geneid | 2909 |
---|---|
ensemblid | ENSG00000160007.20 |
hgncid | 4591 |
symbol | ARHGAP35 |
name | Rho GTPase activating protein 35 |
refseq_nuc | NM_004491.5 |
refseq_prot | NP_004482.4 |
ensembl_nuc | ENST00000672722.1 |
ensembl_prot | ENSP00000500409.1 |
mane_status | MANE Select |
chr | chr19 |
start | 46860997 |
end | 47005077 |
strand | + |
ver | v1.2 |
region | chr19:46860997-47005077 |
region5000 | chr19:46855997-47010077 |
regionname0 | ARHGAP35_chr19_46860997_47005077 |
regionname5000 | ARHGAP35_chr19_46855997_47010077 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1499 | 292 | 87 | 49 | 116 | 10 | 28 | 84 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0002 | 0/0 | 1499 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0003 | 0/0 | 1499 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0004 | 0/0 | 1499 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0005 | 0/0 | 1499 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0006 | 0/0 | 1499 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 4500 | 271 | 70 | 46 | 116 | 10 | 27 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
c0002 | 0/0 | 4500 | 14 | 12 | 2 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
c0003 | 0/0 | 4500 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
c0004 | 0/0 | 4500 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
c0005 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
c0006 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
c0007 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
c0008 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
c0009 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
c0010 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
c0011 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
c0012 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
c0013 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 4791 | 65 | 20 | 14 | 22 | 5 | 3 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0002 | 0/0 | 4793 | 38 | 1 | 4 | 26 | 0 | 7 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0003 | 0/0 | 4789 | 33 | 7 | 11 | 11 | 2 | 2 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0004 | 0/0 | 4787 | 30 | 4 | 1 | 21 | 0 | 4 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0005 | 0/0 | 4792 | 17 | 0 | 6 | 7 | 2 | 2 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0006 | 0/0 | 4789 | 13 | 11 | 2 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0007 | 0/0 | 4791 | 10 | 7 | 0 | 3 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0008 | 0/1 | 4794 | 5 | 0 | 2 | 1 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0009 | 0/0 | 4795 | 5 | 0 | 2 | 2 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0010 | 0/0 | 4789 | 5 | 0 | 4 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0011 | 0/0 | 4789 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0012 | 0/0 | 4792 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0013 | 0/0 | 4789 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0014 | 0/0 | 4786 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0015 | 0/0 | 4789 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0016 | 0/0 | 4791 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0017 | 0/0 | 4782 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0018 | 0/0 | 4789 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0019 | 0/0 | 4795 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0020 | 0/0 | 4790 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0021 | 0/0 | 4796 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0022 | 0/0 | 4789 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0023 | 0/0 | 4795 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0024 | 0/0 | 4789 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0025 | 0/0 | 4793 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0026 | 0/0 | 4791 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0027 | 0/0 | 4791 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0028 | 0/0 | 4784 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0029 | 0/0 | 4795 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0030 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0031 | 0/0 | 4789 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0032 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0033 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0034 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0035 | 0/0 | 4792 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0036 | 0/0 | 4787 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0037 | 0/0 | 4793 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0038 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0039 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0040 | 0/0 | 4789 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0041 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0042 | 0/0 | 4795 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0043 | 0/0 | 4791 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0044 | 0/0 | 4781 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0045 | 0/0 | 4787 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0046 | 0/0 | 4791 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0047 | 0/0 | 4791 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0048 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0049 | 0/0 | 4789 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0050 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0051 | 0/0 | 4793 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0052 | 0/0 | 4789 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0053 | 0/0 | 4793 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0054 | 0/0 | 4803 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0055 | 0/0 | 4786 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0056 | 0/0 | 4782 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
t0057 | 0/0 | 4788 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4500 | 271 | 70 | 46 | 116 | 10 | 27 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0002 | 0/0 | 4500 | 14 | 12 | 2 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0003 | 0/0 | 4500 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0005 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0006 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0007 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0009 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0011 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0002c0004 | 0/0 | 4500 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0003c0013 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0004c0008 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0005c0012 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0006c0010 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 9290 | 64 | 19 | 14 | 22 | 5 | 3 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0002 | 0/0 | 9292 | 37 | 1 | 4 | 26 | 0 | 6 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0003 | 0/0 | 9288 | 31 | 7 | 11 | 9 | 2 | 2 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0004 | 0/0 | 9286 | 27 | 2 | 0 | 21 | 0 | 4 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0005 | 0/0 | 9291 | 17 | 0 | 6 | 7 | 2 | 2 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0007 | 0/0 | 9290 | 10 | 7 | 0 | 3 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0008 | 0/1 | 9293 | 5 | 0 | 2 | 1 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0009 | 0/0 | 9294 | 5 | 0 | 2 | 2 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0010 | 0/0 | 9288 | 4 | 0 | 3 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0011 | 0/0 | 9288 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0012 | 0/0 | 9291 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0013 | 0/0 | 9288 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0014 | 0/0 | 9285 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0015 | 0/0 | 9288 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0016 | 0/0 | 9290 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0017 | 0/0 | 9281 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0018 | 0/0 | 9288 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0019 | 0/0 | 9294 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0020 | 0/0 | 9289 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0021 | 0/0 | 9295 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0022 | 0/0 | 9288 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0023 | 0/0 | 9294 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0024 | 0/0 | 9288 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0025 | 0/0 | 9292 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0026 | 0/0 | 9290 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0027 | 0/0 | 9290 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0028 | 0/0 | 9283 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0029 | 0/0 | 9294 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0030 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0031 | 0/0 | 9288 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0032 | 0/0 | 9286 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0033 | 0/0 | 9295 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0034 | 0/0 | 9293 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0035 | 0/0 | 9291 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0037 | 0/0 | 9292 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0038 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0039 | 0/0 | 9286 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0040 | 0/0 | 9288 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0041 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0042 | 0/0 | 9294 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0043 | 0/0 | 9290 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0044 | 0/0 | 9280 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0045 | 0/0 | 9286 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0046 | 0/0 | 9290 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0047 | 0/0 | 9290 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0048 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0049 | 0/0 | 9288 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0050 | 0/0 | 9300 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0051 | 0/0 | 9292 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0052 | 0/0 | 9288 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0054 | 0/0 | 9302 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0055 | 0/0 | 9285 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0056 | 0/0 | 9281 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0001t0057 | 0/0 | 9287 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0002t0001 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0002t0006 | 0/0 | 9288 | 11 | 9 | 2 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0002t0036 | 0/0 | 9286 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0002t0053 | 0/0 | 9292 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0003t0004 | 0/0 | 9286 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0003t0022 | 0/0 | 9288 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0005t0006 | 0/0 | 9288 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0006t0006 | 0/0 | 9288 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0007t0015 | 0/0 | 9288 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0009t0010 | 0/0 | 9288 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0001c0011t0002 | 0/0 | 9292 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0002c0004t0003 | 0/0 | 9288 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0003c0013t0004 | 0/0 | 9286 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0004c0008t0015 | 0/0 | 9288 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0005c0012t0011 | 0/0 | 9288 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
a0006c0010t0004 | 0/0 | 9286 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | copy fasta | chr19 | 46855997 | 47010077 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0008g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0008g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0009g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0009g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0009g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0009g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0009g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0010g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0010g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0010g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0010g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0012g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0012g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0012g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0012g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0013g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0013g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0013g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0013g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0014g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0014g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0014g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0015g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0016g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0016g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0016g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0017g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0017g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0017g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0018g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0018g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0019g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0019g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0020g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0020g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0021g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0021g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0022g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0023g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0023g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0024g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0024g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0025g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0025g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0026g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0026g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0027g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0027g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0028g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0028g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0029g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0030g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0031g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0032g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0033g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0034g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0035g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0037g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0038g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0039g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0040g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0041g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0042g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0043g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0044g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0045g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0046g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0047g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0048g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0049g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0050g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0051g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0052g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0054g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0055g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0056g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0057g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0036g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0053g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0003t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0003t0022g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0005t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0006t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0007t0015g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0009t0010g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0011t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0002c0004t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0002c0004t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0003c0013t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0004c0008t0015g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0005c0012t0011g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0006c0010t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0009 | g0143 | EUR | GBR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0100 | EUR | GBR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | FIN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0099 | EUR | FIN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00408 | hp2 | a0001 | c0001 | t0013 | g0226 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00558 | hp2 | a0001 | c0001 | t0026 | g0187 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00597 | hp1 | a0001 | c0001 | t0017 | g0250 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00597 | hp2 | a0001 | c0001 | t0026 | g0288 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0263 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00642 | hp1 | a0001 | c0002 | t0006 | g0207 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00642 | hp2 | a0001 | c0009 | t0010 | g0228 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00735 | hp1 | a0001 | c0001 | t0054 | g0287 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0116 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01070 | hp1 | a0001 | c0001 | t0019 | g0024 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01071 | hp2 | a0001 | c0001 | t0019 | g0219 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01099 | hp1 | a0001 | c0001 | t0021 | g0109 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01099 | hp2 | a0001 | c0001 | t0009 | g0290 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0107 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0106 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01192 | hp1 | a0001 | c0001 | t0009 | g0270 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0260 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01243 | hp2 | a0001 | c0002 | t0006 | g0217 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0102 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01256 | hp1 | a0001 | c0001 | t0008 | g0097 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01257 | hp1 | a0001 | c0001 | t0010 | g0035 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01346 | hp1 | a0001 | c0001 | t0005 | g0124 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01433 | hp2 | a0003 | c0013 | t0004 | g0244 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0096 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0259 | EUR | IBS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0117 | EUR | IBS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01891 | hp1 | a0001 | c0001 | t0011 | g0056 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01891 | hp2 | a0001 | c0001 | t0016 | g0092 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01928 | hp1 | a0001 | c0001 | t0010 | g0052 | AMR | PEL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02004 | hp2 | a0001 | c0001 | t0010 | g0222 | AMR | PEL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02015 | hp2 | a0002 | c0004 | t0003 | g0003 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02027 | hp1 | a0002 | c0004 | t0003 | g0008 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02027 | hp2 | a0001 | c0001 | t0012 | g0113 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02055 | hp2 | a0001 | c0002 | t0006 | g0213 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02071 | hp2 | a0001 | c0001 | t0046 | g0043 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02080 | hp1 | a0001 | c0001 | t0056 | g0090 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02135 | hp1 | a0001 | c0001 | t0009 | g0268 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02135 | hp2 | a0001 | c0001 | t0021 | g0254 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02145 | hp1 | a0001 | c0001 | t0029 | g0025 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | CDX | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CDX | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02257 | hp2 | a0001 | c0001 | t0030 | g0277 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02258 | hp1 | a0001 | c0001 | t0027 | g0221 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02258 | hp2 | a0001 | c0002 | t0006 | g0298 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02280 | hp2 | a0001 | c0006 | t0006 | g0296 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02572 | hp2 | a0001 | c0001 | t0045 | g0053 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02622 | hp1 | a0001 | c0001 | t0024 | g0032 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02622 | hp2 | a0001 | c0001 | t0011 | g0059 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02630 | hp2 | a0001 | c0001 | t0014 | g0069 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02647 | hp1 | a0005 | c0012 | t0011 | g0261 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02647 | hp2 | a0001 | c0001 | t0051 | g0229 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0110 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0082 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0095 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02809 | hp1 | a0001 | c0003 | t0004 | g0234 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02886 | hp2 | a0001 | c0001 | t0041 | g0028 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02895 | hp1 | a0001 | c0002 | t0006 | g0212 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0058 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02922 | hp1 | a0001 | c0002 | t0006 | g0211 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02922 | hp2 | a0001 | c0001 | t0016 | g0089 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02965 | hp2 | a0006 | c0010 | t0004 | g0027 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02970 | hp2 | a0001 | c0002 | t0006 | g0297 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02976 | hp2 | a0001 | c0002 | t0006 | g0209 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03098 | hp1 | a0001 | c0002 | t0053 | g0127 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03098 | hp2 | a0001 | c0001 | t0020 | g0258 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03130 | hp1 | a0001 | c0001 | t0027 | g0034 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03130 | hp2 | a0001 | c0001 | t0023 | g0039 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03139 | hp1 | a0001 | c0001 | t0014 | g0248 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03195 | hp1 | a0004 | c0008 | t0015 | g0036 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03195 | hp2 | a0001 | c0002 | t0036 | g0210 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03209 | hp2 | a0001 | c0001 | t0014 | g0247 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03225 | hp1 | a0001 | c0001 | t0048 | g0018 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03225 | hp2 | a0001 | c0001 | t0040 | g0029 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0235 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03239 | hp2 | a0001 | c0001 | t0035 | g0105 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03453 | hp1 | a0001 | c0001 | t0015 | g0037 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03486 | hp1 | a0001 | c0001 | t0025 | g0067 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03486 | hp2 | a0001 | c0001 | t0038 | g0252 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03516 | hp1 | a0001 | c0002 | t0006 | g0215 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03516 | hp2 | a0001 | c0001 | t0023 | g0055 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03540 | hp1 | a0001 | c0001 | t0011 | g0057 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03579 | hp1 | a0001 | c0002 | t0006 | g0214 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03669 | hp2 | a0001 | c0001 | t0043 | g0243 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03688 | hp1 | a0001 | c0001 | t0028 | g0246 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03688 | hp2 | a0001 | c0011 | t0002 | g0274 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0257 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03710 | hp2 | a0001 | c0001 | t0052 | g0066 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | BEB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0081 | SAS | BEB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0061 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04115 | hp2 | a0001 | c0001 | t0008 | g0122 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04204 | hp1 | a0001 | c0001 | t0049 | g0225 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04204 | hp2 | a0001 | c0001 | t0047 | g0230 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04228 | hp1 | a0001 | c0001 | t0033 | g0103 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0271 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18522 | hp1 | a0001 | c0005 | t0006 | g0208 | AFR | YRI | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18522 | hp2 | a0001 | c0001 | t0016 | g0094 | AFR | YRI | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | CHB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18906 | hp1 | a0001 | c0002 | t0006 | g0216 | AFR | YRI | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18906 | hp2 | a0001 | c0001 | t0018 | g0040 | AFR | YRI | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18942 | hp1 | a0001 | c0001 | t0057 | g0091 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18943 | hp2 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18947 | hp1 | a0001 | c0001 | t0028 | g0093 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18950 | hp1 | a0001 | c0001 | t0025 | g0062 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18951 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18953 | hp2 | a0001 | c0001 | t0013 | g0223 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18960 | hp2 | a0001 | c0001 | t0009 | g0135 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18961 | hp2 | a0001 | c0001 | t0012 | g0114 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18964 | hp1 | a0001 | c0001 | t0007 | g0046 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18968 | hp1 | a0001 | c0001 | t0012 | g0112 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18970 | hp1 | a0001 | c0001 | t0044 | g0063 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18971 | hp1 | a0001 | c0001 | t0013 | g0047 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18971 | hp2 | a0001 | c0001 | t0034 | g0111 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18972 | hp1 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18984 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18994 | hp1 | a0001 | c0001 | t0013 | g0049 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19002 | hp2 | a0001 | c0001 | t0007 | g0060 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19007 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19009 | hp1 | a0001 | c0001 | t0005 | g0256 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19009 | hp2 | a0001 | c0001 | t0017 | g0088 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19012 | hp1 | a0001 | c0001 | t0012 | g0255 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19030 | hp1 | a0001 | c0001 | t0050 | g0251 | AFR | LWK | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19030 | hp2 | a0001 | c0001 | t0018 | g0227 | AFR | LWK | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19057 | hp2 | a0001 | c0001 | t0022 | g0074 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19060 | hp1 | a0001 | c0001 | t0032 | g0232 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19062 | hp1 | a0001 | c0001 | t0039 | g0077 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19064 | hp1 | a0001 | c0001 | t0055 | g0129 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19064 | hp2 | a0001 | c0001 | t0017 | g0249 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19066 | hp2 | a0001 | c0001 | t0008 | g0125 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19070 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | YRI | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19240 | hp2 | a0001 | c0003 | t0022 | g0073 | AFR | YRI | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ASW | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ASW | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA20905 | hp1 | a0001 | c0001 | t0037 | g0144 | SAS | GIH | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA20905 | hp2 | a0001 | c0001 | t0010 | g0023 | SAS | GIH | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02109 | hp1 | a0001 | c0001 | t0020 | g0115 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02559 | hp1 | a0001 | c0001 | t0014 | g0087 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | USA | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG06807 | hp2 | a0001 | c0001 | t0042 | g0026 | AFR | USA | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA20300 | hp1 | a0001 | c0007 | t0015 | g0038 | AFR | USA | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA20300 | hp2 | a0001 | c0001 | t0031 | g0041 | AFR | USA | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0083 | AFR | LWK | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA21309 | hp2 | a0001 | c0001 | t0024 | g0220 | AFR | LWK | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0008 | g0108 | REF | REF | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0151 | REF | REF | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:46920929
|
A | G | 1 | a0003 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.2254A>G | p.Ser752Gly | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 2655/9290 | 2254/4500 | 752/1499 | chr19 | 46920929 | ||
chr19:46921181
|
T | G | 1 | a0002 | 2 | HG02015.hp2 HG02027.hp1 |
missense_variant | MODERATE | c.2506T>G | p.Ser836Ala | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 2907/9290 | 2506/4500 | 836/1499 | chr19 | 46921181 | ||
chr19:46921224
|
G | A | 1 | a0004 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.2549G>A | p.Arg850Gln | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 2950/9290 | 2549/4500 | 850/1499 | chr19 | 46921224 | ||
chr19:46921636
|
A | C | 1 | a0005 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.2961A>C | p.Glu987Asp | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 3362/9290 | 2961/4500 | 987/1499 | chr19 | 46921636 | ||
chr19:47000641
|
A | G | 1 | a0006 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.4453A>G | p.Met1485Val | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 4854/9290 | 4453/4500 | 1485/1499 | chr19 | 47000641 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:46919983
|
T | C | 1 | a0001c0003 | 2 | HG02809.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1308T>C | p.Phe436Phe | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 1709/9290 | 1308/4500 | 436/1499 | chr19 | 46919983 | ||
chr19:46920418
|
G | A | 3 | a0001c0002a0001c0005a0001c0006 | 16 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(13): Show |
synonymous_variant | LOW | c.1743G>A | p.Pro581Pro | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 2144/9290 | 1743/4500 | 581/1499 | chr19 | 46920418 | ||
chr19:46920790
|
G | A | 1 | a0001c0007 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.2115G>A | p.Lys705Lys | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 2516/9290 | 2115/4500 | 705/1499 | chr19 | 46920790 | ||
chr19:46921642
|
C | T | 1 | a0001c0006 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.2967C>T | p.Ile989Ile | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 3368/9290 | 2967/4500 | 989/1499 | chr19 | 46921642 | ||
chr19:46921675
|
A | G | 1 | a0001c0005 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.3000A>G | p.Thr1000Thr | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 3401/9290 | 3000/4500 | 1000/1499 | chr19 | 46921675 | ||
chr19:46922296
|
C | T | 1 | a0001c0011 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.3621C>T | p.Tyr1207Tyr | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 4022/9290 | 3621/4500 | 1207/1499 | chr19 | 46922296 | ||
chr19:47000604
|
G | A | 1 | a0001c0009 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.4416G>A | p.Ser1472Ser | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 4817/9290 | 4416/4500 | 1472/1499 | chr19 | 47000604 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:46861077
|
GGCCCCCC | G | 6 | a0001c0001t0014a0001c0001t0017a0001c0001t0028others(3): Show | 12 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-317_-311delCCCCGC others(1): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/7 | 57589 | INFO_REALIGN_3_PRIME | chr19 | 46861077 | ||||
chr19:46861082
|
C | CCCGCCGC others(5): Show |
1 | a0001c0001t0054 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-306_-295dupGAGCCG others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/7 | 57572 | INFO_REALIGN_3_PRIME | chr19 | 46861082 | ||||
chr19:47000723
|
C | G | 1 | a0001c0002t0053 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*35C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 35 | chr19 | 47000723 | |||||
chr19:47001002
|
G | A | 1 | a0001c0001t0029 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*314G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 314 | chr19 | 47001002 | |||||
chr19:47001032
|
C | A | 1 | a0001c0001t0030 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 344 | chr19 | 47001032 | |||||
chr19:47001033
|
G | A | 1 | a0001c0001t0031 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*345G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 345 | chr19 | 47001033 | |||||
chr19:47001240
|
C | T | 1 | a0001c0001t0052 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 552 | chr19 | 47001240 | |||||
chr19:47001638
|
G | A | 1 | a0001c0001t0018 | 2 | NA18906.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*950G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 950 | chr19 | 47001638 | |||||
chr19:47001794
|
C | T | 1 | a0001c0001t0027 | 2 | HG02258.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1106C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 1106 | chr19 | 47001794 | |||||
chr19:47001886
|
A | G | 1 | a0001c0001t0052 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1198A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 1198 | chr19 | 47001886 | |||||
chr19:47001910
|
G | A | 1 | a0001c0001t0032 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1222G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 1222 | chr19 | 47001910 | |||||
chr19:47001977
|
G | A | 1 | a0001c0001t0019 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1289G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 1289 | chr19 | 47001977 | |||||
chr19:47002012
|
C | G | 1 | a0001c0001t0026 | 2 | HG00558.hp2 HG00597.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1324C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 1324 | chr19 | 47002012 | |||||
chr19:47002290
|
C | T | 1 | a0001c0001t0052 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1602C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 1602 | chr19 | 47002290 | |||||
chr19:47002707
|
TG | T | 8 | a0001c0001t0005a0001c0001t0008a0001c0001t0012others(5): Show | 33 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2021delG | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2021 | INFO_REALIGN_3_PRIME | chr19 | 47002707 | ||||
chr19:47002720
|
T | C | 1 | a0001c0001t0033 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2032T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2032 | chr19 | 47002720 | |||||
chr19:47002869
|
C | A | 5 | a0001c0001t0027a0001c0002t0006a0001c0002t0036others(2): Show | 16 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2181C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2181 | chr19 | 47002869 | |||||
chr19:47003095
|
A | G | 20 | a0001c0001t0005a0001c0001t0008a0001c0001t0014others(17): Show | 61 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2407A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2407 | chr19 | 47003095 | |||||
chr19:47003106
|
C | T | 18 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(15): Show | 69 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2418C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2418 | chr19 | 47003106 | |||||
chr19:47003166
|
C | T | 1 | a0001c0001t0014 | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2478C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2478 | chr19 | 47003166 | |||||
chr19:47003177
|
G | A | 1 | a0001c0001t0035 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2489G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2489 | chr19 | 47003177 | |||||
chr19:47003234
|
C | T | 5 | a0001c0001t0027a0001c0002t0006a0001c0002t0036others(2): Show | 16 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2546C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2546 | chr19 | 47003234 | |||||
chr19:47003329
|
A | G | 1 | a0001c0001t0049 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2641A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2641 | chr19 | 47003329 | |||||
chr19:47003410
|
C | T | 1 | a0001c0001t0048 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2722C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2722 | chr19 | 47003410 | |||||
chr19:47003416
|
C | T | 1 | a0001c0001t0024 | 2 | HG02622.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2728C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2728 | chr19 | 47003416 | |||||
chr19:47003497
|
C | T | 1 | a0001c0001t0051 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2809C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2809 | chr19 | 47003497 | |||||
chr19:47003512
|
C | T | 17 | a0001c0001t0005a0001c0001t0008a0001c0001t0012others(14): Show | 50 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2824C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2824 | chr19 | 47003512 | |||||
chr19:47003520
|
G | A | 1 | a0001c0001t0037 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2832G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2832 | chr19 | 47003520 | |||||
chr19:47003567
|
G | T | 1 | a0001c0001t0018 | 2 | NA18906.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2879G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2879 | chr19 | 47003567 | |||||
chr19:47003584
|
C | T | 2 | a0001c0001t0011a0005c0012t0011 | 5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2896C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2896 | chr19 | 47003584 | |||||
chr19:47003594
|
G | A | 1 | a0001c0001t0038 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2906G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2906 | chr19 | 47003594 | |||||
chr19:47003913
|
G | GAC | 7 | a0001c0001t0005a0001c0001t0012a0001c0001t0014others(4): Show | 30 | HG00639.hp2 HG00735.hp2 HG01167.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3228_*3229dupAC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003913 | ||||
chr19:47003913
|
G | GACAC | 7 | a0001c0001t0008a0001c0001t0019a0001c0001t0023others(4): Show | 13 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3226_*3229dupACAC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003913 | ||||
chr19:47003913
|
G | GACACAC | 2 | a0001c0001t0021a0001c0001t0033 | 3 | HG01099.hp1 HG02135.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3229_*3230insACAC others(2): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003913 | ||||
chr19:47003913
|
G | GACACACA others(3): Show |
1 | a0001c0001t0050 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3229_*3230insACAC others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003913 | ||||
chr19:47003913
|
GACACGCA others(3): Show |
G | 1 | a0001c0001t0044 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3230_*3239delGCAC others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003913 | ||||
chr19:47003914
|
ACACG | A | 8 | a0001c0001t0004a0001c0001t0032a0001c0001t0039others(5): Show | 34 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3230_*3233delGCAC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003914 | ||||
chr19:47003916
|
ACG | A | 23 | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(20): Show | 77 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3230_*3231delGC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003916 | ||||
chr19:47003918
|
G | A | 27 | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(24): Show | 71 | HG00639.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*3230G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | chr19 | 47003918 | |||||
chr19:47003918
|
G | GCA | 4 | a0001c0001t0002a0001c0001t0037a0001c0001t0055others(1): Show | 40 | HG00438.hp1 HG01069.hp2 HG01261.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*3261_*3262dupCA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3263 | INFO_REALIGN_3_PRIME | chr19 | 47003918 | ||||
chr19:47003918
|
G | GCACA | 1 | a0001c0001t0009 | 5 | HG00099.hp1 HG01099.hp2 HG01192.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3259_*3262dupCACA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3263 | INFO_REALIGN_3_PRIME | chr19 | 47003918 | ||||
chr19:47004134
|
G | A | 1 | a0001c0001t0043 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3446G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3446 | chr19 | 47004134 | |||||
chr19:47004177
|
C | T | 24 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(21): Show | 77 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3489C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3489 | chr19 | 47004177 | |||||
chr19:47004207
|
G | A | 1 | a0001c0001t0040 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3519G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3519 | chr19 | 47004207 | |||||
chr19:47004211
|
G | A | 24 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(21): Show | 74 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*3523G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3523 | chr19 | 47004211 | |||||
chr19:47004268
|
G | A | 1 | a0001c0001t0040 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3580G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3580 | chr19 | 47004268 | |||||
chr19:47004288
|
T | C | 1 | a0001c0001t0039 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3600T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3600 | chr19 | 47004288 | |||||
chr19:47004299
|
C | T | 1 | a0001c0001t0056 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3611C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3611 | chr19 | 47004299 | |||||
chr19:47004324
|
C | T | 1 | a0001c0001t0050 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3636C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3636 | chr19 | 47004324 | |||||
chr19:47004347
|
G | A | 3 | a0001c0001t0010a0001c0001t0047a0001c0009t0010 | 6 | HG00642.hp2 HG01257.hp1 HG01928.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3659G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3659 | chr19 | 47004347 | |||||
chr19:47004423
|
G | T | 5 | a0001c0001t0014a0001c0001t0017a0001c0001t0028others(2): Show | 11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3735G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3735 | chr19 | 47004423 | |||||
chr19:47004574
|
A | G | 1 | a0001c0001t0056 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3886A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3886 | chr19 | 47004574 | |||||
chr19:47004852
|
A | T | 1 | a0001c0001t0029 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4164A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 4164 | chr19 | 47004852 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:46861296
|
C | A | 10 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0004others(7): Show | 10 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.-189+87C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861296 | ||||||
chr19:46861343
|
G | C | 11 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0021others(8): Show | 11 | HG00639.hp1 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-189+134G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861343 | ||||||
chr19:46861343
|
G | GC | 82 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280others(79): Show | 82 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.-189+144dupC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46861343 | |||||
chr19:46861503
|
T | G | 1 | a0001c0001t0004g0022 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-189+294T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861503 | ||||||
chr19:46861553
|
T | C | 1 | a0001c0001t0010g0023 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-189+344T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861553 | ||||||
chr19:46861865
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-189+656C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861865 | ||||||
chr19:46861885
|
G | T | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+676G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861885 | ||||||
chr19:46861927
|
CT | C | 187 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(184): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-189+720delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46861927 | |||||
chr19:46861936
|
C | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+727C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861936 | ||||||
chr19:46861936
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-189+727C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861936 | ||||||
chr19:46862040
|
G | A | 1 | a0006c0010t0004g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-189+831G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46862040 | ||||||
chr19:46862908
|
ATTACGAT others(6): Show |
A | 1 | a0001c0001t0002g0264 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-189+1703_-189+171 others(17): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46862908 | |||||
chr19:46863144
|
C | T | 54 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(51): Show | 54 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-189+1935C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863144 | ||||||
chr19:46863186
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0294 | 2 | NA18951.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-189+1977A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863186 | ||||||
chr19:46863697
|
A | G | 1 | a0001c0001t0003g0128 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-189+2488A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863697 | ||||||
chr19:46863732
|
C | G | 16 | a0001c0001t0002g0295a0001c0002t0006g0207a0001c0002t0006g0209others(13): Show | 16 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-189+2523C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863732 | ||||||
chr19:46863768
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0279 | 2 | HG02056.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-189+2559G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863768 | ||||||
chr19:46863828
|
C | T | 35 | a0001c0001t0001g0119a0001c0001t0003g0104a0001c0001t0005g0102others(32): Show | 35 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-189+2619C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863828 | ||||||
chr19:46863858
|
A | C | 1 | a0001c0001t0001g0205 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-189+2649A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863858 | ||||||
chr19:46863903
|
C | T | 7 | a0001c0001t0003g0096a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+2694C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863903 | ||||||
chr19:46863916
|
A | G | 1 | a0001c0001t0038g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-189+2707A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863916 | ||||||
chr19:46864194
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-189+2985T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864194 | ||||||
chr19:46864248
|
T | TG | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+3041dupG | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46864248 | |||||
chr19:46864306
|
G | T | 1 | a0001c0001t0002g0295 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-189+3097G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864306 | ||||||
chr19:46864433
|
A | G | 1 | a0001c0001t0050g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-189+3224A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864433 | ||||||
chr19:46864459
|
G | C | 2 | a0001c0001t0040g0029a0001c0001t0041g0028 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-189+3250G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864459 | ||||||
chr19:46864590
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-189+3381A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864590 | ||||||
chr19:46864763
|
C | G | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+3554C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864763 | ||||||
chr19:46864920
|
T | C | 1 | a0001c0001t0004g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-189+3711T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864920 | ||||||
chr19:46864973
|
A | T | 1 | a0001c0001t0042g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-189+3764A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864973 | ||||||
chr19:46865044
|
A | G | 50 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-189+3835A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865044 | ||||||
chr19:46865094
|
A | G | 1 | a0001c0001t0005g0126 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-189+3885A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865094 | ||||||
chr19:46865139
|
G | T | 1 | a0001c0001t0004g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-189+3930G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865139 | ||||||
chr19:46865398
|
C | T | 1 | a0001c0001t0005g0263 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-189+4189C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865398 | ||||||
chr19:46865808
|
C | A | 1 | a0001c0001t0014g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-189+4599C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865808 | ||||||
chr19:46865878
|
T | A | 1 | a0001c0001t0003g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-189+4669T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865878 | ||||||
chr19:46865963
|
C | T | 15 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(12): Show | 15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-189+4754C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865963 | ||||||
chr19:46866123
|
G | A | 3 | a0001c0001t0004g0070a0001c0001t0004g0071a0001c0001t0032g0232 | 3 | NA18969.hp1 NA18982.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-189+4914G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866123 | ||||||
chr19:46866332
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0003g0231a0001c0001t0025g0067 | 3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-189+5123C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866332 | ||||||
chr19:46866496
|
G | C | 35 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(32): Show | 35 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-189+5287G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866496 | ||||||
chr19:46866577
|
G | A | 1 | a0001c0001t0050g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-189+5368G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866577 | ||||||
chr19:46866672
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-189+5463C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866672 | ||||||
chr19:46866792
|
A | G | 3 | a0001c0001t0004g0070a0001c0001t0004g0071a0001c0001t0032g0232 | 3 | NA18969.hp1 NA18982.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-189+5583A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866792 | ||||||
chr19:46866993
|
G | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+5784G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866993 | ||||||
chr19:46867046
|
A | G | 1 | a0001c0001t0016g0094 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-189+5837A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867046 | ||||||
chr19:46867384
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0280others(1): Show | 4 | HG01433.hp1 HG01928.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+6175G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867384 | ||||||
chr19:46867482
|
T | C | 1 | a0001c0001t0003g0009 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-189+6273T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867482 | ||||||
chr19:46867500
|
A | G | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+6291A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867500 | ||||||
chr19:46867545
|
G | A | 1 | a0001c0001t0050g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-189+6336G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867545 | ||||||
chr19:46867557
|
C | T | 1 | a0001c0002t0006g0298 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-189+6348C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867557 | ||||||
chr19:46867699
|
G | C | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+6490G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867699 | ||||||
chr19:46867758
|
T | G | 10 | a0001c0001t0003g0104a0001c0001t0005g0102a0001c0001t0005g0106others(7): Show | 10 | HG00639.hp2 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-189+6549T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867758 | ||||||
chr19:46867761
|
G | T | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-189+6552G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867761 | ||||||
chr19:46867779
|
T | G | 16 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(13): Show | 16 | HG00597.hp1 HG01891.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.-189+6570T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867779 | ||||||
chr19:46867867
|
T | A | 1 | a0001c0001t0005g0102 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-189+6658T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867867 | ||||||
chr19:46867903
|
A | G | 1 | a0001c0001t0047g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-189+6694A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867903 | ||||||
chr19:46868157
|
C | G | 7 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+6948C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46868157 | ||||||
chr19:46868359
|
G | A | 187 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(184): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-189+7150G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46868359 | ||||||
chr19:46868372
|
CAATT | C | 3 | a0001c0001t0024g0032a0001c0001t0024g0220a0001c0001t0038g0252 | 3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-189+7166_-189+716 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46868372 | |||||
chr19:46868477
|
A | G | 1 | a0001c0001t0052g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-189+7268A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46868477 | ||||||
chr19:46868587
|
C | T | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+7378C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46868587 | ||||||
chr19:46868857
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-189+7648C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46868857 | ||||||
chr19:46868893
|
A | AT | 116 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0153others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-189+7713dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46868893 | |||||
chr19:46868893
|
A | ATT | 40 | a0001c0001t0001g0294a0001c0001t0002g0156a0001c0001t0002g0293others(37): Show | 40 | HG00408.hp2 HG00642.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.-189+7712_-189+771 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46868893 | |||||
chr19:46868893
|
A | ATTT | 12 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(9): Show | 12 | HG00438.hp1 HG01243.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-189+7711_-189+771 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46868893 | |||||
chr19:46868893
|
AT | A | 35 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0002g0265others(32): Show | 35 | HG00408.hp1 HG00438.hp2 HG02015.hp1 others(32): Show |
intron_variant | MODIFIER | c.-189+7713delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46868893 | |||||
chr19:46868893
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0004g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-189+7703_-189+771 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46868893 | |||||
chr19:46869095
|
T | A | 269 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(266): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-189+7886T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46869095 | ||||||
chr19:46869182
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-189+7973C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46869182 | ||||||
chr19:46869476
|
T | TTG | 83 | a0001c0001t0001g0068a0001c0001t0001g0134a0001c0001t0001g0167others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.-189+8299_-189+830 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | |||||
chr19:46869476
|
T | TTGTG | 30 | a0001c0001t0001g0191a0001c0001t0002g0141a0001c0001t0002g0155others(27): Show | 30 | HG00597.hp1 HG00639.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.-189+8297_-189+830 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | |||||
chr19:46869476
|
T | TTGTGTG | 10 | a0001c0001t0003g0021a0001c0001t0003g0054a0001c0001t0004g0082others(7): Show | 10 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-189+8295_-189+830 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | |||||
chr19:46869476
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0007g0019a0001c0001t0048g0018 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-189+8291_-189+830 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | |||||
chr19:46869476
|
TTG | T | 18 | a0001c0001t0001g0142a0001c0001t0001g0160a0001c0001t0001g0162others(15): Show | 18 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-189+8299_-189+830 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | |||||
chr19:46869476
|
TTGTG | T | 8 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0012g0112others(5): Show | 8 | HG01255.hp2 HG01496.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.-189+8297_-189+830 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | |||||
chr19:46869476
|
TTGTGTGT others(3): Show |
T | 8 | a0001c0001t0015g0037a0001c0001t0023g0039a0001c0001t0023g0055others(5): Show | 8 | HG02886.hp1 HG02886.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-189+8291_-189+830 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | |||||
chr19:46869476
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-189+8289_-189+830 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | |||||
chr19:46869734
|
G | C | 2 | a0001c0001t0001g0142a0001c0001t0002g0265 | 2 | NA18612.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-189+8525G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46869734 | ||||||
chr19:46869803
|
G | C | 31 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(28): Show | 31 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.-189+8594G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46869803 | ||||||
chr19:46869943
|
C | CT | 6 | a0001c0001t0002g0276a0001c0001t0003g0050a0001c0001t0003g0064others(3): Show | 6 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-189+8755dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869943 | |||||
chr19:46869943
|
CT | C | 111 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0171others(108): Show | 111 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-189+8755delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869943 | |||||
chr19:46869943
|
CTT | C | 35 | a0001c0001t0003g0001a0001c0001t0004g0022a0001c0001t0004g0030others(32): Show | 35 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-189+8754_-189+875 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869943 | |||||
chr19:46869972
|
A | T | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+8763A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46869972 | ||||||
chr19:46869985
|
C | T | 1 | a0001c0001t0002g0133 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-189+8776C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46869985 | ||||||
chr19:46870091
|
C | T | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-189+8882C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870091 | ||||||
chr19:46870139
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-189+8930C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870139 | ||||||
chr19:46870281
|
G | A | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-189+9072G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870281 | ||||||
chr19:46870350
|
C | T | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+9141C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870350 | ||||||
chr19:46870605
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-189+9396T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870605 | ||||||
chr19:46870846
|
A | T | 1 | a0001c0001t0001g0292 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-189+9637A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870846 | ||||||
chr19:46870891
|
T | G | 1 | a0001c0001t0004g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-189+9682T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870891 | ||||||
chr19:46870988
|
A | T | 1 | a0001c0001t0002g0264 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-189+9779A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870988 | ||||||
chr19:46871306
|
A | G | 2 | a0001c0001t0026g0187a0001c0001t0026g0288 | 2 | HG00558.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.-189+10097A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871306 | ||||||
chr19:46871321
|
C | T | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+10112C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871321 | ||||||
chr19:46871355
|
T | G | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+10146T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871355 | ||||||
chr19:46871588
|
C | T | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+10379C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871588 | ||||||
chr19:46871623
|
G | A | 2 | a0001c0001t0007g0042a0001c0001t0046g0043 | 2 | HG02071.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.-189+10414G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871623 | ||||||
chr19:46871645
|
C | T | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+10436C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871645 | ||||||
chr19:46871754
|
G | A | 1 | a0001c0001t0037g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-189+10545G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871754 | ||||||
chr19:46871776
|
C | T | 7 | a0001c0001t0015g0037a0001c0001t0023g0039a0001c0001t0023g0055others(4): Show | 7 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+10567C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871776 | ||||||
chr19:46871793
|
A | C | 1 | a0001c0001t0002g0264 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-189+10584A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871793 | ||||||
chr19:46871904
|
C | T | 3 | a0001c0001t0014g0087a0001c0001t0014g0247a0001c0001t0014g0248 | 3 | HG02559.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-189+10695C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871904 | ||||||
chr19:46872015
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-189+10806G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872015 | ||||||
chr19:46872113
|
C | T | 4 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+10904C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872113 | ||||||
chr19:46872251
|
A | G | 1 | a0001c0001t0043g0243 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-189+11042A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872251 | ||||||
chr19:46872705
|
T | C | 187 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(184): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-189+11496T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872705 | ||||||
chr19:46872707
|
C | T | 1 | a0001c0001t0002g0152 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-189+11498C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872707 | ||||||
chr19:46872844
|
A | G | 187 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(184): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-189+11635A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872844 | ||||||
chr19:46872859
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-189+11650C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872859 | ||||||
chr19:46872866
|
G | A | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-189+11657G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872866 | ||||||
chr19:46872875
|
C | T | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-189+11666C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872875 | ||||||
chr19:46872880
|
C | CA | 161 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(158): Show | 161 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-189+11686dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46872880 | |||||
chr19:46872905
|
A | C | 1 | a0001c0001t0002g0295 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-189+11696A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872905 | ||||||
chr19:46872994
|
C | G | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-189+11785C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872994 | ||||||
chr19:46873129
|
C | T | 115 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(112): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-189+11920C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873129 | ||||||
chr19:46873198
|
C | A | 1 | a0001c0001t0002g0156 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-189+11989C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873198 | ||||||
chr19:46873353
|
T | C | 297 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.-189+12144T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873353 | ||||||
chr19:46873410
|
T | C | 1 | a0001c0001t0013g0226 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-189+12201T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873410 | ||||||
chr19:46873636
|
C | CA | 117 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0281others(114): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-189+12441dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46873636 | |||||
chr19:46873835
|
G | A | 2 | a0001c0001t0024g0032a0001c0001t0024g0220 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-189+12626G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873835 | ||||||
chr19:46873844
|
G | A | 1 | a0001c0001t0004g0233 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-189+12635G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873844 | ||||||
chr19:46873911
|
G | C | 3 | a0001c0001t0024g0032a0001c0001t0024g0220a0001c0001t0038g0252 | 3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-189+12702G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873911 | ||||||
chr19:46873983
|
GGTGATCT others(1055): Show |
G | 1 | a0001c0001t0005g0256 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-189+12788_-189+13 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46873983 | |||||
chr19:46874069
|
T | C | 1 | a0001c0001t0031g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-189+12860T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874069 | ||||||
chr19:46874162
|
C | G | 34 | a0001c0001t0001g0119a0001c0001t0003g0104a0001c0001t0005g0102others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-189+12953C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874162 | ||||||
chr19:46874501
|
C | CT | 117 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0170others(114): Show | 117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-189+13312dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46874501 | |||||
chr19:46874501
|
C | CTT | 11 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0005others(8): Show | 11 | HG02015.hp2 HG02027.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.-189+13311_-189+13 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46874501 | |||||
chr19:46874501
|
CT | C | 6 | a0001c0001t0002g0145a0001c0001t0002g0155a0001c0001t0002g0159others(3): Show | 6 | HG02145.hp1 HG02293.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.-189+13312delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46874501 | |||||
chr19:46874507
|
T | G | 1 | a0001c0001t0001g0192 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-189+13298T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874507 | ||||||
chr19:46874574
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0026g0187a0001c0001t0026g0288 | 3 | HG00558.hp2 HG00597.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-189+13365G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874574 | ||||||
chr19:46874620
|
TCAGCCTC others(17): Show |
T | 1 | a0001c0002t0006g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-189+13415_-189+13 others(30): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46874620 | |||||
chr19:46874661
|
T | C | 271 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(268): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.-189+13452T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874661 | ||||||
chr19:46874719
|
G | C | 1 | a0001c0001t0001g0280 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-189+13510G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874719 | ||||||
chr19:46874810
|
C | CT | 11 | a0001c0001t0001g0190a0001c0001t0001g0201a0001c0001t0001g0294others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-189+13620dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46874810 | |||||
chr19:46874810
|
CT | C | 168 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0179others(165): Show | 168 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.-189+13620delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46874810 | |||||
chr19:46874835
|
G | A | 1 | a0004c0008t0015g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-189+13626G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874835 | ||||||
chr19:46875056
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-189+13847C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875056 | ||||||
chr19:46875187
|
G | A | 1 | a0001c0001t0005g0263 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-189+13978G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875187 | ||||||
chr19:46875212
|
T | C | 3 | a0001c0001t0024g0032a0001c0001t0024g0220a0001c0001t0038g0252 | 3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-189+14003T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875212 | ||||||
chr19:46875343
|
G | T | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | NA18942.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.-189+14134G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875343 | ||||||
chr19:46875430
|
T | C | 1 | a0001c0001t0004g0079 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-189+14221T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875430 | ||||||
chr19:46875600
|
G | A | 35 | a0001c0001t0001g0119a0001c0001t0003g0104a0001c0001t0005g0102others(32): Show | 35 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-189+14391G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875600 | ||||||
chr19:46875650
|
AT | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+14446delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46875650 | |||||
chr19:46875715
|
A | C | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+14506A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875715 | ||||||
chr19:46875757
|
G | A | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-189+14548G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875757 | ||||||
chr19:46875768
|
G | A | 186 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(183): Show | 186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-189+14559G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875768 | ||||||
chr19:46876044
|
C | T | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+14835C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46876044 | ||||||
chr19:46876088
|
G | A | 1 | a0001c0002t0006g0214 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-189+14879G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46876088 | ||||||
chr19:46876126
|
G | T | 2 | a0001c0001t0003g0054a0001c0001t0045g0053 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-189+14917G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46876126 | ||||||
chr19:46876193
|
AT | A | 6 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0005g0257others(3): Show | 6 | HG02258.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-189+14996delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46876193 | |||||
chr19:46876623
|
G | A | 1 | a0001c0001t0020g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-189+15414G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46876623 | ||||||
chr19:46876866
|
T | G | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-189+15657T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46876866 | ||||||
chr19:46877248
|
C | CA | 11 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0181others(8): Show | 11 | HG00733.hp2 HG01243.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-189+16061dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46877248 | |||||
chr19:46877248
|
CA | C | 79 | a0001c0001t0001g0068a0001c0001t0003g0001a0001c0001t0003g0002others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.-189+16061delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46877248 | |||||
chr19:46877248
|
CAA | C | 81 | a0001c0001t0001g0119a0001c0001t0003g0104a0001c0001t0004g0022others(78): Show | 81 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-189+16060_-189+16 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46877248 | |||||
chr19:46877284
|
T | C | 1 | a0001c0001t0014g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-189+16075T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877284 | ||||||
chr19:46877288
|
C | T | 1 | a0001c0001t0007g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-189+16079C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877288 | ||||||
chr19:46877305
|
G | C | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-189+16096G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877305 | ||||||
chr19:46877388
|
C | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+16179C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877388 | ||||||
chr19:46877569
|
AAATAAC | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+16366_-189+16 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46877569 | |||||
chr19:46877571
|
A | C | 1 | a0001c0001t0003g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-189+16362A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877571 | ||||||
chr19:46877665
|
C | T | 1 | a0001c0007t0015g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-189+16456C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877665 | ||||||
chr19:46877916
|
C | G | 4 | a0001c0001t0016g0089a0001c0001t0016g0092a0001c0001t0016g0094others(1): Show | 4 | HG01891.hp2 HG02922.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-189+16707C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877916 | ||||||
chr19:46878004
|
G | A | 1 | a0001c0001t0055g0129 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-189+16795G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878004 | ||||||
chr19:46878084
|
T | G | 12 | a0001c0001t0001g0130a0001c0001t0001g0160a0001c0001t0001g0162others(9): Show | 12 | HG00733.hp2 HG00738.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-189+16875T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878084 | ||||||
chr19:46878376
|
G | A | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+17167G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878376 | ||||||
chr19:46878410
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-189+17201G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878410 | ||||||
chr19:46878583
|
T | G | 1 | a0001c0001t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-189+17374T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878583 | ||||||
chr19:46878640
|
G | T | 12 | a0001c0001t0001g0130a0001c0001t0001g0160a0001c0001t0001g0162others(9): Show | 12 | HG00733.hp2 HG00738.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-189+17431G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878640 | ||||||
chr19:46878876
|
A | G | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+17667A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878876 | ||||||
chr19:46878960
|
T | C | 1 | a0001c0001t0021g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-189+17751T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878960 | ||||||
chr19:46879044
|
T | A | 1 | a0001c0001t0002g0157 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-189+17835T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879044 | ||||||
chr19:46879168
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-189+17959C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879168 | ||||||
chr19:46879236
|
T | G | 7 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(4): Show | 7 | HG01433.hp1 HG01928.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+18027T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879236 | ||||||
chr19:46879271
|
A | G | 1 | a0001c0001t0002g0150 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-189+18062A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879271 | ||||||
chr19:46879333
|
A | T | 31 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(28): Show | 31 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.-189+18124A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879333 | ||||||
chr19:46879352
|
G | C | 1 | a0005c0012t0011g0261 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-189+18143G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879352 | ||||||
chr19:46879534
|
C | T | 2 | a0001c0001t0002g0200a0001c0001t0002g0293 | 2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-189+18325C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879534 | ||||||
chr19:46879587
|
A | AAAAT | 3 | a0001c0001t0004g0086a0001c0002t0036g0210a0001c0002t0053g0127 | 3 | HG02071.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-189+18406_-189+18 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | |||||
chr19:46879587
|
A | AAAATAAA others(1): Show |
6 | a0001c0001t0002g0295a0001c0001t0012g0112a0001c0001t0012g0113others(3): Show | 6 | HG02027.hp2 HG02074.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.-189+18402_-189+18 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | |||||
chr19:46879587
|
A | AAAATAAA others(5): Show |
7 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0289others(4): Show | 7 | HG00621.hp2 HG00735.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-189+18398_-189+18 others(18): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | |||||
chr19:46879587
|
A | AAAATAAA others(9): Show |
68 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0142others(65): Show | 68 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.-189+18394_-189+18 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | |||||
chr19:46879587
|
A | AAAATAAA others(86): Show |
3 | a0001c0001t0001g0068a0001c0001t0003g0012a0001c0001t0007g0014 | 3 | HG03041.hp1 HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-189+18397_-189+18 others(99): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | |||||
chr19:46879587
|
A | AAAATAAA others(90): Show |
3 | a0001c0001t0003g0044a0001c0001t0003g0231a0001c0001t0025g0067 | 3 | HG02895.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-189+18397_-189+18 others(103): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | |||||
chr19:46879587
|
A | AAAATAAA others(94): Show |
39 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0004others(36): Show | 39 | HG00408.hp2 HG00733.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-189+18397_-189+18 others(107): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | |||||
chr19:46879587
|
A | AAAATAAA others(98): Show |
22 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0009others(19): Show | 22 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.-189+18397_-189+18 others(111): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | |||||
chr19:46879587
|
A | AAAATAAA others(102): Show |
3 | a0001c0001t0003g0061a0001c0001t0010g0222a0001c0001t0018g0227 | 3 | HG02004.hp2 HG04115.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-189+18397_-189+18 others(115): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | |||||
chr19:46879587
|
A | AAAATAAA others(13): Show |
37 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(34): Show | 37 | HG00280.hp1 HG00558.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-189+18390_-189+18 others(26): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | |||||
chr19:46879587
|
A | AAAATAAA others(17): Show |
17 | a0001c0001t0001g0130a0001c0001t0001g0165a0001c0001t0001g0173others(14): Show | 17 | HG00597.hp2 HG00735.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.-189+18386_-189+18 others(30): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | |||||
chr19:46879587
|
A | AAAATAAA others(21): Show |
1 | a0001c0001t0002g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-189+18382_-189+18 others(34): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | |||||
chr19:46879615
|
T | TAAATAAA others(17): Show |
1 | a0001c0001t0001g0286 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-189+18409_-189+18 others(30): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879615 | |||||
chr19:46879619
|
A | T | 4 | a0001c0001t0001g0068a0001c0001t0003g0231a0001c0001t0007g0014others(1): Show | 4 | HG03041.hp1 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-189+18410A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879619 | ||||||
chr19:46879708
|
C | T | 1 | a0001c0001t0003g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-189+18499C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879708 | ||||||
chr19:46879780
|
G | A | 18 | a0001c0001t0001g0134a0001c0001t0001g0142a0001c0001t0002g0131others(15): Show | 18 | HG01069.hp2 HG01261.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.-189+18571G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879780 | ||||||
chr19:46879784
|
C | CA | 49 | a0001c0001t0001g0189a0001c0001t0001g0197a0001c0001t0002g0273others(46): Show | 49 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-189+18593dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879784 | |||||
chr19:46879784
|
C | CAA | 6 | a0001c0001t0004g0095a0001c0001t0004g0235a0001c0001t0004g0236others(3): Show | 6 | HG00621.hp1 HG02738.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-189+18592_-189+18 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879784 | |||||
chr19:46879784
|
CA | C | 22 | a0001c0001t0001g0146a0001c0001t0002g0145a0001c0001t0002g0147others(19): Show | 22 | HG00438.hp1 HG02129.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.-189+18593delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879784 | |||||
chr19:46879833
|
C | T | 7 | a0001c0001t0003g0096a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+18624C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879833 | ||||||
chr19:46879944
|
GGCATGGT others(339): Show |
G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+18746_-189+19 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879944 | |||||
chr19:46880000
|
T | G | 1 | a0001c0001t0042g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-189+18791T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46880000 | ||||||
chr19:46880163
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-189+18954T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46880163 | ||||||
chr19:46880215
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-189+19006C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46880215 | ||||||
chr19:46880250
|
T | C | 1 | a0001c0001t0003g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-189+19041T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46880250 | ||||||
chr19:46880548
|
CTT | C | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+19341_-189+19 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46880548 | |||||
chr19:46880690
|
T | G | 1 | a0001c0001t0050g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-189+19481T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46880690 | ||||||
chr19:46880786
|
C | T | 1 | a0001c0001t0009g0290 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-189+19577C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46880786 | ||||||
chr19:46880947
|
C | CT | 34 | a0001c0001t0001g0130a0001c0001t0001g0193a0001c0001t0001g0291others(31): Show | 34 | HG00642.hp1 HG01099.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-189+19757dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46880947 | |||||
chr19:46881069
|
C | T | 1 | a0001c0001t0024g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-189+19860C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881069 | ||||||
chr19:46881168
|
C | T | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-189+19959C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881168 | ||||||
chr19:46881242
|
A | G | 56 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0004others(53): Show | 56 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-189+20033A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881242 | ||||||
chr19:46881265
|
T | C | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-189+20056T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881265 | ||||||
chr19:46881541
|
C | T | 1 | a0001c0001t0004g0022 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-189+20332C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881541 | ||||||
chr19:46881638
|
A | G | 1 | a0001c0001t0002g0149 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-189+20429A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881638 | ||||||
chr19:46881886
|
T | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0294 | 2 | NA18951.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-189+20677T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881886 | ||||||
chr19:46882026
|
G | A | 5 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0006others(2): Show | 5 | HG02015.hp2 HG02027.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189+20817G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46882026 | ||||||
chr19:46882064
|
A | G | 1 | a0001c0001t0005g0263 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-189+20855A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46882064 | ||||||
chr19:46882178
|
G | C | 1 | a0001c0001t0016g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-189+20969G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46882178 | ||||||
chr19:46882254
|
C | T | 1 | a0001c0001t0024g0032 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-189+21045C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46882254 | ||||||
chr19:46882447
|
T | C | 115 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(112): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-189+21238T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46882447 | ||||||
chr19:46882669
|
C | T | 2 | a0001c0001t0003g0098a0001c0001t0008g0097 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-189+21460C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46882669 | ||||||
chr19:46883125
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+21916C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883125 | ||||||
chr19:46883158
|
G | A | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+21949G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883158 | ||||||
chr19:46883261
|
A | AT | 69 | a0001c0001t0001g0068a0001c0001t0002g0295a0001c0001t0003g0001others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.-189+22067dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46883261 | |||||
chr19:46883274
|
T | G | 10 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 10 | HG02015.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-189+22065T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883274 | ||||||
chr19:46883442
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-189+22233G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883442 | ||||||
chr19:46883512
|
A | G | 1 | a0001c0001t0002g0272 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-189+22303A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883512 | ||||||
chr19:46883568
|
C | T | 27 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0004others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.-189+22359C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883568 | ||||||
chr19:46883607
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-189+22398G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883607 | ||||||
chr19:46883740
|
C | T | 1 | a0005c0012t0011g0261 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-189+22531C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883740 | ||||||
chr19:46883766
|
G | A | 1 | a0001c0001t0007g0017 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-189+22557G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883766 | ||||||
chr19:46883844
|
C | T | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-189+22635C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883844 | ||||||
chr19:46884003
|
C | T | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+22794C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884003 | ||||||
chr19:46884110
|
G | T | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-189+22901G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884110 | ||||||
chr19:46884116
|
A | T | 13 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0021others(10): Show | 13 | HG00639.hp1 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-189+22907A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884116 | ||||||
chr19:46884210
|
C | T | 1 | a0003c0013t0004g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-189+23001C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884210 | ||||||
chr19:46884250
|
A | G | 7 | a0001c0001t0017g0088a0001c0001t0017g0249a0001c0001t0017g0250others(4): Show | 7 | HG00597.hp1 HG02080.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+23041A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884250 | ||||||
chr19:46884408
|
A | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-189+23199A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884408 | ||||||
chr19:46884493
|
C | CT | 20 | a0001c0001t0001g0181a0001c0001t0002g0158a0001c0001t0002g0295others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-189+23307dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46884493 | |||||
chr19:46884493
|
CT | C | 11 | a0001c0001t0001g0130a0001c0001t0005g0102a0001c0001t0011g0058others(8): Show | 11 | HG00408.hp2 HG01255.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.-189+23307delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46884493 | |||||
chr19:46884516
|
T | C | 13 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(10): Show | 13 | HG00642.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-189+23307T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884516 | ||||||
chr19:46884585
|
C | T | 1 | a0001c0001t0004g0245 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-189+23376C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884585 | ||||||
chr19:46884641
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+23432C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884641 | ||||||
chr19:46884657
|
G | T | 1 | a0001c0001t0050g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-189+23448G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884657 | ||||||
chr19:46884733
|
C | T | 1 | a0001c0001t0003g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-189+23524C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884733 | ||||||
chr19:46885024
|
T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+23815T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885024 | ||||||
chr19:46885049
|
G | A | 267 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-189+23840G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885049 | ||||||
chr19:46885053
|
G | T | 1 | a0001c0001t0002g0269 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-189+23844G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885053 | ||||||
chr19:46885481
|
A | C | 1 | a0001c0001t0002g0159 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-189+24272A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885481 | ||||||
chr19:46885576
|
C | T | 5 | a0001c0001t0004g0022a0001c0001t0004g0079a0001c0001t0004g0080others(2): Show | 5 | HG02015.hp1 HG02523.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189+24367C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885576 | ||||||
chr19:46885786
|
A | G | 5 | a0001c0001t0017g0088a0001c0001t0017g0249a0001c0001t0017g0250others(2): Show | 5 | HG00597.hp1 NA18942.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189+24577A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885786 | ||||||
chr19:46885799
|
T | A | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-189+24590T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885799 | ||||||
chr19:46885941
|
T | G | 1 | a0001c0001t0044g0063 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-189+24732T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885941 | ||||||
chr19:46886056
|
C | T | 115 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(112): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-189+24847C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886056 | ||||||
chr19:46886113
|
A | G | 29 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0004others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.-189+24904A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886113 | ||||||
chr19:46886365
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+25156A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886365 | ||||||
chr19:46886381
|
G | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+25172G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886381 | ||||||
chr19:46886493
|
T | G | 1 | a0001c0001t0005g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-189+25284T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886493 | ||||||
chr19:46886529
|
C | T | 1 | a0001c0001t0005g0121 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-189+25320C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886529 | ||||||
chr19:46886602
|
T | C | 1 | a0006c0010t0004g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-189+25393T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886602 | ||||||
chr19:46886620
|
G | A | 1 | a0001c0001t0004g0078 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-189+25411G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886620 | ||||||
chr19:46886781
|
CTTA | C | 82 | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0001g0142others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-189+25573_-189+25 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886781 | ||||||
chr19:46886784
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-189+25575A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886784 | ||||||
chr19:46886903
|
T | G | 1 | a0001c0001t0042g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-189+25694T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886903 | ||||||
chr19:46887171
|
T | C | 1 | a0001c0001t0007g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-189+25962T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46887171 | ||||||
chr19:46887416
|
C | T | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-189+26207C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46887416 | ||||||
chr19:46887509
|
C | T | 2 | a0001c0001t0004g0072a0001c0001t0004g0240 | 2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-189+26300C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46887509 | ||||||
chr19:46887640
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-189+26431C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46887640 | ||||||
chr19:46887758
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-189+26549C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46887758 | ||||||
chr19:46888038
|
G | A | 1 | a0001c0001t0004g0235 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-189+26829G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888038 | ||||||
chr19:46888058
|
T | C | 35 | a0001c0001t0001g0119a0001c0001t0003g0104a0001c0001t0005g0102others(32): Show | 35 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-189+26849T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888058 | ||||||
chr19:46888096
|
C | T | 2 | a0001c0001t0005g0262a0001c0001t0008g0125 | 2 | NA18972.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-189+26887C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888096 | ||||||
chr19:46888101
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-189+26892G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888101 | ||||||
chr19:46888195
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0003g0098a0001c0001t0008g0097 | 3 | HG01256.hp1 HG01258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-189+26986G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888195 | ||||||
chr19:46888234
|
A | G | 5 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0149others(2): Show | 5 | NA18612.hp1 NA18950.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-189+27025A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888234 | ||||||
chr19:46888241
|
C | T | 5 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0149others(2): Show | 5 | NA18612.hp1 NA18950.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-189+27032C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888241 | ||||||
chr19:46888261
|
A | AAT | 14 | a0001c0001t0001g0178a0001c0001t0001g0184a0001c0001t0001g0203others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+27108_-189+27 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
A | AATAT | 12 | a0001c0001t0001g0164a0001c0001t0002g0266a0001c0001t0002g0295others(9): Show | 12 | HG01257.hp1 HG01261.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.-189+27106_-189+27 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
A | AATATAT | 6 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0096others(3): Show | 6 | HG01192.hp2 HG01496.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.-189+27104_-189+27 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
A | AATATATA others(3): Show |
3 | a0001c0001t0003g0098a0001c0001t0008g0097a0001c0001t0008g0108 | 3 | HG01256.hp1 HG01258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-189+27100_-189+27 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AAT | A | 25 | a0001c0001t0001g0068a0001c0001t0001g0168a0001c0001t0001g0170others(22): Show | 25 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-189+27108_-189+27 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATAT | A | 39 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0165others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.-189+27106_-189+27 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATAT | A | 33 | a0001c0001t0001g0146a0001c0001t0001g0153a0001c0001t0001g0171others(30): Show | 33 | HG00140.hp2 HG00621.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-189+27104_-189+27 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(1): Show |
A | 21 | a0001c0001t0001g0162a0001c0001t0001g0191a0001c0001t0001g0194others(18): Show | 21 | HG00408.hp2 HG00639.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.-189+27102_-189+27 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(3): Show |
A | 16 | a0001c0001t0001g0186a0001c0001t0002g0267a0001c0001t0003g0021others(13): Show | 16 | HG00597.hp1 HG00738.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-189+27100_-189+27 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(5): Show |
A | 13 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0202others(10): Show | 13 | HG00280.hp1 HG00733.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-189+27098_-189+27 others(18): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(7): Show |
A | 7 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0183others(4): Show | 7 | HG01255.hp2 HG01496.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+27096_-189+27 others(20): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(9): Show |
A | 5 | a0001c0001t0004g0080a0001c0001t0004g0082a0001c0001t0004g0233others(2): Show | 5 | HG01433.hp2 HG02155.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189+27094_-189+27 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(11): Show |
A | 10 | a0001c0001t0001g0169a0001c0001t0001g0278a0001c0001t0004g0022others(7): Show | 10 | HG01891.hp2 HG02015.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.-189+27092_-189+27 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(13): Show |
A | 9 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0078others(6): Show | 9 | HG00438.hp2 HG02071.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-189+27090_-189+27 others(26): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(15): Show |
A | 10 | a0001c0001t0001g0195a0001c0001t0004g0072a0001c0001t0004g0235others(7): Show | 10 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.-189+27088_-189+27 others(28): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(17): Show |
A | 6 | a0001c0001t0003g0054a0001c0001t0004g0070a0001c0001t0004g0071others(3): Show | 6 | HG02451.hp2 HG02572.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.-189+27086_-189+27 others(30): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(19): Show |
A | 7 | a0001c0001t0034g0111a0001c0001t0038g0252a0001c0002t0006g0207others(4): Show | 7 | HG00642.hp1 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-189+27084_-189+27 others(32): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(21): Show |
A | 12 | a0001c0001t0005g0102a0001c0001t0007g0019a0001c0001t0024g0032others(9): Show | 12 | HG01243.hp2 HG01255.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-189+27082_-189+27 others(34): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(23): Show |
A | 9 | a0001c0001t0001g0134a0001c0001t0001g0181a0001c0001t0002g0137others(6): Show | 9 | HG02055.hp1 HG02280.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.-189+27080_-189+27 others(36): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(25): Show |
A | 1 | a0001c0001t0005g0123 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-189+27078_-189+27 others(38): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(27): Show |
A | 2 | a0001c0001t0030g0277a0001c0002t0053g0127 | 2 | HG02257.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-189+27076_-189+27 others(40): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(29): Show |
A | 2 | a0001c0002t0001g0033a0001c0011t0002g0274 | 2 | HG02886.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-189+27074_-189+27 others(42): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888261
|
AATATATA others(33): Show |
A | 1 | a0001c0001t0020g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-189+27070_-189+27 others(46): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | |||||
chr19:46888315
|
T | A | 1 | a0001c0001t0027g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-189+27106T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888315 | ||||||
chr19:46888317
|
T | A | 2 | a0001c0001t0001g0284a0001c0001t0016g0094 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-189+27108T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888317 | ||||||
chr19:46888333
|
T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+27124T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888333 | ||||||
chr19:46888333
|
T | TAC | 24 | a0001c0001t0001g0130a0001c0001t0001g0153a0001c0001t0001g0165others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.-189+27155_-189+27 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888333 | |||||
chr19:46888333
|
T | TACAC | 15 | a0001c0001t0027g0034a0001c0001t0027g0221a0001c0002t0006g0207others(12): Show | 15 | HG00642.hp1 HG01243.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-189+27153_-189+27 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888333 | |||||
chr19:46888333
|
T | TACACAC | 4 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0283others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-189+27151_-189+27 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888333 | |||||
chr19:46888333
|
TAC | T | 103 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(100): Show | 103 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.-189+27155_-189+27 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888333 | |||||
chr19:46888333
|
TACAC | T | 22 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0078others(19): Show | 22 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-189+27153_-189+27 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888333 | |||||
chr19:46888333
|
TACACACA others(3): Show |
T | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+27147_-189+27 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888333 | |||||
chr19:46888365
|
C | CA | 3 | a0001c0001t0001g0203a0001c0001t0002g0154a0001c0001t0009g0290 | 3 | HG01099.hp2 NA18943.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-189+27156_-189+27 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888365 | ||||||
chr19:46888540
|
A | ATT | 5 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0149others(2): Show | 5 | NA18612.hp1 NA18950.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-189+27334_-189+27 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888540 | |||||
chr19:46888746
|
C | T | 1 | a0001c0001t0002g0148 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-189+27537C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888746 | ||||||
chr19:46888829
|
T | C | 31 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(28): Show | 31 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.-189+27620T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888829 | ||||||
chr19:46888837
|
C | CA | 49 | a0001c0001t0001g0167a0001c0001t0001g0193a0001c0001t0002g0137others(46): Show | 49 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-189+27650dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888837 | |||||
chr19:46888837
|
C | CAA | 7 | a0001c0001t0002g0273a0001c0001t0004g0081a0001c0001t0004g0095others(4): Show | 7 | HG00621.hp1 HG01891.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-189+27649_-189+27 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888837 | |||||
chr19:46888837
|
CA | C | 22 | a0001c0001t0001g0142a0001c0001t0001g0172a0001c0001t0001g0173others(19): Show | 22 | HG01069.hp2 HG01261.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-189+27650delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888837 | |||||
chr19:46888837
|
CAAAAAAA | C | 6 | a0001c0001t0003g0054a0001c0001t0018g0040a0001c0001t0018g0227others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-189+27644_-189+27 others(13): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888837 | |||||
chr19:46888837
|
CAAAAAAA others(2): Show |
C | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+27642_-189+27 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888837 | |||||
chr19:46888891
|
A | G | 1 | a0001c0001t0005g0120 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-189+27682A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888891 | ||||||
chr19:46888957
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-189+27748G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888957 | ||||||
chr19:46889045
|
A | G | 200 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(197): Show | 200 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.-189+27836A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46889045 | ||||||
chr19:46889068
|
C | T | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+27859C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46889068 | ||||||
chr19:46889328
|
G | A | 2 | a0001c0001t0024g0032a0001c0001t0024g0220 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-189+28119G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46889328 | ||||||
chr19:46889487
|
T | A | 165 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(162): Show | 165 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.-189+28278T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46889487 | ||||||
chr19:46889534
|
C | T | 1 | a0001c0001t0004g0071 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-189+28325C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46889534 | ||||||
chr19:46889750
|
C | CA | 152 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0286others(149): Show | 152 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.-189+28562dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46889750 | |||||
chr19:46889750
|
C | CAA | 6 | a0001c0001t0004g0095a0001c0001t0005g0262a0001c0001t0018g0227others(3): Show | 6 | HG02622.hp1 HG02738.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.-189+28561_-189+28 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46889750 | |||||
chr19:46890087
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-188-28401A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46890087 | ||||||
chr19:46890267
|
T | G | 1 | a0001c0001t0003g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-188-28221T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46890267 | ||||||
chr19:46890535
|
T | C | 4 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0283others(1): Show | 4 | HG01099.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-188-27953T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46890535 | ||||||
chr19:46890752
|
G | T | 11 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(8): Show | 11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-188-27736G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46890752 | ||||||
chr19:46891274
|
T | G | 1 | a0001c0001t0024g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-188-27214T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891274 | ||||||
chr19:46891421
|
G | GT | 10 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0003g0021others(7): Show | 10 | HG01255.hp1 HG02258.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-188-27055dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46891421 | |||||
chr19:46891431
|
T | G | 54 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(51): Show | 54 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-188-27057T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891431 | ||||||
chr19:46891434
|
G | T | 2 | a0001c0001t0003g0061a0001c0001t0018g0227 | 2 | HG04115.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-188-27054G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891434 | ||||||
chr19:46891459
|
G | T | 1 | a0001c0001t0002g0275 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-188-27029G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891459 | ||||||
chr19:46891508
|
C | A | 1 | a0001c0001t0004g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-188-26980C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891508 | ||||||
chr19:46891586
|
C | G | 1 | a0001c0001t0022g0074 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-188-26902C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891586 | ||||||
chr19:46891635
|
C | T | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG01261.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-188-26853C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891635 | ||||||
chr19:46891638
|
G | A | 3 | a0001c0001t0001g0142a0001c0001t0002g0265a0001c0001t0009g0268 | 3 | HG02135.hp1 NA18612.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-188-26850G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891638 | ||||||
chr19:46891749
|
T | C | 5 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0185others(2): Show | 5 | HG01433.hp1 HG01928.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-188-26739T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891749 | ||||||
chr19:46891790
|
A | G | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-26698A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891790 | ||||||
chr19:46891968
|
C | A | 1 | a0001c0001t0009g0270 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-188-26520C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891968 | ||||||
chr19:46892026
|
A | C | 187 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(184): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-188-26462A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892026 | ||||||
chr19:46892101
|
C | T | 1 | a0001c0001t0025g0062 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-188-26387C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892101 | ||||||
chr19:46892123
|
T | TA | 49 | a0001c0001t0001g0173a0001c0001t0001g0176a0001c0001t0001g0182others(46): Show | 49 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-188-26341dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892123 | |||||
chr19:46892123
|
TA | T | 7 | a0001c0001t0002g0265a0001c0001t0004g0030a0001c0001t0004g0235others(4): Show | 7 | HG00099.hp1 HG02071.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-26341delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892123 | |||||
chr19:46892124
|
A | G | 1 | a0001c0001t0004g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-188-26364A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892124 | ||||||
chr19:46892140
|
A | G | 3 | a0001c0001t0003g0050a0001c0001t0003g0064a0001c0001t0003g0224 | 3 | HG00738.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-188-26348A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892140 | ||||||
chr19:46892148
|
G | A | 3 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0042g0026 | 3 | HG01070.hp1 HG01071.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-188-26340G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892148 | ||||||
chr19:46892156
|
A | T | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-188-26332A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892156 | ||||||
chr19:46892282
|
G | A | 32 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(29): Show | 32 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.-188-26206G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892282 | ||||||
chr19:46892302
|
C | CA | 10 | a0001c0001t0003g0045a0001c0001t0012g0255a0001c0001t0015g0037others(7): Show | 10 | HG01261.hp1 HG02145.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-188-26172dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892302 | |||||
chr19:46892334
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-188-26154G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892334 | ||||||
chr19:46892366
|
T | G | 1 | a0001c0001t0001g0173 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-188-26122T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892366 | ||||||
chr19:46892420
|
A | G | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-188-26068A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892420 | ||||||
chr19:46892468
|
C | CA | 53 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(50): Show | 53 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-188-25999dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892468 | |||||
chr19:46892468
|
CA | C | 6 | a0001c0001t0001g0283a0001c0001t0002g0148a0001c0001t0003g0096others(3): Show | 6 | HG01257.hp2 HG01496.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-188-25999delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892468 | |||||
chr19:46892621
|
A | G | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-25867A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892621 | ||||||
chr19:46892646
|
C | CT | 7 | a0001c0001t0001g0190a0001c0001t0002g0266a0001c0001t0002g0275others(4): Show | 7 | HG01192.hp1 HG01261.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-188-25825dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892646 | |||||
chr19:46892646
|
CT | C | 120 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0179others(117): Show | 120 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-188-25825delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892646 | |||||
chr19:46892663
|
T | C | 1 | a0001c0001t0038g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-188-25825T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892663 | ||||||
chr19:46892702
|
T | C | 1 | a0001c0001t0056g0090 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-188-25786T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892702 | ||||||
chr19:46892776
|
G | A | 1 | a0006c0010t0004g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-188-25712G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892776 | ||||||
chr19:46892940
|
T | C | 5 | a0001c0001t0017g0088a0001c0001t0017g0249a0001c0001t0017g0250others(2): Show | 5 | HG00597.hp1 NA18942.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.-188-25548T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892940 | ||||||
chr19:46893615
|
C | A | 1 | a0001c0002t0006g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-188-24873C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46893615 | ||||||
chr19:46893780
|
T | C | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-24708T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46893780 | ||||||
chr19:46893886
|
C | CT | 31 | a0001c0001t0001g0119a0001c0001t0001g0285a0001c0001t0002g0265others(28): Show | 31 | HG00735.hp2 HG01070.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.-188-24583dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46893886 | |||||
chr19:46893886
|
CT | C | 26 | a0001c0001t0001g0177a0001c0001t0001g0184a0001c0001t0001g0193others(23): Show | 26 | HG00408.hp1 HG01070.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.-188-24583delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46893886 | |||||
chr19:46893915
|
A | G | 188 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(185): Show | 188 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.-188-24573A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46893915 | ||||||
chr19:46893932
|
T | C | 35 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(32): Show | 35 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-188-24556T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46893932 | ||||||
chr19:46894216
|
C | T | 1 | a0001c0001t0048g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-188-24272C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894216 | ||||||
chr19:46894238
|
C | T | 25 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0048others(22): Show | 25 | HG00408.hp2 HG00642.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-188-24250C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894238 | ||||||
chr19:46894332
|
T | G | 1 | a0001c0001t0004g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-188-24156T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894332 | ||||||
chr19:46894445
|
G | GT | 24 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0185others(21): Show | 24 | HG00621.hp2 HG00733.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-188-24024dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46894445 | |||||
chr19:46894445
|
GT | G | 141 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0282others(138): Show | 141 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.-188-24024delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46894445 | |||||
chr19:46894448
|
T | G | 1 | a0001c0001t0001g0193 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-188-24040T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894448 | ||||||
chr19:46894454
|
T | C | 1 | a0001c0001t0003g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-188-24034T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894454 | ||||||
chr19:46894465
|
G | T | 1 | a0001c0001t0002g0161 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-188-24023G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894465 | ||||||
chr19:46894476
|
C | T | 2 | a0001c0001t0005g0106a0001c0001t0005g0107 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-188-24012C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894476 | ||||||
chr19:46894509
|
G | A | 1 | a0001c0001t0049g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-188-23979G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894509 | ||||||
chr19:46894677
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-188-23811C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894677 | ||||||
chr19:46894967
|
C | A | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-188-23521C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894967 | ||||||
chr19:46895103
|
A | G | 1 | a0004c0008t0015g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-188-23385A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895103 | ||||||
chr19:46895165
|
C | CT | 10 | a0001c0001t0002g0158a0001c0001t0003g0051a0001c0001t0003g0061others(7): Show | 10 | HG02738.hp1 HG03130.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.-188-23307dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46895165 | |||||
chr19:46895257
|
G | A | 1 | a0001c0001t0004g0233 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-188-23231G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895257 | ||||||
chr19:46895288
|
C | T | 1 | a0001c0001t0038g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-188-23200C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895288 | ||||||
chr19:46895416
|
C | T | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-188-23072C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895416 | ||||||
chr19:46895542
|
T | C | 1 | a0001c0001t0012g0113 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-188-22946T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895542 | ||||||
chr19:46895619
|
A | G | 1 | a0001c0009t0010g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-188-22869A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895619 | ||||||
chr19:46895794
|
C | T | 50 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-188-22694C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895794 | ||||||
chr19:46895878
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-188-22610G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895878 | ||||||
chr19:46896014
|
A | G | 46 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(43): Show | 46 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.-188-22474A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896014 | ||||||
chr19:46896102
|
C | CA | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-22377dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46896102 | |||||
chr19:46896132
|
A | G | 187 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(184): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-188-22356A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896132 | ||||||
chr19:46896202
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0003g0231a0001c0001t0025g0067 | 3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-188-22286C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896202 | ||||||
chr19:46896288
|
G | A | 2 | a0001c0001t0002g0200a0001c0001t0002g0293 | 2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-188-22200G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896288 | ||||||
chr19:46896298
|
G | A | 13 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(10): Show | 13 | HG00597.hp1 HG02080.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-188-22190G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896298 | ||||||
chr19:46896503
|
C | G | 3 | a0001c0001t0024g0032a0001c0001t0024g0220a0001c0001t0038g0252 | 3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-188-21985C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896503 | ||||||
chr19:46896526
|
A | G | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-21962A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896526 | ||||||
chr19:46896734
|
A | T | 15 | a0001c0001t0001g0134a0001c0001t0002g0131a0001c0001t0002g0132others(12): Show | 15 | HG01069.hp2 HG01261.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-188-21754A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896734 | ||||||
chr19:46896810
|
A | G | 35 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(32): Show | 35 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-188-21678A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896810 | ||||||
chr19:46896955
|
G | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-21533G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896955 | ||||||
chr19:46897060
|
A | AT | 36 | a0001c0001t0001g0146a0001c0001t0001g0191a0001c0001t0001g0194others(33): Show | 36 | HG00408.hp2 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.-188-21409dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46897060 | |||||
chr19:46897060
|
AT | A | 51 | a0001c0001t0002g0265a0001c0001t0004g0022a0001c0001t0004g0030others(48): Show | 51 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-188-21409delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46897060 | |||||
chr19:46897089
|
A | G | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-188-21399A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46897089 | ||||||
chr19:46897145
|
C | T | 1 | a0005c0012t0011g0261 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-188-21343C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46897145 | ||||||
chr19:46897189
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-188-21299G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46897189 | ||||||
chr19:46897407
|
T | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-188-21081T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46897407 | ||||||
chr19:46897447
|
C | CT | 41 | a0001c0001t0002g0161a0001c0001t0004g0022a0001c0001t0004g0030others(38): Show | 41 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.-188-21026dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46897447 | |||||
chr19:46897447
|
CT | C | 7 | a0001c0001t0001g0198a0001c0001t0001g0283a0001c0001t0007g0015others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-188-21026delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46897447 | |||||
chr19:46897462
|
T | C | 1 | a0001c0001t0007g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-188-21026T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46897462 | ||||||
chr19:46897681
|
G | A | 1 | a0001c0009t0010g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-188-20807G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46897681 | ||||||
chr19:46897695
|
C | CA | 115 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0189others(112): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-188-20778dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46897695 | |||||
chr19:46898098
|
C | T | 7 | a0001c0001t0003g0096a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-20390C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898098 | ||||||
chr19:46898206
|
C | T | 1 | a0001c0001t0038g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-188-20282C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898206 | ||||||
chr19:46898214
|
C | G | 3 | a0001c0001t0001g0068a0001c0001t0003g0231a0001c0001t0025g0067 | 3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-188-20274C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898214 | ||||||
chr19:46898240
|
C | CA | 12 | a0001c0001t0001g0282a0001c0001t0003g0065a0001c0001t0010g0052others(9): Show | 12 | HG01243.hp2 HG01928.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.-188-20233dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46898240 | |||||
chr19:46898249
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-188-20239A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898249 | ||||||
chr19:46898256
|
C | A | 7 | a0001c0001t0017g0088a0001c0001t0017g0249a0001c0001t0017g0250others(4): Show | 7 | HG00597.hp1 HG02080.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-20232C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898256 | ||||||
chr19:46898452
|
G | A | 8 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0015others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-188-20036G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898452 | ||||||
chr19:46898552
|
T | C | 15 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(12): Show | 15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-188-19936T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898552 | ||||||
chr19:46898744
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-188-19744G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898744 | ||||||
chr19:46898775
|
A | AGCT | 52 | a0001c0001t0001g0192a0001c0001t0003g0001a0001c0001t0003g0002others(49): Show | 52 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-188-19678_-188-19 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46898775 | |||||
chr19:46898775
|
A | AGCTGCT | 4 | a0001c0001t0001g0173a0001c0001t0003g0012a0001c0001t0004g0233others(1): Show | 4 | HG02004.hp1 HG02155.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.-188-19681_-188-19 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46898775 | |||||
chr19:46898775
|
AGCTGCT | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0289 | 3 | HG00621.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-188-19681_-188-19 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46898775 | |||||
chr19:46898775
|
AGCTGCTG others(11): Show |
A | 1 | a0001c0001t0001g0284 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-188-19693_-188-19 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46898775 | |||||
chr19:46899017
|
T | A | 3 | a0001c0001t0011g0057a0001c0001t0011g0058a0001c0001t0011g0059 | 3 | HG02622.hp2 HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-188-19471T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899017 | ||||||
chr19:46899106
|
G | A | 1 | a0001c0001t0003g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-188-19382G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899106 | ||||||
chr19:46899132
|
T | C | 1 | a0001c0001t0003g0004 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-188-19356T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899132 | ||||||
chr19:46899247
|
C | T | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG01261.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-188-19241C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899247 | ||||||
chr19:46899277
|
A | G | 1 | a0001c0001t0003g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-188-19211A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899277 | ||||||
chr19:46899329
|
T | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0283 | 3 | HG01257.hp2 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-188-19159T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899329 | ||||||
chr19:46899432
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-188-19056C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899432 | ||||||
chr19:46899517
|
A | C | 32 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(29): Show | 32 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.-188-18971A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899517 | ||||||
chr19:46899628
|
AGGT | A | 4 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-18859_-188-18 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899628 | ||||||
chr19:46899646
|
G | C | 2 | a0001c0001t0024g0032a0001c0001t0024g0220 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-188-18842G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899646 | ||||||
chr19:46899648
|
C | T | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-188-18840C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899648 | ||||||
chr19:46899698
|
C | CA | 53 | a0001c0001t0001g0203a0001c0001t0002g0264a0001c0001t0004g0022others(50): Show | 53 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-188-18781dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46899698 | |||||
chr19:46899726
|
C | T | 1 | a0001c0001t0052g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-188-18762C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899726 | ||||||
chr19:46900097
|
T | C | 1 | a0001c0001t0005g0118 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-188-18391T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900097 | ||||||
chr19:46900222
|
G | GT | 65 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0172others(62): Show | 65 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.-188-18249dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46900222 | |||||
chr19:46900222
|
G | GTT | 27 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0048others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-188-18250_-188-18 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46900222 | |||||
chr19:46900222
|
G | GTTT | 6 | a0001c0001t0003g0065a0001c0001t0013g0049a0001c0001t0013g0226others(3): Show | 6 | HG00408.hp2 HG00642.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-188-18251_-188-18 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46900222 | |||||
chr19:46900239
|
T | G | 1 | a0001c0001t0020g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-188-18249T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900239 | ||||||
chr19:46900290
|
C | T | 165 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(162): Show | 165 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.-188-18198C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900290 | ||||||
chr19:46900441
|
G | A | 4 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-18047G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900441 | ||||||
chr19:46900483
|
A | G | 3 | a0001c0001t0004g0070a0001c0001t0004g0071a0001c0001t0032g0232 | 3 | NA18969.hp1 NA18982.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-188-18005A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900483 | ||||||
chr19:46900581
|
A | G | 1 | a0001c0001t0044g0063 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-188-17907A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900581 | ||||||
chr19:46900597
|
T | C | 188 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0189others(185): Show | 188 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.-188-17891T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900597 | ||||||
chr19:46900598
|
G | A | 2 | a0001c0001t0004g0237a0001c0001t0004g0242 | 2 | HG00408.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.-188-17890G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900598 | ||||||
chr19:46900768
|
G | GA | 188 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0189others(185): Show | 188 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.-188-17710dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46900768 | |||||
chr19:46900831
|
G | A | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-188-17657G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900831 | ||||||
chr19:46901299
|
T | G | 1 | a0001c0001t0003g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-188-17189T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46901299 | ||||||
chr19:46901754
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-188-16734G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46901754 | ||||||
chr19:46901777
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-188-16711T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46901777 | ||||||
chr19:46901919
|
C | G | 1 | a0001c0001t0054g0287 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-188-16569C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46901919 | ||||||
chr19:46901922
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-188-16566G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46901922 | ||||||
chr19:46902681
|
T | G | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-15807T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46902681 | ||||||
chr19:46902725
|
T | A | 2 | a0001c0001t0004g0072a0001c0001t0004g0240 | 2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-188-15763T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46902725 | ||||||
chr19:46902749
|
A | G | 1 | a0001c0001t0007g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-188-15739A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46902749 | ||||||
chr19:46902829
|
C | T | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-15659C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46902829 | ||||||
chr19:46902891
|
T | G | 1 | a0001c0001t0001g0286 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-188-15597T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46902891 | ||||||
chr19:46903193
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-188-15295T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903193 | ||||||
chr19:46903368
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-188-15120C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903368 | ||||||
chr19:46903429
|
G | A | 1 | a0001c0011t0002g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-188-15059G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903429 | ||||||
chr19:46903479
|
G | A | 1 | a0001c0007t0015g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-188-15009G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903479 | ||||||
chr19:46903585
|
G | C | 3 | a0001c0001t0024g0032a0001c0001t0024g0220a0001c0001t0038g0252 | 3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-188-14903G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903585 | ||||||
chr19:46903674
|
A | G | 1 | a0001c0001t0038g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-188-14814A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903674 | ||||||
chr19:46903685
|
G | A | 7 | a0001c0001t0015g0037a0001c0001t0023g0039a0001c0001t0023g0055others(4): Show | 7 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-14803G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903685 | ||||||
chr19:46903791
|
T | C | 1 | a0001c0001t0012g0113 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-188-14697T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903791 | ||||||
chr19:46903899
|
G | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-14589G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903899 | ||||||
chr19:46903950
|
G | C | 3 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0042g0026 | 3 | HG01070.hp1 HG01071.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-188-14538G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903950 | ||||||
chr19:46904159
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-188-14329C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904159 | ||||||
chr19:46904239
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-188-14249C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904239 | ||||||
chr19:46904445
|
G | A | 1 | a0001c0001t0015g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-188-14043G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904445 | ||||||
chr19:46904499
|
G | A | 14 | a0001c0001t0001g0130a0001c0001t0001g0160a0001c0001t0001g0162others(11): Show | 14 | HG00733.hp2 HG00738.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-188-13989G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904499 | ||||||
chr19:46904815
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-188-13673G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904815 | ||||||
chr19:46904850
|
G | A | 2 | a0001c0001t0003g0253a0001c0001t0007g0014 | 2 | HG00733.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-188-13638G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904850 | ||||||
chr19:46904910
|
C | T | 115 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(112): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-188-13578C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904910 | ||||||
chr19:46904938
|
G | A | 1 | a0001c0001t0007g0017 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-188-13550G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904938 | ||||||
chr19:46904947
|
G | A | 1 | a0001c0001t0029g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-188-13541G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904947 | ||||||
chr19:46905251
|
G | C | 115 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(112): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-188-13237G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905251 | ||||||
chr19:46905253
|
C | T | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-188-13235C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905253 | ||||||
chr19:46905270
|
A | G | 2 | a0001c0001t0009g0143a0001c0001t0009g0270 | 2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-188-13218A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905270 | ||||||
chr19:46905288
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-188-13200G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905288 | ||||||
chr19:46905372
|
CT | C | 8 | a0001c0001t0001g0160a0001c0001t0001g0184a0001c0001t0001g0204others(5): Show | 8 | HG00735.hp1 HG01099.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-188-13097delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46905372 | |||||
chr19:46905391
|
T | A | 116 | a0001c0001t0001g0119a0001c0001t0003g0031a0001c0001t0003g0104others(113): Show | 116 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.-188-13097T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905391 | ||||||
chr19:46905391
|
T | TA | 71 | a0001c0001t0001g0068a0001c0001t0003g0001a0001c0001t0003g0002others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.-188-13095dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46905391 | |||||
chr19:46905435
|
G | T | 50 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-188-13053G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905435 | ||||||
chr19:46905475
|
A | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-13013A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905475 | ||||||
chr19:46905504
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-188-12984T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905504 | ||||||
chr19:46905537
|
A | G | 1 | a0001c0001t0002g0141 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-188-12951A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905537 | ||||||
chr19:46905555
|
A | AC | 48 | a0001c0001t0001g0146a0001c0001t0001g0165a0001c0001t0001g0170others(45): Show | 48 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-188-12921dupC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46905555 | |||||
chr19:46905555
|
A | ACC | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0194others(10): Show | 13 | HG00621.hp2 HG02055.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.-188-12922_-188-12 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46905555 | |||||
chr19:46905557
|
C | CG | 10 | a0001c0001t0003g0009a0001c0001t0005g0263a0001c0001t0010g0052others(7): Show | 10 | HG00639.hp2 HG00642.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.-188-12931_-188-12 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905557 | ||||||
chr19:46905558
|
C | G | 105 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.-188-12930C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905558 | ||||||
chr19:46905562
|
C | CG | 32 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(29): Show | 32 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.-188-12926_-188-12 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905562 | ||||||
chr19:46905563
|
C | G | 2 | a0001c0001t0019g0024a0001c0001t0019g0219 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-188-12925C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905563 | ||||||
chr19:46905565
|
C | G | 1 | a0001c0001t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-188-12923C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905565 | ||||||
chr19:46905566
|
C | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0021 | 2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-188-12922C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905566 | ||||||
chr19:46905612
|
C | A | 1 | a0001c0001t0038g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-188-12876C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905612 | ||||||
chr19:46905740
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-188-12748C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905740 | ||||||
chr19:46905805
|
G | C | 1 | a0001c0001t0004g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-188-12683G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905805 | ||||||
chr19:46905830
|
G | A | 32 | a0001c0001t0001g0119a0001c0001t0003g0104a0001c0001t0005g0102others(29): Show | 32 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-188-12658G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905830 | ||||||
chr19:46906032
|
A | G | 7 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-12456A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906032 | ||||||
chr19:46906367
|
A | T | 3 | a0001c0001t0001g0205a0001c0001t0026g0187a0001c0001t0026g0288 | 3 | HG00558.hp2 HG00597.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-188-12121A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906367 | ||||||
chr19:46906491
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-188-11997C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906491 | ||||||
chr19:46906518
|
A | C | 1 | a0001c0001t0002g0150 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-188-11970A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906518 | ||||||
chr19:46906549
|
C | T | 2 | a0001c0001t0005g0256a0001c0001t0049g0225 | 2 | HG04204.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-188-11939C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906549 | ||||||
chr19:46906851
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-188-11637G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906851 | ||||||
chr19:46906870
|
C | A | 1 | a0001c0001t0002g0158 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-188-11618C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906870 | ||||||
chr19:46906887
|
G | A | 7 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-11601G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906887 | ||||||
chr19:46906932
|
T | A | 2 | a0001c0001t0040g0029a0001c0001t0041g0028 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-188-11556T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906932 | ||||||
chr19:46906950
|
G | A | 11 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(8): Show | 11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-188-11538G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906950 | ||||||
chr19:46907091
|
A | G | 3 | a0001c0001t0014g0087a0001c0001t0014g0247a0001c0001t0014g0248 | 3 | HG02559.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-188-11397A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46907091 | ||||||
chr19:46907478
|
T | TTTTG | 118 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0189others(115): Show | 118 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.-188-10986_-188-10 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46907478 | |||||
chr19:46907767
|
G | A | 5 | a0001c0001t0004g0022a0001c0001t0004g0079a0001c0001t0004g0080others(2): Show | 5 | HG02015.hp1 HG02523.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.-188-10721G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46907767 | ||||||
chr19:46908080
|
T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-188-10408T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46908080 | ||||||
chr19:46908173
|
T | G | 1 | a0001c0001t0004g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-188-10315T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46908173 | ||||||
chr19:46908189
|
T | A | 2 | a0001c0001t0009g0143a0001c0001t0009g0270 | 2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-188-10299T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46908189 | ||||||
chr19:46908482
|
TTTG | T | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-9997_-188-999 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46908482 | |||||
chr19:46908793
|
C | T | 4 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-9695C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46908793 | ||||||
chr19:46908967
|
T | C | 115 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(112): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-188-9521T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46908967 | ||||||
chr19:46909054
|
CTT | C | 22 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0027g0034others(19): Show | 22 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-188-9432_-188-943 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46909054 | |||||
chr19:46909079
|
C | T | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-9409C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909079 | ||||||
chr19:46909149
|
A | T | 1 | a0001c0001t0033g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-188-9339A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909149 | ||||||
chr19:46909164
|
G | A | 1 | a0001c0001t0037g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-188-9324G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909164 | ||||||
chr19:46909346
|
C | T | 2 | a0001c0001t0002g0154a0001c0001t0002g0264 | 2 | NA18968.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-188-9142C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909346 | ||||||
chr19:46909365
|
C | T | 1 | a0001c0001t0003g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-188-9123C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909365 | ||||||
chr19:46909416
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-188-9072T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909416 | ||||||
chr19:46909468
|
A | G | 1 | a0001c0001t0025g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-188-9020A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909468 | ||||||
chr19:46909487
|
C | G | 1 | a0001c0001t0004g0235 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-188-9001C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909487 | ||||||
chr19:46909495
|
G | A | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-8993G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909495 | ||||||
chr19:46909659
|
C | T | 1 | a0006c0010t0004g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-188-8829C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909659 | ||||||
chr19:46909727
|
T | G | 2 | a0001c0001t0004g0072a0001c0001t0004g0240 | 2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-188-8761T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909727 | ||||||
chr19:46910017
|
C | T | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-8471C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910017 | ||||||
chr19:46910030
|
T | A | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-188-8458T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910030 | ||||||
chr19:46910456
|
G | A | 50 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-188-8032G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910456 | ||||||
chr19:46910467
|
T | C | 1 | a0001c0001t0004g0076 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-188-8021T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910467 | ||||||
chr19:46910685
|
G | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-7803G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910685 | ||||||
chr19:46910752
|
G | A | 2 | a0001c0001t0026g0187a0001c0001t0026g0288 | 2 | HG00558.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.-188-7736G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910752 | ||||||
chr19:46910918
|
C | G | 4 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-7570C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910918 | ||||||
chr19:46911059
|
G | A | 1 | a0001c0007t0015g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-188-7429G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46911059 | ||||||
chr19:46911327
|
C | A | 4 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-7161C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46911327 | ||||||
chr19:46911567
|
G | A | 1 | a0001c0002t0006g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-188-6921G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46911567 | ||||||
chr19:46911729
|
G | A | 253 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(250): Show | 253 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.-188-6759G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46911729 | ||||||
chr19:46911767
|
C | G | 1 | a0001c0001t0004g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-188-6721C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46911767 | ||||||
chr19:46912065
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-188-6423C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912065 | ||||||
chr19:46912179
|
G | T | 1 | a0001c0009t0010g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-188-6309G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912179 | ||||||
chr19:46912514
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-188-5974C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912514 | ||||||
chr19:46912608
|
G | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | NA19004.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-188-5880G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912608 | ||||||
chr19:46912659
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-188-5829T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912659 | ||||||
chr19:46912721
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-188-5767A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912721 | ||||||
chr19:46912722
|
T | A | 49 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(46): Show | 49 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-188-5766T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912722 | ||||||
chr19:46912983
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-188-5505C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912983 | ||||||
chr19:46913126
|
T | C | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-188-5362T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46913126 | ||||||
chr19:46913177
|
G | T | 4 | a0001c0001t0004g0072a0001c0001t0004g0240a0001c0001t0004g0241others(1): Show | 4 | HG00558.hp1 NA18978.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-188-5311G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46913177 | ||||||
chr19:46913232
|
C | T | 1 | a0001c0001t0016g0094 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-188-5256C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46913232 | ||||||
chr19:46913353
|
C | T | 34 | a0001c0001t0001g0119a0001c0001t0003g0104a0001c0001t0005g0102others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-188-5135C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46913353 | ||||||
chr19:46914023
|
AATGT | A | 5 | a0001c0001t0007g0013a0001c0001t0007g0016a0001c0001t0007g0017others(2): Show | 5 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-188-4462_-188-445 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46914023 | |||||
chr19:46914110
|
G | A | 1 | a0001c0001t0004g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-188-4378G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46914110 | ||||||
chr19:46914444
|
C | A | 1 | a0001c0001t0050g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-188-4044C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46914444 | ||||||
chr19:46914446
|
A | AAAT | 12 | a0001c0001t0005g0118a0001c0001t0014g0069a0001c0001t0014g0087others(9): Show | 12 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-188-4024_-188-402 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46914446 | |||||
chr19:46914446
|
AAAT | A | 5 | a0001c0001t0015g0037a0001c0001t0023g0039a0001c0001t0023g0055others(2): Show | 5 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-188-4024_-188-402 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46914446 | |||||
chr19:46914701
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-188-3787T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46914701 | ||||||
chr19:46914894
|
C | T | 1 | a0001c0001t0052g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-188-3594C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46914894 | ||||||
chr19:46915338
|
G | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-3150G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46915338 | ||||||
chr19:46915455
|
A | G | 2 | a0001c0001t0007g0015a0001c0001t0007g0019 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-188-3033A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46915455 | ||||||
chr19:46915499
|
C | T | 1 | a0001c0001t0009g0268 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-188-2989C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46915499 | ||||||
chr19:46915791
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0283 | 3 | HG01257.hp2 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-188-2697G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46915791 | ||||||
chr19:46915929
|
C | CT | 22 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0152others(19): Show | 22 | HG00438.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-188-2535dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46915929 | |||||
chr19:46915929
|
C | CTT | 7 | a0001c0001t0004g0078a0001c0001t0017g0088a0001c0001t0017g0249others(4): Show | 7 | HG00597.hp1 HG02080.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-2536_-188-253 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46915929 | |||||
chr19:46915929
|
CT | C | 10 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0169others(7): Show | 10 | HG00733.hp1 HG00733.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.-188-2535delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46915929 | |||||
chr19:46915993
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-188-2495T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46915993 | ||||||
chr19:46916380
|
A | G | 2 | a0001c0001t0024g0032a0001c0001t0024g0220 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-188-2108A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46916380 | ||||||
chr19:46916382
|
T | TCTGTCCC others(311): Show |
1 | a0001c0001t0057g0091 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-188-2091_-188-209 others(322): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916382 | |||||
chr19:46916382
|
T | TCTGTCCC others(312): Show |
14 | a0001c0001t0004g0030a0001c0001t0016g0089a0001c0001t0016g0092others(11): Show | 14 | HG00597.hp1 HG01891.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.-188-2091_-188-209 others(323): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916382 | |||||
chr19:46916382
|
T | TCTGTCCC others(313): Show |
30 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(27): Show | 30 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.-188-2091_-188-209 others(324): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916382 | |||||
chr19:46916382
|
T | TCTGTCCC others(314): Show |
5 | a0001c0001t0004g0081a0001c0001t0004g0085a0001c0001t0004g0245others(2): Show | 5 | HG02523.hp2 HG02630.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.-188-2091_-188-209 others(325): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916382 | |||||
chr19:46916646
|
A | ATT | 48 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(45): Show | 48 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-188-1834_-188-183 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916646 | |||||
chr19:46916727
|
A | AT | 49 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(46): Show | 49 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-188-1750dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916727 | |||||
chr19:46916727
|
AT | A | 117 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0170others(114): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-188-1750delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916727 | |||||
chr19:46917033
|
C | A | 15 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(12): Show | 15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-188-1455C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46917033 | ||||||
chr19:46917623
|
A | C | 1 | a0001c0001t0003g0001 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-188-865A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46917623 | ||||||
chr19:46917721
|
T | G | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-767T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46917721 | ||||||
chr19:46917806
|
C | G | 1 | a0001c0001t0037g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-188-682C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46917806 | ||||||
chr19:46917956
|
C | T | 1 | a0001c0001t0021g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-188-532C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46917956 | ||||||
chr19:46917994
|
G | A | 31 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(28): Show | 31 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.-188-494G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46917994 | ||||||
chr19:46918066
|
G | T | 272 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(269): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.-188-422G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46918066 | ||||||
chr19:46918349
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0003g0231a0001c0001t0025g0067 | 3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-188-139C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46918349 | ||||||
chr19:46922450
|
T | TA | 11 | a0001c0001t0002g0137a0001c0001t0002g0140a0001c0001t0002g0276others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.3681+104dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46922450 | |||||
chr19:46922488
|
A | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+132A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46922488 | ||||||
chr19:46922752
|
C | T | 1 | a0001c0001t0007g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3681+396C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46922752 | ||||||
chr19:46923010
|
A | T | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3681+654A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923010 | ||||||
chr19:46923011
|
T | C | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3681+655T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923011 | ||||||
chr19:46923012
|
G | T | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3681+656G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923012 | ||||||
chr19:46923013
|
G | C | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3681+657G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923013 | ||||||
chr19:46923102
|
C | CT | 64 | a0001c0001t0001g0130a0001c0001t0001g0162a0001c0001t0001g0163others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.3681+766dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46923102 | |||||
chr19:46923102
|
C | CTT | 14 | a0001c0001t0011g0058a0001c0002t0006g0207a0001c0002t0006g0209others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3681+765_3681+766d others(4): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46923102 | |||||
chr19:46923102
|
CT | C | 7 | a0001c0001t0001g0171a0001c0001t0002g0136a0001c0001t0005g0256others(4): Show | 7 | HG01069.hp2 HG01070.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3681+766delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46923102 | |||||
chr19:46923104
|
T | C | 1 | a0001c0001t0017g0088 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3681+748T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923104 | ||||||
chr19:46923161
|
G | A | 50 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3681+805G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923161 | ||||||
chr19:46923316
|
G | A | 2 | a0001c0001t0002g0200a0001c0001t0002g0293 | 2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.3681+960G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923316 | ||||||
chr19:46923443
|
T | C | 1 | a0001c0001t0028g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3681+1087T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923443 | ||||||
chr19:46923523
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3681+1167G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923523 | ||||||
chr19:46923627
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+1271A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923627 | ||||||
chr19:46923672
|
A | C | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3681+1316A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923672 | ||||||
chr19:46923748
|
A | G | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3681+1392A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923748 | ||||||
chr19:46923920
|
C | CA | 47 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(44): Show | 47 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.3681+1576dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46923920 | |||||
chr19:46923953
|
G | A | 186 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(183): Show | 186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3681+1597G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923953 | ||||||
chr19:46923997
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3681+1641G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923997 | ||||||
chr19:46924101
|
C | G | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3681+1745C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46924101 | ||||||
chr19:46924294
|
C | T | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3681+1938C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46924294 | ||||||
chr19:46924302
|
G | A | 1 | a0004c0008t0015g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3681+1946G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46924302 | ||||||
chr19:46924306
|
G | A | 1 | a0001c0001t0004g0245 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3681+1950G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46924306 | ||||||
chr19:46924493
|
C | A | 1 | a0003c0013t0004g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3681+2137C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46924493 | ||||||
chr19:46924649
|
G | A | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3681+2293G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46924649 | ||||||
chr19:46925074
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3681+2718C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46925074 | ||||||
chr19:46925246
|
G | A | 1 | a0001c0006t0006g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3681+2890G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46925246 | ||||||
chr19:46925580
|
A | G | 2 | a0001c0001t0002g0136a0001c0001t0002g0266 | 2 | HG01069.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.3681+3224A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46925580 | ||||||
chr19:46925682
|
G | A | 1 | a0001c0001t0045g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3681+3326G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46925682 | ||||||
chr19:46925711
|
T | C | 50 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3681+3355T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46925711 | ||||||
chr19:46926021
|
G | A | 3 | a0001c0001t0017g0088a0001c0001t0028g0093a0001c0001t0057g0091 | 3 | NA18942.hp1 NA18947.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3681+3665G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46926021 | ||||||
chr19:46926260
|
A | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+3904A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46926260 | ||||||
chr19:46926351
|
G | T | 2 | a0001c0001t0002g0200a0001c0001t0002g0293 | 2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.3681+3995G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46926351 | ||||||
chr19:46926541
|
G | C | 114 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(111): Show | 114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.3681+4185G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46926541 | ||||||
chr19:46926629
|
T | TA | 19 | a0001c0001t0004g0030a0001c0001t0014g0069a0001c0001t0014g0087others(16): Show | 19 | HG00597.hp1 HG01891.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.3681+4284dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46926629 | |||||
chr19:46927201
|
A | G | 1 | a0001c0001t0005g0256 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3681+4845A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46927201 | ||||||
chr19:46927367
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3681+5011G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46927367 | ||||||
chr19:46927982
|
C | A | 1 | a0001c0001t0003g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3681+5626C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46927982 | ||||||
chr19:46928044
|
T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+5688T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928044 | ||||||
chr19:46928173
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3681+5817G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928173 | ||||||
chr19:46928572
|
C | T | 5 | a0001c0001t0001g0134a0001c0001t0002g0137a0001c0001t0002g0140others(2): Show | 5 | NA18953.hp1 NA18960.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.3681+6216C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928572 | ||||||
chr19:46928575
|
C | T | 1 | a0001c0001t0004g0242 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3681+6219C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928575 | ||||||
chr19:46928594
|
G | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3681+6238G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928594 | ||||||
chr19:46928616
|
T | G | 14 | a0001c0001t0001g0130a0001c0001t0001g0160a0001c0001t0001g0162others(11): Show | 14 | HG00733.hp2 HG00738.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3681+6260T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928616 | ||||||
chr19:46928660
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3681+6304G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928660 | ||||||
chr19:46928927
|
C | CT | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3681+6572dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46928927 | |||||
chr19:46928929
|
C | A | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3681+6573C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928929 | ||||||
chr19:46928967
|
T | C | 1 | a0001c0001t0051g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3681+6611T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928967 | ||||||
chr19:46929007
|
T | TAAG | 297 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.3681+6653_3681+665 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46929007 | |||||
chr19:46929101
|
G | A | 1 | a0001c0001t0052g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3681+6745G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929101 | ||||||
chr19:46929427
|
A | G | 5 | a0001c0001t0017g0088a0001c0001t0017g0249a0001c0001t0017g0250others(2): Show | 5 | HG00597.hp1 NA18942.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.3681+7071A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929427 | ||||||
chr19:46929454
|
T | C | 3 | a0001c0001t0027g0034a0001c0001t0027g0221a0001c0001t0030g0277 | 3 | HG02257.hp2 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3681+7098T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929454 | ||||||
chr19:46929499
|
G | A | 1 | a0006c0010t0004g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3681+7143G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929499 | ||||||
chr19:46929591
|
C | CT | 39 | a0001c0001t0001g0146a0001c0001t0001g0171a0001c0001t0001g0175others(36): Show | 39 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.3681+7261dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46929591 | |||||
chr19:46929591
|
C | CTT | 27 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(24): Show | 27 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.3681+7260_3681+726 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46929591 | |||||
chr19:46929591
|
CT | C | 42 | a0001c0001t0001g0119a0001c0001t0002g0136a0001c0001t0002g0148others(39): Show | 42 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.3681+7261delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46929591 | |||||
chr19:46929658
|
A | G | 1 | a0001c0001t0002g0152 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3681+7302A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929658 | ||||||
chr19:46929790
|
G | A | 1 | a0001c0001t0004g0080 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3681+7434G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929790 | ||||||
chr19:46929843
|
G | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3682-7421G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929843 | ||||||
chr19:46929897
|
A | G | 1 | a0006c0010t0004g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3682-7367A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929897 | ||||||
chr19:46929914
|
C | CA | 52 | a0001c0001t0003g0231a0001c0001t0004g0022a0001c0001t0004g0030others(49): Show | 52 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.3682-7335dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46929914 | |||||
chr19:46929939
|
T | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3682-7325T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929939 | ||||||
chr19:46930021
|
C | T | 1 | a0001c0001t0003g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3682-7243C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930021 | ||||||
chr19:46930065
|
T | C | 1 | a0001c0001t0016g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3682-7199T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930065 | ||||||
chr19:46930126
|
G | A | 1 | a0001c0001t0004g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3682-7138G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930126 | ||||||
chr19:46930177
|
G | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3682-7087G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930177 | ||||||
chr19:46930249
|
G | T | 11 | a0001c0001t0001g0134a0001c0001t0002g0136a0001c0001t0002g0137others(8): Show | 11 | HG01069.hp2 HG01261.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.3682-7015G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930249 | ||||||
chr19:46930526
|
T | C | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3682-6738T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930526 | ||||||
chr19:46930855
|
G | A | 1 | a0001c0001t0020g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3682-6409G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930855 | ||||||
chr19:46930956
|
C | T | 4 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3682-6308C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930956 | ||||||
chr19:46930999
|
C | T | 3 | a0001c0001t0027g0034a0001c0001t0027g0221a0001c0001t0030g0277 | 3 | HG02257.hp2 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3682-6265C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930999 | ||||||
chr19:46931220
|
A | G | 9 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0078others(6): Show | 9 | HG00438.hp2 HG02071.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.3682-6044A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46931220 | ||||||
chr19:46931542
|
C | A | 3 | a0001c0001t0001g0119a0001c0001t0008g0122a0001c0001t0008g0260 | 3 | HG01070.hp2 HG01192.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3682-5722C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46931542 | ||||||
chr19:46931576
|
A | C | 1 | a0001c0001t0003g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3682-5688A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46931576 | ||||||
chr19:46931896
|
G | A | 1 | a0001c0001t0002g0265 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3682-5368G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46931896 | ||||||
chr19:46932405
|
T | C | 1 | a0001c0001t0003g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3682-4859T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46932405 | ||||||
chr19:46932488
|
G | T | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3682-4776G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46932488 | ||||||
chr19:46932676
|
C | T | 5 | a0001c0001t0012g0112a0001c0001t0012g0113a0001c0001t0012g0114others(2): Show | 5 | HG02027.hp2 NA18961.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.3682-4588C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46932676 | ||||||
chr19:46932931
|
G | A | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3682-4333G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46932931 | ||||||
chr19:46932998
|
G | A | 1 | a0001c0001t0038g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3682-4266G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46932998 | ||||||
chr19:46933137
|
C | CT | 157 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0167others(154): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.3682-4105dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46933137 | |||||
chr19:46933137
|
C | CTT | 30 | a0001c0001t0001g0189a0001c0001t0004g0078a0001c0001t0004g0240others(27): Show | 30 | HG00642.hp1 HG01346.hp1 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.3682-4106_3682-410 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46933137 | |||||
chr19:46933137
|
C | CTTT | 7 | a0001c0001t0004g0233a0001c0001t0030g0277a0001c0001t0040g0029others(4): Show | 7 | HG01243.hp2 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.3682-4107_3682-410 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46933137 | |||||
chr19:46933211
|
T | C | 1 | a0001c0001t0051g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3682-4053T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46933211 | ||||||
chr19:46933350
|
C | T | 11 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0021others(8): Show | 11 | HG00639.hp1 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3682-3914C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46933350 | ||||||
chr19:46934044
|
G | C | 1 | a0001c0001t0002g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3682-3220G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934044 | ||||||
chr19:46934197
|
A | C | 30 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(27): Show | 30 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.3682-3067A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934197 | ||||||
chr19:46934280
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3682-2984A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934280 | ||||||
chr19:46934374
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3682-2890C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934374 | ||||||
chr19:46934409
|
C | T | 1 | a0001c0001t0002g0145 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3682-2855C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934409 | ||||||
chr19:46934454
|
A | G | 71 | a0001c0001t0001g0068a0001c0001t0001g0177a0001c0001t0003g0001others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.3682-2810A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934454 | ||||||
chr19:46934529
|
G | A | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3682-2735G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934529 | ||||||
chr19:46934551
|
G | A | 1 | a0001c0001t0005g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3682-2713G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934551 | ||||||
chr19:46934694
|
G | T | 1 | a0001c0001t0010g0023 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3682-2570G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934694 | ||||||
chr19:46934699
|
G | T | 186 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(183): Show | 186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3682-2565G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934699 | ||||||
chr19:46934791
|
T | G | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3682-2473T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934791 | ||||||
chr19:46934805
|
G | A | 1 | a0001c0001t0021g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3682-2459G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934805 | ||||||
chr19:46934818
|
C | T | 2 | a0001c0001t0004g0072a0001c0001t0004g0240 | 2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3682-2446C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934818 | ||||||
chr19:46934886
|
T | C | 1 | a0003c0013t0004g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3682-2378T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934886 | ||||||
chr19:46934912
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3682-2352A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934912 | ||||||
chr19:46934971
|
C | G | 8 | a0001c0001t0005g0118a0001c0001t0005g0120a0001c0001t0005g0121others(5): Show | 8 | NA18972.hp1 NA18973.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.3682-2293C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934971 | ||||||
chr19:46935068
|
G | A | 1 | a0001c0001t0031g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3682-2196G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46935068 | ||||||
chr19:46935070
|
T | A | 15 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(12): Show | 15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3682-2194T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46935070 | ||||||
chr19:46935315
|
T | G | 5 | a0001c0001t0011g0056a0001c0001t0011g0057a0001c0001t0011g0058others(2): Show | 5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3682-1949T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46935315 | ||||||
chr19:46936089
|
G | T | 11 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(8): Show | 11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3682-1175G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46936089 | ||||||
chr19:46936310
|
T | TTGCTGCT others(11): Show |
1 | a0001c0001t0004g0241 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3682-949_3682-932d others(20): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46936310 | |||||
chr19:46936611
|
G | A | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3682-653G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46936611 | ||||||
chr19:46936845
|
C | CT | 13 | a0001c0001t0002g0145a0001c0001t0002g0266a0001c0001t0002g0275others(10): Show | 13 | HG00738.hp1 HG01071.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.3682-401dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46936845 | |||||
chr19:46936845
|
C | CTT | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3682-402_3682-401d others(4): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46936845 | |||||
chr19:46936900
|
C | T | 4 | a0001c0001t0016g0089a0001c0001t0016g0092a0001c0001t0016g0094others(1): Show | 4 | HG01891.hp2 HG02922.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.3682-364C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46936900 | ||||||
chr19:46936901
|
GCAATCTC others(9): Show |
G | 1 | a0001c0001t0002g0265 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3682-355_3682-340d others(18): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46936901 | |||||
chr19:46936934
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3682-330G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46936934 | ||||||
chr19:46936957
|
A | G | 1 | a0001c0001t0004g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3682-307A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46936957 | ||||||
chr19:46937039
|
C | T | 7 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3682-225C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46937039 | ||||||
chr19:46937227
|
C | G | 7 | a0001c0001t0017g0088a0001c0001t0017g0249a0001c0001t0017g0250others(4): Show | 7 | HG00597.hp1 HG02080.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.3682-37C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46937227 | ||||||
chr19:46937939
|
T | C | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3826+531T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46937939 | ||||||
chr19:46938226
|
G | C | 1 | a0001c0001t0004g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3826+818G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938226 | ||||||
chr19:46938322
|
G | A | 1 | a0001c0001t0050g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3826+914G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938322 | ||||||
chr19:46938342
|
A | ATTTTAT | 3 | a0001c0001t0001g0169a0001c0001t0001g0278a0001c0001t0003g0253 | 3 | HG00733.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3826+957_3826+962d others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46938342 | |||||
chr19:46938417
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+1009G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938417 | ||||||
chr19:46938466
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3826+1058G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938466 | ||||||
chr19:46938498
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3826+1090G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938498 | ||||||
chr19:46938530
|
T | C | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3826+1122T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938530 | ||||||
chr19:46938589
|
G | C | 115 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(112): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.3826+1181G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938589 | ||||||
chr19:46938935
|
A | G | 15 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(12): Show | 15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3826+1527A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938935 | ||||||
chr19:46938947
|
G | T | 50 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(47): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3826+1539G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938947 | ||||||
chr19:46939027
|
GAA | G | 16 | a0001c0001t0001g0134a0001c0001t0002g0131a0001c0001t0002g0132others(13): Show | 16 | HG01069.hp2 HG01261.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.3826+1621_3826+162 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46939027 | |||||
chr19:46939178
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3826+1770T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939178 | ||||||
chr19:46939255
|
G | A | 1 | a0001c0001t0049g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3826+1847G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939255 | ||||||
chr19:46939264
|
C | T | 1 | a0001c0001t0003g0004 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3826+1856C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939264 | ||||||
chr19:46939354
|
G | T | 1 | a0001c0001t0004g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3826+1946G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939354 | ||||||
chr19:46939372
|
C | CATTT | 32 | a0001c0001t0001g0134a0001c0001t0001g0153a0001c0001t0001g0175others(29): Show | 32 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.3826+2004_3826+200 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46939372 | |||||
chr19:46939372
|
CATTT | C | 52 | a0001c0001t0001g0204a0001c0001t0002g0147a0001c0001t0002g0148others(49): Show | 52 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.3826+2004_3826+200 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46939372 | |||||
chr19:46939372
|
CATTTATT others(1): Show |
C | 127 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0160others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.3826+2000_3826+200 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46939372 | |||||
chr19:46939372
|
CATTTATT others(5): Show |
C | 4 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+1996_3826+200 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46939372 | |||||
chr19:46939372
|
CATTTATT others(9): Show |
C | 4 | a0001c0001t0003g0054a0001c0001t0018g0040a0001c0001t0018g0227others(1): Show | 4 | HG02451.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3826+1992_3826+200 others(20): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46939372 | |||||
chr19:46939624
|
G | C | 11 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(8): Show | 11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3826+2216G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939624 | ||||||
chr19:46939651
|
A | G | 189 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0189others(186): Show | 189 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.3826+2243A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939651 | ||||||
chr19:46939780
|
A | G | 11 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(8): Show | 11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3826+2372A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939780 | ||||||
chr19:46939919
|
A | AC | 32 | a0001c0001t0001g0204a0001c0001t0004g0022a0001c0001t0004g0070others(29): Show | 32 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.3826+2511_3826+251 others(5): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939919 | ||||||
chr19:46940009
|
A | G | 32 | a0001c0001t0001g0204a0001c0001t0004g0022a0001c0001t0004g0070others(29): Show | 32 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.3826+2601A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940009 | ||||||
chr19:46940063
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3826+2655C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940063 | ||||||
chr19:46940181
|
G | A | 1 | a0001c0001t0004g0082 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3826+2773G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940181 | ||||||
chr19:46940252
|
G | A | 1 | a0001c0002t0006g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3826+2844G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940252 | ||||||
chr19:46940359
|
CA | C | 183 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0179others(180): Show | 183 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.3826+2970delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46940359 | |||||
chr19:46940396
|
C | T | 2 | a0001c0001t0002g0149a0001c0001t0002g0150 | 2 | NA18612.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.3826+2988C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940396 | ||||||
chr19:46940477
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+3069G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940477 | ||||||
chr19:46940550
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3826+3142A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940550 | ||||||
chr19:46940604
|
C | CTT | 15 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(12): Show | 15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3826+3211_3826+321 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46940604 | |||||
chr19:46940604
|
CT | C | 22 | a0001c0001t0001g0171a0001c0001t0001g0185a0001c0001t0002g0140others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.3826+3212delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46940604 | |||||
chr19:46940712
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3826+3304C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940712 | ||||||
chr19:46940750
|
C | G | 1 | a0001c0001t0001g0289 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3826+3342C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940750 | ||||||
chr19:46940750
|
C | T | 1 | a0001c0001t0031g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3826+3342C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940750 | ||||||
chr19:46940788
|
G | A | 2 | a0001c0001t0003g0098a0001c0001t0003g0104 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3826+3380G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940788 | ||||||
chr19:46940795
|
A | G | 15 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(12): Show | 15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3826+3387A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940795 | ||||||
chr19:46940982
|
C | CTTCCCGG others(16): Show |
3 | a0001c0001t0001g0119a0001c0001t0008g0122a0001c0001t0008g0260 | 3 | HG01070.hp2 HG01192.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3826+3575_3826+357 others(27): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46940982 | |||||
chr19:46941004
|
G | A | 5 | a0001c0001t0017g0088a0001c0001t0017g0249a0001c0001t0017g0250others(2): Show | 5 | HG00597.hp1 NA18942.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.3826+3596G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941004 | ||||||
chr19:46941152
|
C | T | 1 | a0001c0001t0013g0047 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3826+3744C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941152 | ||||||
chr19:46941206
|
C | T | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+3798C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941206 | ||||||
chr19:46941399
|
C | G | 1 | a0001c0001t0002g0145 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3826+3991C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941399 | ||||||
chr19:46941519
|
T | C | 6 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3826+4111T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941519 | ||||||
chr19:46941606
|
C | T | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3826+4198C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941606 | ||||||
chr19:46941634
|
G | A | 51 | a0001c0001t0001g0204a0001c0001t0004g0022a0001c0001t0004g0030others(48): Show | 51 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.3826+4226G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941634 | ||||||
chr19:46941657
|
G | A | 5 | a0001c0001t0011g0056a0001c0001t0011g0057a0001c0001t0011g0058others(2): Show | 5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3826+4249G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941657 | ||||||
chr19:46941721
|
G | A | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3826+4313G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941721 | ||||||
chr19:46941819
|
CA | C | 166 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0204others(163): Show | 166 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.3826+4414delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46941819 | |||||
chr19:46941876
|
T | TA | 59 | a0001c0001t0001g0204a0001c0001t0001g0282a0001c0001t0004g0022others(56): Show | 59 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.3826+4492dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46941876 | |||||
chr19:46941876
|
T | TAA | 76 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0002g0159others(73): Show | 76 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.3826+4491_3826+449 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46941876 | |||||
chr19:46941876
|
T | TAAA | 29 | a0001c0001t0001g0189a0001c0001t0003g0021a0001c0001t0003g0044others(26): Show | 29 | HG00738.hp1 HG01071.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.3826+4490_3826+449 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46941876 | |||||
chr19:46941876
|
TA | T | 9 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0179others(6): Show | 9 | HG02258.hp2 HG02683.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.3826+4492delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46941876 | |||||
chr19:46942214
|
C | G | 15 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(12): Show | 15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3826+4806C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942214 | ||||||
chr19:46942251
|
C | A | 1 | a0006c0010t0004g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3826+4843C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942251 | ||||||
chr19:46942569
|
G | A | 4 | a0001c0002t0006g0209a0001c0002t0006g0212a0001c0002t0006g0215others(1): Show | 4 | HG02895.hp1 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+5161G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942569 | ||||||
chr19:46942599
|
T | A | 36 | a0001c0001t0001g0204a0001c0001t0004g0022a0001c0001t0004g0030others(33): Show | 36 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3826+5191T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942599 | ||||||
chr19:46942616
|
G | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0197others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+5208G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942616 | ||||||
chr19:46942718
|
A | G | 22 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0027g0034others(19): Show | 22 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.3826+5310A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942718 | ||||||
chr19:46942757
|
A | C | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3826+5349A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942757 | ||||||
chr19:46942815
|
C | CA | 83 | a0001c0001t0001g0168a0001c0001t0001g0204a0001c0001t0001g0282others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.3826+5408dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46942815 | |||||
chr19:46942815
|
C | CAA | 7 | a0001c0001t0004g0072a0001c0001t0004g0095a0001c0001t0004g0236others(4): Show | 7 | HG00558.hp1 HG02738.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.3826+5408_3826+540 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46942815 | |||||
chr19:46942816
|
AG | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0281a0001c0001t0019g0024 | 3 | HG01070.hp1 HG02155.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.3826+5409delG | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942816 | ||||||
chr19:46942817
|
G | A | 294 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.3826+5409G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942817 | ||||||
chr19:46943010
|
A | G | 1 | a0001c0001t0020g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3826+5602A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943010 | ||||||
chr19:46943039
|
AT | A | 33 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0048others(30): Show | 33 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.3826+5647delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46943039 | |||||
chr19:46943285
|
C | T | 1 | a0001c0001t0035g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3826+5877C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943285 | ||||||
chr19:46943305
|
A | G | 190 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(187): Show | 190 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.3826+5897A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943305 | ||||||
chr19:46943399
|
T | C | 5 | a0001c0001t0011g0056a0001c0001t0011g0057a0001c0001t0011g0058others(2): Show | 5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3826+5991T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943399 | ||||||
chr19:46943434
|
A | G | 113 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0189others(110): Show | 113 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.3826+6026A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943434 | ||||||
chr19:46943901
|
T | C | 181 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0204others(178): Show | 181 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.3826+6493T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943901 | ||||||
chr19:46943995
|
A | G | 1 | a0001c0001t0021g0109 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3826+6587A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943995 | ||||||
chr19:46944100
|
G | A | 1 | a0001c0001t0018g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3826+6692G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944100 | ||||||
chr19:46944277
|
C | T | 1 | a0001c0001t0034g0111 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3826+6869C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944277 | ||||||
chr19:46944311
|
A | G | 7 | a0001c0001t0017g0088a0001c0001t0017g0249a0001c0001t0017g0250others(4): Show | 7 | HG00597.hp1 HG02080.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.3826+6903A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944311 | ||||||
chr19:46944398
|
C | A | 1 | a0001c0001t0004g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3826+6990C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944398 | ||||||
chr19:46944399
|
T | C | 2 | a0001c0001t0004g0071a0001c0001t0032g0232 | 2 | NA18969.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3826+6991T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944399 | ||||||
chr19:46944448
|
G | A | 1 | a0001c0001t0051g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3826+7040G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944448 | ||||||
chr19:46944451
|
C | A | 1 | a0001c0001t0027g0221 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3826+7043C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944451 | ||||||
chr19:46944529
|
T | C | 1 | a0004c0008t0015g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3826+7121T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944529 | ||||||
chr19:46944829
|
C | T | 1 | a0001c0001t0002g0152 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3826+7421C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944829 | ||||||
chr19:46945158
|
AAGGAGGC others(18): Show |
A | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | NA19004.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3826+7777_3826+780 others(29): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46945158 | |||||
chr19:46945512
|
G | T | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3826+8104G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46945512 | ||||||
chr19:46945770
|
C | G | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3826+8362C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46945770 | ||||||
chr19:46945885
|
C | T | 1 | a0001c0001t0025g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3826+8477C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46945885 | ||||||
chr19:46945965
|
G | A | 3 | a0001c0001t0010g0035a0001c0001t0010g0052a0001c0001t0010g0222 | 3 | HG01257.hp1 HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.3826+8557G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46945965 | ||||||
chr19:46946016
|
C | T | 4 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+8608C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946016 | ||||||
chr19:46946090
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3826+8682C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946090 | ||||||
chr19:46946442
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+9034A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946442 | ||||||
chr19:46946585
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+9177C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946585 | ||||||
chr19:46946741
|
T | TTG | 5 | a0001c0001t0001g0130a0001c0001t0001g0286a0001c0001t0001g0289others(2): Show | 5 | HG00621.hp2 HG01928.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.3826+9353_3826+935 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46946741 | |||||
chr19:46946819
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3826+9411G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946819 | ||||||
chr19:46946920
|
A | G | 1 | a0001c0001t0003g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3826+9512A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946920 | ||||||
chr19:46946985
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3826+9577A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946985 | ||||||
chr19:46947501
|
A | G | 1 | a0001c0001t0003g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3826+10093A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46947501 | ||||||
chr19:46947537
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3826+10129C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46947537 | ||||||
chr19:46947576
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3826+10168C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46947576 | ||||||
chr19:46947674
|
G | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+10266G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46947674 | ||||||
chr19:46947721
|
C | T | 1 | a0001c0001t0002g0272 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3826+10313C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46947721 | ||||||
chr19:46948105
|
G | C | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3826+10697G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46948105 | ||||||
chr19:46948396
|
A | G | 2 | a0001c0001t0003g0054a0001c0001t0045g0053 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.3826+10988A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46948396 | ||||||
chr19:46948681
|
G | A | 1 | a0001c0001t0004g0235 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3826+11273G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46948681 | ||||||
chr19:46948807
|
G | C | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3826+11399G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46948807 | ||||||
chr19:46948885
|
C | T | 1 | a0001c0001t0016g0094 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3826+11477C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46948885 | ||||||
chr19:46949181
|
T | C | 1 | a0001c0002t0006g0211 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3826+11773T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46949181 | ||||||
chr19:46949552
|
G | T | 1 | a0001c0001t0049g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3826+12144G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46949552 | ||||||
chr19:46949676
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0054g0287 | 2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.3826+12268C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46949676 | ||||||
chr19:46949679
|
A | T | 1 | a0001c0001t0039g0077 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3826+12271A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46949679 | ||||||
chr19:46949764
|
A | T | 1 | a0001c0001t0052g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3826+12356A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46949764 | ||||||
chr19:46950524
|
C | T | 1 | a0001c0001t0051g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3826+13116C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46950524 | ||||||
chr19:46950689
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0003g0231a0001c0001t0025g0067 | 3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3826+13281G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46950689 | ||||||
chr19:46950694
|
G | A | 1 | a0001c0001t0003g0010 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3826+13286G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46950694 | ||||||
chr19:46950847
|
G | A | 1 | a0001c0001t0003g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3826+13439G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46950847 | ||||||
chr19:46950974
|
T | C | 15 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(12): Show | 15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3826+13566T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46950974 | ||||||
chr19:46951114
|
G | A | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3826+13706G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951114 | ||||||
chr19:46951185
|
T | G | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+13777T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951185 | ||||||
chr19:46951450
|
C | CT | 34 | a0001c0001t0001g0119a0001c0001t0001g0193a0001c0001t0002g0133others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.3826+14051dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46951450 | |||||
chr19:46951557
|
A | G | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3826+14149A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951557 | ||||||
chr19:46951562
|
T | C | 7 | a0001c0001t0015g0037a0001c0001t0023g0039a0001c0001t0023g0055others(4): Show | 7 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.3826+14154T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951562 | ||||||
chr19:46951612
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3826+14204G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951612 | ||||||
chr19:46951615
|
G | T | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3826+14207G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951615 | ||||||
chr19:46951648
|
T | C | 3 | a0001c0001t0007g0017a0001c0001t0007g0020a0001c0001t0048g0018 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3826+14240T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951648 | ||||||
chr19:46951724
|
T | G | 1 | a0003c0013t0004g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3826+14316T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951724 | ||||||
chr19:46951808
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0202 | 2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3826+14400G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951808 | ||||||
chr19:46952058
|
A | G | 64 | a0001c0001t0001g0068a0001c0001t0003g0001a0001c0001t0003g0002others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.3826+14650A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952058 | ||||||
chr19:46952277
|
CATTT | C | 3 | a0001c0001t0001g0068a0001c0001t0003g0231a0001c0001t0025g0067 | 3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3826+14873_3826+14 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46952277 | |||||
chr19:46952286
|
C | T | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3826+14878C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952286 | ||||||
chr19:46952298
|
T | C | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+14890T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952298 | ||||||
chr19:46952445
|
T | A | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3826+15037T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952445 | ||||||
chr19:46952480
|
T | C | 1 | a0001c0001t0003g0009 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3826+15072T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952480 | ||||||
chr19:46952599
|
T | C | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | NA18993.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.3826+15191T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952599 | ||||||
chr19:46952628
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3826+15220A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952628 | ||||||
chr19:46952639
|
A | T | 36 | a0001c0001t0001g0204a0001c0001t0004g0022a0001c0001t0004g0030others(33): Show | 36 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3826+15231A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952639 | ||||||
chr19:46952700
|
G | A | 2 | a0001c0001t0003g0005a0001c0001t0003g0007 | 2 | NA18983.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.3826+15292G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952700 | ||||||
chr19:46952874
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3826+15466C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952874 | ||||||
chr19:46952877
|
C | T | 1 | a0001c0002t0006g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3826+15469C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952877 | ||||||
chr19:46953193
|
G | C | 11 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(8): Show | 11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3826+15785G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953193 | ||||||
chr19:46953329
|
G | T | 3 | a0001c0001t0024g0032a0001c0001t0024g0220a0001c0001t0038g0252 | 3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3826+15921G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953329 | ||||||
chr19:46953333
|
G | C | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+15925G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953333 | ||||||
chr19:46953676
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+16268G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953676 | ||||||
chr19:46953816
|
T | C | 3 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0289 | 3 | HG00621.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3826+16408T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953816 | ||||||
chr19:46953904
|
T | C | 2 | a0001c0001t0024g0032a0001c0001t0024g0220 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3826+16496T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953904 | ||||||
chr19:46953905
|
G | A | 2 | a0001c0001t0024g0032a0001c0001t0024g0220 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3826+16497G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953905 | ||||||
chr19:46954003
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3826+16595G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46954003 | ||||||
chr19:46954156
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3826+16748G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46954156 | ||||||
chr19:46954408
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3826+17000T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46954408 | ||||||
chr19:46954494
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3826+17086G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46954494 | ||||||
chr19:46954829
|
T | G | 1 | a0001c0001t0002g0154 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3826+17421T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46954829 | ||||||
chr19:46954965
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+17557A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46954965 | ||||||
chr19:46955265
|
A | T | 1 | a0001c0001t0002g0141 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3826+17857A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46955265 | ||||||
chr19:46955470
|
C | G | 1 | a0001c0001t0001g0173 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3826+18062C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46955470 | ||||||
chr19:46956144
|
G | A | 81 | a0001c0001t0001g0068a0001c0001t0001g0189a0001c0001t0003g0001others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.3826+18736G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956144 | ||||||
chr19:46956219
|
A | T | 45 | a0001c0001t0001g0142a0001c0001t0001g0170a0001c0001t0001g0172others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.3826+18811A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956219 | ||||||
chr19:46956233
|
A | G | 190 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0189others(187): Show | 190 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.3826+18825A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956233 | ||||||
chr19:46956238
|
A | G | 1 | a0001c0001t0045g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3826+18830A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956238 | ||||||
chr19:46956493
|
C | G | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3826+19085C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956493 | ||||||
chr19:46956704
|
G | T | 1 | a0001c0001t0005g0123 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3826+19296G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956704 | ||||||
chr19:46956756
|
G | T | 1 | a0001c0001t0021g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3826+19348G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956756 | ||||||
chr19:46956956
|
C | CCTT | 9 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(6): Show | 9 | HG00597.hp1 HG02559.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3826+19548_3826+19 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956956 | ||||||
chr19:46956956
|
C | CT | 132 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(129): Show | 132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.3826+19569dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46956956 | |||||
chr19:46956956
|
C | CTT | 50 | a0001c0001t0001g0181a0001c0001t0003g0009a0001c0001t0003g0051others(47): Show | 50 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.3826+19568_3826+19 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46956956 | |||||
chr19:46956999
|
G | A | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3826+19591G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956999 | ||||||
chr19:46957051
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3826+19643T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957051 | ||||||
chr19:46957109
|
A | C | 190 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0189others(187): Show | 190 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.3826+19701A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957109 | ||||||
chr19:46957118
|
C | T | 1 | a0001c0001t0004g0235 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3826+19710C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957118 | ||||||
chr19:46957587
|
C | T | 1 | a0001c0001t0004g0242 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3826+20179C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957587 | ||||||
chr19:46957603
|
C | T | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3826+20195C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957603 | ||||||
chr19:46957631
|
A | T | 1 | a0001c0001t0034g0111 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3826+20223A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957631 | ||||||
chr19:46957686
|
T | C | 1 | a0001c0001t0007g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3826+20278T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957686 | ||||||
chr19:46957752
|
A | C | 1 | a0001c0001t0001g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3826+20344A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957752 | ||||||
chr19:46957783
|
C | G | 2 | a0001c0001t0004g0072a0001c0001t0004g0240 | 2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3826+20375C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957783 | ||||||
chr19:46957963
|
G | A | 2 | a0001c0001t0007g0015a0001c0001t0007g0019 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3826+20555G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957963 | ||||||
chr19:46957967
|
G | A | 1 | a0001c0001t0004g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3826+20559G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957967 | ||||||
chr19:46957999
|
G | A | 1 | a0001c0001t0003g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3826+20591G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957999 | ||||||
chr19:46958110
|
A | G | 270 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(267): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.3826+20702A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46958110 | ||||||
chr19:46958211
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3826+20803G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46958211 | ||||||
chr19:46958253
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3826+20845G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46958253 | ||||||
chr19:46958256
|
C | T | 2 | a0001c0001t0018g0040a0001c0001t0018g0227 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3826+20848C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46958256 | ||||||
chr19:46958384
|
C | CA | 6 | a0001c0001t0001g0202a0001c0001t0003g0050a0001c0001t0003g0064others(3): Show | 6 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.3826+20993dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46958384 | |||||
chr19:46958575
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3826+21167G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46958575 | ||||||
chr19:46959030
|
G | GTTGT | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3826+21624_3826+21 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46959030 | |||||
chr19:46959090
|
T | C | 1 | a0001c0001t0007g0060 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3826+21682T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959090 | ||||||
chr19:46959107
|
T | C | 188 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0204others(185): Show | 188 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3826+21699T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959107 | ||||||
chr19:46959125
|
C | G | 3 | a0001c0001t0004g0070a0001c0001t0004g0071a0001c0001t0032g0232 | 3 | NA18969.hp1 NA18982.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3826+21717C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959125 | ||||||
chr19:46959307
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3826+21899G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959307 | ||||||
chr19:46959478
|
C | A | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3826+22070C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959478 | ||||||
chr19:46959504
|
A | G | 2 | a0001c0001t0007g0046a0001c0001t0007g0060 | 2 | NA18964.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.3826+22096A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959504 | ||||||
chr19:46959556
|
C | T | 1 | a0001c0001t0003g0004 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3826+22148C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959556 | ||||||
chr19:46959559
|
C | G | 1 | a0001c0001t0025g0062 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3826+22151C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959559 | ||||||
chr19:46959646
|
C | T | 1 | a0001c0001t0004g0233 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3826+22238C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959646 | ||||||
chr19:46959665
|
G | T | 1 | a0001c0007t0015g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3826+22257G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959665 | ||||||
chr19:46959674
|
A | T | 1 | a0001c0001t0002g0139 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3826+22266A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959674 | ||||||
chr19:46959942
|
A | T | 64 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(61): Show | 64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3826+22534A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959942 | ||||||
chr19:46959943
|
T | A | 92 | a0001c0001t0001g0068a0001c0001t0001g0204a0001c0001t0003g0001others(89): Show | 92 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.3826+22535T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959943 | ||||||
chr19:46959964
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0004g0233 | 2 | HG02155.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.3826+22556G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959964 | ||||||
chr19:46960110
|
C | CA | 13 | a0001c0001t0001g0205a0001c0001t0002g0275a0001c0001t0004g0082others(10): Show | 13 | HG00558.hp2 HG00597.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.3826+22719dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46960110 | |||||
chr19:46960166
|
G | A | 1 | a0001c0001t0004g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3826+22758G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960166 | ||||||
chr19:46960226
|
A | G | 9 | a0001c0001t0003g0011a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG00639.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3826+22818A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960226 | ||||||
chr19:46960327
|
G | A | 1 | a0001c0001t0004g0078 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3826+22919G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960327 | ||||||
chr19:46960372
|
C | T | 36 | a0001c0001t0001g0204a0001c0001t0004g0022a0001c0001t0004g0030others(33): Show | 36 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3826+22964C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960372 | ||||||
chr19:46960392
|
G | A | 12 | a0001c0001t0001g0130a0001c0001t0001g0160a0001c0001t0001g0162others(9): Show | 12 | HG00733.hp2 HG00738.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3826+22984G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960392 | ||||||
chr19:46960515
|
A | G | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3826+23107A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960515 | ||||||
chr19:46960881
|
G | A | 2 | a0001c0001t0007g0017a0001c0001t0007g0020 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3826+23473G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960881 | ||||||
chr19:46960893
|
C | CT | 11 | a0001c0001t0001g0181a0001c0001t0001g0282a0001c0001t0003g0009others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.3826+23501dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46960893 | |||||
chr19:46960919
|
A | T | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3826+23511A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960919 | ||||||
chr19:46960996
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+23588G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960996 | ||||||
chr19:46961137
|
C | T | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3826+23729C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961137 | ||||||
chr19:46961163
|
G | C | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3826+23755G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961163 | ||||||
chr19:46961224
|
C | T | 1 | a0001c0001t0003g0128 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3826+23816C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961224 | ||||||
chr19:46961274
|
T | C | 5 | a0001c0001t0012g0112a0001c0001t0012g0113a0001c0001t0012g0114others(2): Show | 5 | HG02027.hp2 NA18961.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.3826+23866T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961274 | ||||||
chr19:46961544
|
G | A | 1 | a0001c0001t0016g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3826+24136G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961544 | ||||||
chr19:46961588
|
T | C | 1 | a0001c0002t0006g0297 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3826+24180T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961588 | ||||||
chr19:46961879
|
G | A | 1 | a0001c0001t0050g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3826+24471G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961879 | ||||||
chr19:46961966
|
GAGAA | G | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+24562_3826+24 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46961966 | |||||
chr19:46962081
|
G | T | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3826+24673G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962081 | ||||||
chr19:46962109
|
T | C | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3826+24701T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962109 | ||||||
chr19:46962153
|
A | C | 1 | a0001c0001t0052g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3826+24745A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962153 | ||||||
chr19:46962196
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3826+24788G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962196 | ||||||
chr19:46962330
|
C | A | 2 | a0001c0001t0016g0092a0001c0001t0016g0094 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3826+24922C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962330 | ||||||
chr19:46962336
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3826+24928C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962336 | ||||||
chr19:46962742
|
T | A | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3827-25247T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962742 | ||||||
chr19:46962851
|
T | C | 1 | a0001c0001t0004g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3827-25138T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962851 | ||||||
chr19:46962857
|
G | A | 2 | a0001c0001t0018g0040a0001c0001t0018g0227 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3827-25132G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962857 | ||||||
chr19:46962884
|
C | T | 1 | a0001c0001t0024g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3827-25105C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962884 | ||||||
chr19:46962960
|
G | A | 1 | a0001c0001t0050g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3827-25029G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962960 | ||||||
chr19:46963226
|
T | C | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-24763T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963226 | ||||||
chr19:46963344
|
G | A | 11 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0004others(8): Show | 11 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.3827-24645G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963344 | ||||||
chr19:46963370
|
T | A | 1 | a0001c0001t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3827-24619T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963370 | ||||||
chr19:46963581
|
C | G | 118 | a0001c0001t0001g0068a0001c0001t0001g0204a0001c0001t0003g0001others(115): Show | 118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.3827-24408C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963581 | ||||||
chr19:46963625
|
T | A | 1 | a0001c0001t0005g0262 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3827-24364T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963625 | ||||||
chr19:46963626
|
A | T | 1 | a0001c0001t0005g0262 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3827-24363A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963626 | ||||||
chr19:46963663
|
C | A | 1 | a0001c0001t0001g0294 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3827-24326C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963663 | ||||||
chr19:46963699
|
C | T | 1 | a0001c0001t0018g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3827-24290C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963699 | ||||||
chr19:46963744
|
G | A | 36 | a0001c0001t0001g0204a0001c0001t0004g0022a0001c0001t0004g0030others(33): Show | 36 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3827-24245G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963744 | ||||||
chr19:46963752
|
C | T | 1 | a0001c0001t0031g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3827-24237C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963752 | ||||||
chr19:46964069
|
T | C | 2 | a0001c0001t0007g0015a0001c0001t0007g0019 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3827-23920T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964069 | ||||||
chr19:46964301
|
A | G | 5 | a0001c0001t0012g0112a0001c0001t0012g0113a0001c0001t0012g0114others(2): Show | 5 | HG02027.hp2 NA18961.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.3827-23688A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964301 | ||||||
chr19:46964362
|
G | A | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3827-23627G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964362 | ||||||
chr19:46964372
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3827-23617A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964372 | ||||||
chr19:46964380
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-23609G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964380 | ||||||
chr19:46964743
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0283 | 3 | HG01257.hp2 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.3827-23246G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964743 | ||||||
chr19:46964984
|
G | T | 2 | a0001c0001t0003g0012a0001c0001t0003g0021 | 2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3827-23005G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964984 | ||||||
chr19:46965075
|
G | A | 1 | a0001c0001t0014g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3827-22914G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965075 | ||||||
chr19:46965087
|
C | T | 1 | a0004c0008t0015g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3827-22902C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965087 | ||||||
chr19:46965168
|
C | T | 2 | a0001c0001t0003g0054a0001c0001t0045g0053 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.3827-22821C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965168 | ||||||
chr19:46965212
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-22777C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965212 | ||||||
chr19:46965466
|
T | TTTTG | 53 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(50): Show | 53 | HG00639.hp2 HG00642.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.3827-22491_3827-22 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46965466 | |||||
chr19:46965466
|
T | TTTTGTTT others(1): Show |
10 | a0001c0001t0008g0125a0001c0001t0014g0069a0001c0001t0017g0088others(7): Show | 10 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3827-22495_3827-22 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46965466 | |||||
chr19:46965466
|
TTTTG | T | 114 | a0001c0001t0001g0068a0001c0001t0001g0204a0001c0001t0002g0267others(111): Show | 114 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.3827-22491_3827-22 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46965466 | |||||
chr19:46965575
|
C | T | 1 | a0001c0002t0006g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3827-22414C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965575 | ||||||
chr19:46965715
|
G | A | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3827-22274G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965715 | ||||||
chr19:46965791
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-22198A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965791 | ||||||
chr19:46965905
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0196 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3827-22084G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965905 | ||||||
chr19:46966082
|
G | T | 1 | a0001c0001t0005g0262 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3827-21907G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966082 | ||||||
chr19:46966319
|
C | T | 3 | a0001c0001t0024g0032a0001c0001t0024g0220a0001c0001t0038g0252 | 3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3827-21670C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966319 | ||||||
chr19:46966513
|
T | C | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-21476T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966513 | ||||||
chr19:46966849
|
A | T | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-21140A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966849 | ||||||
chr19:46966850
|
G | C | 1 | a0001c0001t0007g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3827-21139G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966850 | ||||||
chr19:46966874
|
C | T | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-21115C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966874 | ||||||
chr19:46966986
|
G | A | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3827-21003G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966986 | ||||||
chr19:46967071
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0003g0231a0001c0001t0025g0067 | 3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3827-20918C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967071 | ||||||
chr19:46967097
|
C | T | 2 | a0001c0001t0003g0051a0001c0001t0007g0013 | 2 | HG02717.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3827-20892C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967097 | ||||||
chr19:46967213
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3827-20776G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967213 | ||||||
chr19:46967279
|
C | T | 185 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0204others(182): Show | 185 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3827-20710C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967279 | ||||||
chr19:46967370
|
G | A | 1 | a0001c0001t0002g0265 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3827-20619G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967370 | ||||||
chr19:46967402
|
A | G | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3827-20587A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967402 | ||||||
chr19:46967493
|
T | A | 51 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(48): Show | 51 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.3827-20496T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967493 | ||||||
chr19:46967605
|
T | C | 146 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0003g0001others(143): Show | 146 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.3827-20384T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967605 | ||||||
chr19:46967764
|
G | A | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3827-20225G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967764 | ||||||
chr19:46967815
|
G | C | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-20174G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967815 | ||||||
chr19:46967821
|
C | G | 1 | a0001c0001t0005g0256 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3827-20168C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967821 | ||||||
chr19:46967918
|
C | T | 1 | a0001c0001t0046g0043 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3827-20071C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967918 | ||||||
chr19:46967953
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0294 | 2 | NA18951.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.3827-20036G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967953 | ||||||
chr19:46968419
|
T | C | 1 | a0001c0007t0015g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3827-19570T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46968419 | ||||||
chr19:46968457
|
A | G | 1 | a0001c0001t0042g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3827-19532A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46968457 | ||||||
chr19:46968639
|
C | T | 1 | a0001c0003t0004g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3827-19350C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46968639 | ||||||
chr19:46968808
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3827-19181C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46968808 | ||||||
chr19:46969042
|
G | A | 1 | a0001c0001t0004g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3827-18947G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969042 | ||||||
chr19:46969336
|
T | C | 4 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-18653T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969336 | ||||||
chr19:46969393
|
A | G | 1 | a0001c0001t0005g0124 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3827-18596A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969393 | ||||||
chr19:46969609
|
C | G | 1 | a0001c0001t0001g0190 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3827-18380C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969609 | ||||||
chr19:46969728
|
G | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-18261G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969728 | ||||||
chr19:46969821
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3827-18168T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969821 | ||||||
chr19:46969919
|
C | T | 1 | a0001c0001t0049g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3827-18070C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969919 | ||||||
chr19:46970057
|
T | A | 4 | a0001c0001t0003g0054a0001c0001t0018g0040a0001c0001t0018g0227others(1): Show | 4 | HG02451.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3827-17932T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970057 | ||||||
chr19:46970142
|
A | G | 2 | a0001c0001t0024g0032a0001c0001t0024g0220 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3827-17847A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970142 | ||||||
chr19:46970316
|
C | A | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3827-17673C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970316 | ||||||
chr19:46970387
|
C | A | 3 | a0001c0001t0001g0119a0001c0001t0008g0122a0001c0001t0008g0260 | 3 | HG01070.hp2 HG01192.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3827-17602C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970387 | ||||||
chr19:46970409
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3827-17580G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970409 | ||||||
chr19:46970485
|
T | C | 190 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0204others(187): Show | 190 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.3827-17504T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970485 | ||||||
chr19:46970596
|
C | T | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-17393C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970596 | ||||||
chr19:46970794
|
G | A | 34 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.3827-17195G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970794 | ||||||
chr19:46970921
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-17068G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970921 | ||||||
chr19:46971380
|
C | T | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3827-16609C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46971380 | ||||||
chr19:46971477
|
T | G | 3 | a0001c0001t0001g0170a0001c0001t0007g0042a0001c0001t0046g0043 | 3 | HG02071.hp2 NA18943.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.3827-16512T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46971477 | ||||||
chr19:46971949
|
C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0283 | 3 | HG01257.hp2 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.3827-16040C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46971949 | ||||||
chr19:46972095
|
C | T | 80 | a0001c0001t0002g0145a0001c0001t0003g0001a0001c0001t0003g0002others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.3827-15894C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46972095 | ||||||
chr19:46972117
|
C | T | 35 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(32): Show | 35 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.3827-15872C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46972117 | ||||||
chr19:46972179
|
T | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-15810T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46972179 | ||||||
chr19:46972537
|
C | A | 1 | a0001c0001t0003g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3827-15452C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46972537 | ||||||
chr19:46972875
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3827-15114C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46972875 | ||||||
chr19:46972974
|
C | A | 1 | a0001c0001t0016g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3827-15015C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46972974 | ||||||
chr19:46973021
|
A | AT | 187 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(184): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.3827-14960dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46973021 | |||||
chr19:46973103
|
C | T | 1 | a0001c0007t0015g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3827-14886C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973103 | ||||||
chr19:46973266
|
G | A | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG01261.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.3827-14723G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973266 | ||||||
chr19:46973391
|
T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-14598T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973391 | ||||||
chr19:46973485
|
C | G | 1 | a0001c0001t0003g0045 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3827-14504C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973485 | ||||||
chr19:46973509
|
G | C | 1 | a0001c0001t0002g0158 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3827-14480G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973509 | ||||||
chr19:46973564
|
G | A | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-14425G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973564 | ||||||
chr19:46973646
|
G | A | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3827-14343G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973646 | ||||||
chr19:46973711
|
G | A | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3827-14278G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973711 | ||||||
chr19:46973754
|
G | A | 1 | a0003c0013t0004g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3827-14235G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973754 | ||||||
chr19:46973784
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-14205G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973784 | ||||||
chr19:46973903
|
G | T | 1 | a0001c0001t0045g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3827-14086G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973903 | ||||||
chr19:46973995
|
CA | C | 36 | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(33): Show | 36 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3827-13983delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46973995 | |||||
chr19:46974486
|
A | G | 7 | a0001c0001t0015g0037a0001c0001t0023g0039a0001c0001t0023g0055others(4): Show | 7 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.3827-13503A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46974486 | ||||||
chr19:46974687
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3827-13302T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46974687 | ||||||
chr19:46974895
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3827-13094G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46974895 | ||||||
chr19:46975072
|
A | G | 3 | a0001c0001t0027g0034a0001c0001t0027g0221a0001c0002t0001g0033 | 3 | HG02258.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3827-12917A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975072 | ||||||
chr19:46975122
|
G | A | 1 | a0001c0001t0038g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3827-12867G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975122 | ||||||
chr19:46975171
|
G | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-12818G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975171 | ||||||
chr19:46975193
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3827-12796C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975193 | ||||||
chr19:46975275
|
A | T | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3827-12714A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975275 | ||||||
chr19:46975297
|
A | G | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3827-12692A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975297 | ||||||
chr19:46975304
|
C | G | 1 | a0001c0001t0016g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3827-12685C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975304 | ||||||
chr19:46975410
|
G | A | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3827-12579G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975410 | ||||||
chr19:46975527
|
T | C | 187 | a0001c0001t0001g0119a0001c0001t0001g0130a0001c0001t0003g0001others(184): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.3827-12462T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975527 | ||||||
chr19:46975631
|
C | CAGA | 66 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(63): Show | 66 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.3827-12356_3827-12 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46975631 | |||||
chr19:46975970
|
T | G | 36 | a0001c0001t0001g0130a0001c0001t0004g0022a0001c0001t0004g0030others(33): Show | 36 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3827-12019T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975970 | ||||||
chr19:46976210
|
C | CT | 100 | a0001c0001t0001g0068a0001c0001t0001g0130a0001c0001t0001g0142others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.3827-11759dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46976210 | |||||
chr19:46976210
|
CT | C | 13 | a0001c0001t0003g0050a0001c0001t0003g0064a0001c0001t0003g0224others(10): Show | 13 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.3827-11759delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46976210 | |||||
chr19:46976210
|
CTT | C | 30 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(27): Show | 30 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.3827-11760_3827-11 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46976210 | |||||
chr19:46976325
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-11664A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46976325 | ||||||
chr19:46976591
|
C | T | 1 | a0001c0001t0009g0268 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3827-11398C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46976591 | ||||||
chr19:46976619
|
G | A | 3 | a0001c0001t0014g0087a0001c0001t0014g0247a0001c0001t0014g0248 | 3 | HG02559.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3827-11370G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46976619 | ||||||
chr19:46976679
|
G | A | 1 | a0001c0001t0005g0118 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3827-11310G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46976679 | ||||||
chr19:46976779
|
G | C | 1 | a0001c0001t0050g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3827-11210G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46976779 | ||||||
chr19:46976935
|
T | C | 297 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.3827-11054T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46976935 | ||||||
chr19:46977065
|
C | T | 1 | a0001c0001t0005g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3827-10924C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46977065 | ||||||
chr19:46977417
|
A | G | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-10572A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46977417 | ||||||
chr19:46977603
|
C | T | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-10386C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46977603 | ||||||
chr19:46977617
|
G | T | 1 | a0001c0001t0029g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3827-10372G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46977617 | ||||||
chr19:46978067
|
T | G | 297 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.3827-9922T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978067 | ||||||
chr19:46978084
|
G | A | 1 | a0001c0001t0020g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3827-9905G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978084 | ||||||
chr19:46978425
|
G | A | 25 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0048others(22): Show | 25 | HG00408.hp2 HG00642.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.3827-9564G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978425 | ||||||
chr19:46978474
|
T | G | 1 | a0001c0001t0001g0172 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3827-9515T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978474 | ||||||
chr19:46978607
|
T | A | 1 | a0001c0001t0002g0275 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3827-9382T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978607 | ||||||
chr19:46978607
|
TGTG | T | 49 | a0001c0001t0001g0142a0001c0001t0001g0170a0001c0001t0001g0172others(46): Show | 49 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.3827-9378_3827-937 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46978607 | |||||
chr19:46978686
|
G | GATGTGTG others(11): Show |
186 | a0001c0001t0001g0119a0001c0001t0001g0130a0001c0001t0003g0001others(183): Show | 186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3827-9287_3827-928 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46978686 | |||||
chr19:46978687
|
A | ATGTGTGT others(70): Show |
1 | a0001c0001t0003g0128 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3827-9287_3827-928 others(81): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46978687 | |||||
chr19:46978717
|
G | A | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3827-9272G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978717 | ||||||
chr19:46978796
|
GTGGGATG others(56): Show |
G | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-9189_3827-912 others(67): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46978796 | |||||
chr19:46978893
|
GGGGGTGT others(7): Show |
G | 1 | a0001c0001t0002g0295 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3827-9083_3827-907 others(18): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46978893 | |||||
chr19:46978939
|
G | A | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3827-9050G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978939 | ||||||
chr19:46978968
|
A | G | 296 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.3827-9021A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978968 | ||||||
chr19:46978969
|
A | C | 1 | a0001c0001t0003g0002 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3827-9020A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978969 | ||||||
chr19:46979003
|
G | A | 1 | a0001c0001t0020g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3827-8986G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979003 | ||||||
chr19:46979034
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3827-8955G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979034 | ||||||
chr19:46979054
|
A | G | 1 | a0001c0001t0002g0159 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3827-8935A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979054 | ||||||
chr19:46979062
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-8927G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979062 | ||||||
chr19:46979147
|
G | A | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3827-8842G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979147 | ||||||
chr19:46979321
|
C | T | 1 | a0001c0001t0003g0002 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3827-8668C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979321 | ||||||
chr19:46979322
|
T | C | 1 | a0001c0001t0003g0002 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3827-8667T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979322 | ||||||
chr19:46979323
|
C | T | 1 | a0001c0001t0003g0002 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3827-8666C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979323 | ||||||
chr19:46979334
|
C | T | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3827-8655C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979334 | ||||||
chr19:46979345
|
T | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0218 | 2 | HG01081.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3827-8644T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979345 | ||||||
chr19:46979493
|
T | C | 1 | a0001c0001t0003g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3827-8496T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979493 | ||||||
chr19:46979779
|
T | C | 5 | a0001c0001t0011g0056a0001c0001t0011g0057a0001c0001t0011g0058others(2): Show | 5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3827-8210T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979779 | ||||||
chr19:46979805
|
A | G | 3 | a0001c0001t0027g0034a0001c0001t0027g0221a0001c0002t0001g0033 | 3 | HG02258.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3827-8184A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979805 | ||||||
chr19:46979848
|
A | G | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-8141A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979848 | ||||||
chr19:46980043
|
G | C | 2 | a0001c0001t0002g0180a0001c0001t0002g0265 | 2 | NA18612.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.3827-7946G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980043 | ||||||
chr19:46980046
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3827-7943G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980046 | ||||||
chr19:46980049
|
G | A | 3 | a0001c0001t0003g0231a0001c0001t0025g0067a0001c0001t0029g0025 | 3 | HG02145.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3827-7940G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980049 | ||||||
chr19:46980464
|
C | T | 1 | a0001c0001t0007g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3827-7525C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980464 | ||||||
chr19:46980631
|
C | T | 4 | a0001c0001t0003g0054a0001c0001t0018g0040a0001c0001t0018g0227others(1): Show | 4 | HG02451.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3827-7358C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980631 | ||||||
chr19:46980665
|
G | A | 7 | a0001c0001t0015g0037a0001c0001t0023g0039a0001c0001t0023g0055others(4): Show | 7 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.3827-7324G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980665 | ||||||
chr19:46980738
|
G | A | 2 | a0001c0001t0004g0082a0001c0001t0004g0095 | 2 | HG02698.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3827-7251G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980738 | ||||||
chr19:46980746
|
T | G | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-7243T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980746 | ||||||
chr19:46981247
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3827-6742G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981247 | ||||||
chr19:46981317
|
A | T | 1 | a0001c0001t0003g0065 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3827-6672A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981317 | ||||||
chr19:46981408
|
TAAGC | T | 3 | a0001c0001t0014g0087a0001c0001t0014g0247a0001c0001t0014g0248 | 3 | HG02559.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3827-6577_3827-657 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981408 | |||||
chr19:46981545
|
G | A | 1 | a0001c0001t0004g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3827-6444G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981545 | ||||||
chr19:46981723
|
C | T | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-6266C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981723 | ||||||
chr19:46981824
|
G | T | 1 | a0001c0002t0006g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3827-6165G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981824 | ||||||
chr19:46981825
|
G | GTGTTT | 40 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(37): Show | 40 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.3827-6121_3827-611 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981825 | |||||
chr19:46981825
|
G | GTGTTTTG others(3): Show |
11 | a0001c0001t0012g0113a0001c0001t0021g0254a0001c0001t0051g0229others(8): Show | 11 | HG02027.hp2 HG02055.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.3827-6126_3827-611 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981825 | |||||
chr19:46981825
|
G | GTGTTTTG others(8): Show |
1 | a0001c0005t0006g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3827-6131_3827-611 others(19): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981825 | |||||
chr19:46981825
|
G | T | 1 | a0001c0002t0006g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3827-6164G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981825 | ||||||
chr19:46981825
|
GTGTTT | G | 86 | a0001c0001t0001g0068a0001c0001t0001g0130a0001c0001t0001g0134others(83): Show | 86 | HG00140.hp1 HG00280.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.3827-6121_3827-611 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981825 | |||||
chr19:46981825
|
GTGTTTTG others(3): Show |
G | 118 | a0001c0001t0001g0204a0001c0001t0002g0136a0001c0001t0003g0001others(115): Show | 118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.3827-6126_3827-611 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981825 | |||||
chr19:46981825
|
GTGTTTTG others(13): Show |
G | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3827-6136_3827-611 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981825 | |||||
chr19:46981875
|
A | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | NA19004.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3827-6114A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981875 | ||||||
chr19:46981999
|
A | T | 6 | a0001c0001t0007g0042a0001c0001t0007g0046a0001c0001t0007g0060others(3): Show | 6 | HG02071.hp2 NA18943.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.3827-5990A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981999 | ||||||
chr19:46982070
|
C | T | 51 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(48): Show | 51 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.3827-5919C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982070 | ||||||
chr19:46982095
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3827-5894G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982095 | ||||||
chr19:46982114
|
C | A | 11 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0004others(8): Show | 11 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.3827-5875C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982114 | ||||||
chr19:46982152
|
A | G | 3 | a0001c0001t0001g0205a0001c0001t0026g0187a0001c0001t0026g0288 | 3 | HG00558.hp2 HG00597.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.3827-5837A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982152 | ||||||
chr19:46982203
|
G | A | 1 | a0001c0001t0051g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3827-5786G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982203 | ||||||
chr19:46982281
|
A | C | 1 | a0001c0001t0021g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3827-5708A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982281 | ||||||
chr19:46982524
|
T | TAAAAAGC others(1): Show |
5 | a0001c0001t0007g0013a0001c0001t0007g0016a0001c0001t0007g0017others(2): Show | 5 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3827-5464_3827-545 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46982524 | |||||
chr19:46982936
|
C | T | 7 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3827-5053C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982936 | ||||||
chr19:46983054
|
C | CA | 44 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0146others(41): Show | 44 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.3827-4905dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | |||||
chr19:46983054
|
C | CAA | 30 | a0001c0001t0001g0068a0001c0001t0001g0173a0001c0001t0001g0177others(27): Show | 30 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3827-4906_3827-490 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | |||||
chr19:46983054
|
C | CAAA | 25 | a0001c0001t0001g0172a0001c0001t0001g0185a0001c0001t0001g0186others(22): Show | 25 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.3827-4907_3827-490 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | |||||
chr19:46983054
|
C | CAAAA | 19 | a0001c0001t0003g0031a0001c0001t0003g0045a0001c0001t0003g0048others(16): Show | 19 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.3827-4908_3827-490 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | |||||
chr19:46983054
|
C | CAAAAA | 17 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0007others(14): Show | 17 | HG00408.hp2 HG00642.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.3827-4909_3827-490 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | |||||
chr19:46983054
|
C | CAAAAAAA others(6): Show |
1 | a0002c0004t0003g0003 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3827-4917_3827-490 others(17): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | |||||
chr19:46983054
|
C | CAAAAAAA others(7): Show |
1 | a0002c0004t0003g0008 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3827-4918_3827-490 others(18): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | |||||
chr19:46983054
|
CA | C | 41 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(38): Show | 41 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.3827-4905delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | |||||
chr19:46983054
|
CAA | C | 44 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(41): Show | 44 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.3827-4906_3827-490 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | |||||
chr19:46983054
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0007g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3827-4916_3827-490 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | |||||
chr19:46983054
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0011g0056a0001c0001t0011g0057a0001c0001t0011g0058others(2): Show | 5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3827-4917_3827-490 others(17): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | |||||
chr19:46983151
|
G | A | 1 | a0001c0001t0052g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3827-4838G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983151 | ||||||
chr19:46983240
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3827-4749C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983240 | ||||||
chr19:46983483
|
C | A | 1 | a0001c0001t0004g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3827-4506C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983483 | ||||||
chr19:46983606
|
C | CT | 102 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0184others(99): Show | 102 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.3827-4358dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983606 | |||||
chr19:46983606
|
C | CTT | 22 | a0001c0001t0001g0173a0001c0001t0002g0174a0001c0001t0003g0048others(19): Show | 22 | HG01243.hp2 HG01928.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.3827-4359_3827-435 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983606 | |||||
chr19:46983606
|
CT | C | 6 | a0001c0001t0001g0218a0001c0001t0002g0156a0001c0001t0002g0275others(3): Show | 6 | HG01070.hp1 HG01516.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.3827-4358delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983606 | |||||
chr19:46983606
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0024g0032 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3827-4368_3827-435 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983606 | |||||
chr19:46983706
|
C | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-4283C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983706 | ||||||
chr19:46983861
|
C | T | 1 | a0004c0008t0015g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3827-4128C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983861 | ||||||
chr19:46983882
|
G | A | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3827-4107G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983882 | ||||||
chr19:46983912
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4077G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983912 | ||||||
chr19:46983947
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4042C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983947 | ||||||
chr19:46983950
|
T | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4039T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983950 | ||||||
chr19:46983954
|
A | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4035A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983954 | ||||||
chr19:46983960
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4029G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983960 | ||||||
chr19:46983963
|
A | G | 11 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(8): Show | 11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3827-4026A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983963 | ||||||
chr19:46983968
|
A | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4021A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983968 | ||||||
chr19:46983971
|
T | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4018T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983971 | ||||||
chr19:46983980
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4009G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983980 | ||||||
chr19:46983982
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4007C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983982 | ||||||
chr19:46983998
|
G | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3991G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983998 | ||||||
chr19:46984017
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3972G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984017 | ||||||
chr19:46984032
|
T | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3957T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984032 | ||||||
chr19:46984092
|
T | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3897T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984092 | ||||||
chr19:46984146
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3843G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984146 | ||||||
chr19:46984147
|
T | G | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3842T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984147 | ||||||
chr19:46984153
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3836G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984153 | ||||||
chr19:46984155
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3834G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984155 | ||||||
chr19:46984157
|
C | G | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3832C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984157 | ||||||
chr19:46984165
|
A | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3824A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984165 | ||||||
chr19:46984183
|
T | G | 1 | a0001c0001t0003g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3827-3806T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984183 | ||||||
chr19:46984195
|
T | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3794T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984195 | ||||||
chr19:46984217
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3772G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984217 | ||||||
chr19:46984225
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3764G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984225 | ||||||
chr19:46984231
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3758G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984231 | ||||||
chr19:46984245
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3744G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984245 | ||||||
chr19:46984249
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3740G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984249 | ||||||
chr19:46984252
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3737G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984252 | ||||||
chr19:46984289
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3700C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984289 | ||||||
chr19:46984290
|
G | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3699G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984290 | ||||||
chr19:46984292
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3697G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984292 | ||||||
chr19:46984296
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3693G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984296 | ||||||
chr19:46984301
|
A | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3688A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984301 | ||||||
chr19:46984428
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3561G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984428 | ||||||
chr19:46984452
|
T | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3537T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984452 | ||||||
chr19:46984469
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3520C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984469 | ||||||
chr19:46984478
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3511G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984478 | ||||||
chr19:46984479
|
T | G | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3510T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984479 | ||||||
chr19:46984491
|
T | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3498T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984491 | ||||||
chr19:46984493
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3496C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984493 | ||||||
chr19:46984501
|
G | A | 1 | a0001c0001t0002g0295 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3827-3488G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984501 | ||||||
chr19:46984524
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3465G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984524 | ||||||
chr19:46984525
|
T | G | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3464T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984525 | ||||||
chr19:46984539
|
T | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3450T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984539 | ||||||
chr19:46984548
|
A | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3441A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984548 | ||||||
chr19:46984552
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3437C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984552 | ||||||
chr19:46984553
|
T | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3436T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984553 | ||||||
chr19:46984554
|
A | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3435A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984554 | ||||||
chr19:46984563
|
T | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3426T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984563 | ||||||
chr19:46984597
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3392C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984597 | ||||||
chr19:46984636
|
C | G | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3353C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984636 | ||||||
chr19:46984658
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3331G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984658 | ||||||
chr19:46984691
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3298G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984691 | ||||||
chr19:46984715
|
T | G | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3274T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984715 | ||||||
chr19:46984717
|
A | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3272A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984717 | ||||||
chr19:46984718
|
T | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3271T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984718 | ||||||
chr19:46984737
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3252G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984737 | ||||||
chr19:46984751
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3238C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984751 | ||||||
chr19:46984764
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3225G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984764 | ||||||
chr19:46984766
|
T | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3223T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984766 | ||||||
chr19:46984768
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3221C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984768 | ||||||
chr19:46984780
|
T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-3209T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984780 | ||||||
chr19:46984793
|
A | G | 7 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3827-3196A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984793 | ||||||
chr19:46984814
|
T | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3175T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984814 | ||||||
chr19:46984815
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3174C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984815 | ||||||
chr19:46984816
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3173G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984816 | ||||||
chr19:46984823
|
T | G | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3166T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984823 | ||||||
chr19:46984824
|
G | C | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3165G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984824 | ||||||
chr19:46984828
|
T | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3161T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984828 | ||||||
chr19:46984831
|
G | A | 1 | a0001c0001t0016g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3827-3158G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984831 | ||||||
chr19:46984848
|
G | T | 1 | a0001c0001t0004g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3827-3141G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984848 | ||||||
chr19:46984972
|
C | T | 29 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(26): Show | 29 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.3827-3017C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984972 | ||||||
chr19:46985088
|
G | A | 1 | a0001c0001t0013g0223 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3827-2901G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985088 | ||||||
chr19:46985305
|
A | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0283 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3827-2684A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985305 | ||||||
chr19:46985327
|
G | A | 1 | a0001c0001t0020g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3827-2662G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985327 | ||||||
chr19:46985380
|
T | C | 65 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(62): Show | 65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-2609T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985380 | ||||||
chr19:46985573
|
A | G | 51 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(48): Show | 51 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.3827-2416A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985573 | ||||||
chr19:46985634
|
A | G | 187 | a0001c0001t0001g0119a0001c0001t0001g0130a0001c0001t0003g0001others(184): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.3827-2355A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985634 | ||||||
chr19:46985674
|
C | T | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-2315C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985674 | ||||||
chr19:46985707
|
C | G | 1 | a0001c0001t0002g0275 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3827-2282C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985707 | ||||||
chr19:46985709
|
C | T | 1 | a0001c0001t0003g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3827-2280C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985709 | ||||||
chr19:46985723
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3827-2266C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985723 | ||||||
chr19:46985789
|
C | A | 1 | a0001c0001t0002g0141 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3827-2200C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985789 | ||||||
chr19:46985821
|
C | G | 31 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(28): Show | 31 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.3827-2168C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985821 | ||||||
chr19:46985858
|
T | C | 4 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-2131T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985858 | ||||||
chr19:46985893
|
AC | A | 297 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0130others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.3827-2091delC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46985893 | |||||
chr19:46986076
|
T | C | 2 | a0001c0001t0016g0092a0001c0001t0016g0094 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3827-1913T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986076 | ||||||
chr19:46986245
|
T | G | 6 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0016others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3827-1744T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986245 | ||||||
chr19:46986301
|
C | T | 115 | a0001c0001t0001g0130a0001c0001t0003g0001a0001c0001t0003g0002others(112): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.3827-1688C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986301 | ||||||
chr19:46986633
|
A | G | 1 | a0001c0001t0013g0223 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3827-1356A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986633 | ||||||
chr19:46986635
|
G | A | 1 | a0001c0001t0013g0223 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3827-1354G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986635 | ||||||
chr19:46986799
|
A | G | 5 | a0001c0001t0012g0112a0001c0001t0012g0113a0001c0001t0012g0114others(2): Show | 5 | HG02027.hp2 NA18961.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.3827-1190A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986799 | ||||||
chr19:46986866
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3827-1123T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986866 | ||||||
chr19:46986887
|
G | A | 4 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-1102G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986887 | ||||||
chr19:46987036
|
C | T | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3827-953C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987036 | ||||||
chr19:46987080
|
G | A | 1 | a0003c0013t0004g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3827-909G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987080 | ||||||
chr19:46987162
|
T | C | 1 | a0001c0001t0038g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3827-827T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987162 | ||||||
chr19:46987188
|
C | A | 1 | a0001c0001t0013g0223 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3827-801C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987188 | ||||||
chr19:46987218
|
C | CT | 23 | a0001c0001t0001g0134a0001c0001t0001g0282a0001c0001t0002g0131others(20): Show | 23 | HG01069.hp2 HG01261.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.3827-753dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46987218 | |||||
chr19:46987218
|
CT | C | 40 | a0001c0001t0001g0119a0001c0001t0001g0169a0001c0001t0001g0184others(37): Show | 40 | HG00597.hp1 HG01070.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.3827-753delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46987218 | |||||
chr19:46987362
|
C | T | 1 | a0001c0001t0005g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3827-627C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987362 | ||||||
chr19:46987515
|
A | G | 1 | a0001c0001t0009g0135 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3827-474A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987515 | ||||||
chr19:46987681
|
T | C | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG01261.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.3827-308T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987681 | ||||||
chr19:46987823
|
G | C | 1 | a0001c0001t0005g0126 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.3827-166G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987823 | ||||||
chr19:46988443
|
G | T | 8 | a0001c0001t0005g0118a0001c0001t0005g0120a0001c0001t0005g0121others(5): Show | 8 | NA18972.hp1 NA18973.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.3904+377G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4/6 | chr19 | 46988443 | ||||||
chr19:46988460
|
A | G | 94 | a0001c0001t0001g0119a0001c0001t0001g0130a0001c0001t0004g0022others(91): Show | 94 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.3904+394A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4/6 | chr19 | 46988460 | ||||||
chr19:46989218
|
G | A | 174 | a0001c0001t0001g0119a0001c0001t0001g0130a0001c0001t0003g0001others(171): Show | 174 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.3905-326G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4/6 | chr19 | 46989218 | ||||||
chr19:46989255
|
T | C | 1 | a0001c0001t0017g0250 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3905-289T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4/6 | chr19 | 46989255 | ||||||
chr19:46989473
|
AG | A | 7 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3905-70delG | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4/6 | chr19 | 46989473 | ||||||
chr19:46989478
|
C | T | 1 | a0001c0001t0049g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3905-66C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4/6 | chr19 | 46989478 | ||||||
chr19:46989934
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4036+259C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46989934 | ||||||
chr19:46990021
|
G | A | 1 | a0001c0001t0054g0287 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4036+346G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46990021 | ||||||
chr19:46990192
|
A | C | 2 | a0001c0001t0001g0146a0001c0001t0002g0293 | 2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.4036+517A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46990192 | ||||||
chr19:46990376
|
C | G | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4036+701C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46990376 | ||||||
chr19:46990420
|
C | T | 29 | a0001c0001t0004g0022a0001c0001t0004g0070a0001c0001t0004g0071others(26): Show | 29 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.4036+745C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46990420 | ||||||
chr19:46990567
|
T | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.4036+892T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46990567 | ||||||
chr19:46991414
|
T | G | 1 | a0006c0010t0004g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4036+1739T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991414 | ||||||
chr19:46991481
|
G | C | 1 | a0001c0001t0004g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4036+1806G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991481 | ||||||
chr19:46991485
|
T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4036+1810T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991485 | ||||||
chr19:46991596
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0279 | 2 | HG02056.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.4036+1921G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991596 | ||||||
chr19:46991599
|
G | A | 6 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.4036+1924G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991599 | ||||||
chr19:46991626
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4036+1951G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991626 | ||||||
chr19:46991683
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4036+2008G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991683 | ||||||
chr19:46991688
|
T | G | 187 | a0001c0001t0001g0119a0001c0001t0001g0130a0001c0001t0003g0001others(184): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.4036+2013T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991688 | ||||||
chr19:46991790
|
T | C | 1 | a0001c0001t0016g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4036+2115T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991790 | ||||||
chr19:46992166
|
C | T | 4 | a0001c0001t0004g0072a0001c0001t0004g0240a0001c0001t0004g0241others(1): Show | 4 | HG00558.hp1 NA18978.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.4036+2491C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992166 | ||||||
chr19:46992167
|
G | A | 11 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(8): Show | 11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.4036+2492G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992167 | ||||||
chr19:46992320
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0002g0293 | 2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.4036+2645C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992320 | ||||||
chr19:46992642
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.4036+2967G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992642 | ||||||
chr19:46992679
|
C | T | 1 | a0001c0001t0003g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4036+3004C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992679 | ||||||
chr19:46992690
|
G | T | 21 | a0001c0001t0001g0119a0001c0001t0005g0118a0001c0001t0005g0120others(18): Show | 21 | HG01070.hp2 HG01192.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.4036+3015G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992690 | ||||||
chr19:46992831
|
G | A | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4036+3156G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992831 | ||||||
chr19:46993289
|
G | A | 1 | a0001c0002t0006g0214 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4036+3614G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46993289 | ||||||
chr19:46993497
|
C | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0152 | 3 | NA19004.hp1 NA19012.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.4036+3822C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46993497 | ||||||
chr19:46993498
|
C | T | 1 | a0001c0001t0043g0243 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4036+3823C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46993498 | ||||||
chr19:46993656
|
T | G | 1 | a0001c0001t0003g0051 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4036+3981T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46993656 | ||||||
chr19:46994015
|
C | G | 1 | a0001c0001t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.4036+4340C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994015 | ||||||
chr19:46994155
|
C | T | 1 | a0001c0001t0025g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4036+4480C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994155 | ||||||
chr19:46994219
|
G | T | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4036+4544G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994219 | ||||||
chr19:46994220
|
A | T | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4036+4545A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994220 | ||||||
chr19:46994347
|
G | A | 1 | a0001c0001t0003g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4036+4672G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994347 | ||||||
chr19:46994408
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0002g0293 | 2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.4036+4733G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994408 | ||||||
chr19:46994573
|
C | T | 1 | a0001c0001t0004g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4037-4731C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994573 | ||||||
chr19:46994585
|
G | A | 1 | a0001c0001t0003g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4037-4719G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994585 | ||||||
chr19:46994590
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4037-4714G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994590 | ||||||
chr19:46994614
|
G | A | 14 | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.4037-4690G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994614 | ||||||
chr19:46994621
|
A | G | 187 | a0001c0001t0001g0119a0001c0001t0001g0130a0001c0001t0003g0001others(184): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.4037-4683A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994621 | ||||||
chr19:46994783
|
C | T | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4037-4521C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994783 | ||||||
chr19:46994904
|
C | T | 1 | a0001c0001t0004g0076 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4037-4400C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994904 | ||||||
chr19:46994973
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4037-4331G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994973 | ||||||
chr19:46995114
|
A | C | 1 | a0001c0001t0004g0022 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4037-4190A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46995114 | ||||||
chr19:46995154
|
T | C | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4037-4150T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46995154 | ||||||
chr19:46995155
|
A | G | 2 | a0001c0001t0027g0034a0001c0001t0027g0221 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4037-4149A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46995155 | ||||||
chr19:46995641
|
C | A | 1 | a0001c0001t0004g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4037-3663C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46995641 | ||||||
chr19:46995774
|
T | C | 186 | a0001c0001t0001g0119a0001c0001t0003g0001a0001c0001t0003g0002others(183): Show | 186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.4037-3530T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46995774 | ||||||
chr19:46995877
|
G | T | 1 | a0001c0001t0009g0270 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4037-3427G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46995877 | ||||||
chr19:46996058
|
G | T | 1 | a0001c0001t0014g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4037-3246G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996058 | ||||||
chr19:46996076
|
G | T | 1 | a0001c0001t0003g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4037-3228G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996076 | ||||||
chr19:46996166
|
C | T | 1 | a0001c0001t0003g0051 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4037-3138C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996166 | ||||||
chr19:46996167
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0196 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4037-3137G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996167 | ||||||
chr19:46996221
|
A | G | 1 | a0001c0001t0050g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4037-3083A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996221 | ||||||
chr19:46996252
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4037-3052C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996252 | ||||||
chr19:46996417
|
A | G | 2 | a0001c0001t0002g0155a0001c0001t0002g0269 | 2 | HG02293.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.4037-2887A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996417 | ||||||
chr19:46996470
|
C | T | 1 | a0001c0001t0028g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4037-2834C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996470 | ||||||
chr19:46996529
|
C | T | 1 | a0001c0001t0007g0017 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4037-2775C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996529 | ||||||
chr19:46996591
|
T | C | 2 | a0001c0001t0003g0012a0001c0001t0003g0021 | 2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4037-2713T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996591 | ||||||
chr19:46996929
|
G | A | 5 | a0001c0001t0011g0056a0001c0001t0011g0057a0001c0001t0011g0058others(2): Show | 5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.4037-2375G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996929 | ||||||
chr19:46996934
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4037-2370G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996934 | ||||||
chr19:46997093
|
G | T | 79 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0004others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.4037-2211G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997093 | ||||||
chr19:46997285
|
A | T | 2 | a0001c0003t0004g0234a0001c0003t0022g0073 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4037-2019A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997285 | ||||||
chr19:46997431
|
C | G | 3 | a0001c0001t0001g0205a0001c0001t0026g0187a0001c0001t0026g0288 | 3 | HG00558.hp2 HG00597.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.4037-1873C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997431 | ||||||
chr19:46997505
|
G | A | 50 | a0001c0001t0001g0119a0001c0001t0005g0102a0001c0001t0005g0106others(47): Show | 50 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.4037-1799G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997505 | ||||||
chr19:46997603
|
A | G | 1 | a0006c0010t0004g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4037-1701A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997603 | ||||||
chr19:46997801
|
C | A | 2 | a0001c0001t0023g0039a0001c0001t0023g0055 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4037-1503C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997801 | ||||||
chr19:46997831
|
G | A | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4037-1473G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997831 | ||||||
chr19:46997963
|
G | A | 1 | a0001c0001t0004g0235 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4037-1341G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997963 | ||||||
chr19:46998034
|
G | A | 1 | a0001c0001t0038g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4037-1270G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998034 | ||||||
chr19:46998057
|
G | A | 1 | a0001c0002t0053g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4037-1247G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998057 | ||||||
chr19:46998245
|
C | T | 2 | a0001c0001t0005g0106a0001c0001t0005g0107 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4037-1059C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998245 | ||||||
chr19:46998445
|
G | A | 1 | a0001c0001t0004g0245 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.4037-859G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998445 | ||||||
chr19:46998594
|
T | TG | 5 | a0001c0001t0001g0166a0001c0001t0002g0158a0001c0001t0010g0052others(2): Show | 5 | HG01243.hp2 HG01928.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.4037-706dupG | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 46998594 | |||||
chr19:46998629
|
G | A | 1 | a0001c0001t0030g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4037-675G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998629 | ||||||
chr19:46998920
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4037-384G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998920 | ||||||
chr19:46998924
|
G | A | 3 | a0001c0001t0027g0034a0001c0001t0027g0221a0001c0003t0004g0234 | 3 | HG02258.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4037-380G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998924 | ||||||
chr19:46999179
|
G | A | 2 | a0001c0001t0003g0054a0001c0001t0045g0053 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.4037-125G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46999179 | ||||||
chr19:46999226
|
G | A | 1 | a0001c0001t0003g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4037-78G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46999226 | ||||||
chr19:46999228
|
C | CCAT | 7 | a0001c0001t0015g0037a0001c0001t0023g0039a0001c0001t0023g0055others(4): Show | 7 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.4037-73_4037-71dup others(3): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 46999228 | |||||
chr19:46999241
|
C | T | 1 | a0001c0002t0006g0212 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4037-63C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46999241 | ||||||
chr19:46999416
|
C | T | 1 | a0001c0001t0004g0079 | 1 | HG02015.hp1 | splice_region_variant&intron_variant | LOW | c.4142+7C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999416 | ||||||
chr19:46999530
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4142+121G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999530 | ||||||
chr19:46999635
|
G | A | 1 | a0001c0001t0052g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4142+226G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999635 | ||||||
chr19:46999642
|
C | T | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4142+233C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999642 | ||||||
chr19:46999798
|
A | C | 1 | a0001c0001t0003g0051 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4142+389A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999798 | ||||||
chr19:46999853
|
C | T | 1 | a0001c0001t0005g0262 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.4142+444C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999853 | ||||||
chr19:46999937
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4143-394C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999937 |