geneid | 9411 |
---|---|
ensemblid | ENSG00000137962.13 |
hgncid | 30207 |
symbol | ARHGAP29 |
name | Rho GTPase activating protein 29 |
refseq_nuc | NM_004815.4 |
refseq_prot | NP_004806.3 |
ensembl_nuc | ENST00000260526.11 |
ensembl_prot | ENSP00000260526.6 |
mane_status | MANE Select |
chr | chr1 |
start | 94168905 |
end | 94237584 |
strand | - |
ver | v1.2 |
region | chr1:94168905-94237584 |
region5000 | chr1:94163905-94242584 |
regionname0 | ARHGAP29_chr1_94168905_94237584 |
regionname5000 | ARHGAP29_chr1_94163905_94242584 |
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 | 1261 | 333 | 66 | 64 | 157 | 16 | 29 | 121 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0002 | 1/0 | 1261 | 16 | 15 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0003 | 0/0 | 1261 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0004 | 0/0 | 1261 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0005 | 0/0 | 1261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0006 | 0/0 | 1261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0007 | 0/0 | 1261 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0008 | 0/0 | 1261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0009 | 0/0 | 1261 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
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 | 3786 | 300 | 61 | 48 | 156 | 11 | 23 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0002 | 0/0 | 3786 | 28 | 2 | 16 | 0 | 5 | 5 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0003 | 1/0 | 3786 | 15 | 14 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0004 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0005 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0006 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0007 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0008 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0009 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0010 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0011 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0012 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0013 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0014 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0015 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
c0016 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5169 | 74 | 4 | 17 | 40 | 4 | 9 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0002 | 0/0 | 5173 | 54 | 7 | 12 | 29 | 2 | 4 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0003 | 0/1 | 5169 | 46 | 10 | 8 | 20 | 4 | 3 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0004 | 0/0 | 5171 | 36 | 11 | 2 | 23 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0005 | 0/0 | 5169 | 23 | 1 | 1 | 18 | 1 | 2 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0006 | 0/0 | 5175 | 16 | 2 | 4 | 8 | 2 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0007 | 0/0 | 5171 | 15 | 4 | 5 | 0 | 0 | 6 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0008 | 1/0 | 5167 | 9 | 8 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0009 | 0/0 | 5171 | 8 | 0 | 4 | 3 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0010 | 0/0 | 5149 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0011 | 0/0 | 5173 | 6 | 4 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0012 | 0/0 | 5171 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0013 | 0/0 | 5169 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0014 | 0/0 | 5171 | 4 | 0 | 2 | 1 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0015 | 0/0 | 5167 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0016 | 0/0 | 5169 | 4 | 0 | 1 | 0 | 2 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0017 | 0/0 | 5169 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0018 | 0/0 | 5167 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0019 | 0/0 | 5171 | 3 | 1 | 2 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0020 | 0/0 | 5173 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0021 | 0/0 | 5177 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0022 | 0/0 | 5173 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0023 | 0/0 | 5171 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0024 | 0/0 | 5167 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0025 | 0/0 | 5169 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0026 | 0/0 | 5169 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0027 | 0/0 | 5169 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0028 | 0/0 | 5179 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0029 | 0/0 | 5173 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0030 | 0/0 | 5173 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0031 | 0/0 | 5169 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0032 | 0/0 | 5175 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0033 | 0/0 | 5173 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0034 | 0/0 | 5169 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0035 | 0/0 | 5169 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0036 | 0/0 | 5169 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0037 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0038 | 0/0 | 5169 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0039 | 0/0 | 5175 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0040 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0041 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0042 | 0/0 | 5171 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0043 | 0/0 | 5167 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
t0044 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
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 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0004 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0006 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
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 | 3786 | 300 | 61 | 48 | 156 | 11 | 23 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0002 | 0/0 | 3786 | 28 | 2 | 16 | 0 | 5 | 5 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0005 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0007 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0009 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0011 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0012 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0002c0003 | 1/0 | 3786 | 15 | 14 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0002c0015 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0003c0004 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0004c0006 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0005c0014 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0006c0008 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0007c0013 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0008c0010 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0009c0016 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8954 | 53 | 2 | 8 | 38 | 1 | 4 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0002 | 0/0 | 8958 | 54 | 7 | 12 | 29 | 2 | 4 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0003 | 0/1 | 8954 | 44 | 8 | 8 | 20 | 4 | 3 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0004 | 0/0 | 8956 | 36 | 11 | 2 | 23 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0005 | 0/0 | 8954 | 23 | 1 | 1 | 18 | 1 | 2 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0006 | 0/0 | 8960 | 15 | 2 | 4 | 7 | 2 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0007 | 0/0 | 8956 | 14 | 3 | 5 | 0 | 0 | 6 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0009 | 0/0 | 8956 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0010 | 0/0 | 8934 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0011 | 0/0 | 8958 | 5 | 3 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0012 | 0/0 | 8956 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0013 | 0/0 | 8954 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0014 | 0/0 | 8956 | 4 | 0 | 2 | 1 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0017 | 0/0 | 8954 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0018 | 0/0 | 8952 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0019 | 0/0 | 8956 | 3 | 1 | 2 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0020 | 0/0 | 8958 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0021 | 0/0 | 8962 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0022 | 0/0 | 8958 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0023 | 0/0 | 8956 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0025 | 0/0 | 8954 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0026 | 0/0 | 8954 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0028 | 0/0 | 8964 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0029 | 0/0 | 8958 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0030 | 0/0 | 8958 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0031 | 0/0 | 8954 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0032 | 0/0 | 8960 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0034 | 0/0 | 8954 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0035 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0036 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0037 | 0/0 | 8956 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0038 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0039 | 0/0 | 8960 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0041 | 0/0 | 8952 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0042 | 0/0 | 8956 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0001t0043 | 0/0 | 8952 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0002t0001 | 0/0 | 8954 | 18 | 2 | 9 | 0 | 3 | 4 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0002t0009 | 0/0 | 8956 | 5 | 0 | 4 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0002t0016 | 0/0 | 8954 | 3 | 0 | 1 | 0 | 2 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0002t0027 | 0/0 | 8954 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0002t0033 | 0/0 | 8958 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0005t0013 | 0/0 | 8954 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0007t0001 | 0/0 | 8954 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0009t0003 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0011t0040 | 0/0 | 8956 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0001c0012t0007 | 0/0 | 8956 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0002c0003t0008 | 1/0 | 8952 | 9 | 8 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0002c0003t0015 | 0/0 | 8952 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0002c0003t0024 | 0/0 | 8952 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0002c0003t0044 | 0/0 | 8952 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0002c0015t0024 | 0/0 | 8952 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0003c0004t0001 | 0/0 | 8954 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0004c0006t0001 | 0/0 | 8954 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0005c0014t0011 | 0/0 | 8958 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0006c0008t0003 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0007c0013t0006 | 0/0 | 8960 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0008c0010t0022 | 0/0 | 8958 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
a0009c0016t0016 | 0/0 | 8954 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | copy fasta | chr1 | 94163905 | 94242584 |
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 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0004 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0009g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0009g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0010g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0010g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0010g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0010g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0011g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0011g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0012g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0012g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0012g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0013g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0013g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0013g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0014g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0014g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0014g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0017g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0017g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0017g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0018g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0018g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0018g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0019g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0019g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0020g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0020g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0021g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0021g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0022g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0023g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0023g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0025g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0025g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0026g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0028g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0029g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0030g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0031g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0032g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0034g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0035g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0036g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0037g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0038g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0039g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0041g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0042g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0001t0043g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0009g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0009g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0009g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0009g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0009g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0016g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0016g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0016g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0027g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0002t0033g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0005t0013g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0007t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0009t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0011t0040g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0001c0012t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0008g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0008g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0008g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0015g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0015g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0015g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0015g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0024g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0003t0044g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0002c0015t0024g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0003c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0004c0006t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0005c0014t0011g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0006c0008t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0007c0013t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0008c0010t0022g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
a0009c0016t0016g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0016 | g0084 | EUR | GBR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | GBR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0021 | EUR | FIN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0229 | EUR | FIN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0078 | EUR | FIN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00323 | hp2 | a0001 | c0001 | t0014 | g0019 | EUR | FIN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00423 | hp2 | a0007 | c0013 | t0006 | g0249 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00544 | hp1 | a0001 | c0001 | t0013 | g0195 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00597 | hp1 | a0001 | c0001 | t0011 | g0147 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00597 | hp2 | a0001 | c0001 | t0020 | g0031 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00621 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00639 | hp2 | a0001 | c0001 | t0014 | g0307 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0235 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00733 | hp1 | a0001 | c0002 | t0027 | g0072 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00735 | hp1 | a0001 | c0002 | t0033 | g0079 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00735 | hp2 | a0001 | c0001 | t0007 | g0283 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01069 | hp1 | a0001 | c0001 | t0006 | g0232 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01071 | hp2 | a0001 | c0001 | t0007 | g0281 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01074 | hp1 | a0001 | c0001 | t0014 | g0019 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01106 | hp1 | a0001 | c0002 | t0009 | g0081 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01109 | hp1 | a0001 | c0001 | t0007 | g0275 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01109 | hp2 | a0001 | c0002 | t0009 | g0073 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01168 | hp1 | a0001 | c0002 | t0009 | g0071 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01243 | hp2 | a0001 | c0001 | t0025 | g0164 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0237 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01256 | hp2 | a0001 | c0001 | t0023 | g0100 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01257 | hp1 | a0001 | c0001 | t0019 | g0103 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0230 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01258 | hp2 | a0001 | c0001 | t0019 | g0012 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01358 | hp1 | a0001 | c0001 | t0017 | g0167 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01433 | hp1 | a0001 | c0002 | t0009 | g0075 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0160 | EUR | IBS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0231 | EUR | IBS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01516 | hp2 | a0001 | c0002 | t0016 | g0083 | EUR | IBS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0234 | EUR | IBS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01884 | hp2 | a0001 | c0001 | t0012 | g0178 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0290 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0126 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01952 | hp1 | a0001 | c0001 | t0007 | g0219 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01981 | hp2 | a0001 | c0001 | t0028 | g0268 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01993 | hp1 | a0001 | c0001 | t0007 | g0220 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02015 | hp2 | a0001 | c0001 | t0014 | g0138 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02040 | hp2 | a0001 | c0001 | t0023 | g0170 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02056 | hp1 | a0001 | c0001 | t0009 | g0110 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02074 | hp1 | a0001 | c0001 | t0017 | g0180 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02129 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02135 | hp1 | a0001 | c0001 | t0006 | g0301 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02145 | hp1 | a0001 | c0001 | t0036 | g0032 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02165 | hp2 | a0001 | c0001 | t0034 | g0111 | EAS | CDX | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0288 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02258 | hp1 | a0006 | c0008 | t0003 | g0177 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0274 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0276 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02280 | hp2 | a0005 | c0014 | t0011 | g0133 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0179 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02451 | hp2 | a0001 | c0001 | t0019 | g0012 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02523 | hp1 | a0001 | c0001 | t0031 | g0047 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0295 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02572 | hp2 | a0001 | c0001 | t0035 | g0292 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02630 | hp2 | a0001 | c0001 | t0022 | g0036 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0215 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02698 | hp1 | a0001 | c0001 | t0026 | g0057 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02698 | hp2 | a0001 | c0002 | t0009 | g0074 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02717 | hp2 | a0001 | c0001 | t0021 | g0310 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02723 | hp1 | a0002 | c0003 | t0015 | g0166 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0299 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0279 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02738 | hp2 | a0001 | c0001 | t0007 | g0277 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02809 | hp2 | a0001 | c0012 | t0007 | g0105 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02886 | hp1 | a0001 | c0001 | t0032 | g0131 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02895 | hp2 | a0001 | c0001 | t0018 | g0152 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0132 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02896 | hp2 | a0002 | c0003 | t0008 | g0210 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02897 | hp1 | a0001 | c0001 | t0011 | g0134 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02897 | hp2 | a0001 | c0001 | t0018 | g0153 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02922 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02922 | hp2 | a0002 | c0003 | t0008 | g0212 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02970 | hp1 | a0002 | c0003 | t0015 | g0043 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0154 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02976 | hp2 | a0002 | c0003 | t0044 | g0211 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03041 | hp2 | a0001 | c0001 | t0012 | g0184 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03098 | hp2 | a0002 | c0003 | t0015 | g0165 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0308 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03139 | hp1 | a0002 | c0003 | t0008 | g0207 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03139 | hp2 | a0001 | c0001 | t0010 | g0304 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0144 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03209 | hp2 | a0002 | c0003 | t0024 | g0161 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0278 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03225 | hp2 | a0001 | c0001 | t0038 | g0293 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0289 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0294 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03486 | hp2 | a0002 | c0003 | t0008 | g0214 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03491 | hp1 | a0001 | c0001 | t0007 | g0280 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03491 | hp2 | a0001 | c0001 | t0025 | g0163 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03579 | hp1 | a0001 | c0001 | t0012 | g0187 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03579 | hp2 | a0002 | c0003 | t0008 | g0213 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03710 | hp2 | a0009 | c0016 | t0016 | g0076 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0077 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03831 | hp2 | a0001 | c0001 | t0043 | g0205 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0157 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG04115 | hp1 | a0001 | c0001 | t0007 | g0218 | SAS | STU | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG04115 | hp2 | a0001 | c0007 | t0001 | g0037 | SAS | STU | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | STU | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0284 | SAS | STU | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG04228 | hp1 | a0001 | c0001 | t0007 | g0217 | SAS | STU | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG04228 | hp2 | a0001 | c0001 | t0005 | g0050 | SAS | STU | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18522 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | YRI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | YRI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18612 | hp1 | a0003 | c0004 | t0001 | g0102 | EAS | CHB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18612 | hp2 | a0001 | c0001 | t0005 | g0054 | EAS | CHB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18906 | hp1 | a0002 | c0003 | t0015 | g0042 | AFR | YRI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | YRI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18941 | hp1 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18943 | hp1 | a0001 | c0001 | t0013 | g0169 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18952 | hp2 | a0001 | c0001 | t0021 | g0260 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18965 | hp1 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18966 | hp1 | a0001 | c0001 | t0009 | g0121 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18970 | hp2 | a0001 | c0001 | t0006 | g0264 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18971 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18973 | hp1 | a0001 | c0001 | t0030 | g0247 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18975 | hp1 | a0001 | c0005 | t0013 | g0168 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18984 | hp1 | a0001 | c0001 | t0006 | g0242 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18991 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18995 | hp2 | a0001 | c0001 | t0017 | g0181 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19000 | hp1 | a0001 | c0001 | t0006 | g0267 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19000 | hp2 | a0001 | c0001 | t0011 | g0104 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19009 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19009 | hp2 | a0001 | c0001 | t0029 | g0228 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19011 | hp2 | a0001 | c0001 | t0006 | g0253 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19030 | hp1 | a0002 | c0003 | t0008 | g0208 | AFR | LWK | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19030 | hp2 | a0001 | c0011 | t0040 | g0101 | AFR | LWK | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | LWK | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19043 | hp2 | a0008 | c0010 | t0022 | g0035 | AFR | LWK | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19054 | hp1 | a0004 | c0006 | t0001 | g0108 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19054 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19056 | hp1 | a0001 | c0001 | t0020 | g0313 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0262 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19067 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19076 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19081 | hp1 | a0001 | c0001 | t0009 | g0120 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19081 | hp2 | a0001 | c0001 | t0013 | g0171 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19089 | hp2 | a0001 | c0001 | t0039 | g0254 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19090 | hp2 | a0001 | c0001 | t0020 | g0031 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | YRI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | YRI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0240 | EUR | TSI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0085 | EUR | TSI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0004 | EUR | TSI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | TSI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA20905 | hp1 | a0001 | c0001 | t0042 | g0206 | SAS | GIH | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | GIH | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG01123 | hp2 | a0001 | c0002 | t0016 | g0066 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02109 | hp1 | a0001 | c0009 | t0003 | g0191 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02109 | hp2 | a0002 | c0003 | t0008 | g0023 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02486 | hp1 | a0001 | c0001 | t0018 | g0291 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02486 | hp2 | a0001 | c0001 | t0037 | g0306 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0203 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG03471 | hp2 | a0001 | c0001 | t0041 | g0287 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | USA | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
HG06807 | hp2 | a0002 | c0003 | t0008 | g0023 | AFR | USA | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | USA | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | USA | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
NA21309 | hp2 | a0002 | c0015 | t0024 | g0106 | AFR | LWK | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0065 | REF | REF | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
homoSapiens_grch38 | hp1 | a0002 | c0003 | t0008 | g0209 | REF | REF | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:94173891
|
C | T | 8 | a0001a0003a0004others(5): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
missense_variant | MODERATE | c.3764G>A | p.Gly1255Asp | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3966/8952 | 3764/3786 | 1255/1261 | chr1 | 94173891 | ||
chr1:94174051
|
C | A | 1 | a0007 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.3604G>T | p.Val1202Leu | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3806/8952 | 3604/3786 | 1202/1261 | chr1 | 94174051 | ||
chr1:94174698
|
A | G | 1 | a0008 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.2957T>C | p.Ile986Thr | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3159/8952 | 2957/3786 | 986/1261 | chr1 | 94174698 | ||
chr1:94179812
|
C | T | 1 | a0006 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.2393G>A | p.Arg798Gln | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/23 | 2595/8952 | 2393/3786 | 798/1261 | chr1 | 94179812 | ||
chr1:94185416
|
G | A | 1 | a0005 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.1846C>T | p.Arg616Cys | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 17/23 | 2048/8952 | 1846/3786 | 616/1261 | chr1 | 94185416 | ||
chr1:94201749
|
C | T | 1 | a0004 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.1252G>A | p.Val418Ile | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/23 | 1454/8952 | 1252/3786 | 418/1261 | chr1 | 94201749 | ||
chr1:94205174
|
T | C | 1 | a0009 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.584A>G | p.Asp195Gly | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/23 | 786/8952 | 584/3786 | 195/1261 | chr1 | 94205174 | ||
chr1:94220347
|
C | T | 1 | a0003 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.251G>A | p.Arg84His | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/23 | 453/8952 | 251/3786 | 84/1261 | chr1 | 94220347 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:94174289
|
A | T | 1 | a0002c0015 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.3366T>A | p.Thr1122Thr | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3568/8952 | 3366/3786 | 1122/1261 | chr1 | 94174289 | ||
chr1:94174310
|
C | T | 1 | a0001c0012 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.3345G>A | p.Gly1115Gly | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3547/8952 | 3345/3786 | 1115/1261 | chr1 | 94174310 | ||
chr1:94174373
|
A | G | 1 | a0001c0011 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.3282T>C | p.Thr1094Thr | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3484/8952 | 3282/3786 | 1094/1261 | chr1 | 94174373 | ||
chr1:94177640
|
C | T | 1 | a0001c0009 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.2877G>A | p.Ala959Ala | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/23 | 3079/8952 | 2877/3786 | 959/1261 | chr1 | 94177640 | ||
chr1:94177975
|
T | C | 2 | a0001c0002a0009c0016 | 29 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(26): Show |
synonymous_variant | LOW | c.2673A>G | p.Gln891Gln | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 21/23 | 2875/8952 | 2673/3786 | 891/1261 | chr1 | 94177975 | ||
chr1:94186506
|
T | C | 1 | a0002c0015 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1773A>G | p.Ser591Ser | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/23 | 1975/8952 | 1773/3786 | 591/1261 | chr1 | 94186506 | ||
chr1:94190075
|
A | C | 1 | a0001c0007 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.1290T>G | p.Val430Val | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 13/23 | 1492/8952 | 1290/3786 | 430/1261 | chr1 | 94190075 | ||
chr1:94205669
|
A | G | 1 | a0001c0005 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.525T>C | p.Val175Val | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 6/23 | 727/8952 | 525/3786 | 175/1261 | chr1 | 94205669 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:94168920
|
G | A | 3 | a0001c0001t0010a0001c0001t0041a0001c0011t0040 | 9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4949C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4949 | chr1 | 94168920 | |||||
chr1:94169054
|
C | T | 1 | a0001c0001t0035 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4815G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4815 | chr1 | 94169054 | |||||
chr1:94169106
|
A | C | 1 | a0001c0011t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4763T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4763 | chr1 | 94169106 | |||||
chr1:94169108
|
G | A | 1 | a0001c0001t0018 | 3 | HG02486.hp1 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4761C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4761 | chr1 | 94169108 | |||||
chr1:94169144
|
C | T | 1 | a0001c0001t0010 | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4725G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4725 | chr1 | 94169144 | |||||
chr1:94169407
|
C | A | 17 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(14): Show | 124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*4462G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4462 | chr1 | 94169407 | |||||
chr1:94169472
|
G | A | 17 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(14): Show | 124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*4397C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4397 | chr1 | 94169472 | |||||
chr1:94169609
|
TGAC | T | 1 | a0001c0001t0010 | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4257_*4259delGTC | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4257 | chr1 | 94169609 | |||||
chr1:94169637
|
C | T | 2 | a0001c0001t0017a0002c0003t0044 | 4 | HG01358.hp1 HG02074.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4232G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4232 | chr1 | 94169637 | |||||
chr1:94169638
|
G | A | 1 | a0001c0001t0041 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4231C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4231 | chr1 | 94169638 | |||||
chr1:94169706
|
T | C | 3 | a0001c0001t0010a0001c0001t0041a0001c0011t0040 | 9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4163A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4163 | chr1 | 94169706 | |||||
chr1:94169793
|
G | T | 1 | a0001c0001t0029 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4076C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4076 | chr1 | 94169793 | |||||
chr1:94170370
|
C | G | 1 | a0001c0001t0010 | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3499G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3499 | chr1 | 94170370 | |||||
chr1:94170430
|
T | C | 24 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(21): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*3439A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3439 | chr1 | 94170430 | |||||
chr1:94170498
|
A | C | 1 | a0001c0011t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3371T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3371 | chr1 | 94170498 | |||||
chr1:94170615
|
T | C | 1 | a0001c0001t0014 | 4 | HG00323.hp2 HG00639.hp2 HG01074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3254A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3254 | chr1 | 94170615 | |||||
chr1:94170703
|
A | T | 10 | a0001c0001t0003a0001c0001t0012a0001c0001t0013others(7): Show | 64 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3166T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3166 | chr1 | 94170703 | |||||
chr1:94171133
|
T | C | 2 | a0001c0001t0042a0001c0001t0043 | 2 | HG03831.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2736A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2736 | chr1 | 94171133 | |||||
chr1:94171160
|
G | C | 1 | a0001c0001t0030 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2709C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2709 | chr1 | 94171160 | |||||
chr1:94171231
|
T | C | 1 | a0001c0001t0031 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2638A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2638 | chr1 | 94171231 | |||||
chr1:94171280
|
A | G | 12 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(9): Show | 97 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2589T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2589 | chr1 | 94171280 | |||||
chr1:94171298
|
A | G | 1 | a0001c0001t0034 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2571T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2571 | chr1 | 94171298 | |||||
chr1:94171436
|
T | A | 1 | a0002c0003t0015 | 4 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2433A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2433 | chr1 | 94171436 | |||||
chr1:94171502
|
C | T | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(22): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2367G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2367 | chr1 | 94171502 | |||||
chr1:94171520
|
G | A | 1 | a0001c0001t0041 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2349C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2349 | chr1 | 94171520 | |||||
chr1:94171759
|
C | G | 1 | a0001c0011t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2110G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2110 | chr1 | 94171759 | |||||
chr1:94172164
|
G | C | 1 | a0001c0001t0012 | 5 | HG01884.hp2 HG02451.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1705C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1705 | chr1 | 94172164 | |||||
chr1:94172612
|
G | GAT | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(19): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1255_*1256dupAT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | 94172612 | |||||
chr1:94172612
|
G | GATAT | 12 | a0001c0001t0004a0001c0001t0007a0001c0001t0009others(9): Show | 76 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1253_*1256dupATAT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | 94172612 | |||||
chr1:94172612
|
G | GATATAT | 9 | a0001c0001t0002a0001c0001t0011a0001c0001t0020others(6): Show | 68 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1251_*1256dupATAT others(2): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | 94172612 | |||||
chr1:94172612
|
G | GATATATA others(1): Show |
4 | a0001c0001t0006a0001c0001t0032a0001c0001t0039others(1): Show | 18 | HG00423.hp2 HG00642.hp1 HG01069.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1249_*1256dupATAT others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | 94172612 | |||||
chr1:94172612
|
G | GATATATA others(3): Show |
1 | a0001c0001t0021 | 2 | HG02717.hp2 NA18952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1247_*1256dupATAT others(6): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | 94172612 | |||||
chr1:94172612
|
G | GATATATA others(5): Show |
1 | a0001c0001t0028 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1245_*1256dupATAT others(8): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | 94172612 | |||||
chr1:94172612
|
GATATATA others(5): Show |
G | 1 | a0001c0001t0010 | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1245_*1256delATAT others(8): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1245 | chr1 | 94172612 | |||||
chr1:94172633
|
T | A | 2 | a0001c0001t0042a0001c0001t0043 | 2 | HG03831.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1236A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1236 | chr1 | 94172633 | |||||
chr1:94172651
|
C | T | 1 | a0001c0001t0038 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1218G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1218 | chr1 | 94172651 | |||||
chr1:94172720
|
T | C | 2 | a0001c0002t0016a0009c0016t0016 | 4 | HG00140.hp1 HG01123.hp2 HG01516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1149A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1149 | chr1 | 94172720 | |||||
chr1:94172792
|
T | C | 1 | a0001c0001t0037 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1077A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1077 | chr1 | 94172792 | |||||
chr1:94172817
|
T | C | 1 | a0001c0001t0038 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1052A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1052 | chr1 | 94172817 | |||||
chr1:94172883
|
A | C | 15 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(12): Show | 122 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*986T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 986 | chr1 | 94172883 | |||||
chr1:94172891
|
C | T | 2 | a0001c0001t0013a0001c0005t0013 | 4 | HG00544.hp1 NA18943.hp1 NA18975.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*978G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 978 | chr1 | 94172891 | |||||
chr1:94173155
|
C | T | 17 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(14): Show | 124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*714G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 714 | chr1 | 94173155 | |||||
chr1:94173172
|
T | C | 1 | a0001c0001t0019 | 3 | HG01257.hp1 HG01258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*697A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 697 | chr1 | 94173172 | |||||
chr1:94173202
|
G | T | 1 | a0001c0011t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*667C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 667 | chr1 | 94173202 | |||||
chr1:94173233
|
T | A | 1 | a0001c0001t0039 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*636A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 636 | chr1 | 94173233 | |||||
chr1:94173408
|
C | A | 5 | a0001c0001t0010a0001c0001t0041a0001c0001t0042others(2): Show | 11 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*461G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 461 | chr1 | 94173408 | |||||
chr1:94173431
|
G | A | 1 | a0001c0001t0025 | 2 | HG01243.hp2 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*438C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 438 | chr1 | 94173431 | |||||
chr1:94173445
|
C | T | 1 | a0001c0002t0027 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*424G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 424 | chr1 | 94173445 | |||||
chr1:94173545
|
A | G | 1 | a0001c0001t0026 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*324T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 324 | chr1 | 94173545 | |||||
chr1:94173781
|
A | G | 56 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(53): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
3_prime_UTR_variant | MODIFIER | c.*88T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 88 | chr1 | 94173781 | |||||
chr1:94173832
|
CACA | C | 1 | a0001c0001t0010 | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*34_*36delTGT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 34 | chr1 | 94173832 | |||||
chr1:94237571
|
G | C | 1 | a0001c0001t0020 | 3 | HG00597.hp2 NA19056.hp1 NA19090.hp2 |
5_prime_UTR_variant | MODIFIER | c.-189C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/23 | 5960 | chr1 | 94237571 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:94174838
|
A | G | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2906-89T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94174838 | ||||||
chr1:94174996
|
C | T | 1 | a0001c0001t0004g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2906-247G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94174996 | ||||||
chr1:94175169
|
C | T | 1 | a0001c0001t0003g0038 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2906-420G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175169 | ||||||
chr1:94175233
|
T | C | 2 | a0001c0001t0004g0127a0001c0001t0011g0104 | 2 | NA18989.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2906-484A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175233 | ||||||
chr1:94175239
|
T | C | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2906-490A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175239 | ||||||
chr1:94175267
|
C | G | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2906-518G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175267 | ||||||
chr1:94175293
|
C | T | 1 | a0001c0001t0002g0026 | 2 | HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2906-544G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175293 | ||||||
chr1:94175332
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(46): Show | 61 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2906-583C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175332 | ||||||
chr1:94175375
|
A | C | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2906-626T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175375 | ||||||
chr1:94175434
|
G | T | 1 | a0001c0001t0007g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2906-685C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175434 | ||||||
chr1:94175524
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2906-775G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175524 | ||||||
chr1:94175641
|
A | C | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.2906-892T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175641 | ||||||
chr1:94175689
|
G | C | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2906-940C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175689 | ||||||
chr1:94175858
|
C | T | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2906-1109G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175858 | ||||||
chr1:94176007
|
G | C | 1 | a0001c0001t0038g0293 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2906-1258C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176007 | ||||||
chr1:94176122
|
A | G | 1 | a0002c0003t0024g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2906-1373T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176122 | ||||||
chr1:94176701
|
G | A | 1 | a0001c0001t0036g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2905+911C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176701 | ||||||
chr1:94176720
|
G | A | 1 | a0001c0001t0003g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2905+892C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176720 | ||||||
chr1:94176721
|
C | G | 1 | a0001c0001t0003g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2905+891G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176721 | ||||||
chr1:94176887
|
G | A | 1 | a0001c0001t0003g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2905+725C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176887 | ||||||
chr1:94176939
|
T | C | 1 | a0001c0001t0038g0293 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2905+673A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176939 | ||||||
chr1:94177107
|
G | A | 1 | a0001c0001t0036g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2905+505C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177107 | ||||||
chr1:94177142
|
GTGTTTAA others(9): Show |
G | 1 | a0001c0001t0004g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2905+454_2905+469d others(18): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177142 | ||||||
chr1:94177179
|
C | T | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2905+433G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177179 | ||||||
chr1:94177199
|
A | T | 3 | a0001c0001t0004g0033a0001c0001t0004g0044a0001c0001t0004g0125 | 3 | HG02559.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2905+413T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177199 | ||||||
chr1:94177230
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(285): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.2905+382A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177230 | ||||||
chr1:94177288
|
C | T | 3 | a0001c0001t0004g0136a0001c0001t0004g0148a0001c0001t0004g0271 | 3 | NA18949.hp2 NA18967.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2905+324G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177288 | ||||||
chr1:94177475
|
T | C | 1 | a0001c0001t0005g0050 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2905+137A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177475 | ||||||
chr1:94178224
|
G | A | 1 | a0001c0001t0021g0260 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2481-57C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94178224 | ||||||
chr1:94178419
|
G | GA | 3 | a0001c0001t0003g0022a0001c0001t0003g0189a0001c0001t0003g0193 | 4 | HG02965.hp2 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2481-253dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94178419 | ||||||
chr1:94178498
|
CATT | C | 57 | a0001c0001t0003g0006a0001c0001t0003g0020a0001c0001t0003g0021others(54): Show | 63 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.2481-334_2481-332d others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94178498 | ||||||
chr1:94178885
|
T | G | 1 | a0001c0001t0013g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2481-718A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94178885 | ||||||
chr1:94179391
|
C | T | 3 | a0001c0001t0007g0277a0001c0001t0007g0280a0001c0001t0007g0284 | 3 | HG02738.hp2 HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2480+334G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179391 | ||||||
chr1:94179492
|
G | A | 1 | a0002c0003t0008g0210 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2480+233C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179492 | ||||||
chr1:94179549
|
T | C | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2480+176A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179549 | ||||||
chr1:94179592
|
C | CA | 12 | a0001c0001t0004g0044a0001c0001t0004g0128a0001c0001t0004g0129others(9): Show | 12 | HG02145.hp1 HG02572.hp1 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.2480+132dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179592 | ||||||
chr1:94179592
|
C | CAA | 29 | a0001c0001t0004g0002a0001c0001t0004g0018a0001c0001t0004g0025others(26): Show | 35 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.2480+131_2480+132d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179592 | ||||||
chr1:94179592
|
C | CAAA | 8 | a0001c0001t0004g0017a0001c0001t0004g0033a0001c0001t0004g0041others(5): Show | 9 | HG01928.hp1 HG02523.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2480+130_2480+132d others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179592 | ||||||
chr1:94179592
|
CA | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(209): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.2480+132delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179592 | ||||||
chr1:94179592
|
CAA | C | 11 | a0001c0001t0002g0239a0001c0001t0002g0305a0001c0001t0003g0183others(8): Show | 12 | HG01168.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2480+131_2480+132d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179592 | ||||||
chr1:94180151
|
GT | G | 8 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(5): Show | 9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2248-195delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180151 | ||||||
chr1:94180243
|
A | T | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2248-286T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180243 | ||||||
chr1:94180320
|
C | T | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2248-363G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180320 | ||||||
chr1:94180421
|
T | A | 1 | a0001c0001t0004g0128 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2248-464A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180421 | ||||||
chr1:94180440
|
A | G | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0009others(14): Show | 24 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2248-483T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180440 | ||||||
chr1:94180496
|
G | T | 1 | a0002c0003t0024g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2248-539C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180496 | ||||||
chr1:94180572
|
C | T | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2248-615G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180572 | ||||||
chr1:94180711
|
C | T | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2248-754G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180711 | ||||||
chr1:94180790
|
T | C | 39 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(36): Show | 46 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.2248-833A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180790 | ||||||
chr1:94180883
|
G | A | 37 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(34): Show | 44 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2248-926C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180883 | ||||||
chr1:94180958
|
G | A | 34 | a0001c0001t0003g0006a0001c0001t0003g0020a0001c0001t0003g0021others(31): Show | 38 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.2248-1001C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180958 | ||||||
chr1:94181047
|
G | A | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2248-1090C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181047 | ||||||
chr1:94181080
|
C | T | 1 | a0001c0001t0007g0283 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2248-1123G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181080 | ||||||
chr1:94181116
|
A | G | 1 | a0001c0001t0037g0306 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2248-1159T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181116 | ||||||
chr1:94181124
|
A | C | 1 | a0001c0001t0038g0293 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2248-1167T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181124 | ||||||
chr1:94181324
|
C | G | 1 | a0001c0001t0001g0122 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2248-1367G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181324 | ||||||
chr1:94181353
|
C | T | 1 | a0001c0007t0001g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2248-1396G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181353 | ||||||
chr1:94181449
|
T | C | 1 | a0001c0001t0004g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2248-1492A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181449 | ||||||
chr1:94181494
|
G | A | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2248-1537C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181494 | ||||||
chr1:94181603
|
G | A | 10 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(7): Show | 11 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.2248-1646C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181603 | ||||||
chr1:94181678
|
A | T | 1 | a0001c0001t0003g0173 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2248-1721T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181678 | ||||||
chr1:94181744
|
AAAC | A | 3 | a0001c0001t0003g0021a0001c0001t0003g0176a0001c0001t0005g0046 | 4 | HG00280.hp1 HG02738.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.2248-1790_2248-178 others(7): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181744 | ||||||
chr1:94181774
|
T | C | 8 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(5): Show | 9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2248-1817A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181774 | ||||||
chr1:94182100
|
T | TA | 295 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(292): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.2247+2050dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182100 | ||||||
chr1:94182129
|
T | C | 2 | a0001c0001t0006g0274a0001c0001t0006g0276 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2247+2022A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182129 | ||||||
chr1:94182146
|
G | A | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2247+2005C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182146 | ||||||
chr1:94182239
|
G | A | 8 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(5): Show | 9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2247+1912C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182239 | ||||||
chr1:94182273
|
A | T | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2247+1878T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182273 | ||||||
chr1:94182284
|
A | G | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2247+1867T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182284 | ||||||
chr1:94182315
|
A | G | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2247+1836T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182315 | ||||||
chr1:94182389
|
A | T | 29 | a0001c0002t0001g0063a0001c0002t0001g0064a0001c0002t0001g0067others(26): Show | 29 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.2247+1762T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182389 | ||||||
chr1:94182577
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(245): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.2247+1574T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182577 | ||||||
chr1:94182580
|
A | G | 304 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(301): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.2247+1571T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182580 | ||||||
chr1:94182619
|
A | C | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2247+1532T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182619 | ||||||
chr1:94182736
|
C | T | 1 | a0001c0001t0004g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2247+1415G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182736 | ||||||
chr1:94182811
|
T | TAAAAC | 131 | a0001c0001t0001g0123a0001c0001t0001g0151a0001c0001t0002g0003others(128): Show | 152 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.2247+1335_2247+133 others(9): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182811 | ||||||
chr1:94182811
|
T | TAAAACAA others(3): Show |
20 | a0001c0001t0001g0156a0001c0001t0002g0223a0001c0001t0002g0236others(17): Show | 22 | HG00741.hp1 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2247+1330_2247+133 others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182811 | ||||||
chr1:94182811
|
T | TAAAACAA others(8): Show |
1 | a0001c0001t0012g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2247+1325_2247+133 others(19): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182811 | ||||||
chr1:94182811
|
T | TAAAACAA others(13): Show |
2 | a0001c0001t0018g0152a0001c0001t0018g0153 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2247+1320_2247+133 others(24): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182811 | ||||||
chr1:94182811
|
TAAAAC | T | 6 | a0002c0003t0008g0207a0002c0003t0015g0042a0002c0003t0015g0043others(3): Show | 6 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2247+1335_2247+133 others(9): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182811 | ||||||
chr1:94182811
|
TAAAACAA others(3): Show |
T | 9 | a0001c0001t0001g0150a0001c0001t0010g0029a0001c0001t0010g0288others(6): Show | 10 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2247+1330_2247+133 others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182811 | ||||||
chr1:94183138
|
A | T | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2247+1013T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183138 | ||||||
chr1:94183196
|
TA | T | 108 | a0001c0001t0001g0151a0001c0001t0002g0003a0001c0001t0002g0026others(105): Show | 124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.2247+954delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183196 | ||||||
chr1:94183204
|
A | T | 9 | a0001c0001t0002g0222a0001c0001t0002g0257a0001c0001t0010g0029others(6): Show | 10 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2247+947T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183204 | ||||||
chr1:94183204
|
AT | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.2247+946delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183204 | ||||||
chr1:94183206
|
T | A | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2247+945A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183206 | ||||||
chr1:94183292
|
T | C | 1 | a0001c0001t0004g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2247+859A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183292 | ||||||
chr1:94183357
|
G | A | 1 | a0001c0001t0007g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2247+794C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183357 | ||||||
chr1:94183401
|
T | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0266 | 2 | HG04184.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2247+750A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183401 | ||||||
chr1:94183430
|
T | C | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2247+721A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183430 | ||||||
chr1:94183693
|
C | T | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2247+458G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183693 | ||||||
chr1:94184036
|
C | A | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2247+115G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94184036 | ||||||
chr1:94184040
|
T | C | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2247+111A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94184040 | ||||||
chr1:94184044
|
G | A | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2247+107C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94184044 | ||||||
chr1:94184092
|
CA | C | 7 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(4): Show | 8 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2247+58delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94184092 | ||||||
chr1:94184520
|
A | C | 18 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0009others(15): Show | 25 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.2110-232T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184520 | ||||||
chr1:94184556
|
C | T | 2 | a0001c0001t0004g0033a0001c0001t0036g0032 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2110-268G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184556 | ||||||
chr1:94184589
|
A | T | 3 | a0001c0001t0004g0294a0001c0001t0004g0295a0002c0003t0008g0212 | 3 | HG02572.hp1 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2109+283T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184589 | ||||||
chr1:94184590
|
T | A | 10 | a0001c0001t0001g0298a0001c0001t0007g0275a0001c0001t0010g0029others(7): Show | 11 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2109+282A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184590 | ||||||
chr1:94184624
|
C | T | 1 | a0001c0001t0005g0049 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2109+248G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184624 | ||||||
chr1:94184838
|
T | A | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2109+34A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184838 | ||||||
chr1:94184849
|
A | C | 1 | a0008c0010t0022g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2109+23T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184849 | ||||||
chr1:94185175
|
T | C | 1 | a0002c0015t0024g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1921-115A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 17/22 | chr1 | 94185175 | ||||||
chr1:94185249
|
T | C | 2 | a0001c0001t0004g0033a0001c0001t0036g0032 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1920+93A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 17/22 | chr1 | 94185249 | ||||||
chr1:94185321
|
A | C | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1920+21T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 17/22 | chr1 | 94185321 | ||||||
chr1:94185676
|
G | C | 8 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(5): Show | 9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1781-195C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94185676 | ||||||
chr1:94185690
|
A | G | 1 | a0001c0001t0031g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1781-209T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94185690 | ||||||
chr1:94185795
|
G | C | 1 | a0001c0001t0004g0125 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1781-314C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94185795 | ||||||
chr1:94185835
|
A | G | 4 | a0002c0003t0015g0042a0002c0003t0015g0043a0002c0003t0015g0165others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1781-354T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94185835 | ||||||
chr1:94186086
|
C | T | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1780+413G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94186086 | ||||||
chr1:94186091
|
A | C | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1780+408T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94186091 | ||||||
chr1:94186120
|
T | C | 1 | a0001c0001t0037g0306 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1780+379A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94186120 | ||||||
chr1:94186230
|
T | C | 2 | a0001c0001t0022g0036a0008c0010t0022g0035 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1780+269A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94186230 | ||||||
chr1:94186615
|
A | C | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1682-18T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94186615 | ||||||
chr1:94186955
|
A | T | 31 | a0001c0001t0025g0163a0001c0001t0025g0164a0001c0002t0001g0063others(28): Show | 31 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1682-358T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94186955 | ||||||
chr1:94186972
|
T | A | 2 | a0001c0001t0004g0033a0001c0001t0036g0032 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1682-375A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94186972 | ||||||
chr1:94187027
|
A | G | 2 | a0001c0001t0004g0033a0001c0001t0036g0032 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1682-430T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187027 | ||||||
chr1:94187187
|
C | T | 4 | a0002c0003t0015g0042a0002c0003t0015g0043a0002c0003t0015g0165others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1682-590G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187187 | ||||||
chr1:94187250
|
A | T | 2 | a0002c0003t0015g0165a0002c0003t0015g0166 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1682-653T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187250 | ||||||
chr1:94187279
|
T | C | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1682-682A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187279 | ||||||
chr1:94187291
|
C | T | 2 | a0001c0001t0018g0152a0001c0001t0018g0153 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1682-694G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187291 | ||||||
chr1:94187376
|
T | C | 2 | a0001c0001t0006g0253a0001c0001t0006g0267 | 2 | NA19000.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1682-779A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187376 | ||||||
chr1:94187382
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1682-785C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187382 | ||||||
chr1:94187439
|
G | A | 1 | a0001c0001t0005g0056 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1682-842C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187439 | ||||||
chr1:94187444
|
A | G | 8 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(5): Show | 9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1682-847T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187444 | ||||||
chr1:94187699
|
A | T | 1 | a0001c0001t0001g0297 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1682-1102T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187699 | ||||||
chr1:94187764
|
G | A | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1681+1073C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187764 | ||||||
chr1:94187806
|
A | G | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1681+1031T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187806 | ||||||
chr1:94187892
|
T | A | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1681+945A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187892 | ||||||
chr1:94188126
|
C | A | 2 | a0001c0001t0004g0294a0001c0001t0004g0295 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1681+711G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94188126 | ||||||
chr1:94188470
|
A | G | 2 | a0001c0001t0022g0036a0008c0010t0022g0035 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1681+367T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94188470 | ||||||
chr1:94188594
|
G | A | 1 | a0001c0001t0036g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1681+243C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94188594 | ||||||
chr1:94188602
|
T | C | 1 | a0001c0001t0003g0176 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1681+235A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94188602 | ||||||
chr1:94188669
|
C | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1681+168G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94188669 | ||||||
chr1:94189025
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1577-84A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 14/22 | chr1 | 94189025 | ||||||
chr1:94189510
|
T | C | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1440-158A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 13/22 | chr1 | 94189510 | ||||||
chr1:94189528
|
T | G | 1 | a0001c0001t0038g0293 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1440-176A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 13/22 | chr1 | 94189528 | ||||||
chr1:94189539
|
G | A | 7 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(4): Show | 8 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1440-187C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 13/22 | chr1 | 94189539 | ||||||
chr1:94189802
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1439+124A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 13/22 | chr1 | 94189802 | ||||||
chr1:94190153
|
T | G | 1 | a0001c0001t0004g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1282-70A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94190153 | ||||||
chr1:94190397
|
C | A | 1 | a0001c0001t0004g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1282-314G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94190397 | ||||||
chr1:94190808
|
C | T | 3 | a0001c0001t0042g0206a0001c0001t0043g0205a0001c0002t0016g0083 | 3 | HG01516.hp2 HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1282-725G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94190808 | ||||||
chr1:94190811
|
G | A | 4 | a0002c0003t0015g0042a0002c0003t0015g0043a0002c0003t0015g0165others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-728C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94190811 | ||||||
chr1:94190816
|
A | G | 1 | a0002c0003t0024g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1282-733T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94190816 | ||||||
chr1:94190977
|
A | G | 9 | a0001c0001t0002g0229a0001c0001t0002g0233a0001c0001t0002g0236others(6): Show | 9 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1282-894T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94190977 | ||||||
chr1:94191282
|
G | A | 1 | a0001c0001t0003g0065 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1282-1199C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94191282 | ||||||
chr1:94191462
|
T | C | 1 | a0001c0001t0037g0306 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1282-1379A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94191462 | ||||||
chr1:94191492
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0003g0189a0001c0001t0003g0190others(4): Show | 8 | HG02109.hp1 HG02965.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-1409G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94191492 | ||||||
chr1:94191679
|
G | C | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1282-1596C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94191679 | ||||||
chr1:94192202
|
C | T | 2 | a0001c0001t0004g0294a0001c0001t0004g0295 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1282-2119G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192202 | ||||||
chr1:94192213
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(136): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1282-2130C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192213 | ||||||
chr1:94192297
|
T | C | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1282-2214A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192297 | ||||||
chr1:94192422
|
C | G | 41 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(38): Show | 48 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1282-2339G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192422 | ||||||
chr1:94192631
|
A | T | 1 | a0001c0001t0007g0278 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1282-2548T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192631 | ||||||
chr1:94192738
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1282-2655G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192738 | ||||||
chr1:94192772
|
A | G | 1 | a0001c0001t0004g0136 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1282-2689T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192772 | ||||||
chr1:94193013
|
A | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1282-2930T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193013 | ||||||
chr1:94193137
|
G | A | 1 | a0001c0001t0017g0180 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1282-3054C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193137 | ||||||
chr1:94193153
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1282-3070T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193153 | ||||||
chr1:94193185
|
G | T | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1282-3102C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193185 | ||||||
chr1:94193236
|
A | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0113others(8): Show | 14 | HG00438.hp2 HG00558.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1282-3153T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193236 | ||||||
chr1:94193302
|
A | G | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1282-3219T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193302 | ||||||
chr1:94193368
|
C | CA | 10 | a0001c0001t0001g0092a0001c0001t0002g0229a0001c0001t0002g0263others(7): Show | 10 | HG00280.hp2 HG01993.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1282-3286dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193368 | ||||||
chr1:94193368
|
CA | C | 79 | a0001c0001t0001g0116a0001c0001t0001g0226a0001c0001t0002g0175others(76): Show | 93 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1282-3286delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193368 | ||||||
chr1:94193388
|
A | T | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1282-3305T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193388 | ||||||
chr1:94193415
|
T | C | 58 | a0001c0001t0001g0226a0001c0001t0002g0175a0001c0001t0003g0006others(55): Show | 64 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1282-3332A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193415 | ||||||
chr1:94193493
|
T | C | 1 | a0001c0001t0007g0283 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1282-3410A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193493 | ||||||
chr1:94193677
|
G | A | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1282-3594C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193677 | ||||||
chr1:94193717
|
C | T | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1282-3634G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193717 | ||||||
chr1:94193772
|
C | A | 1 | a0001c0001t0026g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1282-3689G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193772 | ||||||
chr1:94193803
|
G | A | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1282-3720C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193803 | ||||||
chr1:94193838
|
C | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1282-3755G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193838 | ||||||
chr1:94193839
|
T | C | 1 | a0001c0001t0003g0227 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1282-3756A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193839 | ||||||
chr1:94194327
|
A | T | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1282-4244T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94194327 | ||||||
chr1:94194404
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1282-4321A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94194404 | ||||||
chr1:94194577
|
CTT | C | 58 | a0001c0001t0001g0226a0001c0001t0002g0175a0001c0001t0003g0006others(55): Show | 64 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1282-4496_1282-449 others(6): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94194577 | ||||||
chr1:94194770
|
T | A | 304 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(301): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.1282-4687A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94194770 | ||||||
chr1:94194959
|
CAAAAGTA | C | 39 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(36): Show | 46 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1282-4883_1282-487 others(11): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94194959 | ||||||
chr1:94195006
|
A | C | 4 | a0002c0003t0015g0042a0002c0003t0015g0043a0002c0003t0015g0165others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-4923T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195006 | ||||||
chr1:94195053
|
C | T | 41 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(38): Show | 48 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1282-4970G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195053 | ||||||
chr1:94195123
|
T | C | 1 | a0001c0002t0009g0081 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1282-5040A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195123 | ||||||
chr1:94195126
|
T | C | 1 | a0001c0001t0004g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1282-5043A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195126 | ||||||
chr1:94195215
|
A | C | 2 | a0001c0001t0005g0052a0001c0001t0005g0055 | 2 | NA18941.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1282-5132T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195215 | ||||||
chr1:94195231
|
T | C | 4 | a0001c0002t0001g0077a0001c0002t0001g0078a0001c0002t0001g0157others(1): Show | 4 | HG00323.hp1 HG02683.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282-5148A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195231 | ||||||
chr1:94195246
|
G | GA | 4 | a0001c0001t0001g0116a0001c0001t0002g0263a0001c0001t0004g0142others(1): Show | 4 | HG01109.hp1 NA18961.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-5164dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195246 | ||||||
chr1:94195273
|
C | T | 1 | a0001c0001t0003g0196 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1282-5190G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195273 | ||||||
chr1:94195299
|
T | C | 1 | a0001c0001t0002g0221 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1282-5216A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195299 | ||||||
chr1:94195322
|
C | T | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0009others(14): Show | 24 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1282-5239G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195322 | ||||||
chr1:94195446
|
T | C | 2 | a0001c0001t0025g0163a0001c0001t0025g0164 | 2 | HG01243.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1282-5363A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195446 | ||||||
chr1:94195588
|
T | C | 29 | a0001c0002t0001g0063a0001c0002t0001g0064a0001c0002t0001g0067others(26): Show | 29 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1282-5505A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195588 | ||||||
chr1:94195594
|
A | C | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1282-5511T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195594 | ||||||
chr1:94195712
|
T | C | 9 | a0001c0001t0004g0128a0001c0001t0007g0281a0001c0001t0010g0029others(6): Show | 10 | HG01071.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1282-5629A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195712 | ||||||
chr1:94195720
|
T | A | 8 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(5): Show | 9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1282-5637A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195720 | ||||||
chr1:94195920
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1281+5800C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195920 | ||||||
chr1:94196053
|
C | A | 2 | a0001c0001t0018g0152a0001c0001t0018g0153 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1281+5667G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196053 | ||||||
chr1:94196061
|
G | A | 108 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0027others(105): Show | 124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1281+5659C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196061 | ||||||
chr1:94196065
|
A | T | 1 | a0001c0001t0017g0167 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1281+5655T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196065 | ||||||
chr1:94196082
|
T | A | 6 | a0001c0001t0002g0030a0001c0001t0002g0309a0001c0001t0002g0311others(3): Show | 7 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1281+5638A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196082 | ||||||
chr1:94196248
|
G | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(187): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1281+5472C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196248 | ||||||
chr1:94196249
|
TG | T | 85 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0027others(82): Show | 101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1281+5470delC | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196249 | ||||||
chr1:94196250
|
G | T | 21 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0224others(18): Show | 21 | HG00621.hp2 HG01109.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.1281+5470C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196250 | ||||||
chr1:94196254
|
T | C | 19 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0224others(16): Show | 19 | HG00621.hp2 HG01109.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1281+5466A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196254 | ||||||
chr1:94196255
|
T | C | 85 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0027others(82): Show | 101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1281+5465A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196255 | ||||||
chr1:94196256
|
C | CT | 72 | a0001c0001t0001g0226a0001c0001t0002g0175a0001c0001t0003g0006others(69): Show | 78 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1281+5463dupA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196256 | ||||||
chr1:94196256
|
C | CTT | 15 | a0001c0001t0003g0038a0001c0001t0003g0099a0001c0001t0003g0176others(12): Show | 15 | HG01192.hp1 HG01975.hp2 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+5462_1281+546 others(6): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196256 | ||||||
chr1:94196256
|
C | T | 106 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0027others(103): Show | 122 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1281+5464G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196256 | ||||||
chr1:94196256
|
CT | C | 11 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(8): Show | 12 | HG01891.hp2 HG02257.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1281+5463delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196256 | ||||||
chr1:94196259
|
T | TC | 44 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(41): Show | 56 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1281+5460_1281+546 others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196259 | ||||||
chr1:94196260
|
T | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0116a0001c0001t0009g0121 | 3 | NA18961.hp2 NA18966.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1281+5460A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196260 | ||||||
chr1:94196262
|
T | C | 1 | a0001c0001t0002g0285 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1281+5458A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196262 | ||||||
chr1:94196263
|
T | TC | 38 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(35): Show | 45 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1281+5456_1281+545 others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196263 | ||||||
chr1:94196264
|
T | C | 1 | a0001c0001t0011g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1281+5456A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196264 | ||||||
chr1:94196293
|
G | C | 1 | a0001c0001t0006g0301 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1281+5427C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196293 | ||||||
chr1:94196348
|
A | G | 1 | a0001c0001t0029g0228 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1281+5372T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196348 | ||||||
chr1:94196386
|
C | A | 2 | a0001c0001t0022g0036a0008c0010t0022g0035 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1281+5334G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196386 | ||||||
chr1:94196422
|
C | T | 9 | a0001c0001t0004g0002a0001c0001t0004g0025a0001c0001t0004g0041others(6): Show | 13 | NA18941.hp2 NA18942.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.1281+5298G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196422 | ||||||
chr1:94196451
|
C | T | 1 | a0001c0001t0038g0293 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1281+5269G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196451 | ||||||
chr1:94196507
|
C | T | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1281+5213G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196507 | ||||||
chr1:94196616
|
T | C | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1281+5104A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196616 | ||||||
chr1:94196867
|
T | G | 1 | a0002c0015t0024g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1281+4853A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196867 | ||||||
chr1:94196916
|
G | A | 1 | a0001c0001t0017g0181 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1281+4804C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196916 | ||||||
chr1:94197007
|
T | C | 2 | a0001c0001t0003g0182a0001c0001t0003g0183 | 2 | NA18962.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1281+4713A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197007 | ||||||
chr1:94197071
|
T | C | 2 | a0002c0003t0015g0165a0002c0003t0015g0166 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1281+4649A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197071 | ||||||
chr1:94197113
|
T | C | 1 | a0001c0001t0023g0100 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1281+4607A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197113 | ||||||
chr1:94197151
|
T | C | 1 | a0001c0001t0003g0174 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1281+4569A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197151 | ||||||
chr1:94197168
|
G | A | 1 | a0001c0001t0022g0036 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1281+4552C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197168 | ||||||
chr1:94197429
|
C | T | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1281+4291G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197429 | ||||||
chr1:94197623
|
T | C | 1 | a0001c0001t0004g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1281+4097A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197623 | ||||||
chr1:94197884
|
C | A | 1 | a0001c0001t0001g0116 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1281+3836G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197884 | ||||||
chr1:94197954
|
C | T | 9 | a0001c0001t0004g0017a0001c0001t0004g0128a0001c0001t0004g0129others(6): Show | 10 | HG02148.hp2 HG02280.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.1281+3766G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197954 | ||||||
chr1:94198184
|
CAATT | C | 115 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0027others(112): Show | 132 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1281+3532_1281+353 others(8): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198184 | ||||||
chr1:94198409
|
T | G | 1 | a0002c0015t0024g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1281+3311A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198409 | ||||||
chr1:94198564
|
T | TA | 4 | a0001c0001t0011g0132a0001c0001t0011g0134a0001c0001t0032g0131others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281+3155dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198564 | ||||||
chr1:94198602
|
G | A | 302 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1281+3118C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198602 | ||||||
chr1:94198704
|
T | C | 1 | a0001c0001t0005g0053 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1281+3016A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198704 | ||||||
chr1:94198732
|
A | G | 4 | a0001c0002t0001g0077a0001c0002t0001g0078a0001c0002t0001g0157others(1): Show | 4 | HG00323.hp1 HG02683.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281+2988T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198732 | ||||||
chr1:94198786
|
A | G | 1 | a0001c0001t0003g0186 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1281+2934T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198786 | ||||||
chr1:94198826
|
G | A | 1 | a0001c0001t0036g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1281+2894C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198826 | ||||||
chr1:94198857
|
G | A | 4 | a0002c0003t0015g0042a0002c0003t0015g0043a0002c0003t0015g0165others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+2863C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198857 | ||||||
chr1:94198964
|
G | A | 303 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1281+2756C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198964 | ||||||
chr1:94198994
|
G | A | 1 | a0001c0001t0025g0164 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1281+2726C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198994 | ||||||
chr1:94199119
|
A | G | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1281+2601T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199119 | ||||||
chr1:94199213
|
A | G | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1281+2507T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199213 | ||||||
chr1:94199249
|
A | G | 39 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(36): Show | 46 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1281+2471T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199249 | ||||||
chr1:94199266
|
G | A | 39 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(36): Show | 46 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1281+2454C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199266 | ||||||
chr1:94199390
|
AT | A | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1281+2329delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199390 | ||||||
chr1:94199460
|
C | T | 2 | a0002c0003t0015g0165a0002c0003t0015g0166 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1281+2260G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199460 | ||||||
chr1:94199668
|
ATGC | A | 5 | a0001c0001t0010g0288a0001c0001t0010g0289a0001c0001t0010g0290others(2): Show | 5 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+2049_1281+205 others(7): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199668 | ||||||
chr1:94199693
|
C | T | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1281+2027G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199693 | ||||||
chr1:94199772
|
C | T | 1 | a0001c0001t0006g0267 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1281+1948G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199772 | ||||||
chr1:94199882
|
T | C | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1281+1838A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199882 | ||||||
chr1:94199907
|
C | A | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1281+1813G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199907 | ||||||
chr1:94199998
|
C | T | 4 | a0001c0001t0002g0221a0001c0001t0002g0239a0001c0001t0002g0240others(1): Show | 4 | HG01168.hp2 HG01192.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281+1722G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199998 | ||||||
chr1:94200025
|
T | C | 1 | a0001c0001t0004g0062 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1281+1695A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200025 | ||||||
chr1:94200279
|
T | C | 3 | a0001c0001t0007g0154a0001c0001t0019g0012a0001c0001t0019g0103 | 4 | HG01257.hp1 HG01258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+1441A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200279 | ||||||
chr1:94200312
|
C | T | 2 | a0001c0001t0022g0036a0008c0010t0022g0035 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1281+1408G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200312 | ||||||
chr1:94200391
|
C | T | 303 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1281+1329G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200391 | ||||||
chr1:94200392
|
G | A | 2 | a0002c0003t0015g0165a0002c0003t0015g0166 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1281+1328C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200392 | ||||||
chr1:94200587
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0112 | 3 | HG00609.hp2 NA18953.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1281+1133T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200587 | ||||||
chr1:94200639
|
G | A | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1281+1081C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200639 | ||||||
chr1:94201126
|
CT | C | 37 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(34): Show | 44 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1281+593delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201126 | ||||||
chr1:94201348
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1281+372G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201348 | ||||||
chr1:94201394
|
T | C | 1 | a0002c0003t0008g0210 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1281+326A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201394 | ||||||
chr1:94201401
|
T | C | 1 | a0001c0001t0004g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1281+319A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201401 | ||||||
chr1:94201434
|
T | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0118a0001c0001t0009g0110others(1): Show | 5 | HG00621.hp1 HG02040.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1281+286A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201434 | ||||||
chr1:94201457
|
C | G | 1 | a0002c0003t0024g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1281+263G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201457 | ||||||
chr1:94201459
|
TCCTTCCT others(5): Show |
T | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1281+249_1281+260d others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201459 | ||||||
chr1:94201477
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0003g0192 | 2 | HG02135.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1281+243A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201477 | ||||||
chr1:94201506
|
TTCTCTCT others(1): Show |
T | 3 | a0001c0001t0041g0287a0001c0001t0042g0206a0001c0001t0043g0205 | 3 | HG03471.hp2 HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1281+206_1281+213d others(10): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201506 | ||||||
chr1:94201506
|
TTCTCTCT others(5): Show |
T | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1281+202_1281+213d others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201506 | ||||||
chr1:94201506
|
TTCTCTCT others(7): Show |
T | 288 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(285): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.1281+200_1281+213d others(16): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201506 | ||||||
chr1:94201506
|
TTCTCTCT others(9): Show |
T | 1 | a0001c0002t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1281+198_1281+213d others(18): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201506 | ||||||
chr1:94201874
|
G | GA | 296 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(293): Show | 338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.1144-18dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94201874 | ||||||
chr1:94201892
|
G | C | 1 | a0001c0001t0002g0233 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1144-35C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94201892 | ||||||
chr1:94202067
|
T | C | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-210A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94202067 | ||||||
chr1:94202073
|
A | G | 3 | a0001c0001t0006g0252a0001c0001t0029g0228a0007c0013t0006g0249 | 3 | HG00423.hp2 NA18965.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1144-216T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94202073 | ||||||
chr1:94202366
|
C | T | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1143+178G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94202366 | ||||||
chr1:94202414
|
T | C | 60 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0027others(57): Show | 67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1143+130A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94202414 | ||||||
chr1:94202468
|
C | T | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1143+76G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94202468 | ||||||
chr1:94202490
|
C | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(287): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.1143+54G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94202490 | ||||||
chr1:94202810
|
T | C | 2 | a0001c0001t0006g0262a0001c0001t0006g0264 | 2 | NA18970.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.955-78A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 10/22 | chr1 | 94202810 | ||||||
chr1:94203676
|
A | C | 1 | a0001c0001t0017g0167 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.762+254T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 8/22 | chr1 | 94203676 | ||||||
chr1:94203739
|
C | T | 8 | a0001c0001t0002g0027a0001c0001t0002g0256a0001c0001t0002g0263others(5): Show | 9 | HG02135.hp1 HG03831.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.762+191G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 8/22 | chr1 | 94203739 | ||||||
chr1:94203751
|
C | T | 42 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(39): Show | 49 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.762+179G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 8/22 | chr1 | 94203751 | ||||||
chr1:94203826
|
T | C | 1 | a0005c0014t0011g0133 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.762+104A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 8/22 | chr1 | 94203826 | ||||||
chr1:94204144
|
CT | C | 15 | a0001c0001t0002g0273a0001c0001t0002g0302a0001c0001t0004g0128others(12): Show | 16 | HG01069.hp1 HG01891.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.698-151delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204144 | ||||||
chr1:94204160
|
T | A | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.698-166A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204160 | ||||||
chr1:94204161
|
A | T | 20 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0005g0004others(17): Show | 27 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.698-167T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204161 | ||||||
chr1:94204202
|
G | C | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.698-208C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204202 | ||||||
chr1:94204305
|
T | C | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.698-311A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204305 | ||||||
chr1:94204535
|
T | TTTAAGCA others(16): Show |
6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.697+503_697+525dup others(23): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204535 | ||||||
chr1:94204678
|
A | G | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.697+383T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204678 | ||||||
chr1:94204722
|
TTC | T | 41 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(38): Show | 48 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.697+337_697+338del others(2): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204722 | ||||||
chr1:94204774
|
T | C | 3 | a0001c0001t0018g0152a0001c0001t0018g0153a0001c0001t0018g0291 | 3 | HG02486.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.697+287A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204774 | ||||||
chr1:94204842
|
A | T | 1 | a0001c0001t0002g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.697+219T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204842 | ||||||
chr1:94204848
|
T | C | 1 | a0002c0015t0024g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.697+213A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204848 | ||||||
chr1:94205228
|
T | C | 108 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0027others(105): Show | 124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.560-30A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 6/22 | chr1 | 94205228 | ||||||
chr1:94205270
|
G | A | 18 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0009others(15): Show | 25 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.560-72C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 6/22 | chr1 | 94205270 | ||||||
chr1:94205335
|
T | C | 1 | a0001c0001t0028g0268 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.560-137A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 6/22 | chr1 | 94205335 | ||||||
chr1:94205838
|
A | G | 41 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(38): Show | 48 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.511-155T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94205838 | ||||||
chr1:94205855
|
T | C | 3 | a0001c0001t0003g0093a0001c0001t0003g0096a0001c0001t0003g0099 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.511-172A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94205855 | ||||||
chr1:94205935
|
A | G | 1 | a0001c0001t0035g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.511-252T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94205935 | ||||||
chr1:94206213
|
C | A | 1 | a0001c0001t0002g0233 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.511-530G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206213 | ||||||
chr1:94206293
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 11 | HG02074.hp2 NA18747.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.511-610C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206293 | ||||||
chr1:94206313
|
G | A | 29 | a0001c0002t0001g0063a0001c0002t0001g0064a0001c0002t0001g0067others(26): Show | 29 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.511-630C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206313 | ||||||
chr1:94206347
|
T | C | 1 | a0001c0001t0005g0054 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.511-664A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206347 | ||||||
chr1:94206641
|
A | C | 1 | a0001c0001t0004g0135 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.511-958T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206641 | ||||||
chr1:94206645
|
A | C | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.511-962T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206645 | ||||||
chr1:94206861
|
A | ACT | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.511-1179_511-1178i others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206861 | ||||||
chr1:94206909
|
T | A | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.511-1226A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206909 | ||||||
chr1:94206925
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.511-1242A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206925 | ||||||
chr1:94206966
|
A | AAT | 4 | a0001c0002t0016g0066a0001c0002t0016g0083a0001c0002t0016g0084others(1): Show | 4 | HG00140.hp1 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-1285_511-1284d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206966 | ||||||
chr1:94206976
|
T | G | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.511-1293A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206976 | ||||||
chr1:94206978
|
T | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(67): Show | 83 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.511-1295A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206978 | ||||||
chr1:94206980
|
G | T | 49 | a0001c0001t0001g0286a0001c0001t0002g0255a0001c0001t0002g0285others(46): Show | 50 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.511-1297C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206980 | ||||||
chr1:94206982
|
G | T | 1 | a0001c0002t0001g0067 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.511-1299C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206982 | ||||||
chr1:94207001
|
T | TTTTA | 16 | a0001c0001t0004g0017a0001c0001t0004g0033a0001c0001t0004g0044others(13): Show | 17 | HG02145.hp1 HG02148.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.511-1322_511-1319d others(6): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207001 | ||||||
chr1:94207001
|
T | TTTTATTT others(1): Show |
23 | a0001c0001t0004g0002a0001c0001t0004g0018a0001c0001t0004g0025others(20): Show | 28 | HG00558.hp2 HG00597.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.511-1326_511-1319d others(10): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207001 | ||||||
chr1:94207001
|
T | TTTTATTT others(5): Show |
2 | a0001c0001t0004g0124a0001c0001t0014g0019 | 3 | HG00323.hp2 HG01074.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.511-1330_511-1319d others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207001 | ||||||
chr1:94207066
|
C | T | 2 | a0001c0001t0005g0010a0001c0001t0005g0050 | 3 | HG02056.hp2 HG02129.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.511-1383G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207066 | ||||||
chr1:94207113
|
A | AT | 290 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(287): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.511-1431dupA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207113 | ||||||
chr1:94207119
|
G | A | 60 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0027others(57): Show | 67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.511-1436C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207119 | ||||||
chr1:94207260
|
C | T | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+1572G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207260 | ||||||
chr1:94207301
|
C | T | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+1531G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207301 | ||||||
chr1:94207389
|
C | T | 1 | a0001c0001t0014g0307 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.510+1443G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207389 | ||||||
chr1:94207550
|
CCA | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(287): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.510+1280_510+1281d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207550 | ||||||
chr1:94207581
|
T | C | 1 | a0001c0007t0001g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.510+1251A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207581 | ||||||
chr1:94207622
|
T | G | 1 | a0001c0001t0002g0303 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.510+1210A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207622 | ||||||
chr1:94207631
|
G | A | 41 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(38): Show | 48 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.510+1201C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207631 | ||||||
chr1:94207787
|
G | A | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.510+1045C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207787 | ||||||
chr1:94207838
|
T | G | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510+994A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207838 | ||||||
chr1:94207841
|
T | G | 1 | a0001c0001t0004g0126 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.510+991A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207841 | ||||||
chr1:94207844
|
G | T | 2 | a0001c0001t0005g0009a0001c0001t0005g0049 | 3 | NA18971.hp2 NA18986.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.510+988C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207844 | ||||||
chr1:94207871
|
G | A | 1 | a0002c0003t0015g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.510+961C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207871 | ||||||
chr1:94207879
|
C | T | 1 | a0001c0001t0035g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.510+953G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207879 | ||||||
chr1:94207895
|
G | A | 1 | a0001c0001t0007g0277 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.510+937C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207895 | ||||||
chr1:94208071
|
C | G | 1 | a0002c0003t0008g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.510+761G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94208071 | ||||||
chr1:94208382
|
T | A | 1 | a0001c0001t0026g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.510+450A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94208382 | ||||||
chr1:94208639
|
T | C | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510+193A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94208639 | ||||||
chr1:94208656
|
C | A | 2 | a0001c0001t0004g0294a0001c0001t0004g0295 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.510+176G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94208656 | ||||||
chr1:94209000
|
T | C | 1 | a0001c0001t0010g0290 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.438-96A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 4/22 | chr1 | 94209000 | ||||||
chr1:94209167
|
G | A | 304 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(301): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.437+87C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 4/22 | chr1 | 94209167 | ||||||
chr1:94209170
|
T | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 72 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.437+84A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 4/22 | chr1 | 94209170 | ||||||
chr1:94209524
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0109a0001c0001t0001g0118others(2): Show | 6 | HG00621.hp1 HG02040.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-174G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94209524 | ||||||
chr1:94209711
|
G | A | 1 | a0001c0002t0009g0075 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.341-361C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94209711 | ||||||
chr1:94209764
|
T | C | 1 | a0001c0001t0002g0246 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.341-414A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94209764 | ||||||
chr1:94209812
|
TATATAC | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(287): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.341-468_341-463del others(6): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94209812 | ||||||
chr1:94210149
|
T | C | 2 | a0001c0001t0022g0036a0008c0010t0022g0035 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.341-799A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210149 | ||||||
chr1:94210163
|
C | T | 1 | a0001c0001t0036g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.341-813G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210163 | ||||||
chr1:94210237
|
G | A | 1 | a0001c0001t0007g0279 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.341-887C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210237 | ||||||
chr1:94210243
|
T | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.341-893A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210243 | ||||||
chr1:94210259
|
G | C | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.341-909C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210259 | ||||||
chr1:94210395
|
T | C | 1 | a0001c0001t0011g0144 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.341-1045A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210395 | ||||||
chr1:94210445
|
G | C | 1 | a0001c0001t0004g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.341-1095C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210445 | ||||||
chr1:94210602
|
C | G | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.341-1252G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210602 | ||||||
chr1:94210606
|
CAAAAAG | C | 4 | a0001c0002t0016g0066a0001c0002t0016g0083a0001c0002t0016g0084others(1): Show | 4 | HG00140.hp1 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-1262_341-1257d others(8): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210606 | ||||||
chr1:94210712
|
T | G | 40 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(37): Show | 47 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.341-1362A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210712 | ||||||
chr1:94210787
|
C | T | 1 | a0001c0002t0001g0063 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.341-1437G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210787 | ||||||
chr1:94210802
|
G | C | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.341-1452C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210802 | ||||||
chr1:94210904
|
TA | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(280): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.341-1555delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210904 | ||||||
chr1:94210904
|
TAA | T | 7 | a0001c0001t0004g0127a0001c0001t0004g0128a0001c0001t0007g0217others(4): Show | 7 | HG02895.hp2 HG03471.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.341-1556_341-1555d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210904 | ||||||
chr1:94210943
|
C | A | 1 | a0001c0001t0035g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.341-1593G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210943 | ||||||
chr1:94210948
|
G | T | 1 | a0001c0001t0001g0296 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.341-1598C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210948 | ||||||
chr1:94211093
|
T | C | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.341-1743A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211093 | ||||||
chr1:94211287
|
C | CA | 8 | a0001c0001t0001g0159a0001c0001t0003g0093a0001c0001t0018g0152others(5): Show | 8 | HG00438.hp2 HG01069.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.341-1938dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | ||||||
chr1:94211287
|
C | CAA | 35 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(32): Show | 47 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.341-1939_341-1938d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | ||||||
chr1:94211287
|
C | CAAA | 33 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0040others(30): Show | 35 | HG00621.hp1 HG00733.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.341-1940_341-1938d others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | ||||||
chr1:94211287
|
C | CAAAA | 73 | a0001c0001t0001g0151a0001c0001t0002g0003a0001c0001t0002g0026others(70): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.341-1941_341-1938d others(6): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | ||||||
chr1:94211287
|
C | CAAAAA | 37 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0030others(34): Show | 42 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.341-1942_341-1938d others(7): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | ||||||
chr1:94211287
|
C | CAAAAAA | 9 | a0001c0001t0002g0149a0001c0001t0002g0265a0001c0001t0007g0219others(6): Show | 10 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.341-1943_341-1938d others(8): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | ||||||
chr1:94211287
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0006g0267 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.341-1949_341-1938d others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | ||||||
chr1:94211287
|
C | CCA | 4 | a0001c0001t0010g0029a0001c0001t0010g0290a0001c0001t0010g0299others(1): Show | 5 | HG01891.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-1938_341-1937i others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | ||||||
chr1:94211287
|
CAA | C | 9 | a0001c0001t0003g0061a0001c0001t0003g0172a0001c0001t0003g0199others(6): Show | 9 | HG01358.hp1 HG02027.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-1939_341-1938d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | ||||||
chr1:94211287
|
CAAA | C | 36 | a0001c0001t0001g0226a0001c0001t0002g0175a0001c0001t0003g0020others(33): Show | 40 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.341-1940_341-1938d others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | ||||||
chr1:94211287
|
CAAAAAAA others(4): Show |
C | 1 | a0004c0006t0001g0108 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.341-1948_341-1938d others(13): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | ||||||
chr1:94211287
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0002g0251a0001c0001t0002g0273 | 2 | HG00609.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.341-1949_341-1938d others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | ||||||
chr1:94211299
|
A | AAAAAC | 35 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(32): Show | 42 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.341-1950_341-1949i others(7): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211299 | ||||||
chr1:94211305
|
A | C | 40 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(37): Show | 47 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.341-1955T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211305 | ||||||
chr1:94211319
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(136): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.341-1969A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211319 | ||||||
chr1:94211387
|
C | T | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-2037G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211387 | ||||||
chr1:94211599
|
T | C | 1 | a0001c0001t0003g0185 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.341-2249A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211599 | ||||||
chr1:94211641
|
T | C | 1 | a0001c0001t0002g0248 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.341-2291A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211641 | ||||||
chr1:94211745
|
T | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(287): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.341-2395A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211745 | ||||||
chr1:94211911
|
A | C | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.341-2561T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211911 | ||||||
chr1:94211936
|
G | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(287): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.341-2586C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211936 | ||||||
chr1:94212142
|
G | A | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.341-2792C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212142 | ||||||
chr1:94212176
|
A | G | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-2826T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212176 | ||||||
chr1:94212212
|
C | G | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.341-2862G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212212 | ||||||
chr1:94212419
|
C | T | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.341-3069G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212419 | ||||||
chr1:94212538
|
T | C | 1 | a0002c0015t0024g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.341-3188A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212538 | ||||||
chr1:94212562
|
G | A | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.341-3212C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212562 | ||||||
chr1:94212587
|
T | C | 1 | a0001c0001t0003g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.341-3237A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212587 | ||||||
chr1:94212669
|
C | T | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.341-3319G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212669 | ||||||
chr1:94212726
|
T | C | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-3376A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212726 | ||||||
chr1:94212956
|
T | C | 88 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0027others(85): Show | 97 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.341-3606A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212956 | ||||||
chr1:94213038
|
C | T | 1 | a0001c0001t0004g0126 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.341-3688G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213038 | ||||||
chr1:94213081
|
G | A | 2 | a0001c0001t0002g0244a0001c0001t0002g0270 | 2 | NA18967.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.341-3731C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213081 | ||||||
chr1:94213192
|
T | C | 1 | a0001c0001t0004g0145 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.341-3842A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213192 | ||||||
chr1:94213242
|
T | C | 2 | a0002c0003t0015g0042a0002c0003t0015g0043 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.341-3892A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213242 | ||||||
chr1:94213338
|
C | T | 1 | a0001c0001t0037g0306 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.341-3988G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213338 | ||||||
chr1:94213364
|
A | G | 2 | a0001c0001t0004g0033a0001c0001t0036g0032 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.341-4014T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213364 | ||||||
chr1:94213455
|
T | C | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.341-4105A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213455 | ||||||
chr1:94213542
|
G | A | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.341-4192C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213542 | ||||||
chr1:94213633
|
T | A | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.341-4283A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213633 | ||||||
chr1:94214007
|
T | G | 2 | a0001c0001t0004g0033a0001c0001t0036g0032 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.341-4657A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214007 | ||||||
chr1:94214042
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 72 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.341-4692C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214042 | ||||||
chr1:94214083
|
A | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.341-4733T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214083 | ||||||
chr1:94214099
|
G | A | 1 | a0002c0003t0024g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.341-4749C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214099 | ||||||
chr1:94214179
|
T | C | 1 | a0001c0001t0023g0100 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.341-4829A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214179 | ||||||
chr1:94214292
|
G | A | 7 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(4): Show | 8 | HG00639.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.341-4942C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214292 | ||||||
chr1:94214587
|
T | G | 1 | a0002c0015t0024g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.341-5237A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214587 | ||||||
chr1:94214629
|
A | G | 29 | a0001c0002t0001g0063a0001c0002t0001g0064a0001c0002t0001g0067others(26): Show | 29 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.341-5279T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214629 | ||||||
chr1:94214719
|
T | C | 298 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.341-5369A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214719 | ||||||
chr1:94214753
|
A | C | 1 | a0001c0001t0002g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.341-5403T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214753 | ||||||
chr1:94214765
|
C | T | 2 | a0001c0001t0007g0154a0001c0001t0036g0032 | 2 | HG02145.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.341-5415G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214765 | ||||||
chr1:94214773
|
A | T | 1 | a0001c0001t0004g0062 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.341-5423T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214773 | ||||||
chr1:94215104
|
G | GA | 63 | a0001c0001t0001g0122a0001c0001t0004g0002a0001c0001t0004g0017others(60): Show | 72 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.340+5153dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94215104 | ||||||
chr1:94215104
|
GA | G | 10 | a0001c0001t0001g0226a0001c0001t0002g0175a0001c0001t0003g0024others(7): Show | 11 | HG01258.hp1 HG01981.hp1 HG04204.hp1 others(8): Show |
intron_variant | MODIFIER | c.340+5153delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94215104 | ||||||
chr1:94215135
|
C | T | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.340+5123G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94215135 | ||||||
chr1:94215329
|
A | C | 1 | a0002c0015t0024g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.340+4929T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94215329 | ||||||
chr1:94215544
|
AG | A | 18 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0009others(15): Show | 25 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.340+4713delC | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94215544 | ||||||
chr1:94215938
|
C | CAAATG | 302 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.340+4319_340+4320i others(7): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94215938 | ||||||
chr1:94216210
|
T | C | 49 | a0001c0001t0001g0226a0001c0001t0002g0175a0001c0001t0003g0020others(46): Show | 53 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.340+4048A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94216210 | ||||||
chr1:94216247
|
T | G | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.340+4011A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94216247 | ||||||
chr1:94216378
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.340+3880G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94216378 | ||||||
chr1:94216392
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0107 | 4 | NA18968.hp2 NA18974.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+3866G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94216392 | ||||||
chr1:94216438
|
T | C | 1 | a0001c0001t0041g0287 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.340+3820A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94216438 | ||||||
chr1:94217367
|
C | T | 1 | a0001c0001t0004g0125 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.340+2891G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217367 | ||||||
chr1:94217471
|
C | T | 1 | a0001c0001t0037g0306 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.340+2787G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217471 | ||||||
chr1:94217508
|
G | A | 1 | a0001c0001t0018g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.340+2750C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217508 | ||||||
chr1:94217508
|
G | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.340+2750C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217508 | ||||||
chr1:94217529
|
C | CA | 6 | a0001c0001t0004g0146a0001c0001t0004g0148a0001c0001t0011g0147others(3): Show | 6 | HG00597.hp1 HG02970.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+2728dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217529 | ||||||
chr1:94217529
|
CA | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(232): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.340+2728delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217529 | ||||||
chr1:94217547
|
C | A | 1 | a0001c0001t0018g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.340+2711G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217547 | ||||||
chr1:94217549
|
C | T | 1 | a0001c0001t0018g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.340+2709G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217549 | ||||||
chr1:94217746
|
C | T | 1 | a0001c0001t0005g0048 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.340+2512G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217746 | ||||||
chr1:94217779
|
T | G | 1 | a0002c0015t0024g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.340+2479A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217779 | ||||||
chr1:94217842
|
C | T | 5 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0069others(2): Show | 5 | HG01433.hp2 HG01496.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+2416G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217842 | ||||||
chr1:94217860
|
CA | C | 9 | a0001c0001t0002g0269a0001c0001t0003g0045a0001c0001t0004g0295others(6): Show | 9 | HG02572.hp1 HG02723.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.340+2397delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217860 | ||||||
chr1:94217860
|
CAA | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(291): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.340+2396_340+2397d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217860 | ||||||
chr1:94217862
|
A | C | 1 | a0001c0001t0010g0288 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.340+2396T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217862 | ||||||
chr1:94217871
|
A | C | 50 | a0001c0001t0001g0226a0001c0001t0002g0175a0001c0001t0003g0020others(47): Show | 54 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.340+2387T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217871 | ||||||
chr1:94217872
|
A | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(287): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.340+2386T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217872 | ||||||
chr1:94218199
|
A | G | 49 | a0001c0001t0001g0226a0001c0001t0002g0175a0001c0001t0003g0020others(46): Show | 53 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.340+2059T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218199 | ||||||
chr1:94218262
|
T | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(286): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.340+1996A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218262 | ||||||
chr1:94218495
|
C | G | 1 | a0001c0001t0002g0250 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.340+1763G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218495 | ||||||
chr1:94218562
|
A | G | 1 | a0001c0001t0003g0089 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.340+1696T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218562 | ||||||
chr1:94218581
|
T | A | 4 | a0001c0001t0002g0221a0001c0001t0002g0239a0001c0001t0002g0240others(1): Show | 4 | HG01168.hp2 HG01192.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+1677A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218581 | ||||||
chr1:94218763
|
A | T | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.340+1495T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218763 | ||||||
chr1:94218784
|
G | A | 1 | a0001c0001t0026g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.340+1474C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218784 | ||||||
chr1:94218849
|
T | C | 1 | a0001c0001t0002g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.340+1409A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218849 | ||||||
chr1:94218950
|
G | T | 1 | a0002c0015t0024g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.340+1308C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218950 | ||||||
chr1:94219011
|
C | G | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+1247G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219011 | ||||||
chr1:94219056
|
T | C | 1 | a0001c0001t0035g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.340+1202A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219056 | ||||||
chr1:94219136
|
C | T | 2 | a0001c0001t0002g0309a0001c0001t0007g0308 | 2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.340+1122G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219136 | ||||||
chr1:94219259
|
A | ACCCTGCA others(10): Show |
295 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(292): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.340+998_340+999ins others(17): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219259 | ||||||
chr1:94219440
|
C | T | 1 | a0007c0013t0006g0249 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.340+818G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219440 | ||||||
chr1:94219631
|
C | G | 1 | a0001c0001t0004g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.340+627G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219631 | ||||||
chr1:94219791
|
A | G | 1 | a0001c0001t0036g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.340+467T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219791 | ||||||
chr1:94219806
|
A | C | 1 | a0001c0002t0016g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.340+452T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219806 | ||||||
chr1:94219918
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(292): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.340+340A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219918 | ||||||
chr1:94219919
|
T | A | 304 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(301): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.340+339A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219919 | ||||||
chr1:94219966
|
C | A | 1 | a0001c0012t0007g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.340+292G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219966 | ||||||
chr1:94220029
|
T | G | 46 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(43): Show | 53 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.340+229A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94220029 | ||||||
chr1:94220039
|
T | A | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.340+219A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94220039 | ||||||
chr1:94220487
|
T | C | 1 | a0001c0001t0002g0285 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.206-95A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94220487 | ||||||
chr1:94220554
|
A | T | 111 | a0001c0001t0001g0238a0001c0001t0001g0266a0001c0001t0002g0003others(108): Show | 127 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.206-162T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94220554 | ||||||
chr1:94220570
|
A | G | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-178T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94220570 | ||||||
chr1:94220735
|
A | AT | 51 | a0001c0001t0001g0008a0001c0001t0001g0202a0001c0001t0001g0226others(48): Show | 57 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.206-344dupA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94220735 | ||||||
chr1:94220871
|
G | GA | 29 | a0001c0002t0001g0063a0001c0002t0001g0064a0001c0002t0001g0067others(26): Show | 29 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.206-480dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94220871 | ||||||
chr1:94220984
|
A | G | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-592T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94220984 | ||||||
chr1:94221021
|
A | G | 1 | a0001c0001t0020g0313 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.206-629T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221021 | ||||||
chr1:94221059
|
C | G | 6 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-667G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221059 | ||||||
chr1:94221093
|
C | T | 1 | a0001c0011t0040g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.206-701G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221093 | ||||||
chr1:94221111
|
C | T | 8 | a0001c0001t0002g0222a0001c0001t0002g0224a0001c0001t0002g0245others(5): Show | 8 | NA18947.hp1 NA18949.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-719G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221111 | ||||||
chr1:94221357
|
GGTGTTTA others(3): Show |
G | 1 | a0001c0001t0005g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.206-975_206-966del others(10): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221357 | ||||||
chr1:94221524
|
A | G | 1 | a0002c0003t0024g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.206-1132T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221524 | ||||||
chr1:94221565
|
A | AT | 258 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(255): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.206-1174dupA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221565 | ||||||
chr1:94221919
|
A | C | 1 | a0001c0001t0005g0048 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.206-1527T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221919 | ||||||
chr1:94221974
|
T | TA | 94 | a0001c0001t0001g0226a0001c0001t0001g0238a0001c0001t0001g0266others(91): Show | 104 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.206-1583dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221974 | ||||||
chr1:94222018
|
A | C | 7 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(4): Show | 8 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-1626T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222018 | ||||||
chr1:94222056
|
G | A | 1 | a0001c0001t0003g0038 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.206-1664C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222056 | ||||||
chr1:94222119
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(125): Show | 147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.206-1727T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222119 | ||||||
chr1:94222206
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.206-1814A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222206 | ||||||
chr1:94222280
|
T | C | 1 | a0001c0001t0002g0223 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.206-1888A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222280 | ||||||
chr1:94222391
|
G | C | 1 | a0001c0001t0028g0268 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.206-1999C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222391 | ||||||
chr1:94222404
|
T | A | 1 | a0001c0001t0037g0306 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.206-2012A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222404 | ||||||
chr1:94222445
|
G | A | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.206-2053C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222445 | ||||||
chr1:94222495
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(257): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.206-2103A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222495 | ||||||
chr1:94222705
|
G | A | 2 | a0002c0003t0015g0165a0002c0003t0015g0166 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.206-2313C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222705 | ||||||
chr1:94222784
|
T | TAATACAG others(6052): Show |
1 | a0001c0001t0001g0151 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.206-2393_206-2392i others(6061): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222784 | ||||||
chr1:94222849
|
C | A | 304 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(301): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.206-2457G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222849 | ||||||
chr1:94222948
|
A | AT | 236 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(233): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.206-2557dupA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222948 | ||||||
chr1:94222948
|
A | ATT | 23 | a0001c0001t0001g0058a0001c0001t0003g0034a0001c0001t0003g0060others(20): Show | 30 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.206-2558_206-2557d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222948 | ||||||
chr1:94223045
|
G | A | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.206-2653C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223045 | ||||||
chr1:94223075
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(257): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.206-2683A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223075 | ||||||
chr1:94223088
|
C | T | 6 | a0001c0001t0010g0288a0001c0001t0010g0289a0001c0001t0010g0290others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-2696G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223088 | ||||||
chr1:94223172
|
C | T | 1 | a0001c0001t0036g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.206-2780G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223172 | ||||||
chr1:94223235
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.206-2843G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223235 | ||||||
chr1:94223414
|
T | C | 1 | a0001c0001t0005g0059 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.206-3022A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223414 | ||||||
chr1:94223465
|
G | A | 7 | a0001c0001t0003g0022a0001c0001t0003g0189a0001c0001t0003g0190others(4): Show | 8 | HG02109.hp1 HG02965.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-3073C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223465 | ||||||
chr1:94223471
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(255): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.206-3079T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223471 | ||||||
chr1:94223502
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(251): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.206-3110C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223502 | ||||||
chr1:94223550
|
G | T | 1 | a0001c0001t0025g0163 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.206-3158C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223550 | ||||||
chr1:94223584
|
A | G | 7 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(4): Show | 8 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-3192T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223584 | ||||||
chr1:94223733
|
G | T | 1 | a0001c0001t0006g0242 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.206-3341C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223733 | ||||||
chr1:94223808
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(257): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.206-3416G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223808 | ||||||
chr1:94223820
|
C | T | 1 | a0001c0001t0002g0224 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.206-3428G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223820 | ||||||
chr1:94223821
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.206-3429A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223821 | ||||||
chr1:94223847
|
G | A | 2 | a0001c0001t0018g0152a0001c0001t0018g0153 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.206-3455C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223847 | ||||||
chr1:94223872
|
A | G | 1 | a0001c0001t0002g0241 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.206-3480T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223872 | ||||||
chr1:94224032
|
C | T | 4 | a0001c0001t0002g0221a0001c0001t0002g0239a0001c0001t0002g0240others(1): Show | 4 | HG01168.hp2 HG01192.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-3640G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224032 | ||||||
chr1:94224088
|
C | A | 32 | a0001c0001t0003g0006a0001c0001t0003g0034a0001c0001t0003g0065others(29): Show | 34 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.206-3696G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224088 | ||||||
chr1:94224151
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.206-3759G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224151 | ||||||
chr1:94224178
|
A | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0095a0001c0001t0001g0097others(8): Show | 13 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.206-3786T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224178 | ||||||
chr1:94224388
|
G | T | 9 | a0001c0001t0002g0229a0001c0001t0002g0233a0001c0001t0002g0236others(6): Show | 9 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.206-3996C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224388 | ||||||
chr1:94224432
|
A | G | 1 | a0001c0001t0035g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.206-4040T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224432 | ||||||
chr1:94224631
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(257): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.206-4239T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224631 | ||||||
chr1:94224715
|
T | C | 1 | a0002c0003t0008g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.206-4323A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224715 | ||||||
chr1:94224885
|
T | C | 2 | a0001c0001t0003g0060a0001c0001t0003g0061 | 2 | NA18963.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.206-4493A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224885 | ||||||
chr1:94224905
|
T | C | 1 | a0001c0001t0003g0194 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.206-4513A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224905 | ||||||
chr1:94224908
|
G | A | 2 | a0001c0002t0001g0087a0001c0002t0001g0088 | 2 | HG01358.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.206-4516C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224908 | ||||||
chr1:94225175
|
A | T | 8 | a0001c0001t0003g0172a0001c0001t0013g0169a0001c0001t0013g0171others(5): Show | 9 | HG00544.hp1 HG00597.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.206-4783T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225175 | ||||||
chr1:94225239
|
T | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(251): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.206-4847A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225239 | ||||||
chr1:94225306
|
A | C | 1 | a0001c0001t0031g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.206-4914T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225306 | ||||||
chr1:94225418
|
C | T | 304 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(301): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.206-5026G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225418 | ||||||
chr1:94225473
|
A | T | 7 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(4): Show | 8 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-5081T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225473 | ||||||
chr1:94225522
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(92): Show | 112 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.206-5130G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225522 | ||||||
chr1:94225543
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 9 | NA18952.hp1 NA18970.hp1 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.206-5151T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225543 | ||||||
chr1:94225684
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(125): Show | 147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.206-5292A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225684 | ||||||
chr1:94225995
|
T | C | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+5412A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225995 | ||||||
chr1:94226106
|
A | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(254): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.205+5301T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94226106 | ||||||
chr1:94226357
|
T | A | 1 | a0001c0001t0002g0269 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.205+5050A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94226357 | ||||||
chr1:94226388
|
T | A | 1 | a0001c0001t0002g0270 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.205+5019A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94226388 | ||||||
chr1:94226583
|
T | A | 32 | a0001c0001t0003g0006a0001c0001t0003g0034a0001c0001t0003g0065others(29): Show | 34 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.205+4824A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94226583 | ||||||
chr1:94226820
|
T | C | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+4587A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94226820 | ||||||
chr1:94226912
|
A | G | 32 | a0001c0001t0003g0006a0001c0001t0003g0034a0001c0001t0003g0065others(29): Show | 34 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.205+4495T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94226912 | ||||||
chr1:94227128
|
AT | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(124): Show | 146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.205+4278delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94227128 | ||||||
chr1:94227518
|
T | C | 1 | a0001c0001t0007g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.205+3889A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94227518 | ||||||
chr1:94227589
|
T | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(251): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.205+3818A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94227589 | ||||||
chr1:94228024
|
G | C | 1 | a0001c0001t0004g0155 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.205+3383C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94228024 | ||||||
chr1:94228147
|
C | T | 87 | a0001c0001t0001g0226a0001c0001t0001g0238a0001c0001t0001g0266others(84): Show | 96 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.205+3260G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94228147 | ||||||
chr1:94228148
|
G | A | 1 | a0001c0001t0010g0299 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.205+3259C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94228148 | ||||||
chr1:94228480
|
C | A | 1 | a0001c0001t0001g0156 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.205+2927G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94228480 | ||||||
chr1:94228584
|
C | T | 1 | a0001c0001t0036g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.205+2823G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94228584 | ||||||
chr1:94228799
|
T | C | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+2608A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94228799 | ||||||
chr1:94229107
|
A | G | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+2300T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94229107 | ||||||
chr1:94229158
|
G | C | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+2249C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94229158 | ||||||
chr1:94229264
|
G | C | 2 | a0001c0002t0001g0063a0001c0002t0001g0064 | 2 | HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.205+2143C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94229264 | ||||||
chr1:94229265
|
C | T | 2 | a0001c0002t0001g0063a0001c0002t0001g0064 | 2 | HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.205+2142G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94229265 | ||||||
chr1:94229612
|
C | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(257): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.205+1795G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94229612 | ||||||
chr1:94229684
|
TCCATACA others(4): Show |
T | 1 | a0001c0001t0017g0167 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.205+1712_205+1722d others(13): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94229684 | ||||||
chr1:94230200
|
T | C | 1 | a0001c0001t0013g0195 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.205+1207A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230200 | ||||||
chr1:94230505
|
CTTAAA | C | 24 | a0001c0001t0001g0058a0001c0001t0003g0060a0001c0001t0003g0061others(21): Show | 31 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.205+897_205+901del others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230505 | ||||||
chr1:94230574
|
A | G | 1 | a0001c0001t0004g0271 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.205+833T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230574 | ||||||
chr1:94230583
|
T | C | 44 | a0001c0001t0001g0008a0001c0001t0001g0202a0001c0001t0002g0175others(41): Show | 50 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.205+824A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230583 | ||||||
chr1:94230594
|
A | C | 1 | a0001c0001t0036g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.205+813T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230594 | ||||||
chr1:94230657
|
G | A | 21 | a0001c0001t0001g0058a0001c0001t0003g0060a0001c0001t0003g0061others(18): Show | 28 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.205+750C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230657 | ||||||
chr1:94230687
|
T | C | 2 | a0001c0001t0007g0219a0001c0001t0007g0220 | 2 | HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.205+720A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230687 | ||||||
chr1:94230757
|
C | T | 2 | a0001c0001t0004g0025a0001c0001t0029g0228 | 3 | NA19004.hp2 NA19009.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.205+650G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230757 | ||||||
chr1:94230930
|
G | A | 1 | a0001c0002t0001g0157 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.205+477C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230930 | ||||||
chr1:94230958
|
T | TA | 11 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0202others(8): Show | 13 | HG00438.hp2 HG00544.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.205+448dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230958 | ||||||
chr1:94230958
|
TA | T | 6 | a0001c0001t0001g0226a0001c0001t0003g0024a0001c0001t0003g0227others(3): Show | 7 | HG03831.hp2 NA18949.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.205+448delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230958 | ||||||
chr1:94231050
|
T | C | 1 | a0002c0003t0024g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.205+357A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94231050 | ||||||
chr1:94231141
|
G | A | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+266C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94231141 | ||||||
chr1:94231188
|
A | G | 21 | a0001c0001t0001g0058a0001c0001t0003g0060a0001c0001t0003g0061others(18): Show | 28 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.205+219T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94231188 | ||||||
chr1:94231195
|
T | C | 1 | a0001c0002t0001g0160 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.205+212A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94231195 | ||||||
chr1:94231349
|
C | T | 1 | a0001c0001t0005g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.205+58G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94231349 | ||||||
chr1:94231887
|
T | C | 1 | a0002c0003t0024g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-32-244A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94231887 | ||||||
chr1:94232024
|
C | G | 63 | a0001c0001t0001g0226a0001c0001t0001g0238a0001c0001t0001g0266others(60): Show | 71 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-32-381G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232024 | ||||||
chr1:94232193
|
A | G | 90 | a0001c0001t0001g0226a0001c0001t0001g0238a0001c0001t0001g0266others(87): Show | 99 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-32-550T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232193 | ||||||
chr1:94232202
|
T | C | 1 | a0001c0001t0012g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32-559A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232202 | ||||||
chr1:94232263
|
G | GATT | 260 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(257): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.-32-623_-32-621dup others(3): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232263 | ||||||
chr1:94232573
|
G | A | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-32-930C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232573 | ||||||
chr1:94232578
|
A | G | 3 | a0001c0001t0004g0044a0002c0003t0015g0042a0002c0003t0015g0043 | 3 | HG02970.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-32-935T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232578 | ||||||
chr1:94232932
|
G | GT | 13 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0225others(10): Show | 13 | HG02135.hp2 HG02300.hp2 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32-1290dupA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232932 | ||||||
chr1:94232978
|
G | A | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-32-1335C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232978 | ||||||
chr1:94233003
|
G | A | 1 | a0001c0001t0042g0206 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-32-1360C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233003 | ||||||
chr1:94233094
|
A | G | 44 | a0001c0001t0001g0008a0001c0001t0001g0202a0001c0001t0002g0175others(41): Show | 50 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.-32-1451T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233094 | ||||||
chr1:94233259
|
G | A | 260 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(257): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.-32-1616C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233259 | ||||||
chr1:94233298
|
T | A | 1 | a0001c0002t0001g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-32-1655A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233298 | ||||||
chr1:94233334
|
C | T | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-32-1691G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233334 | ||||||
chr1:94233411
|
T | TAGCAGTA others(1): Show |
258 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(255): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.-32-1769_-32-1768i others(10): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233411 | ||||||
chr1:94233562
|
T | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(257): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.-32-1919A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233562 | ||||||
chr1:94233606
|
C | G | 2 | a0001c0001t0022g0036a0008c0010t0022g0035 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-32-1963G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233606 | ||||||
chr1:94233627
|
A | G | 44 | a0001c0001t0001g0008a0001c0001t0001g0202a0001c0001t0002g0175others(41): Show | 50 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.-32-1984T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233627 | ||||||
chr1:94233743
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-32-2100T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233743 | ||||||
chr1:94233777
|
G | C | 1 | a0001c0001t0002g0300 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-32-2134C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233777 | ||||||
chr1:94234911
|
C | A | 2 | a0001c0001t0025g0163a0001c0001t0025g0164 | 2 | HG01243.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-33+2504G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94234911 | ||||||
chr1:94234998
|
T | C | 2 | a0002c0003t0015g0165a0002c0003t0015g0166 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-33+2417A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94234998 | ||||||
chr1:94235090
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(257): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.-33+2325A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235090 | ||||||
chr1:94235128
|
A | G | 4 | a0001c0001t0007g0217a0001c0001t0007g0218a0001c0001t0007g0219others(1): Show | 4 | HG01952.hp1 HG01993.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+2287T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235128 | ||||||
chr1:94235301
|
C | A | 1 | a0001c0001t0006g0301 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-33+2114G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235301 | ||||||
chr1:94235322
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(257): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.-33+2093G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235322 | ||||||
chr1:94235386
|
G | A | 1 | a0001c0001t0003g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-33+2029C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235386 | ||||||
chr1:94235653
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(255): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.-33+1762G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235653 | ||||||
chr1:94235711
|
T | C | 2 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-33+1704A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235711 | ||||||
chr1:94235893
|
T | C | 1 | a0001c0001t0002g0302 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-33+1522A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235893 | ||||||
chr1:94236402
|
C | T | 304 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(301): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.-33+1013G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236402 | ||||||
chr1:94236530
|
G | C | 1 | a0001c0002t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-33+885C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236530 | ||||||
chr1:94236547
|
T | C | 1 | a0001c0001t0002g0303 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-33+868A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236547 | ||||||
chr1:94236678
|
A | C | 1 | a0001c0001t0002g0216 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-33+737T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236678 | ||||||
chr1:94236683
|
A | T | 1 | a0001c0001t0003g0034 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-33+732T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236683 | ||||||
chr1:94236684
|
T | A | 106 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0238others(103): Show | 116 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-33+731A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236684 | ||||||
chr1:94236685
|
T | A | 1 | a0001c0001t0010g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-33+730A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236685 | ||||||
chr1:94236693
|
T | A | 1 | a0001c0001t0002g0305 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-33+722A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236693 | ||||||
chr1:94236704
|
T | G | 1 | a0001c0001t0037g0306 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-33+711A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236704 | ||||||
chr1:94236893
|
A | C | 2 | a0001c0001t0004g0033a0001c0001t0036g0032 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-33+522T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236893 | ||||||
chr1:94237121
|
G | C | 1 | a0001c0001t0014g0307 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-33+294C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94237121 | ||||||
chr1:94237147
|
T | C | 6 | a0001c0001t0002g0030a0001c0001t0002g0309a0001c0001t0002g0311others(3): Show | 7 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+268A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94237147 |