Show | 30 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.64-9564T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448538 | ||||||
chr17:38448633
|
C | G | 3 | a0001c0004t0001g0060a0004c0019t0004g0058a0004c0019t0004g0061 | 3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-9469C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448633 | ||||||
chr17:38448641
|
G | GT | 63 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0078others(60): Show | 63 | HG00323.hp2 HG00621.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.64-9439dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448641 | |||||
chr17:38448641
|
G | GTT | 8 | a0001c0004t0001g0054a0001c0004t0001g0057a0001c0005t0001g0031others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-9440_64-9439dup others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448641 | |||||
chr17:38448641
|
GT | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(101): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.64-9439delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448641 | |||||
chr17:38448801
|
A | ATCCCCGA others(317): Show |
2 | a0001c0011t0001g0067a0003c0014t0001g0066 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.64-9285_64-9284ins others(324): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448801 | |||||
chr17:38448801
|
A | ATCCCCGA others(318): Show |
5 | a0001c0004t0001g0052a0001c0004t0001g0054a0001c0004t0001g0059others(2): Show | 5 | HG01891.hp1 HG03486.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-9285_64-9284ins others(325): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448801 | |||||
chr17:38448801
|
A | ATCCCCGA others(319): Show |
2 | a0001c0004t0001g0053a0001c0009t0003g0159 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.64-9285_64-9284ins others(326): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448801 | |||||
chr17:38448858
|
C | CT | 7 | a0001c0001t0001g0077a0001c0001t0001g0231a0001c0004t0001g0029others(4): Show | 7 | HG01243.hp1 HG01346.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-9227dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448858 | |||||
chr17:38448858
|
C | CTTTTT | 36 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(33): Show | 36 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.64-9231_64-9227dup others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448858 | |||||
chr17:38448858
|
C | CTTTTTTT | 7 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(4): Show | 7 | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-9233_64-9227dup others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448858 | |||||
chr17:38448858
|
C | T | 2 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.64-9244C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448858 | ||||||
chr17:38448911
|
G | T | 3 | a0001c0004t0001g0060a0004c0019t0004g0058a0004c0019t0004g0061 | 3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-9191G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448911 | ||||||
chr17:38449157
|
C | T | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-8945C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449157 | ||||||
chr17:38449246
|
G | A | 59 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(56): Show | 59 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.64-8856G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449246 | ||||||
chr17:38449314
|
G | A | 5 | a0001c0011t0006g0071a0001c0011t0006g0074a0001c0032t0001g0201others(2): Show | 5 | HG01358.hp1 HG01884.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-8788G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449314 | ||||||
chr17:38449412
|
C | T | 1 | a0001c0007t0003g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-8690C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449412 | ||||||
chr17:38449417
|
C | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(228): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.64-8685C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449417 | ||||||
chr17:38449475
|
G | A | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-8627G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449475 | ||||||
chr17:38449550
|
C | A | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-8552C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449550 | ||||||
chr17:38449650
|
C | T | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-8452C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449650 | ||||||
chr17:38449895
|
T | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(168): Show | 173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.64-8207T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449895 | ||||||
chr17:38449903
|
C | T | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-8199C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449903 | ||||||
chr17:38449947
|
C | G | 1 | a0001c0024t0001g0103 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.64-8155C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449947 | ||||||
chr17:38449988
|
C | T | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-8114C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449988 | ||||||
chr17:38450101
|
C | T | 2 | a0001c0002t0002g0229a0001c0054t0002g0230 | 2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.64-8001C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450101 | ||||||
chr17:38450181
|
C | T | 1 | a0001c0007t0003g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-7921C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450181 | ||||||
chr17:38450347
|
G | T | 4 | a0001c0011t0006g0071a0001c0011t0006g0074a0003c0014t0001g0072others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-7755G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450347 | ||||||
chr17:38450444
|
C | T | 1 | a0001c0031t0003g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-7658C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450444 | ||||||
chr17:38450471
|
A | AATGGCGT others(1): Show |
12 | a0001c0004t0001g0057a0001c0004t0001g0069a0001c0004t0001g0170others(9): Show | 12 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-7629_64-7628ins others(8): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38450471 | |||||
chr17:38450472
|
A | G | 9 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(6): Show | 9 | HG02071.hp2 HG02074.hp2 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-7630A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450472 | ||||||
chr17:38450617
|
G | A | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-7485G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450617 | ||||||
chr17:38450778
|
T | G | 1 | a0001c0009t0003g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-7324T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450778 | ||||||
chr17:38451064
|
T | G | 1 | a0001c0001t0001g0112 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-7038T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451064 | ||||||
chr17:38451239
|
G | A | 8 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(5): Show | 8 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-6863G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451239 | ||||||
chr17:38451322
|
T | A | 1 | a0001c0001t0001g0112 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-6780T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451322 | ||||||
chr17:38451343
|
G | A | 51 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-6759G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451343 | ||||||
chr17:38451364
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.64-6738A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451364 | ||||||
chr17:38451453
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-6649C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451453 | ||||||
chr17:38451458
|
C | T | 1 | a0002c0036t0003g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64-6644C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451458 | ||||||
chr17:38451498
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.64-6604C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451498 | ||||||
chr17:38451534
|
G | C | 2 | a0001c0004t0001g0029a0004c0055t0004g0302 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-6568G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451534 | ||||||
chr17:38451662
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.64-6440T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451662 | ||||||
chr17:38451846
|
C | G | 1 | a0001c0001t0001g0112 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-6256C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451846 | ||||||
chr17:38451847
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-6255G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451847 | ||||||
chr17:38451887
|
C | T | 3 | a0001c0008t0001g0188a0001c0008t0001g0195a0002c0015t0001g0189 | 3 | NA18983.hp1 NA18985.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.64-6215C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451887 | ||||||
chr17:38451966
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.64-6136C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451966 | ||||||
chr17:38452083
|
C | A | 3 | a0001c0004t0006g0008a0001c0020t0005g0009a0001c0020t0005g0141 | 3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.64-6019C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452083 | ||||||
chr17:38452141
|
C | T | 2 | a0001c0004t0001g0029a0004c0055t0004g0302 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-5961C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452141 | ||||||
chr17:38452247
|
C | T | 1 | a0001c0002t0002g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.64-5855C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452247 | ||||||
chr17:38452292
|
C | G | 6 | a0001c0001t0001g0283a0001c0004t0001g0170a0001c0004t0001g0171others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-5810C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452292 | ||||||
chr17:38452392
|
C | A | 1 | a0001c0003t0001g0113 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.64-5710C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452392 | ||||||
chr17:38452433
|
T | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(287): Show | 292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.64-5669T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452433 | ||||||
chr17:38452438
|
C | T | 1 | a0002c0023t0001g0239 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64-5664C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452438 | ||||||
chr17:38452555
|
A | G | 28 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(25): Show | 28 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.64-5547A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452555 | ||||||
chr17:38452896
|
C | T | 28 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(25): Show | 28 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.64-5206C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452896 | ||||||
chr17:38452916
|
T | C | 28 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(25): Show | 28 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.64-5186T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452916 | ||||||
chr17:38452945
|
C | T | 1 | a0001c0031t0003g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-5157C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452945 | ||||||
chr17:38453021
|
T | G | 3 | a0001c0004t0001g0060a0004c0019t0004g0058a0004c0019t0004g0061 | 3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-5081T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453021 | ||||||
chr17:38453037
|
T | A | 2 | a0001c0004t0001g0029a0004c0055t0004g0302 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-5065T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453037 | ||||||
chr17:38453040
|
A | G | 9 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(6): Show | 9 | HG01891.hp1 HG02647.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-5062A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453040 | ||||||
chr17:38453107
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.64-4995G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453107 | ||||||
chr17:38453244
|
T | G | 16 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(13): Show | 16 | HG01358.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-4858T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453244 | ||||||
chr17:38453261
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(129): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.64-4841T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453261 | ||||||
chr17:38453359
|
A | T | 2 | a0001c0001t0001g0017a0001c0001t0003g0174 | 2 | HG04184.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.64-4743A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453359 | ||||||
chr17:38453382
|
TTCTC | T | 28 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(25): Show | 28 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.64-4718_64-4715del others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453382 | |||||
chr17:38453415
|
ATGCG | A | 3 | a0001c0009t0003g0172a0001c0009t0003g0173a0001c0040t0002g0135 | 3 | HG00735.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.64-4680_64-4677del others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453415 | |||||
chr17:38453418
|
CGTGCGT | C | 7 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(4): Show | 7 | HG01891.hp1 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-4680_64-4675del others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453418 | |||||
chr17:38453418
|
CGTGCGTG others(3): Show |
C | 3 | a0001c0004t0006g0008a0001c0020t0005g0009a0001c0020t0005g0141 | 3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.64-4680_64-4671del others(10): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453418 | |||||
chr17:38453418
|
CGTGCGTG others(5): Show |
C | 2 | a0001c0031t0003g0065a0006c0021t0003g0070 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.64-4680_64-4669del others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453418 | |||||
chr17:38453418
|
CGTGCGTG others(7): Show |
C | 6 | a0001c0011t0006g0071a0001c0011t0006g0074a0001c0032t0001g0201others(3): Show | 6 | HG01358.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-4680_64-4667del others(14): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453418 | |||||
chr17:38453419
|
G | A | 5 | a0001c0016t0003g0045a0001c0016t0003g0301a0001c0037t0003g0137others(2): Show | 5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-4683G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453419 | ||||||
chr17:38453422
|
C | CGT | 23 | a0001c0001t0001g0064a0001c0001t0001g0091a0001c0001t0001g0092others(20): Show | 23 | HG00558.hp1 HG01071.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.64-4642_64-4641dup others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | |||||
chr17:38453422
|
C | CGTGT | 4 | a0001c0001t0001g0285a0001c0004t0001g0131a0003c0028t0001g0015others(1): Show | 4 | HG01433.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-4644_64-4641dup others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | |||||
chr17:38453422
|
C | CGTGTGT | 3 | a0001c0004t0001g0280a0001c0006t0002g0177a0001c0010t0001g0014 | 3 | HG02071.hp1 NA18522.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.64-4646_64-4641dup others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | |||||
chr17:38453422
|
C | T | 3 | a0001c0004t0001g0170a0001c0004t0001g0171a0001c0010t0001g0169 | 3 | HG01070.hp1 HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.64-4680C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453422 | ||||||
chr17:38453422
|
CGT | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0075others(14): Show | 17 | HG00099.hp1 HG00741.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-4642_64-4641del others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | |||||
chr17:38453422
|
CGTGT | C | 27 | a0001c0001t0001g0056a0001c0001t0001g0079a0001c0001t0001g0093others(24): Show | 27 | HG00609.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.64-4644_64-4641del others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | |||||
chr17:38453422
|
CGTGTGT | C | 21 | a0001c0001t0001g0023a0001c0001t0001g0078a0001c0001t0001g0098others(18): Show | 21 | HG00621.hp2 HG01175.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.64-4646_64-4641del others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | |||||
chr17:38453422
|
CGTGTGTG others(1): Show |
C | 10 | a0001c0001t0007g0104a0001c0001t0011g0062a0001c0003t0001g0113others(7): Show | 10 | HG00597.hp2 HG01952.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-4648_64-4641del others(8): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | |||||
chr17:38453422
|
CGTGTGTG others(3): Show |
C | 3 | a0001c0002t0002g0013a0001c0002t0002g0255a0001c0003t0001g0012 | 3 | HG01169.hp1 HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.64-4650_64-4641del others(10): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | |||||
chr17:38453422
|
CGTGTGTG others(5): Show |
C | 9 | a0001c0002t0002g0114a0001c0002t0002g0121a0001c0002t0002g0306others(6): Show | 9 | HG02886.hp2 HG03017.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-4652_64-4641del others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | |||||
chr17:38453450
|
TGTGTGTG others(5): Show |
T | 2 | a0001c0001t0001g0213a0001c0004t0001g0057 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.64-4650_64-4639del others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453450 | |||||
chr17:38453452
|
TGTGTGTG others(3): Show |
T | 1 | a0001c0001t0001g0150 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-4648_64-4639del others(10): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453452 | |||||
chr17:38453456
|
TGTGTGC | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0081a0001c0001t0001g0165others(21): Show | 25 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.64-4644_64-4639del others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453456 | |||||
chr17:38453458
|
T | C | 58 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(55): Show | 58 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.64-4644T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453458 | ||||||
chr17:38453458
|
TGTGC | T | 24 | a0001c0001t0001g0006a0001c0001t0001g0148a0001c0001t0001g0203others(21): Show | 24 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.64-4642_64-4639del others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453458 | |||||
chr17:38453460
|
T | C | 62 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(59): Show | 62 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.64-4642T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453460 | ||||||
chr17:38453460
|
TGC | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(46): Show | 50 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.64-4631_64-4630del others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453460 | |||||
chr17:38453462
|
C | T | 45 | a0001c0001t0001g0032a0001c0001t0001g0064a0001c0001t0001g0083others(42): Show | 45 | HG00140.hp1 HG00558.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.64-4640C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453462 | ||||||
chr17:38453524
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0213a0001c0001t0001g0214others(19): Show | 23 | HG00280.hp2 HG00639.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.64-4578G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453524 | ||||||
chr17:38453649
|
C | T | 2 | a0001c0004t0001g0029a0004c0055t0004g0302 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-4453C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453649 | ||||||
chr17:38453708
|
C | T | 1 | a0001c0004t0001g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-4394C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453708 | ||||||
chr17:38453715
|
C | A | 1 | a0001c0010t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.64-4387C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453715 | ||||||
chr17:38453796
|
TCCGGGGG others(32): Show |
T | 1 | a0001c0031t0003g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-4297_64-4259del others(39): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453796 | |||||
chr17:38453815
|
C | T | 1 | a0001c0043t0001g0178 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.64-4287C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453815 | ||||||
chr17:38453866
|
G | T | 1 | a0001c0001t0001g0268 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.64-4236G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453866 | ||||||
chr17:38453955
|
C | T | 3 | a0001c0004t0006g0008a0001c0020t0005g0009a0001c0020t0005g0141 | 3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.64-4147C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453955 | ||||||
chr17:38454152
|
G | A | 1 | a0005c0041t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-3950G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454152 | ||||||
chr17:38454306
|
G | T | 23 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(20): Show | 23 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.64-3796G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454306 | ||||||
chr17:38454435
|
G | A | 1 | a0001c0007t0003g0018 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.64-3667G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454435 | ||||||
chr17:38454436
|
T | A | 5 | a0001c0011t0006g0071a0001c0011t0006g0074a0001c0032t0001g0201others(2): Show | 5 | HG01358.hp1 HG01884.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-3666T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454436 | ||||||
chr17:38454514
|
G | T | 1 | a0001c0003t0001g0099 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64-3588G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454514 | ||||||
chr17:38454625
|
C | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0075others(47): Show | 50 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.64-3477C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454625 | ||||||
chr17:38454663
|
G | A | 5 | a0001c0016t0003g0045a0001c0016t0003g0301a0001c0037t0003g0137others(2): Show | 5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-3439G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454663 | ||||||
chr17:38454732
|
G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(83): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.64-3370G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454732 | ||||||
chr17:38454779
|
C | T | 1 | a0001c0007t0003g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-3323C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454779 | ||||||
chr17:38454784
|
G | C | 5 | a0001c0001t0001g0187a0001c0001t0001g0227a0001c0001t0001g0234others(2): Show | 5 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-3318G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454784 | ||||||
chr17:38454838
|
G | A | 5 | a0001c0011t0006g0071a0001c0011t0006g0074a0001c0032t0001g0201others(2): Show | 5 | HG01358.hp1 HG01884.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-3264G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454838 | ||||||
chr17:38455031
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.64-3071C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455031 | ||||||
chr17:38455045
|
G | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG00642.hp2 HG01256.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-3057G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455045 | ||||||
chr17:38455169
|
A | G | 3 | a0001c0008t0001g0197a0001c0008t0001g0198a0001c0010t0001g0168 | 3 | HG00099.hp1 HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.64-2933A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455169 | ||||||
chr17:38455207
|
G | A | 3 | a0001c0002t0002g0114a0001c0002t0002g0121a0001c0002t0012g0106 | 3 | HG03017.hp2 HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.64-2895G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455207 | ||||||
chr17:38455469
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(166): Show | 171 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.64-2633A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455469 | ||||||
chr17:38455487
|
G | C | 3 | a0001c0004t0001g0060a0004c0019t0004g0058a0004c0019t0004g0061 | 3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-2615G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455487 | ||||||
chr17:38455560
|
G | T | 1 | a0017c0057t0001g0282 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.64-2542G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455560 | ||||||
chr17:38455618
|
T | C | 1 | a0015c0039t0001g0186 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.64-2484T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455618 | ||||||
chr17:38455721
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.64-2381G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455721 | ||||||
chr17:38455727
|
G | T | 1 | a0001c0009t0003g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-2375G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455727 | ||||||
chr17:38455741
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.64-2361G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455741 | ||||||
chr17:38455755
|
C | T | 1 | a0001c0010t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.64-2347C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455755 | ||||||
chr17:38455815
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.64-2287G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455815 | ||||||
chr17:38456054
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.64-2048C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456054 | ||||||
chr17:38456080
|
G | T | 1 | a0001c0004t0001g0304 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.64-2022G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456080 | ||||||
chr17:38456118
|
G | A | 1 | a0001c0032t0001g0201 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64-1984G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456118 | ||||||
chr17:38456249
|
C | G | 21 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(18): Show | 21 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-1853C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456249 | ||||||
chr17:38456297
|
C | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(102): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.64-1805C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456297 | ||||||
chr17:38456345
|
A | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(102): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.64-1757A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456345 | ||||||
chr17:38456590
|
G | A | 7 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(4): Show | 7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1512G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456590 | ||||||
chr17:38456602
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.64-1500G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456602 | ||||||
chr17:38456632
|
T | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(102): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.64-1470T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456632 | ||||||
chr17:38456694
|
C | T | 27 | a0001c0004t0006g0008a0001c0005t0001g0031a0001c0005t0001g0034others(24): Show | 27 | HG00733.hp1 HG01081.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.64-1408C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456694 | ||||||
chr17:38456704
|
C | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(160): Show | 165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.64-1398C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456704 | ||||||
chr17:38456829
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.64-1273C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456829 | ||||||
chr17:38457018
|
T | G | 2 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.64-1084T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457018 | ||||||
chr17:38457019
|
C | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(102): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.64-1083C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457019 | ||||||
chr17:38457101
|
G | C | 1 | a0001c0007t0003g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-1001G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457101 | ||||||
chr17:38457364
|
T | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(105): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.64-738T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457364 | ||||||
chr17:38457492
|
G | T | 30 | a0001c0004t0001g0057a0001c0005t0001g0031a0001c0005t0001g0034others(27): Show | 30 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-610G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457492 | ||||||
chr17:38457496
|
T | C | 1 | a0001c0009t0003g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64-606T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457496 | ||||||
chr17:38457566
|
G | A | 5 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 5 | HG02132.hp2 HG02165.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-536G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457566 | ||||||
chr17:38457768
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.64-334A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457768 | ||||||
chr17:38457893
|
G | C | 1 | a0001c0032t0001g0201 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64-209G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457893 | ||||||
chr17:38458280
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(100): Show | 105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.225+17G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458280 | ||||||
chr17:38458319
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(102): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.225+56C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458319 | ||||||
chr17:38458387
|
C | T | 1 | a0001c0032t0001g0201 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.225+124C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458387 | ||||||
chr17:38458455
|
A | G | 24 | a0001c0005t0001g0031a0001c0005t0001g0034a0001c0005t0001g0035others(21): Show | 24 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.225+192A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458455 | ||||||
chr17:38458486
|
G | C | 1 | a0013c0044t0001g0192 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.225+223G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458486 | ||||||
chr17:38458605
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(102): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.225+342G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458605 | ||||||
chr17:38458637
|
CT | C | 5 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | NA18960.hp1 NA18979.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+375delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458637 | ||||||
chr17:38458763
|
C | T | 3 | a0001c0004t0001g0060a0004c0019t0004g0058a0004c0019t0004g0061 | 3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.225+500C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458763 | ||||||
chr17:38458806
|
C | T | 7 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(4): Show | 7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.225+543C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458806 | ||||||
chr17:38458807
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.225+544G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458807 | ||||||
chr17:38458819
|
A | G | 1 | a0001c0003t0001g0107 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.225+556A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458819 | ||||||
chr17:38459190
|
A | G | 1 | a0001c0002t0002g0306 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.225+927A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459190 | ||||||
chr17:38459208
|
G | C | 2 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.225+945G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459208 | ||||||
chr17:38459331
|
T | C | 1 | a0001c0004t0001g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.225+1068T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459331 | ||||||
chr17:38459338
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(102): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.225+1075T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459338 | ||||||
chr17:38459389
|
C | T | 4 | a0001c0004t0001g0057a0001c0004t0001g0060a0004c0019t0004g0058others(1): Show | 4 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+1126C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459389 | ||||||
chr17:38459460
|
G | C | 1 | a0001c0004t0001g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225+1197G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459460 | ||||||
chr17:38459649
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(108): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.226-1256A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459649 | ||||||
chr17:38459723
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(115): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.226-1182A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459723 | ||||||
chr17:38459740
|
T | G | 25 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(22): Show | 25 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.226-1165T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459740 | ||||||
chr17:38459815
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(129): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.226-1090T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459815 | ||||||
chr17:38459822
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.226-1083C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459822 | ||||||
chr17:38459845
|
C | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(154): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.226-1060C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459845 | ||||||
chr17:38459955
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.226-950G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459955 | ||||||
chr17:38459983
|
T | C | 2 | a0001c0002t0002g0242a0001c0003t0001g0185 | 2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.226-922T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459983 | ||||||
chr17:38460222
|
G | T | 3 | a0001c0001t0001g0208a0013c0044t0001g0192a0017c0057t0001g0282 | 3 | HG02135.hp1 HG02165.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.226-683G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460222 | ||||||
chr17:38460314
|
C | T | 1 | a0019c0058t0002g0202 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.226-591C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460314 | ||||||
chr17:38460472
|
G | A | 1 | a0001c0002t0002g0117 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.226-433G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460472 | ||||||
chr17:38460582
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0083 | 2 | HG02165.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.226-323C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460582 | ||||||
chr17:38460583
|
G | A | 1 | a0008c0050t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.226-322G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460583 | ||||||
chr17:38460621
|
C | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.226-284C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460621 | ||||||
chr17:38460692
|
G | A | 7 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(4): Show | 7 | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.226-213G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460692 | ||||||
chr17:38460704
|
G | A | 1 | a0001c0007t0015g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.226-201G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460704 | ||||||
chr17:38460766
|
C | T | 4 | a0001c0004t0001g0057a0001c0004t0001g0060a0004c0019t0004g0058others(1): Show | 4 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-139C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460766 | ||||||
chr17:38460832
|
C | T | 3 | a0001c0004t0006g0008a0001c0020t0005g0009a0001c0020t0005g0141 | 3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.226-73C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460832 | ||||||
chr17:38460966
|
G | A | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(108): Show | 111 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.253+34G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38460966 | ||||||
chr17:38461183
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.253+251C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38461183 | ||||||
chr17:38461234
|
G | C | 7 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(4): Show | 7 | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.253+302G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38461234 | ||||||
chr17:38461480
|
G | A | 2 | a0003c0028t0001g0303a0004c0055t0004g0302 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.253+548G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38461480 | ||||||
chr17:38461565
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.253+633C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38461565 | ||||||
chr17:38461584
|
G | A | 11 | a0001c0001t0001g0032a0001c0001t0001g0143a0001c0001t0001g0147others(8): Show | 11 | HG02145.hp2 HG02280.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+652G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38461584 | ||||||
chr17:38461710
|
CT | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.253+780delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr17 | 38461710 | |||||
chr17:38461782
|
T | A | 1 | a0001c0008t0001g0028 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.253+850T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38461782 | ||||||
chr17:38462040
|
C | A | 2 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.254-806C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38462040 | ||||||
chr17:38462046
|
G | A | 24 | a0001c0005t0001g0031a0001c0005t0001g0034a0001c0005t0001g0035others(21): Show | 24 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.254-800G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38462046 | ||||||
chr17:38462199
|
C | T | 24 | a0001c0005t0001g0031a0001c0005t0001g0034a0001c0005t0001g0035others(21): Show | 24 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.254-647C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38462199 | ||||||
chr17:38462247
|
CT | C | 21 | a0001c0001t0001g0271a0001c0001t0011g0062a0001c0002t0002g0114others(18): Show | 21 | HG01071.hp2 HG01081.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.254-575delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr17 | 38462247 | |||||
chr17:38462247
|
CTT | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.254-576_254-575del others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr17 | 38462247 | |||||
chr17:38462247
|
CTTT | C | 35 | a0001c0001t0001g0081a0001c0001t0001g0112a0001c0001t0001g0214others(32): Show | 35 | HG00733.hp1 HG01256.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.254-577_254-575del others(3): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr17 | 38462247 | |||||
chr17:38462247
|
CTTTT | C | 7 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(4): Show | 7 | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.254-578_254-575del others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr17 | 38462247 | |||||
chr17:38462546
|
A | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.254-300A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38462546 | ||||||
chr17:38462744
|
C | T | 2 | a0001c0001t0001g0290a0008c0049t0001g0266 | 2 | NA18963.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.254-102C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38462744 | ||||||
chr17:38462794
|
T | C | 1 | a0001c0010t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.254-52T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38462794 | ||||||
chr17:38462960
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.349+19C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4/23 | chr17 | 38462960 | ||||||
chr17:38462985
|
C | G | 1 | a0001c0004t0001g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.349+44C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4/23 | chr17 | 38462985 | ||||||
chr17:38463214
|
C | T | 7 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(4): Show | 7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+18C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 5/23 | chr17 | 38463214 | ||||||
chr17:38463277
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.429-51C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 5/23 | chr17 | 38463277 | ||||||
chr17:38463540
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0211a0001c0001t0001g0233others(7): Show | 11 | HG00609.hp1 HG02040.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.483+158C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38463540 | ||||||
chr17:38463650
|
C | T | 2 | a0003c0028t0001g0303a0004c0055t0004g0302 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.483+268C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38463650 | ||||||
chr17:38463750
|
G | A | 5 | a0001c0016t0003g0045a0001c0016t0003g0301a0001c0037t0003g0137others(2): Show | 5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+368G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38463750 | ||||||
chr17:38464062
|
C | T | 53 | a0001c0001t0001g0151a0001c0004t0001g0052a0001c0004t0001g0053others(50): Show | 53 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.483+680C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464062 | ||||||
chr17:38464086
|
C | T | 2 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.483+704C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464086 | ||||||
chr17:38464107
|
A | G | 2 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.483+725A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464107 | ||||||
chr17:38464228
|
C | T | 7 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(4): Show | 7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+846C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464228 | ||||||
chr17:38464258
|
G | A | 7 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(4): Show | 7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+876G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464258 | ||||||
chr17:38464290
|
C | CCA | 35 | a0001c0001t0001g0151a0001c0001t0001g0283a0001c0001t0014g0274others(32): Show | 35 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.483+926_483+927dup others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 38464290 | |||||
chr17:38464290
|
CCA | C | 5 | a0001c0016t0003g0045a0001c0016t0003g0301a0001c0037t0003g0137others(2): Show | 5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+926_483+927del others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 38464290 | |||||
chr17:38464354
|
C | T | 1 | a0001c0002t0002g0244 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.483+972C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464354 | ||||||
chr17:38464355
|
G | A | 1 | a0002c0023t0001g0239 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.483+973G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464355 | ||||||
chr17:38464384
|
C | T | 1 | a0001c0012t0003g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.483+1002C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464384 | ||||||
chr17:38464424
|
T | G | 7 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(4): Show | 7 | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+1042T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464424 | ||||||
chr17:38464526
|
T | G | 1 | a0018c0047t0001g0016 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.483+1144T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464526 | ||||||
chr17:38464592
|
G | C | 2 | a0001c0001t0001g0098a0001c0003t0001g0099 | 2 | HG03492.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.483+1210G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464592 | ||||||
chr17:38464593
|
G | C | 1 | a0005c0041t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.483+1211G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464593 | ||||||
chr17:38464652
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.483+1270C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464652 | ||||||
chr17:38464679
|
C | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.483+1297C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464679 | ||||||
chr17:38464922
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.484-1245A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464922 | ||||||
chr17:38464927
|
C | T | 1 | a0001c0048t0002g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.484-1240C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464927 | ||||||
chr17:38464933
|
G | A | 3 | a0001c0001t0001g0292a0001c0003t0001g0293a0001c0052t0001g0291 | 3 | NA18960.hp1 NA18979.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.484-1234G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464933 | ||||||
chr17:38464970
|
C | A | 5 | a0001c0016t0003g0045a0001c0016t0003g0301a0001c0037t0003g0137others(2): Show | 5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-1197C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464970 | ||||||
chr17:38464986
|
C | T | 1 | a0001c0003t0001g0099 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.484-1181C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464986 | ||||||
chr17:38465034
|
G | A | 1 | a0001c0037t0003g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.484-1133G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465034 | ||||||
chr17:38465080
|
C | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(267): Show | 272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.484-1087C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465080 | ||||||
chr17:38465165
|
G | A | 2 | a0001c0001t0001g0098a0001c0003t0001g0099 | 2 | HG03492.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.484-1002G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465165 | ||||||
chr17:38465204
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(99): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.484-963T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465204 | ||||||
chr17:38465271
|
C | CCTGGGAC others(21): Show |
24 | a0001c0005t0001g0031a0001c0005t0001g0034a0001c0005t0001g0035others(21): Show | 24 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.484-895_484-868dup others(28): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 38465271 | |||||
chr17:38465315
|
C | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.484-852C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465315 | ||||||
chr17:38465318
|
CTG | C | 45 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(42): Show | 45 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.484-835_484-834del others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 38465318 | |||||
chr17:38465339
|
G | T | 1 | a0001c0003t0001g0099 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.484-828G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465339 | ||||||
chr17:38465363
|
T | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.484-804T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465363 | ||||||
chr17:38465685
|
C | T | 2 | a0001c0001t0001g0077a0001c0003t0001g0063 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.484-482C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465685 | ||||||
chr17:38465794
|
C | T | 6 | a0001c0016t0003g0045a0001c0016t0003g0301a0001c0031t0003g0065others(3): Show | 6 | HG02723.hp2 HG02886.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-373C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465794 | ||||||
chr17:38465897
|
T | G | 1 | a0001c0001t0001g0236 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.484-270T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465897 | ||||||
chr17:38465932
|
A | G | 45 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(42): Show | 45 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.484-235A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465932 | ||||||
chr17:38465950
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.484-217A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465950 | ||||||
chr17:38467361
|
G | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.1648+30G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467361 | ||||||
chr17:38467393
|
G | A | 2 | a0003c0028t0001g0303a0004c0055t0004g0302 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1648+62G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467393 | ||||||
chr17:38467497
|
G | A | 2 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1648+166G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467497 | ||||||
chr17:38467557
|
T | C | 3 | a0001c0002t0002g0085a0001c0002t0002g0086a0001c0002t0002g0090 | 3 | NA18943.hp1 NA18980.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1648+226T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467557 | ||||||
chr17:38467557
|
T | TTATCCTT others(3): Show |
1 | a0001c0001t0001g0007 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1648+227_1648+236d others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr17 | 38467557 | |||||
chr17:38467579
|
C | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.1648+248C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467579 | ||||||
chr17:38467648
|
C | T | 1 | a0001c0010t0001g0168 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1648+317C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467648 | ||||||
chr17:38467758
|
A | C | 1 | a0008c0050t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1648+427A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467758 | ||||||
chr17:38467856
|
T | C | 7 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(4): Show | 7 | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1648+525T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467856 | ||||||
chr17:38468010
|
G | T | 4 | a0001c0011t0006g0071a0001c0011t0006g0074a0003c0014t0001g0072others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648+679G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468010 | ||||||
chr17:38468033
|
C | A | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1648+702C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468033 | ||||||
chr17:38468249
|
C | A | 2 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1649-895C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468249 | ||||||
chr17:38468254
|
G | A | 1 | a0004c0019t0004g0061 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1649-890G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468254 | ||||||
chr17:38468355
|
G | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(100): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1649-789G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468355 | ||||||
chr17:38468367
|
A | G | 2 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1649-777A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468367 | ||||||
chr17:38468383
|
TGA | T | 7 | a0001c0011t0001g0067a0001c0011t0006g0071a0001c0011t0006g0074others(4): Show | 7 | HG01358.hp1 HG01884.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1649-757_1649-756d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr17 | 38468383 | |||||
chr17:38468587
|
G | A | 2 | a0001c0005t0001g0036a0012c0034t0001g0037 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1649-557G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468587 | ||||||
chr17:38468614
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1649-530C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468614 | ||||||
chr17:38468669
|
A | G | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(159): Show | 162 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.1649-475A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468669 | ||||||
chr17:38469110
|
C | T | 2 | a0006c0021t0003g0068a0006c0021t0003g0070 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1649-34C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38469110 | ||||||
chr17:38469505
|
G | A | 7 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(4): Show | 7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1805-19G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 8/23 | chr17 | 38469505 | ||||||
chr17:38469678
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1916+43C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 9/23 | chr17 | 38469678 | ||||||
chr17:38469678
|
C | T | 31 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0054others(28): Show | 31 | HG00733.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.1916+43C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 9/23 | chr17 | 38469678 | ||||||
chr17:38469821
|
C | T | 38 | a0001c0001t0001g0064a0001c0004t0001g0052a0001c0004t0001g0053others(35): Show | 38 | HG00733.hp1 HG01243.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.1917-26C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 9/23 | chr17 | 38469821 | ||||||
chr17:38469915
|
C | A | 6 | a0001c0004t0001g0057a0001c0004t0001g0060a0004c0019t0004g0058others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1974+11C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38469915 | ||||||
chr17:38469998
|
C | T | 1 | a0002c0035t0001g0237 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1974+94C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38469998 | ||||||
chr17:38470057
|
G | A | 1 | a0001c0011t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1974+153G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470057 | ||||||
chr17:38470066
|
C | G | 1 | a0001c0001t0001g0268 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1974+162C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470066 | ||||||
chr17:38470201
|
G | A | 1 | a0001c0043t0001g0178 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1974+297G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470201 | ||||||
chr17:38470352
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG00099.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.1974+448T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470352 | ||||||
chr17:38470605
|
T | C | 2 | a0001c0001t0008g0260a0001c0007t0003g0018 | 2 | HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1974+701T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470605 | ||||||
chr17:38470622
|
C | T | 3 | a0001c0001t0001g0093a0001c0003t0001g0105a0001c0003t0001g0191 | 3 | NA18959.hp2 NA18999.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1974+718C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470622 | ||||||
chr17:38470627
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(125): Show | 128 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.1974+723C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470627 | ||||||
chr17:38470682
|
G | A | 1 | a0001c0042t0001g0261 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1974+778G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470682 | ||||||
chr17:38470725
|
C | G | 4 | a0001c0007t0003g0051a0003c0014t0001g0066a0003c0028t0001g0303others(1): Show | 4 | HG02486.hp1 HG02896.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1974+821C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470725 | ||||||
chr17:38470775
|
G | C | 1 | a0001c0003t0001g0206 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1974+871G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470775 | ||||||
chr17:38470807
|
G | A | 5 | a0001c0011t0001g0067a0001c0011t0006g0071a0001c0011t0006g0074others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1974+903G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470807 | ||||||
chr17:38470826
|
C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(83): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1974+922C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470826 | ||||||
chr17:38470895
|
G | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(131): Show | 134 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.1975-968G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470895 | ||||||
chr17:38470928
|
C | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(132): Show | 135 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.1975-935C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470928 | ||||||
chr17:38470941
|
T | A | 7 | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(4): Show | 7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1975-922T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470941 | ||||||
chr17:38470957
|
C | CTT | 8 | a0001c0001t0001g0163a0001c0004t0001g0052a0001c0004t0001g0053others(5): Show | 8 | HG01891.hp1 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1975-894_1975-893d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr17 | 38470957 | |||||
chr17:38470972
|
A | C | 4 | a0001c0004t0001g0057a0001c0004t0001g0060a0004c0019t0004g0058others(1): Show | 4 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975-891A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470972 | ||||||
chr17:38471016
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(115): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1975-847G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38471016 | ||||||
chr17:38471099
|
T | C | 1 | a0002c0035t0001g0237 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1975-764T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38471099 | ||||||
chr17:38471221
|
G | A | 5 | a0001c0001t0001g0187a0001c0001t0001g0227a0001c0001t0001g0234others(2): Show | 5 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975-642G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38471221 | ||||||
chr17:38471533
|
C | T | 1 | a0001c0004t0001g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1975-330C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38471533 | ||||||
chr17:38471681
|
C | T | 7 | a0001c0004t0001g0057a0001c0007t0003g0051a0003c0014t0001g0066others(4): Show | 7 | HG02145.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1975-182C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38471681 | ||||||
chr17:38471750
|
G | A | 1 | a0001c0003t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1975-113G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38471750 | ||||||
chr17:38472186
|
G | T | 1 | a0001c0004t0001g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2118+180G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38472186 | ||||||
chr17:38472236
|
G | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(131): Show | 134 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.2118+230G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38472236 | ||||||
chr17:38472429
|
C | CGGGGGCT others(45): Show |
2 | a0001c0007t0003g0051a0004c0055t0004g0302 | 2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2118+426_2118+477d others(54): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 38472429 | |||||
chr17:38472643
|
A | G | 2 | a0001c0003t0001g0109a0001c0007t0003g0110 | 2 | HG00544.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.2118+637A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38472643 | ||||||
chr17:38472958
|
A | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0205 | 2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2118+952A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38472958 | ||||||
chr17:38472999
|
C | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0079others(46): Show | 49 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.2118+993C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38472999 | ||||||
chr17:38473090
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2118+1084C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473090 | ||||||
chr17:38473103
|
A | AT | 10 | a0001c0001t0001g0093a0001c0001t0001g0271a0001c0002t0002g0013others(7): Show | 10 | HG00323.hp2 HG00735.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2118+1117dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 38473103 | |||||
chr17:38473103
|
AT | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(112): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.2118+1117delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 38473103 | |||||
chr17:38473103
|
ATT | A | 18 | a0001c0001t0001g0081a0001c0001t0001g0150a0001c0004t0001g0053others(15): Show | 18 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2118+1116_2118+111 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 38473103 | |||||
chr17:38473347
|
C | G | 6 | a0001c0001t0001g0154a0001c0007t0013g0146a0001c0012t0003g0043others(3): Show | 6 | HG02145.hp2 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2118+1341C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473347 | ||||||
chr17:38473371
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2118+1365G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473371 | ||||||
chr17:38473400
|
T | C | 1 | a0001c0003t0001g0105 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2118+1394T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473400 | ||||||
chr17:38473424
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0152 | 2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2118+1418G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473424 | ||||||
chr17:38473487
|
G | A | 4 | a0001c0004t0006g0008a0001c0010t0001g0169a0001c0020t0005g0141others(1): Show | 4 | HG01074.hp2 HG02818.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2118+1481G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473487 | ||||||
chr17:38473523
|
G | T | 2 | a0001c0002t0002g0155a0001c0004t0001g0029 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2118+1517G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473523 | ||||||
chr17:38473567
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2118+1561A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473567 | ||||||
chr17:38473582
|
G | A | 1 | a0001c0048t0002g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2118+1576G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473582 | ||||||
chr17:38473649
|
C | A | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0032others(120): Show | 124 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.2118+1643C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473649 | ||||||
chr17:38473778
|
A | G | 27 | a0001c0001t0001g0023a0001c0001t0001g0118a0001c0001t0001g0132others(24): Show | 27 | HG01099.hp2 HG01175.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.2118+1772A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473778 | ||||||
chr17:38474030
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.2118+2024T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474030 | ||||||
chr17:38474161
|
G | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2118+2155G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474161 | ||||||
chr17:38474200
|
C | T | 1 | a0001c0007t0003g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2118+2194C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474200 | ||||||
chr17:38474211
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2118+2205G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474211 | ||||||
chr17:38474266
|
G | A | 1 | a0001c0001t0014g0274 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2118+2260G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474266 | ||||||
chr17:38474270
|
T | C | 25 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0119others(22): Show | 25 | HG00735.hp1 HG01169.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.2118+2264T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474270 | ||||||
chr17:38474328
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2118+2322C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474328 | ||||||
chr17:38474353
|
G | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.2118+2347G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474353 | ||||||
chr17:38474356
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.2118+2350G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474356 | ||||||
chr17:38474471
|
G | T | 4 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0011g0062others(1): Show | 4 | HG02451.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2118+2465G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474471 | ||||||
chr17:38474599
|
A | T | 2 | a0001c0003t0001g0063a0001c0007t0013g0146 | 2 | HG01109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2118+2593A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474599 | ||||||
chr17:38474656
|
C | A | 7 | a0001c0001t0001g0219a0001c0001t0001g0245a0001c0001t0001g0246others(4): Show | 7 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2118+2650C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474656 | ||||||
chr17:38474674
|
T | A | 58 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0118others(55): Show | 58 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.2118+2668T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474674 | ||||||
chr17:38474757
|
T | TG | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(116): Show | 120 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.2118+2758dupG | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 38474757 | |||||
chr17:38475077
|
T | G | 1 | a0001c0003t0001g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2119-2502T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475077 | ||||||
chr17:38475286
|
C | T | 1 | a0001c0042t0001g0261 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2119-2293C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475286 | ||||||
chr17:38475321
|
G | T | 2 | a0001c0031t0003g0065a0008c0050t0003g0136 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2119-2258G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475321 | ||||||
chr17:38475730
|
T | G | 7 | a0001c0011t0006g0071a0001c0011t0006g0074a0003c0014t0001g0066others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2119-1849T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475730 | ||||||
chr17:38475737
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2119-1842G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475737 | ||||||
chr17:38475933
|
G | A | 1 | a0008c0049t0001g0266 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2119-1646G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475933 | ||||||
chr17:38475987
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2119-1592C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475987 | ||||||
chr17:38476229
|
G | A | 1 | a0003c0028t0001g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2119-1350G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476229 | ||||||
chr17:38476258
|
C | A | 6 | a0001c0003t0001g0109a0001c0024t0001g0096a0001c0024t0001g0103others(3): Show | 6 | HG02040.hp1 HG02071.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2119-1321C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476258 | ||||||
chr17:38476282
|
C | T | 29 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0119others(26): Show | 29 | HG00735.hp1 HG01169.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.2119-1297C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476282 | ||||||
chr17:38476283
|
G | A | 1 | a0001c0032t0001g0201 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2119-1296G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476283 | ||||||
chr17:38476568
|
C | T | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2119-1011C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476568 | ||||||
chr17:38476569
|
T | G | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2119-1010T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476569 | ||||||
chr17:38476588
|
G | A | 1 | a0004c0017t0004g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2119-991G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476588 | ||||||
chr17:38476610
|
A | G | 1 | a0004c0055t0004g0302 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2119-969A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476610 | ||||||
chr17:38476791
|
T | TTGTGCAA | 3 | a0001c0004t0001g0052a0001c0004t0001g0059a0001c0009t0003g0159 | 3 | HG01891.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2119-784_2119-778d others(9): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 38476791 | |||||
chr17:38476808
|
G | A | 1 | a0001c0005t0001g0041 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2119-771G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476808 | ||||||
chr17:38476869
|
T | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2119-710T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476869 | ||||||
chr17:38477146
|
A | G | 1 | a0001c0001t0011g0062 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2119-433A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38477146 | ||||||
chr17:38477172
|
G | A | 1 | a0001c0003t0001g0113 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2119-407G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38477172 | ||||||
chr17:38477268
|
G | A | 2 | a0001c0004t0001g0052a0001c0004t0001g0059 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2119-311G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38477268 | ||||||
chr17:38477365
|
G | C | 1 | a0001c0007t0003g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2119-214G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38477365 | ||||||
chr17:38477445
|
G | A | 1 | a0001c0004t0001g0287 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2119-134G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38477445 | ||||||
chr17:38477972
|
C | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.2436+76C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38477972 | ||||||
chr17:38478042
|
A | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2436+146A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478042 | ||||||
chr17:38478092
|
C | T | 1 | a0001c0051t0003g0270 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2436+196C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478092 | ||||||
chr17:38478103
|
G | A | 1 | a0001c0001t0011g0062 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2436+207G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478103 | ||||||
chr17:38478108
|
G | T | 8 | a0001c0001t0001g0118a0001c0001t0001g0132a0001c0001t0001g0133others(5): Show | 8 | HG00642.hp1 HG01175.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.2436+212G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478108 | ||||||
chr17:38478233
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2436+337G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478233 | ||||||
chr17:38478399
|
G | A | 7 | a0001c0005t0001g0031a0001c0005t0001g0035a0001c0005t0001g0038others(4): Show | 7 | HG02055.hp2 HG02886.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2436+503G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478399 | ||||||
chr17:38478417
|
A | AT | 97 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0064others(94): Show | 97 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.2436+536dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr17 | 38478417 | |||||
chr17:38478417
|
A | ATT | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.2436+535_2436+536d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr17 | 38478417 | |||||
chr17:38478460
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2436+564G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478460 | ||||||
chr17:38478700
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2437-736T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478700 | ||||||
chr17:38478800
|
C | G | 3 | a0001c0002t0002g0164a0002c0023t0001g0180a0007c0029t0001g0289 | 3 | HG02155.hp2 NA18940.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2437-636C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478800 | ||||||
chr17:38478826
|
G | T | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-610G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478826 | ||||||
chr17:38478830
|
C | T | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-606C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478830 | ||||||
chr17:38478831
|
C | A | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-605C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478831 | ||||||
chr17:38478832
|
C | G | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-604C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478832 | ||||||
chr17:38478833
|
A | T | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-603A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478833 | ||||||
chr17:38478834
|
C | G | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-602C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478834 | ||||||
chr17:38478836
|
C | G | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-600C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478836 | ||||||
chr17:38478837
|
A | T | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-599A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478837 | ||||||
chr17:38478838
|
A | T | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-598A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478838 | ||||||
chr17:38479043
|
C | G | 25 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0119others(22): Show | 25 | HG00735.hp1 HG01169.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.2437-393C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38479043 | ||||||
chr17:38479044
|
T | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2437-392T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38479044 | ||||||
chr17:38479283
|
G | A | 1 | a0001c0012t0003g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2437-153G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38479283 | ||||||
chr17:38479307
|
C | G | 2 | a0001c0001t0001g0098a0015c0039t0001g0186 | 2 | HG01255.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2437-129C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38479307 | ||||||
chr17:38479407
|
A | G | 3 | a0001c0010t0001g0014a0001c0011t0001g0067a0001c0012t0003g0049 | 3 | HG03209.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2437-29A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38479407 | ||||||
chr17:38479559
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2498+62G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479559 | ||||||
chr17:38479583
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2498+86G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479583 | ||||||
chr17:38479732
|
C | A | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-21C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479732 | ||||||
chr17:38479734
|
C | A | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-19C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479734 | ||||||
chr17:38479736
|
C | A | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-17C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479736 | ||||||
chr17:38479737
|
C | T | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-16C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479737 | ||||||
chr17:38479738
|
C | A | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-15C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479738 | ||||||
chr17:38479739
|
T | G | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-14T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479739 | ||||||
chr17:38479742
|
T | G | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-11T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479742 | ||||||
chr17:38479743
|
T | C | 1 | a0001c0002t0002g0117 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2499-10T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479743 | ||||||
chr17:38479744
|
C | T | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-9C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479744 | ||||||
chr17:38479943
|
G | A | 1 | a0018c0047t0001g0016 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2629+60G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38479943 | ||||||
chr17:38479952
|
T | A | 1 | a0001c0001t0001g0208 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2629+69T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38479952 | ||||||
chr17:38480034
|
G | T | 1 | a0008c0049t0001g0266 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2629+151G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480034 | ||||||
chr17:38480077
|
G | A | 8 | a0001c0001t0001g0118a0001c0001t0001g0132a0001c0001t0001g0133others(5): Show | 8 | HG00642.hp1 HG01175.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.2629+194G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480077 | ||||||
chr17:38480086
|
T | G | 4 | a0001c0001t0001g0056a0001c0001t0001g0154a0004c0055t0004g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2629+203T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480086 | ||||||
chr17:38480255
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.2629+372C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480255 | ||||||
chr17:38480322
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.2629+439T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480322 | ||||||
chr17:38480399
|
C | T | 1 | a0001c0004t0001g0194 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2629+516C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480399 | ||||||
chr17:38480589
|
G | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0011g0062others(1): Show | 4 | HG02451.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2629+706G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480589 | ||||||
chr17:38480678
|
C | T | 1 | a0001c0002t0002g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2629+795C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480678 | ||||||
chr17:38480803
|
C | CA | 22 | a0001c0001t0001g0088a0001c0001t0001g0119a0001c0001t0001g0208others(19): Show | 22 | HG00438.hp2 HG00609.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.2629+941dupA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr17 | 38480803 | |||||
chr17:38480826
|
AAAG | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0011g0062 | 3 | HG02451.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2629+946_2629+948d others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr17 | 38480826 | |||||
chr17:38480828
|
A | G | 1 | a0005c0041t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2629+945A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480828 | ||||||
chr17:38480829
|
G | A | 1 | a0005c0041t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2629+946G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480829 | ||||||
chr17:38480897
|
C | CTGTCCCA others(3): Show |
1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1016_2629+101 others(14): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr17 | 38480897 | |||||
chr17:38480901
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1018G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480901 | ||||||
chr17:38480914
|
C | A | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1031C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480914 | ||||||
chr17:38480916
|
T | A | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1033T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480916 | ||||||
chr17:38480930
|
T | G | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1047T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480930 | ||||||
chr17:38480931
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1048G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480931 | ||||||
chr17:38480934
|
A | C | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1051A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480934 | ||||||
chr17:38480941
|
T | A | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1058T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480941 | ||||||
chr17:38480950
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1067T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480950 | ||||||
chr17:38480951
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1068A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480951 | ||||||
chr17:38480953
|
A | C | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1069A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480953 | ||||||
chr17:38480958
|
T | G | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1064T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480958 | ||||||
chr17:38480961
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1061T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480961 | ||||||
chr17:38480963
|
T | A | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1059T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480963 | ||||||
chr17:38480964
|
C | A | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2630-1058C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480964 | ||||||
chr17:38480964
|
C | G | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1058C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480964 | ||||||
chr17:38480965
|
C | G | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1057C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480965 | ||||||
chr17:38480966
|
C | A | 1 | a0007c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2630-1056C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480966 | ||||||
chr17:38480966
|
C | G | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1056C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480966 | ||||||
chr17:38480967
|
T | A | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1055T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480967 | ||||||
chr17:38480972
|
A | C | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1050A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480972 | ||||||
chr17:38480973
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1049A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480973 | ||||||
chr17:38480975
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1047A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480975 | ||||||
chr17:38480976
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1046T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480976 | ||||||
chr17:38480980
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1042T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480980 | ||||||
chr17:38480984
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1038A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480984 | ||||||
chr17:38480986
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1036A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480986 | ||||||
chr17:38480988
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1034A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480988 | ||||||
chr17:38480991
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1031A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480991 | ||||||
chr17:38480995
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1027A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480995 | ||||||
chr17:38480999
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1023A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480999 | ||||||
chr17:38481011
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1011A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481011 | ||||||
chr17:38481018
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1004T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481018 | ||||||
chr17:38481035
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-987G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481035 | ||||||
chr17:38481154
|
T | A | 1 | a0001c0003t0001g0012 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2630-868T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481154 | ||||||
chr17:38481307
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2630-715T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481307 | ||||||
chr17:38481310
|
C | G | 1 | a0001c0001t0001g0294 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2630-712C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481310 | ||||||
chr17:38481313
|
A | C | 1 | a0001c0001t0001g0294 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2630-709A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481313 | ||||||
chr17:38481318
|
T | A | 1 | a0001c0001t0001g0294 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2630-704T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481318 | ||||||
chr17:38481442
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2630-580C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481442 | ||||||
chr17:38481446
|
C | T | 1 | a0001c0002t0002g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2630-576C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481446 | ||||||
chr17:38481450
|
G | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0011g0062others(1): Show | 4 | HG02451.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2630-572G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481450 | ||||||
chr17:38481600
|
T | A | 2 | a0001c0001t0001g0006a0001c0002t0002g0258 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2630-422T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481600 | ||||||
chr17:38481747
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.2630-275T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481747 | ||||||
chr17:38481881
|
A | T | 1 | a0001c0002t0002g0117 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2630-141A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481881 | ||||||
chr17:38481905
|
C | CAGAT | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2630-116_2630-115i others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr17 | 38481905 | |||||
chr17:38481907
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2630-115T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481907 | ||||||
chr17:38481937
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2630-85C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481937 | ||||||
chr17:38481938
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2630-84G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481938 | ||||||
chr17:38482014
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(108): Show | 112 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(109): Show |
splice_region_variant&intron_variant | LOW | c.2630-8C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38482014 | ||||||
chr17:38482147
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
splice_region_variant&intron_variant | LOW | c.2751+4A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 15/23 | chr17 | 38482147 | ||||||
chr17:38482303
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2751+160C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 15/23 | chr17 | 38482303 | ||||||
chr17:38482454
|
G | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2752-69G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 15/23 | chr17 | 38482454 | ||||||
chr17:38482707
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.2907+29A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38482707 | ||||||
chr17:38483039
|
C | T | 1 | a0001c0001t0011g0062 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2907+361C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483039 | ||||||
chr17:38483040
|
G | A | 4 | a0001c0031t0003g0065a0006c0021t0003g0068a0006c0021t0003g0070others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2907+362G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483040 | ||||||
chr17:38483170
|
G | A | 25 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0119others(22): Show | 25 | HG00735.hp1 HG01169.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.2907+492G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483170 | ||||||
chr17:38483212
|
G | A | 2 | a0001c0001t0001g0077a0018c0047t0001g0016 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2907+534G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483212 | ||||||
chr17:38483403
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2907+725C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483403 | ||||||
chr17:38483696
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(112): Show | 116 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2907+1018T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483696 | ||||||
chr17:38483799
|
T | C | 1 | a0001c0016t0003g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2907+1121T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483799 | ||||||
chr17:38484158
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2907+1480C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484158 | ||||||
chr17:38484230
|
A | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(86): Show | 90 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.2907+1552A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484230 | ||||||
chr17:38484348
|
C | T | 1 | a0001c0003t0001g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2907+1670C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484348 | ||||||
chr17:38484367
|
A | G | 1 | a0001c0011t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2907+1689A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484367 | ||||||
chr17:38484493
|
C | T | 1 | a0001c0002t0002g0117 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2908-1569C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484493 | ||||||
chr17:38484601
|
AGGGCATT others(1): Show |
A | 17 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0119others(14): Show | 17 | HG00735.hp1 HG01169.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2908-1458_2908-145 others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr17 | 38484601 | |||||
chr17:38484618
|
A | G | 5 | a0001c0001t0001g0075a0001c0001t0001g0265a0001c0001t0001g0268others(2): Show | 5 | HG00558.hp2 NA18960.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.2908-1444A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484618 | ||||||
chr17:38484767
|
T | C | 9 | a0001c0001t0001g0118a0001c0001t0001g0132a0001c0001t0001g0133others(6): Show | 9 | HG00642.hp1 HG01175.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.2908-1295T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484767 | ||||||
chr17:38484990
|
T | C | 2 | a0001c0001t0001g0077a0018c0047t0001g0016 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2908-1072T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484990 | ||||||
chr17:38485476
|
C | T | 1 | a0001c0009t0003g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2908-586C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38485476 | ||||||
chr17:38485779
|
A | G | 1 | a0015c0039t0001g0186 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2908-283A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38485779 | ||||||
chr17:38485847
|
A | C | 1 | a0001c0004t0001g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2908-215A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38485847 | ||||||
chr17:38486232
|
CT | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.2986+107delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 38486232 | |||||
chr17:38486255
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2986+115T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486255 | ||||||
chr17:38486337
|
C | G | 1 | a0001c0010t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2986+197C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486337 | ||||||
chr17:38486423
|
G | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2986+283G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486423 | ||||||
chr17:38486452
|
G | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.2986+312G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486452 | ||||||
chr17:38486536
|
C | CT | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(87): Show | 91 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.2986+416dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 38486536 | |||||
chr17:38486536
|
C | CTT | 10 | a0001c0001t0001g0079a0001c0001t0001g0102a0001c0001t0001g0125others(7): Show | 10 | HG00323.hp2 HG00642.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2986+415_2986+416d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 38486536 | |||||
chr17:38486536
|
CT | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.2986+416delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 38486536 | |||||
chr17:38486556
|
T | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0205 | 2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2986+416T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486556 | ||||||
chr17:38486662
|
A | G | 1 | a0004c0055t0004g0302 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2986+522A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486662 | ||||||
chr17:38486834
|
C | T | 29 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0119others(26): Show | 29 | HG00735.hp1 HG01169.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.2986+694C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486834 | ||||||
chr17:38486898
|
T | C | 8 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0011g0062others(5): Show | 8 | HG01081.hp1 HG02451.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2986+758T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486898 | ||||||
chr17:38486987
|
A | G | 1 | a0003c0028t0001g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2986+847A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486987 | ||||||
chr17:38487130
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.2986+990A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487130 | ||||||
chr17:38487213
|
G | A | 2 | a0001c0001t0001g0272a0001c0004t0001g0057 | 2 | HG00642.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2986+1073G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487213 | ||||||
chr17:38487215
|
G | A | 2 | a0001c0001t0001g0019a0001c0003t0001g0022 | 2 | HG01081.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2986+1075G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487215 | ||||||
chr17:38487222
|
C | T | 2 | a0001c0001t0001g0019a0001c0003t0001g0022 | 2 | HG01081.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2986+1082C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487222 | ||||||
chr17:38487289
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2986+1149A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487289 | ||||||
chr17:38487431
|
A | G | 1 | a0001c0005t0001g0034 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2986+1291A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487431 | ||||||
chr17:38487435
|
C | T | 1 | a0001c0010t0001g0169 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2986+1295C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487435 | ||||||
chr17:38487470
|
G | A | 2 | a0001c0001t0001g0163a0001c0004t0006g0008 | 2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2986+1330G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487470 | ||||||
chr17:38487495
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2986+1355G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487495 | ||||||
chr17:38487563
|
A | G | 44 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0112others(41): Show | 44 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.2986+1423A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487563 | ||||||
chr17:38487693
|
G | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0003g0174others(5): Show | 8 | HG01081.hp2 HG01346.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.2986+1553G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487693 | ||||||
chr17:38487728
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2986+1588G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487728 | ||||||
chr17:38487731
|
G | GCAC | 3 | a0001c0001t0001g0118a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG01361.hp2 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2986+1592_2986+159 others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 38487731 | |||||
chr17:38487756
|
A | T | 4 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0011g0062others(1): Show | 4 | HG02451.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2986+1616A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487756 | ||||||
chr17:38487784
|
A | C | 1 | a0001c0002t0002g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2986+1644A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487784 | ||||||
chr17:38487904
|
A | G | 1 | a0018c0047t0001g0016 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2986+1764A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487904 | ||||||
chr17:38488054
|
A | G | 1 | a0018c0047t0001g0016 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2986+1914A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488054 | ||||||
chr17:38488079
|
A | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.2986+1939A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488079 | ||||||
chr17:38488080
|
T | A | 2 | a0004c0019t0004g0058a0004c0019t0004g0061 | 2 | HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2986+1940T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488080 | ||||||
chr17:38488155
|
G | A | 6 | a0001c0001t0001g0077a0001c0020t0005g0009a0001c0020t0005g0141others(3): Show | 6 | HG01081.hp1 HG01891.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2987-1947G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488155 | ||||||
chr17:38488199
|
C | T | 1 | a0001c0010t0001g0169 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2987-1903C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488199 | ||||||
chr17:38488343
|
A | G | 4 | a0001c0020t0005g0009a0001c0020t0005g0141a0001c0027t0005g0144others(1): Show | 4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2987-1759A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488343 | ||||||
chr17:38488362
|
G | A | 4 | a0001c0020t0005g0009a0001c0020t0005g0141a0001c0027t0005g0144others(1): Show | 4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2987-1740G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488362 | ||||||
chr17:38488421
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.2987-1681C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488421 | ||||||
chr17:38488422
|
G | A | 7 | a0001c0011t0006g0071a0001c0011t0006g0074a0003c0014t0001g0066others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2987-1680G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488422 | ||||||
chr17:38488533
|
A | T | 4 | a0001c0020t0005g0009a0001c0020t0005g0141a0001c0027t0005g0144others(1): Show | 4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2987-1569A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488533 | ||||||
chr17:38488548
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2987-1554T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488548 | ||||||
chr17:38489007
|
C | G | 4 | a0001c0020t0005g0009a0001c0020t0005g0141a0001c0027t0005g0144others(1): Show | 4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2987-1095C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489007 | ||||||
chr17:38489020
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2987-1082C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489020 | ||||||
chr17:38489055
|
T | C | 2 | a0001c0001t0001g0163a0001c0004t0006g0008 | 2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2987-1047T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489055 | ||||||
chr17:38489181
|
A | G | 1 | a0001c0003t0001g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2987-921A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489181 | ||||||
chr17:38489425
|
C | T | 8 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0003g0174others(5): Show | 8 | HG01081.hp2 HG01346.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.2987-677C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489425 | ||||||
chr17:38489449
|
A | G | 1 | a0001c0001t0011g0062 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2987-653A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489449 | ||||||
chr17:38489581
|
C | T | 2 | a0001c0001t0001g0077a0018c0047t0001g0016 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2987-521C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489581 | ||||||
chr17:38489688
|
A | G | 12 | a0001c0001t0001g0056a0001c0001t0001g0077a0001c0001t0001g0154others(9): Show | 12 | HG01081.hp1 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2987-414A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489688 | ||||||
chr17:38489726
|
G | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.2987-376G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489726 | ||||||
chr17:38489807
|
C | T | 2 | a0005c0033t0001g0073a0005c0053t0001g0126 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2987-295C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489807 | ||||||
chr17:38489915
|
G | A | 1 | a0001c0018t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2987-187G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489915 | ||||||
chr17:38490020
|
G | A | 2 | a0001c0004t0001g0170a0001c0004t0001g0171 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2987-82G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38490020 | ||||||
chr17:38490050
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.2987-52A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38490050 | ||||||
chr17:38490084
|
G | A | 2 | a0001c0009t0003g0172a0001c0009t0003g0173 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2987-18G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38490084 | ||||||
chr17:38490290
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3060+115C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 18/23 | chr17 | 38490290 | ||||||
chr17:38490367
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3061-95G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 18/23 | chr17 | 38490367 | ||||||
chr17:38490579
|
G | A | 2 | a0001c0010t0001g0014a0001c0011t0001g0067 | 2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3150+28G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490579 | ||||||
chr17:38490778
|
C | T | 6 | a0001c0001t0001g0077a0001c0020t0005g0009a0001c0020t0005g0141others(3): Show | 6 | HG01081.hp1 HG01891.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3150+227C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490778 | ||||||
chr17:38490782
|
C | T | 5 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0011g0062others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3150+231C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490782 | ||||||
chr17:38490811
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.3150+260G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490811 | ||||||
chr17:38490889
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3150+338G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490889 | ||||||
chr17:38490991
|
T | G | 1 | a0001c0002t0002g0306 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3151-416T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490991 | ||||||
chr17:38490992
|
T | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.3151-415T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490992 | ||||||
chr17:38491053
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.3151-354G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38491053 | ||||||
chr17:38491080
|
A | AT | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.3151-325dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr17 | 38491080 | |||||
chr17:38491083
|
A | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.3151-324A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38491083 | ||||||
chr17:38491748
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.3276+216G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38491748 | ||||||
chr17:38491850
|
G | A | 2 | a0005c0033t0001g0073a0005c0053t0001g0126 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3276+318G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38491850 | ||||||
chr17:38492103
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3276+571C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492103 | ||||||
chr17:38492160
|
G | A | 2 | a0001c0001t0001g0077a0018c0047t0001g0016 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3276+628G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492160 | ||||||
chr17:38492162
|
G | A | 5 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0011g0062others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3276+630G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492162 | ||||||
chr17:38492212
|
G | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.3276+680G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492212 | ||||||
chr17:38492262
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.3276+730A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492262 | ||||||
chr17:38492446
|
G | A | 5 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0011g0062others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3276+914G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492446 | ||||||
chr17:38492449
|
G | A | 11 | a0001c0011t0006g0071a0001c0011t0006g0074a0003c0013t0001g0127others(8): Show | 11 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3276+917G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492449 | ||||||
chr17:38492609
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3276+1077G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492609 | ||||||
chr17:38492851
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3276+1319A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492851 | ||||||
chr17:38492917
|
C | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0267 | 2 | HG00438.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.3276+1385C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492917 | ||||||
chr17:38493162
|
G | GC | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.3276+1630_3276+163 others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493162 | ||||||
chr17:38493194
|
C | CT | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0211others(5): Show | 8 | HG01891.hp1 HG02074.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.3276+1671dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38493194 | |||||
chr17:38493194
|
CT | C | 5 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0011g0062others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3276+1671delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38493194 | |||||
chr17:38493211
|
TG | T | 4 | a0003c0013t0001g0127a0003c0013t0001g0128a0003c0013t0001g0130others(1): Show | 4 | HG02895.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3276+1680delG | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493211 | ||||||
chr17:38493212
|
G | GT | 12 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(9): Show | 12 | HG00642.hp1 HG01175.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.3276+1690dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38493212 | |||||
chr17:38493212
|
GT | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.3276+1690delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38493212 | |||||
chr17:38493250
|
T | C | 1 | a0002c0036t0003g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3276+1718T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493250 | ||||||
chr17:38493449
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.3276+1917C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493449 | ||||||
chr17:38493568
|
G | A | 1 | a0001c0003t0001g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3276+2036G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493568 | ||||||
chr17:38493578
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3276+2046G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493578 | ||||||
chr17:38493715
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.3276+2183C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493715 | ||||||
chr17:38493742
|
C | G | 58 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0118others(55): Show | 58 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.3276+2210C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493742 | ||||||
chr17:38493757
|
G | A | 4 | a0001c0031t0003g0065a0006c0021t0003g0068a0006c0021t0003g0070others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.3276+2225G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493757 | ||||||
chr17:38494001
|
A | C | 1 | a0004c0055t0004g0302 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3276+2469A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494001 | ||||||
chr17:38494024
|
CTG | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(84): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.3276+2498_3276+249 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38494024 | |||||
chr17:38494104
|
G | A | 2 | a0001c0004t0001g0054a0001c0005t0001g0042 | 2 | HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3276+2572G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494104 | ||||||
chr17:38494202
|
A | G | 1 | a0001c0002t0002g0164 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3276+2670A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494202 | ||||||
chr17:38494357
|
G | A | 1 | a0001c0007t0013g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3276+2825G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494357 | ||||||
chr17:38494360
|
G | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0119others(1): Show | 4 | HG02135.hp2 NA18944.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.3276+2828G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494360 | ||||||
chr17:38494460
|
G | A | 51 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0118others(48): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.3276+2928G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494460 | ||||||
chr17:38494485
|
G | A | 1 | a0001c0003t0001g0105 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3276+2953G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494485 | ||||||
chr17:38494492
|
G | GGTGGGAG others(6): Show |
1 | a0008c0049t0001g0266 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3276+2964_3276+297 others(17): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38494492 | |||||
chr17:38494520
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3276+2988C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494520 | ||||||
chr17:38494521
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0122others(7): Show | 10 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.3276+2989G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494521 | ||||||
chr17:38494559
|
GAC | G | 5 | a0001c0001t0001g0017a0001c0001t0003g0174a0001c0003t0001g0193others(2): Show | 5 | HG01981.hp2 HG02293.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.3276+3045_3276+304 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38494559 | |||||
chr17:38494564
|
A | G | 1 | a0001c0001t0001g0006 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3276+3032A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494564 | ||||||
chr17:38494575
|
C | A | 1 | a0001c0009t0003g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3276+3043C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494575 | ||||||
chr17:38494577
|
C | A | 1 | a0001c0009t0003g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3276+3045C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494577 | ||||||
chr17:38494579
|
A | C | 1 | a0001c0003t0001g0012 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3276+3047A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494579 | ||||||
chr17:38494588
|
T | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.3276+3056T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494588 | ||||||
chr17:38494594
|
A | C | 1 | a0008c0049t0001g0266 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3276+3062A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494594 | ||||||
chr17:38494703
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.3277-3082C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494703 | ||||||
chr17:38494735
|
T | C | 5 | a0001c0003t0001g0109a0001c0024t0001g0096a0001c0024t0001g0103others(2): Show | 5 | HG02040.hp1 HG02071.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.3277-3050T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494735 | ||||||
chr17:38494782
|
G | T | 2 | a0001c0001t0001g0077a0018c0047t0001g0016 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3277-3003G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494782 | ||||||
chr17:38494882
|
C | T | 1 | a0001c0003t0001g0012 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3277-2903C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494882 | ||||||
chr17:38494904
|
T | G | 4 | a0001c0031t0003g0065a0006c0021t0003g0068a0006c0021t0003g0070others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.3277-2881T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494904 | ||||||
chr17:38494940
|
C | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.3277-2845C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494940 | ||||||
chr17:38494941
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.3277-2844A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494941 | ||||||
chr17:38495020
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.3277-2765A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495020 | ||||||
chr17:38495032
|
C | T | 9 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG02622.hp1 HG02895.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.3277-2753C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495032 | ||||||
chr17:38495228
|
CT | C | 56 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0118others(53): Show | 56 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.3277-2536delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38495228 | |||||
chr17:38495228
|
CTT | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.3277-2537_3277-253 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38495228 | |||||
chr17:38495233
|
T | C | 4 | a0001c0002t0002g0086a0001c0003t0001g0293a0003c0028t0001g0015others(1): Show | 4 | HG02145.hp2 NA18943.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.3277-2552T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495233 | ||||||
chr17:38495234
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.3277-2551T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495234 | ||||||
chr17:38495235
|
T | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0118others(49): Show | 52 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.3277-2550T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495235 | ||||||
chr17:38495426
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3277-2359T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495426 | ||||||
chr17:38495724
|
T | C | 1 | a0001c0004t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3277-2061T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495724 | ||||||
chr17:38495754
|
T | A | 4 | a0001c0001t0001g0082a0001c0001t0001g0200a0001c0001t0001g0290others(1): Show | 4 | HG02132.hp2 NA18963.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.3277-2031T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495754 | ||||||
chr17:38495791
|
T | G | 1 | a0001c0001t0001g0184 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3277-1994T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495791 | ||||||
chr17:38495903
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.3277-1882T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495903 | ||||||
chr17:38495906
|
AT | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(81): Show | 85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.3277-1871delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38495906 | |||||
chr17:38496140
|
C | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0011g0062others(3): Show | 6 | HG02451.hp1 HG02647.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3277-1645C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38496140 | ||||||
chr17:38496145
|
G | C | 1 | a0004c0055t0004g0302 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3277-1640G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38496145 | ||||||
chr17:38496269
|
T | C | 1 | a0004c0055t0004g0302 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3277-1516T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38496269 | ||||||
chr17:38496309
|
ATT | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.3277-1464_3277-146 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38496309 | |||||
chr17:38496358
|
C | T | 1 | a0004c0055t0004g0302 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3277-1427C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38496358 | ||||||
chr17:38496952
|
GA | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.3277-819delA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38496952 | |||||
chr17:38497119
|
A | G | 2 | a0001c0001t0001g0077a0004c0055t0004g0302 | 2 | HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3277-666A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497119 | ||||||
chr17:38497135
|
T | C | 21 | a0001c0003t0001g0063a0001c0004t0001g0054a0001c0005t0001g0031others(18): Show | 21 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3277-650T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497135 | ||||||
chr17:38497169
|
A | C | 54 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0001g0227others(51): Show | 54 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.3277-616A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497169 | ||||||
chr17:38497298
|
G | T | 1 | a0001c0005t0001g0145 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3277-487G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497298 | ||||||
chr17:38497307
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3277-478G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497307 | ||||||
chr17:38497352
|
G | A | 21 | a0001c0003t0001g0063a0001c0004t0001g0054a0001c0005t0001g0031others(18): Show | 21 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3277-433G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497352 | ||||||
chr17:38497368
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0019others(83): Show | 87 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.3277-417T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497368 | ||||||
chr17:38497373
|
C | A | 5 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0011g0062others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3277-412C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497373 | ||||||
chr17:38497398
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(57): Show | 61 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.3277-387C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497398 | ||||||
chr17:38497414
|
C | T | 54 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0001g0227others(51): Show | 54 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.3277-371C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497414 | ||||||
chr17:38497422
|
C | T | 55 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0001g0227others(52): Show | 55 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.3277-363C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497422 | ||||||
chr17:38497446
|
C | T | 58 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0001g0227others(55): Show | 58 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.3277-339C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497446 | ||||||
chr17:38497572
|
C | G | 1 | a0001c0001t0001g0285 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3277-213C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497572 | ||||||
chr17:38497586
|
A | G | 3 | a0001c0001t0001g0077a0001c0009t0003g0055a0004c0055t0004g0302 | 3 | HG02486.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3277-199A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497586 | ||||||
chr17:38497698
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.3277-87G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497698 | ||||||
chr17:38497748
|
A | G | 49 | a0001c0001t0001g0227a0001c0002t0002g0013a0001c0002t0002g0024others(46): Show | 49 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.3277-37A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497748 | ||||||
chr17:38497753
|
G | C | 49 | a0001c0001t0001g0227a0001c0002t0002g0013a0001c0002t0002g0024others(46): Show | 49 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.3277-32G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497753 | ||||||
chr17:38497763
|
C | T | 52 | a0001c0001t0001g0227a0001c0002t0002g0013a0001c0002t0002g0024others(49): Show | 52 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.3277-22C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497763 | ||||||
chr17:38497904
|
C | T | 1 | a0001c0006t0002g0084 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3318+78C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 21/23 | chr17 | 38497904 | ||||||
chr17:38497916
|
C | T | 51 | a0001c0001t0001g0227a0001c0002t0002g0013a0001c0002t0002g0024others(48): Show | 51 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.3318+90C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 21/23 | chr17 | 38497916 | ||||||
chr17:38498036
|
G | A | 1 | a0001c0010t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3318+210G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 21/23 | chr17 | 38498036 | ||||||
chr17:38498070
|
AC | A | 44 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0064others(41): Show | 44 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.3318+247delC | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr17 | 38498070 | |||||
chr17:38498205
|
C | G | 52 | a0001c0001t0001g0227a0001c0002t0002g0013a0001c0002t0002g0024others(49): Show | 52 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.3319-209C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 21/23 | chr17 | 38498205 | ||||||
chr17:38498756
|
C | T | 1 | a0004c0055t0004g0302 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3415+246C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38498756 | ||||||
chr17:38498809
|
T | C | 1 | a0002c0035t0001g0237 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3415+299T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38498809 | ||||||
chr17:38498819
|
G | T | 1 | a0001c0004t0001g0280 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3415+309G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38498819 | ||||||
chr17:38498858
|
C | T | 12 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0132others(9): Show | 12 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.3415+348C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38498858 | ||||||
chr17:38499025
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3415+515C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499025 | ||||||
chr17:38499040
|
C | T | 23 | a0001c0004t0001g0054a0001c0005t0001g0031a0001c0005t0001g0034others(20): Show | 23 | HG00733.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.3415+530C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499040 | ||||||
chr17:38499061
|
G | A | 12 | a0001c0001t0001g0083a0001c0001t0001g0215a0001c0001t0001g0216others(9): Show | 12 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.3415+551G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499061 | ||||||
chr17:38499177
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3415+667C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499177 | ||||||
chr17:38499199
|
C | T | 1 | a0001c0002t0002g0258 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3415+689C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499199 | ||||||
chr17:38499312
|
C | A | 6 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0001g0149others(3): Show | 6 | HG02895.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3415+802C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499312 | ||||||
chr17:38499366
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0154 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3415+856G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499366 | ||||||
chr17:38499377
|
C | T | 1 | a0001c0003t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3415+867C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499377 | ||||||
chr17:38499576
|
C | G | 8 | a0001c0003t0001g0063a0001c0018t0001g0039a0001c0018t0001g0044others(5): Show | 8 | HG01109.hp1 HG02630.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.3416-1021C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499576 | ||||||
chr17:38499785
|
G | A | 1 | a0003c0013t0001g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3416-812G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499785 | ||||||
chr17:38499839
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.3416-758T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499839 | ||||||
chr17:38499906
|
G | A | 1 | a0001c0005t0001g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3416-691G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499906 | ||||||
chr17:38499943
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.3416-654G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499943 | ||||||
chr17:38500207
|
C | A | 9 | a0001c0001t0001g0032a0001c0004t0001g0053a0001c0004t0001g0060others(6): Show | 9 | HG02451.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3416-390C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38500207 | ||||||
chr17:38500553
|
T | C | 1 | a0001c0004t0001g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3416-44T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38500553 | ||||||
chr17:38500636
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03831.hp1 | splice_region_variant&intron_variant | LOW | c.3447+8T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38500636 | ||||||
chr17:38500697
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.3447+69G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38500697 | ||||||
chr17:38500716
|
T | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG00639.hp1 HG01256.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3447+88T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38500716 | ||||||
chr17:38500931
|
G | A | 9 | a0001c0001t0001g0032a0001c0004t0001g0053a0001c0004t0001g0060others(6): Show | 9 | HG02451.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3447+303G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38500931 | ||||||
chr17:38500932
|
C | T | 9 | a0001c0001t0001g0032a0001c0004t0001g0053a0001c0004t0001g0060others(6): Show | 9 | HG02451.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3447+304C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38500932 | ||||||
chr17:38501071
|
T | C | 2 | a0001c0001t0001g0083a0013c0044t0001g0192 | 2 | HG02135.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.3447+443T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38501071 | ||||||
chr17:38501219
|
T | TA | 5 | a0001c0001t0001g0023a0001c0001t0001g0098a0001c0001t0001g0124others(2): Show | 5 | HG01099.hp1 HG01255.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.3447+596dupA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38501219 | |||||
chr17:38501242
|
A | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0032others(23): Show | 26 | HG00544.hp1 HG00733.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.3447+614A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38501242 | ||||||
chr17:38501286
|
GTTATTTT | G | 30 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0002t0002g0013others(27): Show | 30 | HG00735.hp2 HG01169.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.3447+672_3447+678d others(9): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38501286 | |||||
chr17:38501473
|
T | C | 28 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0002t0002g0013others(25): Show | 28 | HG00735.hp2 HG01169.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.3447+845T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38501473 | ||||||
chr17:38501534
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3447+906C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38501534 | ||||||
chr17:38501536
|
C | T | 1 | a0001c0012t0003g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3447+908C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38501536 | ||||||
chr17:38501553
|
GGCCTCC | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.3447+927_3447+932d others(8): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38501553 | |||||
chr17:38501592
|
C | T | 13 | a0001c0004t0001g0054a0001c0005t0001g0031a0001c0005t0001g0034others(10): Show | 13 | HG00733.hp1 HG02055.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.3447+964C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38501592 | ||||||
chr17:38502081
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3447+1453G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38502081 | ||||||
chr17:38502199
|
A | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.3447+1571A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38502199 | ||||||
chr17:38502472
|
G | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.3447+1844G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38502472 | ||||||
chr17:38502473
|
C | T | 3 | a0001c0005t0001g0142a0001c0005t0001g0156a0001c0005t0001g0157 | 3 | HG02257.hp2 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3447+1845C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38502473 | ||||||
chr17:38502729
|
G | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(91): Show | 95 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.3447+2101G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38502729 | ||||||
chr17:38502811
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0009g0003 | 2 | NA18952.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.3447+2183G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38502811 | ||||||
chr17:38503015
|
T | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.3447+2387T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503015 | ||||||
chr17:38503021
|
C | A | 1 | a0001c0006t0002g0084 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3447+2393C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503021 | ||||||
chr17:38503049
|
A | AAAAC | 3 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0004t0001g0057 | 3 | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3447+2441_3447+244 others(8): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38503049 | |||||
chr17:38503079
|
C | T | 4 | a0001c0020t0005g0009a0001c0020t0005g0141a0001c0027t0005g0144others(1): Show | 4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+2451C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503079 | ||||||
chr17:38503401
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0217a0001c0001t0001g0234others(1): Show | 4 | HG00099.hp2 HG00280.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+2773C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503401 | ||||||
chr17:38503545
|
T | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0064others(22): Show | 25 | HG00544.hp1 HG00733.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.3447+2917T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503545 | ||||||
chr17:38503648
|
G | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0078others(113): Show | 117 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.3447+3020G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503648 | ||||||
chr17:38503668
|
T | G | 2 | a0004c0019t0004g0058a0004c0019t0004g0061 | 2 | HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3447+3040T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503668 | ||||||
chr17:38503749
|
AGGAGGCC others(19): Show |
A | 1 | a0001c0006t0002g0084 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3447+3123_3447+314 others(30): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38503749 | |||||
chr17:38503870
|
A | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0004t0001g0057 | 3 | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3447+3242A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503870 | ||||||
chr17:38504085
|
T | C | 1 | a0001c0009t0003g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3447+3457T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504085 | ||||||
chr17:38504256
|
C | T | 4 | a0001c0001t0011g0062a0004c0017t0004g0138a0004c0017t0004g0139others(1): Show | 4 | HG02486.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+3628C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504256 | ||||||
chr17:38504303
|
C | T | 1 | a0013c0044t0001g0192 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3447+3675C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504303 | ||||||
chr17:38504360
|
C | A | 1 | a0001c0009t0003g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3447+3732C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504360 | ||||||
chr17:38504402
|
C | T | 4 | a0001c0001t0011g0062a0004c0017t0004g0138a0004c0017t0004g0139others(1): Show | 4 | HG02486.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+3774C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504402 | ||||||
chr17:38504425
|
G | A | 1 | a0001c0010t0001g0169 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3447+3797G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504425 | ||||||
chr17:38504442
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.3447+3814C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504442 | ||||||
chr17:38504687
|
C | G | 11 | a0001c0004t0001g0054a0001c0005t0001g0031a0001c0005t0001g0034others(8): Show | 11 | HG00733.hp1 HG02055.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.3447+4059C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504687 | ||||||
chr17:38504740
|
C | T | 27 | a0001c0002t0002g0013a0001c0002t0002g0024a0001c0002t0002g0025others(24): Show | 27 | HG00735.hp2 HG01169.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.3447+4112C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504740 | ||||||
chr17:38504816
|
C | T | 4 | a0001c0001t0011g0062a0004c0017t0004g0138a0004c0017t0004g0139others(1): Show | 4 | HG02486.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+4188C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504816 | ||||||
chr17:38504976
|
ATCTTTTT others(13): Show |
A | 1 | a0001c0001t0001g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3447+4350_3447+436 others(24): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504976 | |||||
chr17:38504978
|
C | CT | 12 | a0001c0001t0001g0218a0001c0001t0001g0285a0001c0003t0001g0010others(9): Show | 12 | HG00621.hp1 HG01993.hp2 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.3447+4395dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
C | CTT | 10 | a0001c0001t0001g0254a0001c0001t0001g0259a0001c0001t0001g0272others(7): Show | 10 | HG00609.hp1 HG00642.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.3447+4394_3447+439 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
C | CTTT | 7 | a0001c0001t0001g0118a0001c0001t0001g0133a0001c0001t0001g0298others(4): Show | 7 | HG01074.hp1 HG01361.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.3447+4393_3447+439 others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
C | CTTTT | 7 | a0001c0001t0001g0122a0001c0001t0001g0248a0001c0003t0001g0193others(4): Show | 7 | HG01070.hp1 HG01074.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.3447+4392_3447+439 others(8): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
C | T | 1 | a0001c0008t0001g0198 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3447+4350C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504978 | ||||||
chr17:38504978
|
CT | C | 28 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0098others(25): Show | 28 | HG00438.hp1 HG00621.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.3447+4395delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTT | C | 23 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0124others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.3447+4394_3447+439 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTT | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0082a0001c0001t0001g0184others(3): Show | 6 | HG01884.hp1 HG01943.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.3447+4393_3447+439 others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0166a0001c0001t0001g0187others(4): Show | 7 | HG02280.hp1 HG03239.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.3447+4389_3447+439 others(11): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(1): Show |
C | 29 | a0001c0001t0001g0032a0001c0001t0001g0075a0001c0001t0001g0087others(26): Show | 29 | HG00735.hp1 HG01106.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.3447+4388_3447+439 others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(2): Show |
C | 33 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0081others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.3447+4387_3447+439 others(13): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(3): Show |
C | 22 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0083others(19): Show | 23 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.3447+4386_3447+439 others(14): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0205a0001c0001t0001g0214a0001c0002t0002g0108others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.3447+4385_3447+439 others(15): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(5): Show |
C | 21 | a0001c0001t0001g0017a0001c0001t0001g0216a0001c0001t0001g0238others(18): Show | 21 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.3447+4384_3447+439 others(16): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(6): Show |
C | 35 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0077others(32): Show | 35 | HG00735.hp2 HG01106.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.3447+4383_3447+439 others(17): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(7): Show |
C | 6 | a0001c0001t0001g0152a0001c0002t0002g0306a0001c0031t0003g0065others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3447+4382_3447+439 others(18): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(8): Show |
C | 3 | a0001c0007t0013g0146a0001c0010t0001g0168a0015c0039t0001g0186 | 3 | HG01255.hp2 HG01993.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3447+4381_3447+439 others(19): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(9): Show |
C | 6 | a0001c0009t0003g0173a0004c0017t0004g0138a0004c0017t0004g0139others(3): Show | 6 | HG01243.hp2 HG02486.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.3447+4380_3447+439 others(20): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(10): Show |
C | 5 | a0001c0001t0001g0163a0001c0001t0011g0062a0001c0009t0003g0172others(2): Show | 5 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3447+4379_3447+439 others(21): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0132a0001c0004t0001g0029 | 2 | HG02055.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3447+4378_3447+439 others(22): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0027t0005g0153 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3447+4377_3447+439 others(23): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(13): Show |
C | 4 | a0001c0003t0001g0279a0001c0020t0005g0009a0001c0020t0005g0141others(1): Show | 4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+4376_3447+439 others(24): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(15): Show |
C | 1 | a0001c0007t0015g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3447+4374_3447+439 others(26): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38504978
|
CTTTTTTT others(17): Show |
C | 3 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0004t0001g0057 | 3 | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3447+4372_3447+439 others(28): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | |||||
chr17:38505155
|
C | A | 4 | a0001c0001t0011g0062a0004c0017t0004g0138a0004c0017t0004g0139others(1): Show | 4 | HG02486.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+4527C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505155 | ||||||
chr17:38505184
|
A | T | 34 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0064others(31): Show | 34 | HG00544.hp1 HG00733.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.3447+4556A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505184 | ||||||
chr17:38505375
|
A | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(253): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.3448-4569A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505375 | ||||||
chr17:38505458
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3448-4486G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505458 | ||||||
chr17:38505658
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(86): Show | 90 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.3448-4286G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505658 | ||||||
chr17:38505690
|
A | G | 1 | a0001c0006t0002g0084 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3448-4254A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505690 | ||||||
chr17:38505746
|
TG | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0004t0001g0057 | 3 | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3448-4196delG | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38505746 | |||||
chr17:38505824
|
C | T | 4 | a0001c0020t0005g0009a0001c0020t0005g0141a0001c0027t0005g0144others(1): Show | 4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3448-4120C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505824 | ||||||
chr17:38505971
|
C | G | 2 | a0001c0001t0001g0296a0001c0002t0002g0228 | 2 | NA18952.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.3448-3973C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505971 | ||||||
chr17:38506004
|
C | G | 2 | a0001c0018t0001g0039a0001c0018t0001g0044 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3448-3940C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506004 | ||||||
chr17:38506045
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0004t0001g0057 | 3 | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3448-3899G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506045 | ||||||
chr17:38506162
|
A | G | 9 | a0001c0003t0001g0063a0003c0013t0001g0127a0003c0013t0001g0128others(6): Show | 9 | HG01109.hp1 HG01884.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3448-3782A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506162 | ||||||
chr17:38506481
|
A | C | 3 | a0004c0017t0004g0138a0004c0017t0004g0139a0004c0055t0004g0302 | 3 | HG02486.hp1 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3448-3463A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506481 | ||||||
chr17:38506638
|
C | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.3448-3306C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506638 | ||||||
chr17:38506655
|
G | T | 1 | a0001c0001t0001g0297 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3448-3289G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506655 | ||||||
chr17:38506656
|
C | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(129): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.3448-3288C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506656 | ||||||
chr17:38506694
|
C | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(266): Show | 271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.3448-3250C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506694 | ||||||
chr17:38506989
|
C | T | 29 | a0001c0001t0001g0272a0001c0001t0003g0174a0001c0004t0001g0054others(26): Show | 29 | HG00544.hp1 HG00642.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.3448-2955C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506989 | ||||||
chr17:38506999
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.3448-2945A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506999 | ||||||
chr17:38507067
|
A | C | 1 | a0001c0001t0001g0222 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3448-2877A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38507067 | ||||||
chr17:38507157
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3448-2787C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38507157 | ||||||
chr17:38507227
|
T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(92): Show | 96 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.3448-2717T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38507227 | ||||||
chr17:38507276
|
A | AAAT | 3 | a0001c0001t0001g0056a0001c0003t0001g0193a0001c0004t0001g0057 | 3 | HG02293.hp1 HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3448-2640_3448-263 others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | |||||
chr17:38507276
|
A | AAATAATA others(2): Show |
19 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0112others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.3448-2646_3448-263 others(13): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | |||||
chr17:38507276
|
A | AAATAATA others(5): Show |
101 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(98): Show | 102 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.3448-2649_3448-263 others(16): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | |||||
chr17:38507276
|
A | AAATAATA others(8): Show |
69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(66): Show | 70 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.3448-2652_3448-263 others(19): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | |||||
chr17:38507276
|
A | AAATAATA others(11): Show |
50 | a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0125others(47): Show | 50 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.3448-2655_3448-263 others(22): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | |||||
chr17:38507276
|
A | AAATAATA others(14): Show |
16 | a0001c0001t0001g0143a0001c0001t0001g0271a0001c0001t0001g0294others(13): Show | 16 | HG01257.hp2 HG01258.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.3448-2658_3448-263 others(25): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | |||||
chr17:38507276
|
A | AAATAATA others(13): Show |
1 | a0001c0006t0002g0084 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3448-2652_3448-265 others(24): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | |||||
chr17:38507276
|
A | ATAATAAT others(12): Show |
1 | a0001c0001t0001g0081 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3448-2668_3448-266 others(23): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38507276 | ||||||
chr17:38507300
|
T | TAATAATA others(11): Show |
1 | a0001c0002t0002g0123 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3448-2638_3448-263 others(22): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507300 | |||||
chr17:38507300
|
T | TAATAATA others(14): Show |
4 | a0001c0002t0002g0013a0001c0002t0002g0255a0001c0040t0002g0135others(1): Show | 4 | HG00735.hp2 HG01169.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.3448-2638_3448-263 others(25): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507300 | |||||
chr17:38507753
|
T | C | 10 | a0001c0005t0001g0041a0001c0005t0001g0048a0001c0005t0001g0050others(7): Show | 10 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.3448-2191T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38507753 | ||||||
chr17:38508184
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3448-1760G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508184 | ||||||
chr17:38508505
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3448-1439G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508505 | ||||||
chr17:38508823
|
A | C | 1 | a0001c0011t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3448-1121A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508823 | ||||||
chr17:38508825
|
A | G | 1 | a0001c0011t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3448-1119A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508825 | ||||||
chr17:38508898
|
A | G | 2 | a0001c0012t0003g0043a0001c0031t0003g0065 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3448-1046A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508898 | ||||||
chr17:38508918
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0009g0003 | 2 | NA18952.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.3448-1026G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508918 | ||||||
chr17:38508967
|
A | G | 2 | a0001c0002t0002g0229a0001c0054t0002g0230 | 2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.3448-977A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508967 | ||||||
chr17:38508989
|
C | T | 8 | a0001c0007t0003g0051a0001c0018t0001g0039a0001c0018t0001g0044others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.3448-955C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508989 | ||||||
chr17:38509021
|
TGGGGAAG others(3): Show |
T | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.3448-908_3448-899d others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38509021 | |||||
chr17:38509041
|
A | C | 1 | a0002c0035t0001g0237 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3448-903A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509041 | ||||||
chr17:38509058
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3448-886C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509058 | ||||||
chr17:38509381
|
G | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0004t0001g0057 | 3 | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3448-563G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509381 | ||||||
chr17:38509596
|
C | T | 1 | a0001c0027t0005g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3448-348C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509596 | ||||||
chr17:38509609
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0207 | 2 | HG00544.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.3448-335G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509609 | ||||||
chr17:38509755
|
G | T | 1 | a0001c0001t0001g0267 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3448-189G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509755 | ||||||
chr17:38509761
|
G | C | 2 | a0001c0016t0003g0045a0001c0016t0003g0301 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3448-183G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509761 | ||||||
chr17:38509810
|
G | C | 6 | a0001c0001t0001g0077a0001c0005t0001g0048a0001c0005t0001g0050others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3448-134G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509810 | ||||||
chr17:38509876
|
G | A | 1 | a0001c0020t0005g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3448-68G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509876 | ||||||
chr17:38509888
|
G | A | 2 | a0001c0016t0003g0045a0001c0016t0003g0301 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3448-56G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509888 | ||||||
chr17:38509932
|
T | G | 1 | a0016c0056t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3448-12T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509932 |