Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79658 |
|---|---|
| ensemblid | ENSG00000071205.12 |
| hgncid | 26099 |
| symbol | ARHGAP10 |
| name | Rho GTPase activating protein 10 |
| refseq_nuc | NM_024605.4 |
| refseq_prot | NP_078881.3 |
| ensembl_nuc | ENST00000336498.8 |
| ensembl_prot | ENSP00000336923.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 147732088 |
| end | 148072776 |
| strand | + |
| ver | v1.2 |
| region | chr4:147732088-148072776 |
| region5000 | chr4:147727088-148077776 |
| regionname0 | ARHGAP10_chr4_147732088_148072776 |
| regionname5000 | ARHGAP10_chr4_147727088_148077776 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 786 | 98 | 54 | 13 | 20 | 0 | 9 | 12 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0002 | 0/0 | 786 | 5 | 1 | 1 | 2 | 0 | 1 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0003 | 0/0 | 786 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0004 | 0/0 | 786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2361 | 73 | 38 | 13 | 16 | 0 | 4 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| c0002 | 0/0 | 2361 | 11 | 2 | 0 | 4 | 0 | 5 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| c0003 | 0/0 | 2361 | 5 | 1 | 1 | 2 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| c0004 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| c0005 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| c0006 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| c0007 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| c0008 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| c0009 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| c0010 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| c0011 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 910 | 103 | 57 | 13 | 22 | 0 | 9 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| t0002 | 0/0 | 910 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| t0003 | 0/0 | 910 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2361 | 73 | 38 | 13 | 16 | 0 | 4 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0002 | 0/0 | 2361 | 11 | 2 | 0 | 4 | 0 | 5 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0004 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0005 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0006 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0008 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0009 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0011 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0002c0003 | 0/0 | 2361 | 5 | 1 | 1 | 2 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0003c0007 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0004c0010 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3270 | 70 | 37 | 12 | 16 | 0 | 3 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0001t0002 | 0/0 | 3270 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0001t0003 | 0/0 | 3270 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0002t0001 | 0/0 | 3270 | 11 | 2 | 0 | 4 | 0 | 5 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0004t0001 | 0/0 | 3270 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0005t0001 | 0/0 | 3270 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0006t0001 | 0/0 | 3270 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0008t0001 | 0/0 | 3270 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0009t0001 | 0/0 | 3270 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0001c0011t0001 | 0/0 | 3270 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0002c0003t0001 | 0/0 | 3270 | 5 | 1 | 1 | 2 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0003c0007t0001 | 0/0 | 3270 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| a0004c0010t0001 | 0/0 | 3270 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | copy fasta | chr4 | 147727088 | 148077776 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0005t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0005t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0006t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0008t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0008t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0009t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0009t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0001c0011t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0002c0003t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0002c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0002c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0003c0007t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0003c0007t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| a0004c0010t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0009 | AMR | PUR | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01891 | hp2 | a0003 | c0007 | t0001 | g0079 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02165 | hp1 | a0002 | c0003 | t0001 | g0032 | EAS | CDX | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | CDX | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02258 | hp2 | a0001 | c0006 | t0001 | g0042 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02451 | hp2 | a0001 | c0011 | t0001 | g0092 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0105 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0098 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0074 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02922 | hp2 | a0001 | c0006 | t0001 | g0040 | AFR | ESN | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03041 | hp1 | a0003 | c0007 | t0001 | g0082 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03098 | hp1 | a0001 | c0008 | t0001 | g0060 | AFR | MSL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0102 | AFR | MSL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | MSL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0096 | AFR | MSL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03225 | hp2 | a0001 | c0009 | t0001 | g0008 | AFR | MSL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03516 | hp2 | a0001 | c0005 | t0001 | g0003 | AFR | ESN | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03710 | hp1 | a0002 | c0003 | t0001 | g0064 | SAS | PJL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | BEB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA18522 | hp1 | a0001 | c0009 | t0001 | g0007 | AFR | YRI | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | YRI | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA18612 | hp1 | a0002 | c0003 | t0001 | g0073 | EAS | CHB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA18906 | hp1 | a0004 | c0010 | t0001 | g0048 | AFR | YRI | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA18906 | hp2 | a0001 | c0006 | t0001 | g0071 | AFR | YRI | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03471 | hp1 | a0001 | c0008 | t0001 | g0059 | AFR | MSL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0045 | AFR | MSL | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0011 | REF | REF | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0039 | REF | REF | ARHGAP10_chr4_147727088_148077776 | ARHGAP10 | chr4 | 147727088 | 148077776 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:148023345
|
C | T | 1 | a0004 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.1799C>T | p.Ser600Leu | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/23 | 2013/3270 | 1799/2361 | 600/786 | chr4 | 148023345 | ||
| chr4:148023409
|
A | C | 1 | a0004 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.1863A>C | p.Glu621Asp | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/23 | 2077/3270 | 1863/2361 | 621/786 | chr4 | 148023409 | ||
| chr4:148063170
|
A | G | 1 | a0002 | 5 | HG01169.hp2 HG02165.hp1 HG03225.hp1 others(2): Show |
missense_variant | MODERATE | c.2050A>G | p.Met684Val | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 21/23 | 2264/3270 | 2050/2361 | 684/786 | chr4 | 148063170 | ||
| chr4:148063227
|
A | G | 1 | a0003 | 2 | HG01891.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.2107A>G | p.Thr703Ala | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 21/23 | 2321/3270 | 2107/2361 | 703/786 | chr4 | 148063227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:147875047
|
G | A | 1 | a0001c0004 | 3 | HG02572.hp2 HG03098.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.729G>A | p.Arg243Arg | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/23 | 943/3270 | 729/2361 | 243/786 | chr4 | 147875047 | ||
| chr4:147913126
|
C | T | 1 | a0001c0011 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1215C>T | p.Ala405Ala | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/23 | 1429/3270 | 1215/2361 | 405/786 | chr4 | 147913126 | ||
| chr4:147965034
|
C | T | 2 | a0001c0006a0004c0010 | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
synonymous_variant | LOW | c.1461C>T | p.Ser487Ser | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 17/23 | 1675/3270 | 1461/2361 | 487/786 | chr4 | 147965034 | ||
| chr4:148023316
|
A | G | 1 | a0001c0002 | 11 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(8): Show |
synonymous_variant | LOW | c.1770A>G | p.Ala590Ala | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/23 | 1984/3270 | 1770/2361 | 590/786 | chr4 | 148023316 | ||
| chr4:148023382
|
C | T | 1 | a0001c0005 | 3 | HG02615.hp1 HG02886.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1836C>T | p.Ala612Ala | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/23 | 2050/3270 | 1836/2361 | 612/786 | chr4 | 148023382 | ||
| chr4:148023388
|
C | T | 1 | a0001c0009 | 2 | HG03225.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.1842C>T | p.Tyr614Tyr | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/23 | 2056/3270 | 1842/2361 | 614/786 | chr4 | 148023388 | ||
| chr4:148046962
|
C | T | 1 | a0001c0008 | 2 | HG03098.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.1938C>T | p.Pro646Pro | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/23 | 2152/3270 | 1938/2361 | 646/786 | chr4 | 148046962 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:148072581
|
A | G | 1 | a0001c0001t0003 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*500A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 23/23 | 500 | chr4 | 148072581 | |||||
| chr4:148072706
|
C | G | 1 | a0001c0001t0002 | 2 | HG01070.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*625C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 23/23 | 625 | chr4 | 148072706 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:147732578
|
C | T | 2 | a0001c0001t0001g0106a0001c0004t0001g0105 | 2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154+123C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147732578 | ||||||
| chr4:147732724
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.154+269C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147732724 | ||||||
| chr4:147732818
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+363C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147732818 | ||||||
| chr4:147732987
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.154+532T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147732987 | ||||||
| chr4:147733338
|
A | ATTAGCCC others(6): Show |
8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+893_154+894ins others(13): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147733338 | |||||
| chr4:147733500
|
T | C | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+1045T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147733500 | ||||||
| chr4:147733522
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+1067A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147733522 | ||||||
| chr4:147733537
|
A | C | 8 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+1082A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147733537 | ||||||
| chr4:147733645
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+1190G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147733645 | ||||||
| chr4:147733760
|
C | A | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.154+1305C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147733760 | ||||||
| chr4:147734013
|
GC | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.154+1560delC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147734013 | |||||
| chr4:147734059
|
G | A | 3 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042 | 3 | HG02258.hp2 HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.154+1604G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147734059 | ||||||
| chr4:147734125
|
A | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(35): Show | 38 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.154+1670A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147734125 | ||||||
| chr4:147734327
|
T | A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+1872T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147734327 | ||||||
| chr4:147734591
|
G | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.154+2136G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147734591 | ||||||
| chr4:147734691
|
T | TC | 3 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.154+2240dupC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147734691 | |||||
| chr4:147734924
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.154+2469A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147734924 | ||||||
| chr4:147735379
|
T | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+2924T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147735379 | ||||||
| chr4:147735746
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.154+3291C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147735746 | ||||||
| chr4:147735853
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154+3398G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147735853 | ||||||
| chr4:147736051
|
CA | C | 8 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0091others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+3597delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147736051 | ||||||
| chr4:147736120
|
C | CTG | 22 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0038others(19): Show | 22 | HG01071.hp2 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.154+3698_154+3699d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147736120 | |||||
| chr4:147736120
|
C | CTGTG | 22 | a0001c0001t0001g0034a0001c0001t0001g0049a0001c0001t0001g0050others(19): Show | 22 | HG00558.hp2 HG01261.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.154+3696_154+3699d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147736120 | |||||
| chr4:147736120
|
C | CTGTGTG | 18 | a0001c0001t0001g0035a0001c0001t0001g0061a0001c0001t0001g0062others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.154+3694_154+3699d others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147736120 | |||||
| chr4:147736120
|
C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+3692_154+3699d others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147736120 | |||||
| chr4:147736120
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0001g0036a0001c0005t0001g0098 | 2 | HG02615.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.154+3690_154+3699d others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147736120 | |||||
| chr4:147736120
|
C | CTGTGTGT others(5): Show |
1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+3688_154+3699d others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147736120 | |||||
| chr4:147736150
|
G | GTGTC | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.154+3698_154+3699i others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147736150 | |||||
| chr4:147736150
|
G | GTGTGTC | 2 | a0001c0009t0001g0007a0001c0009t0001g0008 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.154+3699_154+3700i others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147736150 | |||||
| chr4:147736621
|
C | T | 29 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(26): Show | 29 | HG01261.hp1 HG01891.hp1 HG02080.hp1 others(26): Show |
intron_variant | MODIFIER | c.154+4166C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147736621 | ||||||
| chr4:147736793
|
C | A | 32 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(29): Show | 32 | HG01261.hp1 HG01891.hp1 HG02080.hp1 others(29): Show |
intron_variant | MODIFIER | c.154+4338C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147736793 | ||||||
| chr4:147736820
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.154+4365A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147736820 | ||||||
| chr4:147736851
|
G | GGAGACGT | 3 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.154+4399_154+4405d others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147736851 | |||||
| chr4:147736925
|
T | A | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.154+4470T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147736925 | ||||||
| chr4:147736957
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(7): Show | 10 | HG01071.hp2 HG01169.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.154+4502G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147736957 | ||||||
| chr4:147737181
|
C | T | 2 | a0001c0001t0001g0070a0001c0002t0001g0066 | 2 | NA18979.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.154+4726C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147737181 | ||||||
| chr4:147737291
|
C | T | 2 | a0001c0001t0001g0106a0001c0004t0001g0105 | 2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154+4836C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147737291 | ||||||
| chr4:147737326
|
C | CT | 30 | a0001c0001t0001g0027a0001c0001t0001g0034a0001c0001t0001g0044others(27): Show | 30 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.154+4888dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147737326 | |||||
| chr4:147737326
|
C | CTT | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0008t0001g0059others(1): Show | 4 | HG02738.hp1 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+4887_154+4888d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147737326 | |||||
| chr4:147737326
|
CT | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0099a0001c0001t0001g0100others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+4888delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147737326 | |||||
| chr4:147737446
|
C | T | 3 | a0001c0001t0001g0077a0001c0002t0001g0072a0001c0002t0001g0078 | 3 | HG00558.hp2 HG02738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.154+4991C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147737446 | ||||||
| chr4:147737483
|
T | TA | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0037 | 3 | HG01167.hp2 HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.154+5030dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147737483 | |||||
| chr4:147737986
|
C | T | 24 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(21): Show | 24 | HG01261.hp1 HG01891.hp1 HG02080.hp1 others(21): Show |
intron_variant | MODIFIER | c.154+5531C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147737986 | ||||||
| chr4:147738022
|
T | G | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.154+5567T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147738022 | ||||||
| chr4:147738051
|
T | C | 2 | a0001c0001t0001g0106a0001c0004t0001g0105 | 2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154+5596T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147738051 | ||||||
| chr4:147738273
|
T | C | 2 | a0001c0001t0001g0106a0001c0004t0001g0105 | 2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154+5818T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147738273 | ||||||
| chr4:147738291
|
G | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.154+5836G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147738291 | ||||||
| chr4:147738339
|
C | T | 2 | a0001c0001t0001g0006a0001c0002t0001g0005 | 2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.154+5884C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147738339 | ||||||
| chr4:147738482
|
G | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(33): Show | 36 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.154+6027G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147738482 | ||||||
| chr4:147738558
|
C | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0093others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+6103C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147738558 | ||||||
| chr4:147738560
|
C | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(33): Show | 36 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.154+6105C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147738560 | ||||||
| chr4:147738561
|
A | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0086 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.154+6106A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147738561 | ||||||
| chr4:147738637
|
G | A | 8 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0091others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+6182G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147738637 | ||||||
| chr4:147738838
|
T | G | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+6383T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147738838 | ||||||
| chr4:147739079
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.154+6624C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147739079 | ||||||
| chr4:147739186
|
C | CA | 28 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(25): Show | 28 | HG00558.hp2 HG01261.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.154+6748dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147739186 | |||||
| chr4:147739186
|
C | CAA | 9 | a0001c0001t0001g0053a0001c0001t0001g0061a0001c0001t0001g0088others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+6747_154+6748d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147739186 | |||||
| chr4:147739199
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.154+6744A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147739199 | ||||||
| chr4:147739502
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+7047C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147739502 | ||||||
| chr4:147739562
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154+7107G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147739562 | ||||||
| chr4:147739564
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.154+7109A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147739564 | ||||||
| chr4:147739581
|
A | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.154+7126A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147739581 | ||||||
| chr4:147739710
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.154+7255A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147739710 | ||||||
| chr4:147739738
|
C | CT | 9 | a0001c0001t0001g0001a0001c0001t0001g0088a0001c0001t0001g0089others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+7299dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147739738 | |||||
| chr4:147739738
|
CT | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0005t0001g0098others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+7299delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147739738 | |||||
| chr4:147739919
|
A | G | 3 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.154+7464A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147739919 | ||||||
| chr4:147739939
|
T | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+7484T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147739939 | ||||||
| chr4:147740011
|
C | T | 22 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0075others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.154+7556C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147740011 | ||||||
| chr4:147740047
|
C | CT | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(5): Show | 8 | HG02055.hp1 HG02056.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+7611dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147740047 | |||||
| chr4:147740106
|
T | C | 32 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(29): Show | 32 | HG00558.hp2 HG01261.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.154+7651T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147740106 | ||||||
| chr4:147740232
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.154+7777A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147740232 | ||||||
| chr4:147740243
|
A | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.154+7788A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147740243 | ||||||
| chr4:147740393
|
C | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG01261.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+7938C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147740393 | ||||||
| chr4:147740511
|
A | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.154+8056A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147740511 | ||||||
| chr4:147740809
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+8354A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147740809 | ||||||
| chr4:147740864
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.154+8409G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147740864 | ||||||
| chr4:147740995
|
C | A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+8540C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147740995 | ||||||
| chr4:147741051
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154+8596C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741051 | ||||||
| chr4:147741148
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.154+8693G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741148 | ||||||
| chr4:147741232
|
T | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.154+8777T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741232 | ||||||
| chr4:147741584
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+9129A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741584 | ||||||
| chr4:147741647
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.154+9192G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741647 | ||||||
| chr4:147741767
|
TACACACA others(21): Show |
T | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154+9337_154+9364d others(30): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741767 | |||||
| chr4:147741767
|
TACACACA others(27): Show |
T | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.154+9337_154+9370d others(36): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741767 | |||||
| chr4:147741770
|
ACACACAC others(15): Show |
A | 2 | a0001c0001t0001g0051a0004c0010t0001g0048 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.154+9337_154+9358d others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741770 | |||||
| chr4:147741772
|
ACACACAC others(13): Show |
A | 5 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(2): Show | 5 | HG02109.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+9337_154+9356d others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741772 | |||||
| chr4:147741774
|
ACACACAC others(11): Show |
A | 4 | a0001c0001t0001g0002a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+9337_154+9354d others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741774 | |||||
| chr4:147741778
|
ACACACAC others(7): Show |
A | 2 | a0001c0001t0001g0089a0001c0009t0001g0008 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.154+9337_154+9350d others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741778 | |||||
| chr4:147741780
|
ACACACAC others(5): Show |
A | 4 | a0001c0001t0001g0106a0001c0002t0001g0072a0001c0002t0001g0078others(1): Show | 4 | HG02572.hp2 HG02738.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+9337_154+9348d others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741780 | |||||
| chr4:147741782
|
A | ACACACAC others(1): Show |
4 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+9334_154+9335i others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741782 | |||||
| chr4:147741782
|
ACACACAC others(3): Show |
A | 5 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+9337_154+9346d others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741782 | |||||
| chr4:147741784
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.154+9329A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741784 | ||||||
| chr4:147741784
|
ACACACAC others(1): Show |
A | 2 | a0001c0005t0001g0003a0001c0005t0001g0074 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.154+9337_154+9344d others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741784 | |||||
| chr4:147741786
|
A | ACACG | 2 | a0001c0001t0001g0097a0002c0003t0001g0096 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.154+9334_154+9335i others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741786 | |||||
| chr4:147741786
|
ACACACG | A | 8 | a0001c0001t0001g0044a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG02080.hp1 HG03710.hp1 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+9337_154+9342d others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741786 | |||||
| chr4:147741788
|
A | ACACACAC others(5): Show |
1 | a0001c0001t0001g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.154+9336_154+9337i others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741788 | |||||
| chr4:147741788
|
A | ACG | 4 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(1): Show | 4 | HG02258.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+9334_154+9335i others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741788 | |||||
| chr4:147741788
|
A | G | 1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.154+9333A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741788 | ||||||
| chr4:147741788
|
ACACG | A | 15 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0050others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.154+9337_154+9340d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741788 | |||||
| chr4:147741790
|
A | G | 2 | a0001c0001t0001g0095a0001c0005t0001g0098 | 2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.154+9335A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741790 | ||||||
| chr4:147741790
|
ACG | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0088others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+9337_154+9338d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741790 | |||||
| chr4:147741792
|
G | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0052others(13): Show | 16 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.154+9337G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741792 | ||||||
| chr4:147741792
|
G | GCGCA | 2 | a0001c0008t0001g0059a0001c0008t0001g0060 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.154+9338_154+9339i others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741792 | |||||
| chr4:147741794
|
A | G | 14 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0050others(11): Show | 14 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.154+9339A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741794 | ||||||
| chr4:147741796
|
A | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 7 | HG02080.hp1 HG03710.hp1 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+9341A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741796 | ||||||
| chr4:147741798
|
A | ACACG | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG02976.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.154+9346_154+9347i others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741798 | |||||
| chr4:147741798
|
A | G | 1 | a0001c0005t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+9343A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741798 | ||||||
| chr4:147741800
|
A | ACG | 21 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.154+9346_154+9347i others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147741800 | |||||
| chr4:147741800
|
A | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.154+9345A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741800 | ||||||
| chr4:147741802
|
A | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0034others(3): Show | 6 | HG00558.hp1 HG02056.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+9347A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741802 | ||||||
| chr4:147741804
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+9349A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741804 | ||||||
| chr4:147741806
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.154+9351A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741806 | ||||||
| chr4:147741810
|
A | G | 5 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0065others(2): Show | 5 | HG02109.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+9355A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741810 | ||||||
| chr4:147741812
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.154+9357A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741812 | ||||||
| chr4:147741951
|
G | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0080a0001c0001t0001g0084others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+9496G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741951 | ||||||
| chr4:147741995
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+9540C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147741995 | ||||||
| chr4:147742018
|
T | G | 2 | a0001c0001t0001g0106a0001c0004t0001g0105 | 2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154+9563T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147742018 | ||||||
| chr4:147742178
|
C | A | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.154+9723C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147742178 | ||||||
| chr4:147742466
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.154+10011T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147742466 | ||||||
| chr4:147742476
|
C | CT | 42 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(39): Show | 42 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.154+10045dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147742476 | |||||
| chr4:147742476
|
C | CTT | 8 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+10044_154+1004 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147742476 | |||||
| chr4:147742476
|
C | CTTT | 6 | a0001c0001t0001g0024a0001c0001t0001g0091a0001c0001t0001g0099others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.154+10043_154+1004 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147742476 | |||||
| chr4:147742476
|
CT | C | 20 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049others(17): Show | 20 | HG00558.hp2 HG02055.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.154+10045delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147742476 | |||||
| chr4:147742480
|
T | TA | 2 | a0001c0001t0001g0106a0001c0004t0001g0105 | 2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154+10025_154+1002 others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147742480 | ||||||
| chr4:147742484
|
T | A | 2 | a0001c0001t0001g0106a0001c0004t0001g0105 | 2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154+10029T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147742484 | ||||||
| chr4:147742488
|
T | A | 1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.154+10033T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147742488 | ||||||
| chr4:147742514
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.154+10059G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147742514 | ||||||
| chr4:147742609
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.154+10154G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147742609 | ||||||
| chr4:147742677
|
G | A | 25 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0049others(22): Show | 25 | HG01070.hp2 HG01071.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.154+10222G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147742677 | ||||||
| chr4:147742904
|
C | CT | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(95): Show | 98 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(95): Show |
intron_variant | MODIFIER | c.154+10463dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147742904 | |||||
| chr4:147743039
|
T | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0035others(69): Show | 72 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.154+10584T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147743039 | ||||||
| chr4:147743057
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154+10602A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147743057 | ||||||
| chr4:147743269
|
G | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0002t0001g0029others(1): Show | 4 | HG02056.hp2 HG02080.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+10814G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147743269 | ||||||
| chr4:147743279
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.154+10824C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147743279 | ||||||
| chr4:147743280
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+10825G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147743280 | ||||||
| chr4:147743307
|
A | G | 9 | a0001c0001t0001g0043a0001c0001t0001g0088a0001c0001t0001g0089others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+10852A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147743307 | ||||||
| chr4:147743408
|
AC | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+10955delC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147743408 | |||||
| chr4:147743771
|
CCTT | C | 2 | a0001c0001t0001g0106a0001c0004t0001g0105 | 2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154+11319_154+1132 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147743771 | |||||
| chr4:147743868
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.154+11413A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147743868 | ||||||
| chr4:147744045
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0002t0001g0029 | 3 | HG02056.hp2 HG02080.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.154+11590C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147744045 | ||||||
| chr4:147744055
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.154+11600A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147744055 | ||||||
| chr4:147744115
|
A | G | 2 | a0001c0002t0001g0072a0001c0002t0001g0078 | 2 | HG02738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.154+11660A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147744115 | ||||||
| chr4:147744286
|
A | G | 27 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049others(24): Show | 27 | HG00558.hp2 HG01261.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.154+11831A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147744286 | ||||||
| chr4:147744555
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.154+12100G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147744555 | ||||||
| chr4:147744631
|
G | C | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+12176G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147744631 | ||||||
| chr4:147744678
|
G | C | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.154+12223G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147744678 | ||||||
| chr4:147744800
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.154+12345A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147744800 | ||||||
| chr4:147744963
|
A | G | 4 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+12508A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147744963 | ||||||
| chr4:147744995
|
G | A | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.154+12540G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147744995 | ||||||
| chr4:147745288
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.154+12833T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147745288 | ||||||
| chr4:147745324
|
A | C | 4 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+12869A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147745324 | ||||||
| chr4:147745335
|
C | G | 1 | a0001c0001t0002g0023 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.154+12880C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147745335 | ||||||
| chr4:147745483
|
G | GTGTT | 3 | a0001c0001t0001g0077a0001c0008t0001g0059a0001c0008t0001g0060 | 3 | HG00558.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.154+13050_154+1305 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147745483 | |||||
| chr4:147745575
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.154+13120C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147745575 | ||||||
| chr4:147745616
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(7): Show | 10 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.154+13161C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147745616 | ||||||
| chr4:147745633
|
A | C | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.154+13178A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147745633 | ||||||
| chr4:147745687
|
T | G | 32 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049others(29): Show | 32 | HG00558.hp2 HG01891.hp1 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.154+13232T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147745687 | ||||||
| chr4:147745771
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+13316G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147745771 | ||||||
| chr4:147745790
|
C | CT | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 31 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.154+13349dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147745790 | |||||
| chr4:147745828
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.154+13373C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147745828 | ||||||
| chr4:147745909
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+13454C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147745909 | ||||||
| chr4:147746002
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+13547C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147746002 | ||||||
| chr4:147746143
|
C | T | 3 | a0001c0001t0001g0077a0001c0008t0001g0059a0001c0008t0001g0060 | 3 | HG00558.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.154+13688C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147746143 | ||||||
| chr4:147746304
|
A | G | 1 | a0001c0001t0001g0015 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.154+13849A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147746304 | ||||||
| chr4:147746332
|
A | T | 1 | a0001c0002t0001g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.154+13877A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147746332 | ||||||
| chr4:147746349
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+13894G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147746349 | ||||||
| chr4:147746404
|
C | CT | 10 | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0001t0001g0088others(7): Show | 10 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.154+13964dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147746404 | |||||
| chr4:147746404
|
CT | C | 9 | a0001c0001t0001g0052a0001c0001t0001g0075a0001c0001t0001g0076others(6): Show | 9 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.154+13964delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147746404 | |||||
| chr4:147746571
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0004t0001g0045others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+14116G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147746571 | ||||||
| chr4:147746579
|
G | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0097a0001c0005t0001g0098others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+14124G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147746579 | ||||||
| chr4:147746782
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+14327G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147746782 | ||||||
| chr4:147746829
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+14374C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147746829 | ||||||
| chr4:147746884
|
G | T | 18 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(15): Show | 18 | HG01891.hp1 HG02080.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.154+14429G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147746884 | ||||||
| chr4:147746890
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.154+14435C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147746890 | ||||||
| chr4:147746998
|
A | G | 1 | a0001c0009t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.154+14543A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147746998 | ||||||
| chr4:147747166
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154+14711T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147747166 | ||||||
| chr4:147747378
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+14923C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147747378 | ||||||
| chr4:147747524
|
A | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0097a0001c0005t0001g0098others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+15069A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147747524 | ||||||
| chr4:147747647
|
G | GT | 30 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049others(27): Show | 30 | HG00558.hp2 HG01891.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.154+15199dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147747647 | |||||
| chr4:147747757
|
G | A | 2 | a0001c0001t0001g0091a0001c0002t0001g0090 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.154+15302G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147747757 | ||||||
| chr4:147748094
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.154+15639A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147748094 | ||||||
| chr4:147748383
|
G | A | 1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.154+15928G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147748383 | ||||||
| chr4:147748384
|
T | TA | 24 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0049others(21): Show | 24 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.154+15937dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147748384 | |||||
| chr4:147748486
|
A | G | 28 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0041others(25): Show | 28 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.154+16031A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147748486 | ||||||
| chr4:147748594
|
A | T | 27 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0041others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.154+16139A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147748594 | ||||||
| chr4:147748703
|
G | A | 1 | a0001c0005t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+16248G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147748703 | ||||||
| chr4:147748863
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.154+16408G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147748863 | ||||||
| chr4:147748881
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(101): Show | 104 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(101): Show |
intron_variant | MODIFIER | c.154+16426T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147748881 | ||||||
| chr4:147748994
|
AACTTTT | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+16546_154+1655 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147748994 | |||||
| chr4:147749158
|
T | C | 1 | a0001c0005t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+16703T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147749158 | ||||||
| chr4:147749613
|
T | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+17158T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147749613 | ||||||
| chr4:147750094
|
T | G | 1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.154+17639T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147750094 | ||||||
| chr4:147750395
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0002t0001g0021 | 3 | HG01993.hp2 HG02165.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.154+17940C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147750395 | ||||||
| chr4:147750458
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.154+18003G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147750458 | ||||||
| chr4:147750601
|
C | CT | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(6): Show | 9 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.154+18159dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147750601 | |||||
| chr4:147750602
|
T | C | 3 | a0001c0001t0001g0047a0001c0004t0001g0045a0004c0010t0001g0048 | 3 | HG02896.hp2 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.154+18147T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147750602 | ||||||
| chr4:147750647
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.154+18192G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147750647 | ||||||
| chr4:147750663
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.154+18208G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147750663 | ||||||
| chr4:147750704
|
C | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG01070.hp2 HG01071.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.154+18249C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147750704 | ||||||
| chr4:147750843
|
C | T | 24 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0043others(21): Show | 24 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.154+18388C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147750843 | ||||||
| chr4:147750957
|
C | T | 1 | a0001c0005t0001g0003 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.154+18502C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147750957 | ||||||
| chr4:147751069
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154+18614C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147751069 | ||||||
| chr4:147751190
|
CAAA | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+18741_154+1874 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147751190 | |||||
| chr4:147751260
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.154+18805A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147751260 | ||||||
| chr4:147751527
|
CCAT | C | 3 | a0001c0001t0001g0077a0001c0008t0001g0059a0001c0008t0001g0060 | 3 | HG00558.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.154+19073_154+1907 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147751527 | ||||||
| chr4:147751531
|
T | A | 3 | a0001c0001t0001g0077a0001c0008t0001g0059a0001c0008t0001g0060 | 3 | HG00558.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.154+19076T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147751531 | ||||||
| chr4:147751666
|
C | CT | 4 | a0001c0001t0001g0065a0001c0001t0001g0097a0001c0005t0001g0098others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+19218dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147751666 | |||||
| chr4:147751688
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+19233A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147751688 | ||||||
| chr4:147751711
|
CAGTGTTT others(1): Show |
C | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+19257_154+1926 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147751711 | ||||||
| chr4:147751805
|
G | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+19350G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147751805 | ||||||
| chr4:147751883
|
G | GT | 14 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(11): Show | 14 | HG00558.hp2 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.154+19449dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147751883 | |||||
| chr4:147751883
|
G | GTT | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+19448_154+1944 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147751883 | |||||
| chr4:147751883
|
GT | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0084others(2): Show | 5 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+19449delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147751883 | |||||
| chr4:147752031
|
G | A | 4 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+19576G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147752031 | ||||||
| chr4:147752122
|
A | T | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.154+19667A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147752122 | ||||||
| chr4:147752175
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154+19720G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147752175 | ||||||
| chr4:147752188
|
T | C | 2 | a0001c0001t0001g0106a0001c0004t0001g0105 | 2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154+19733T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147752188 | ||||||
| chr4:147752254
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154+19799G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147752254 | ||||||
| chr4:147752488
|
T | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+20033T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147752488 | ||||||
| chr4:147752541
|
C | CTT | 4 | a0001c0001t0001g0065a0001c0001t0001g0097a0001c0005t0001g0098others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+20099_154+2010 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147752541 | |||||
| chr4:147752562
|
G | A | 2 | a0001c0001t0001g0106a0001c0004t0001g0105 | 2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154+20107G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147752562 | ||||||
| chr4:147752588
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+20133C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147752588 | ||||||
| chr4:147752734
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+20279C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147752734 | ||||||
| chr4:147752795
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0005t0001g0003others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+20340G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147752795 | ||||||
| chr4:147752806
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.154+20351C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147752806 | ||||||
| chr4:147752892
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+20437C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147752892 | ||||||
| chr4:147753355
|
C | CT | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+20912dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147753355 | |||||
| chr4:147753498
|
C | G | 25 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0041others(22): Show | 25 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.154+21043C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147753498 | ||||||
| chr4:147753518
|
G | GT | 47 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0041others(44): Show | 47 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.154+21078dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147753518 | |||||
| chr4:147753518
|
G | GTT | 4 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0004t0001g0045others(1): Show | 4 | HG02258.hp2 HG03471.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+21077_154+2107 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147753518 | |||||
| chr4:147753611
|
C | T | 3 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.154+21156C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147753611 | ||||||
| chr4:147753973
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.154+21518G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147753973 | ||||||
| chr4:147754042
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0037 | 3 | HG01167.hp2 HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.154+21587T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147754042 | ||||||
| chr4:147754084
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+21629C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147754084 | ||||||
| chr4:147754112
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+21657C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147754112 | ||||||
| chr4:147754147
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154+21692A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147754147 | ||||||
| chr4:147754277
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154+21822C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147754277 | ||||||
| chr4:147754620
|
A | AT | 5 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0077others(2): Show | 5 | HG00558.hp2 HG01071.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+22176dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147754620 | |||||
| chr4:147754646
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+22191A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147754646 | ||||||
| chr4:147754980
|
G | A | 9 | a0001c0001t0001g0052a0001c0001t0001g0075a0001c0001t0001g0076others(6): Show | 9 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.154+22525G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147754980 | ||||||
| chr4:147755075
|
T | A | 23 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0052others(20): Show | 23 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.154+22620T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147755075 | ||||||
| chr4:147755076
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.154+22621C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147755076 | ||||||
| chr4:147755257
|
A | G | 29 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049others(26): Show | 29 | HG00558.hp2 HG01891.hp1 HG02080.hp1 others(26): Show |
intron_variant | MODIFIER | c.154+22802A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147755257 | ||||||
| chr4:147755277
|
C | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0004t0001g0045others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+22822C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147755277 | ||||||
| chr4:147755741
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154+23286G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147755741 | ||||||
| chr4:147755988
|
A | AT | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+23543dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147755988 | |||||
| chr4:147756130
|
C | CA | 5 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp2 HG02055.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+23690dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147756130 | |||||
| chr4:147756130
|
C | CAA | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+23689_154+2369 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147756130 | |||||
| chr4:147756130
|
CA | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0036others(2): Show | 5 | HG01070.hp1 HG01243.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+23690delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147756130 | |||||
| chr4:147756224
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+23769C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147756224 | ||||||
| chr4:147756460
|
G | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(38): Show | 41 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.154+24005G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147756460 | ||||||
| chr4:147756500
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.154+24045T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147756500 | ||||||
| chr4:147756604
|
C | T | 2 | a0001c0001t0001g0047a0001c0004t0001g0045 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.154+24149C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147756604 | ||||||
| chr4:147756723
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0004t0001g0045 | 3 | HG02896.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.154+24268T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147756723 | ||||||
| chr4:147756883
|
G | GT | 7 | a0001c0001t0001g0046a0001c0001t0001g0095a0001c0001t0001g0097others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+24441dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147756883 | |||||
| chr4:147756908
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+24453A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147756908 | ||||||
| chr4:147757088
|
G | T | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+24633G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757088 | ||||||
| chr4:147757109
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154+24654G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757109 | ||||||
| chr4:147757167
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.154+24712A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757167 | ||||||
| chr4:147757190
|
C | CT | 17 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0053others(14): Show | 17 | HG00558.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.154+24757dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147757190 | |||||
| chr4:147757190
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+24748_154+2475 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147757190 | |||||
| chr4:147757258
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.154+24803C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757258 | ||||||
| chr4:147757302
|
C | T | 1 | a0001c0009t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.154+24847C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757302 | ||||||
| chr4:147757442
|
C | T | 25 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0050others(22): Show | 25 | HG01891.hp1 HG02080.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.154+24987C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757442 | ||||||
| chr4:147757611
|
A | G | 8 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0077others(5): Show | 8 | HG00558.hp2 HG02572.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+25156A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757611 | ||||||
| chr4:147757643
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.154+25188T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757643 | ||||||
| chr4:147757699
|
C | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+25244C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757699 | ||||||
| chr4:147757774
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.154+25319A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757774 | ||||||
| chr4:147757813
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+25358C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757813 | ||||||
| chr4:147757841
|
C | G | 12 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0070others(9): Show | 12 | HG00558.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.154+25386C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757841 | ||||||
| chr4:147757902
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154+25447C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147757902 | ||||||
| chr4:147758107
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154+25652A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147758107 | ||||||
| chr4:147758133
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154+25678C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147758133 | ||||||
| chr4:147758263
|
C | CA | 11 | a0001c0001t0001g0052a0001c0001t0001g0075a0001c0001t0001g0081others(8): Show | 11 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.154+25823dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147758263 | |||||
| chr4:147758409
|
A | G | 2 | a0001c0001t0001g0047a0001c0004t0001g0045 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.154+25954A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147758409 | ||||||
| chr4:147758478
|
C | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.154+26023C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147758478 | ||||||
| chr4:147758671
|
T | A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+26216T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147758671 | ||||||
| chr4:147758776
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.154+26321C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147758776 | ||||||
| chr4:147758933
|
C | T | 22 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0052others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.154+26478C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147758933 | ||||||
| chr4:147758972
|
C | CA | 11 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0027others(8): Show | 11 | HG01243.hp1 HG01261.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.154+26536dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147758972 | |||||
| chr4:147758991
|
A | C | 8 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0077others(5): Show | 8 | HG00558.hp2 HG02572.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+26536A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147758991 | ||||||
| chr4:147759024
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.154+26569A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147759024 | ||||||
| chr4:147759035
|
A | G | 14 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0070others(11): Show | 14 | HG00558.hp2 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.154+26580A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147759035 | ||||||
| chr4:147759154
|
C | G | 1 | a0001c0002t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.154+26699C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147759154 | ||||||
| chr4:147759210
|
G | A | 25 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0050others(22): Show | 25 | HG01891.hp1 HG02080.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.154+26755G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147759210 | ||||||
| chr4:147759225
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.154+26770T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147759225 | ||||||
| chr4:147759426
|
G | A | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.154+26971G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147759426 | ||||||
| chr4:147759432
|
G | A | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.154+26977G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147759432 | ||||||
| chr4:147759580
|
G | GC | 8 | a0001c0001t0001g0038a0001c0001t0001g0052a0001c0001t0001g0075others(5): Show | 8 | HG01243.hp2 HG01261.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+27137dupC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147759580 | |||||
| chr4:147759580
|
GC | G | 33 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(30): Show | 33 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.154+27137delC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147759580 | |||||
| chr4:147759580
|
GCC | G | 21 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0050others(18): Show | 21 | HG01891.hp1 HG02080.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.154+27136_154+2713 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147759580 | |||||
| chr4:147759590
|
C | T | 3 | a0001c0001t0001g0083a0003c0007t0001g0079a0003c0007t0001g0082 | 3 | HG01891.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.154+27135C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147759590 | ||||||
| chr4:147759626
|
A | G | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.154+27171A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147759626 | ||||||
| chr4:147759938
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+27483C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147759938 | ||||||
| chr4:147760234
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.154+27779C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147760234 | ||||||
| chr4:147760297
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.154+27842C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147760297 | ||||||
| chr4:147760298
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.154+27843G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147760298 | ||||||
| chr4:147760400
|
G | T | 4 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+27945G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147760400 | ||||||
| chr4:147760430
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+27975C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147760430 | ||||||
| chr4:147760609
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.154+28154G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147760609 | ||||||
| chr4:147760906
|
A | G | 7 | a0001c0001t0001g0035a0001c0001t0001g0088a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+28451A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147760906 | ||||||
| chr4:147760972
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.154+28517G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147760972 | ||||||
| chr4:147761017
|
C | CT | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(7): Show | 10 | HG02055.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.154+28579dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147761017 | |||||
| chr4:147761017
|
CT | C | 24 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0043others(21): Show | 24 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.154+28579delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147761017 | |||||
| chr4:147761792
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.154+29337T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147761792 | ||||||
| chr4:147761853
|
T | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.154+29398T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147761853 | ||||||
| chr4:147761896
|
G | GC | 11 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.154+29442dupC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147761896 | |||||
| chr4:147762036
|
C | T | 2 | a0001c0004t0001g0105a0004c0010t0001g0048 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.154+29581C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762036 | ||||||
| chr4:147762242
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+29787A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762242 | ||||||
| chr4:147762299
|
C | T | 22 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0050others(19): Show | 22 | HG01891.hp1 HG02080.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.154+29844C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762299 | ||||||
| chr4:147762349
|
A | G | 22 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0050others(19): Show | 22 | HG01891.hp1 HG02080.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.154+29894A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762349 | ||||||
| chr4:147762499
|
C | CTTAT | 15 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(12): Show | 15 | HG01243.hp2 HG02055.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.154+30063_154+3006 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147762499 | |||||
| chr4:147762499
|
C | CTTATTTA others(1): Show |
83 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(80): Show | 83 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.154+30059_154+3006 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147762499 | |||||
| chr4:147762499
|
C | CTTATTTA others(5): Show |
1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.154+30055_154+3006 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147762499 | |||||
| chr4:147762522
|
T | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+30067T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762522 | ||||||
| chr4:147762524
|
A | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+30069A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762524 | ||||||
| chr4:147762536
|
A | ATTT | 3 | a0001c0001t0001g0070a0001c0008t0001g0059a0001c0008t0001g0060 | 3 | HG03098.hp1 HG03471.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.154+30082_154+3008 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147762536 | |||||
| chr4:147762540
|
A | T | 7 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0070others(4): Show | 7 | HG02976.hp2 HG03098.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+30085A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762540 | ||||||
| chr4:147762544
|
T | A | 2 | a0001c0004t0001g0105a0004c0010t0001g0048 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.154+30089T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762544 | ||||||
| chr4:147762636
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.154+30181T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762636 | ||||||
| chr4:147762675
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.154+30220G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762675 | ||||||
| chr4:147762696
|
A | AT | 22 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0052others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.154+30249dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147762696 | |||||
| chr4:147762731
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+30276C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762731 | ||||||
| chr4:147762829
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.154+30374C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762829 | ||||||
| chr4:147762920
|
C | G | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+30465C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762920 | ||||||
| chr4:147762926
|
T | C | 8 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0089others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+30471T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762926 | ||||||
| chr4:147762967
|
T | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+30512T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147762967 | ||||||
| chr4:147763088
|
G | A | 2 | a0001c0001t0001g0047a0001c0004t0001g0045 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.154+30633G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147763088 | ||||||
| chr4:147763301
|
A | C | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.154+30846A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147763301 | ||||||
| chr4:147763315
|
G | GT | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(41): Show | 44 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.154+30877dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147763315 | |||||
| chr4:147763343
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+30888C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147763343 | ||||||
| chr4:147763746
|
C | CT | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(35): Show | 38 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.154+31316dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147763746 | |||||
| chr4:147763746
|
CT | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0043others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.154+31316delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147763746 | |||||
| chr4:147763746
|
CTTTTTTT others(10): Show |
C | 3 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.154+31300_154+3131 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147763746 | |||||
| chr4:147763771
|
T | A | 4 | a0001c0001t0001g0089a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+31316T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147763771 | ||||||
| chr4:147763845
|
T | C | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 31 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.154+31390T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147763845 | ||||||
| chr4:147763907
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.154+31452G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147763907 | ||||||
| chr4:147764002
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+31547G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147764002 | ||||||
| chr4:147764276
|
A | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.154+31821A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147764276 | ||||||
| chr4:147764315
|
G | A | 2 | a0001c0004t0001g0105a0004c0010t0001g0048 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.154+31860G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147764315 | ||||||
| chr4:147764410
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.154+31955C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147764410 | ||||||
| chr4:147764463
|
TG | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.154+32009delG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147764463 | ||||||
| chr4:147764485
|
T | TA | 6 | a0001c0001t0001g0058a0001c0001t0001g0088a0001c0001t0001g0093others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+32042dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147764485 | |||||
| chr4:147764619
|
C | T | 57 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(54): Show | 57 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.154+32164C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147764619 | ||||||
| chr4:147764846
|
T | G | 22 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(19): Show | 22 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.154+32391T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147764846 | ||||||
| chr4:147765154
|
C | T | 3 | a0001c0001t0001g0088a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp1 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.154+32699C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147765154 | ||||||
| chr4:147765323
|
G | GGT | 5 | a0001c0001t0001g0088a0001c0001t0001g0106a0001c0001t0002g0031others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+32882_154+3288 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147765323 | |||||
| chr4:147765323
|
G | GGTGT | 4 | a0001c0001t0001g0012a0001c0001t0001g0034a0001c0001t0001g0093others(1): Show | 4 | HG02056.hp1 HG02056.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+32880_154+3288 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147765323 | |||||
| chr4:147765337
|
T | G | 3 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.154+32882T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147765337 | ||||||
| chr4:147765337
|
T | TG | 11 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0080others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.154+32893dupG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147765337 | |||||
| chr4:147765337
|
T | TGTG | 34 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(31): Show | 34 | HG00558.hp1 HG01070.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.154+32883_154+3288 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147765337 | |||||
| chr4:147765337
|
T | TGTGG | 13 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0053others(10): Show | 13 | HG01243.hp1 HG02738.hp1 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.154+32883_154+3288 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147765337 | |||||
| chr4:147765338
|
G | GT | 5 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0094others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+32883_154+3288 others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147765338 | ||||||
| chr4:147765338
|
G | GTGT | 16 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(13): Show | 16 | HG00558.hp2 HG01071.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.154+32883_154+3288 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147765338 | ||||||
| chr4:147765339
|
G | T | 9 | a0001c0001t0001g0052a0001c0001t0001g0075a0001c0001t0001g0081others(6): Show | 9 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.154+32884G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147765339 | ||||||
| chr4:147765340
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.154+32885G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147765340 | ||||||
| chr4:147765341
|
G | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+32886G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147765341 | ||||||
| chr4:147765347
|
G | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+32892G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147765347 | ||||||
| chr4:147765349
|
T | G | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.154+32894T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147765349 | ||||||
| chr4:147765368
|
A | C | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.154+32913A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147765368 | ||||||
| chr4:147765636
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.154+33181C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147765636 | ||||||
| chr4:147766044
|
T | C | 6 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.154+33589T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766044 | ||||||
| chr4:147766052
|
C | T | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 31 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.154+33597C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766052 | ||||||
| chr4:147766129
|
T | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(7): Show | 10 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.154+33674T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766129 | ||||||
| chr4:147766183
|
A | G | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 31 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.154+33728A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766183 | ||||||
| chr4:147766459
|
A | G | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 31 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.154+34004A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766459 | ||||||
| chr4:147766488
|
T | C | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 31 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.154+34033T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766488 | ||||||
| chr4:147766546
|
CTGTGTGT others(3): Show |
C | 3 | a0001c0001t0001g0089a0001c0004t0001g0105a0004c0010t0001g0048 | 3 | HG01243.hp2 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.154+34110_154+3411 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766546 | |||||
| chr4:147766569
|
T | G | 43 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(40): Show | 43 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.154+34114T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766569 | ||||||
| chr4:147766598
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+34143A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766598 | ||||||
| chr4:147766757
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.154+34302G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766757 | ||||||
| chr4:147766799
|
C | CATAT | 2 | a0001c0001t0001g0080a0001c0001t0003g0087 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.154+34381_154+3438 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766799 | |||||
| chr4:147766799
|
CATAT | C | 4 | a0001c0001t0001g0081a0001c0001t0001g0094a0001c0005t0001g0074others(1): Show | 4 | HG02280.hp2 HG02886.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+34381_154+3438 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766799 | |||||
| chr4:147766799
|
CATATAT | C | 2 | a0001c0001t0001g0038a0002c0003t0001g0073 | 2 | HG02622.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.154+34379_154+3438 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766799 | |||||
| chr4:147766799
|
CATATATA others(1): Show |
C | 4 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0063others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+34377_154+3438 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766799 | |||||
| chr4:147766799
|
CATATATA others(3): Show |
C | 2 | a0001c0001t0001g0062a0001c0001t0001g0065 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.154+34375_154+3438 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766799 | |||||
| chr4:147766799
|
CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0046a0001c0001t0001g0076 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.154+34373_154+3438 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766799 | |||||
| chr4:147766799
|
CATATATA others(7): Show |
C | 7 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+34371_154+3438 others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766799 | |||||
| chr4:147766799
|
CATATATA others(9): Show |
C | 4 | a0001c0001t0001g0088a0001c0001t0001g0097a0001c0001t0001g0106others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+34369_154+3438 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766799 | |||||
| chr4:147766799
|
CATATATA others(11): Show |
C | 2 | a0001c0002t0001g0090a0001c0011t0001g0092 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.154+34367_154+3438 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766799 | |||||
| chr4:147766799
|
CATATATA others(13): Show |
C | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154+34365_154+3438 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766799 | |||||
| chr4:147766799
|
CATATATA others(17): Show |
C | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 30 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.154+34361_154+3438 others(28): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766799 | |||||
| chr4:147766816
|
ATATATAT others(17): Show |
A | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.154+34365_154+3438 others(28): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766816 | |||||
| chr4:147766820
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154+34369_154+3438 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766820 | |||||
| chr4:147766824
|
ATATATAT others(9): Show |
A | 3 | a0001c0001t0001g0043a0001c0001t0001g0089a0001c0004t0001g0102 | 3 | HG01243.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.154+34373_154+3438 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766824 | |||||
| chr4:147766826
|
ATATATAT others(7): Show |
A | 6 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0002t0001g0066others(3): Show | 6 | HG02080.hp1 HG02738.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.154+34375_154+3438 others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766826 | |||||
| chr4:147766828
|
ATATATAT others(5): Show |
A | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG02738.hp1 NA18995.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+34377_154+3438 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766828 | |||||
| chr4:147766830
|
ATATATAT others(3): Show |
A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG01891.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.154+34379_154+3438 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766830 | |||||
| chr4:147766832
|
ATATATAT others(1): Show |
A | 4 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0005t0001g0003others(1): Show | 4 | HG01261.hp1 HG02896.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+34381_154+3438 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766832 | |||||
| chr4:147766832
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.154+34381_154+3439 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766832 | |||||
| chr4:147766834
|
ATATATT | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0104 | 2 | HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.154+34383_154+3438 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766834 | |||||
| chr4:147766836
|
A | ATT | 3 | a0001c0004t0001g0105a0003c0007t0001g0079a0003c0007t0001g0082 | 3 | HG01891.hp2 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.154+34382_154+3438 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766836 | |||||
| chr4:147766836
|
A | T | 9 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0088others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.154+34381A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766836 | ||||||
| chr4:147766836
|
ATATT | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+34403_154+3440 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766836 | |||||
| chr4:147766838
|
ATT | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0005a0001c0004t0001g0045others(3): Show | 6 | HG02895.hp1 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.154+34385_154+3438 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147766838 | |||||
| chr4:147766840
|
T | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0080a0001c0001t0001g0086 | 3 | HG02886.hp2 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.154+34385T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766840 | ||||||
| chr4:147766844
|
T | A | 1 | a0001c0008t0001g0060 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.154+34389T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766844 | ||||||
| chr4:147766934
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.154+34479C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147766934 | ||||||
| chr4:147767107
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.154+34652G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147767107 | ||||||
| chr4:147767367
|
CT | C | 32 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(29): Show | 32 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.154+34925delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147767367 | |||||
| chr4:147767512
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.154+35057T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147767512 | ||||||
| chr4:147767540
|
A | G | 1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.154+35085A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147767540 | ||||||
| chr4:147767820
|
T | C | 2 | a0001c0001t0001g0047a0001c0004t0001g0045 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.154+35365T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147767820 | ||||||
| chr4:147767830
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+35375G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147767830 | ||||||
| chr4:147767998
|
G | A | 1 | a0002c0003t0001g0009 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.154+35543G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147767998 | ||||||
| chr4:147768197
|
T | C | 2 | a0001c0002t0001g0090a0001c0011t0001g0092 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.154+35742T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147768197 | ||||||
| chr4:147768360
|
G | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+35905G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147768360 | ||||||
| chr4:147768495
|
C | A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+36040C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147768495 | ||||||
| chr4:147768522
|
G | A | 2 | a0001c0001t0001g0047a0001c0004t0001g0045 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.154+36067G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147768522 | ||||||
| chr4:147768576
|
A | C | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.154+36121A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147768576 | ||||||
| chr4:147768587
|
ATAAT | A | 3 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.154+36134_154+3613 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147768587 | |||||
| chr4:147768726
|
G | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+36271G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147768726 | ||||||
| chr4:147768741
|
C | CT | 4 | a0001c0001t0001g0058a0001c0004t0001g0102a0001c0004t0001g0105others(1): Show | 4 | HG02572.hp2 HG03098.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+36301dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147768741 | |||||
| chr4:147768741
|
CT | C | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 30 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.154+36301delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147768741 | |||||
| chr4:147768769
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(80): Show | 83 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(80): Show |
intron_variant | MODIFIER | c.154+36314T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147768769 | ||||||
| chr4:147769001
|
G | T | 8 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(5): Show | 8 | HG02080.hp1 HG02738.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+36546G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147769001 | ||||||
| chr4:147769097
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(80): Show | 83 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(80): Show |
intron_variant | MODIFIER | c.154+36642A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147769097 | ||||||
| chr4:147769329
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.154+36874A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147769329 | ||||||
| chr4:147769459
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0095 | 2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.154+37004A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147769459 | ||||||
| chr4:147769512
|
T | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+37057T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147769512 | ||||||
| chr4:147769537
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0094 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.154+37082C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147769537 | ||||||
| chr4:147769563
|
C | A | 2 | a0001c0004t0001g0105a0004c0010t0001g0048 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.154+37108C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147769563 | ||||||
| chr4:147769762
|
A | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+37307A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147769762 | ||||||
| chr4:147769847
|
T | A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+37392T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147769847 | ||||||
| chr4:147769890
|
A | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+37435A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147769890 | ||||||
| chr4:147769994
|
A | G | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.154+37539A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147769994 | ||||||
| chr4:147770109
|
T | C | 2 | a0001c0004t0001g0105a0004c0010t0001g0048 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.154+37654T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147770109 | ||||||
| chr4:147770150
|
G | T | 2 | a0001c0001t0001g0047a0001c0004t0001g0045 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.154+37695G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147770150 | ||||||
| chr4:147770271
|
C | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+37816C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147770271 | ||||||
| chr4:147770398
|
G | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+37943G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147770398 | ||||||
| chr4:147770617
|
A | G | 1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.154+38162A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147770617 | ||||||
| chr4:147770750
|
C | G | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+38295C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147770750 | ||||||
| chr4:147770842
|
A | G | 1 | a0001c0001t0001g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.154+38387A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147770842 | ||||||
| chr4:147770971
|
C | G | 21 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(18): Show | 21 | HG01891.hp1 HG02080.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.154+38516C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147770971 | ||||||
| chr4:147771018
|
C | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+38563C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147771018 | ||||||
| chr4:147771440
|
A | C | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.154+38985A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147771440 | ||||||
| chr4:147771496
|
G | GATTAA | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+39045_154+3904 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147771496 | |||||
| chr4:147771795
|
A | AT | 8 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0077others(5): Show | 8 | HG00558.hp2 HG02572.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+39347dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147771795 | |||||
| chr4:147771827
|
T | G | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+39372T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147771827 | ||||||
| chr4:147772069
|
C | T | 1 | a0001c0009t0001g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.154+39614C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147772069 | ||||||
| chr4:147772079
|
C | T | 27 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 27 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.154+39624C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147772079 | ||||||
| chr4:147772522
|
G | A | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+40067G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147772522 | ||||||
| chr4:147773019
|
C | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+40564C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147773019 | ||||||
| chr4:147773092
|
T | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.154+40637T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147773092 | ||||||
| chr4:147773243
|
A | G | 7 | a0001c0001t0001g0052a0001c0001t0001g0075a0001c0001t0001g0083others(4): Show | 7 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+40788A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147773243 | ||||||
| chr4:147773434
|
G | T | 2 | a0001c0002t0001g0090a0001c0011t0001g0092 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.154+40979G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147773434 | ||||||
| chr4:147773507
|
C | T | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 30 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.154+41052C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147773507 | ||||||
| chr4:147773545
|
G | C | 2 | a0001c0004t0001g0105a0004c0010t0001g0048 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.154+41090G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147773545 | ||||||
| chr4:147773644
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.154+41189T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147773644 | ||||||
| chr4:147774001
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+41546C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147774001 | ||||||
| chr4:147774109
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.154+41654A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147774109 | ||||||
| chr4:147774161
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0002t0001g0029 | 3 | HG02056.hp2 HG02080.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.154+41706C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147774161 | ||||||
| chr4:147774374
|
G | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+41919G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147774374 | ||||||
| chr4:147774805
|
G | T | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 30 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.154+42350G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147774805 | ||||||
| chr4:147774899
|
C | T | 1 | a0001c0005t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+42444C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147774899 | ||||||
| chr4:147774908
|
A | AT | 19 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(16): Show | 19 | HG00558.hp2 HG01243.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.154+42468dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147774908 | |||||
| chr4:147775179
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+42724C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775179 | ||||||
| chr4:147775214
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0037 | 2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.154+42759A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775214 | ||||||
| chr4:147775246
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0097 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.154+42791C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775246 | ||||||
| chr4:147775408
|
A | T | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 30 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.154+42953A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775408 | ||||||
| chr4:147775432
|
TA | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0093a0001c0001t0001g0095 | 3 | HG02055.hp2 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.154+42978delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775432 | ||||||
| chr4:147775443
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(82): Show | 85 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(82): Show |
intron_variant | MODIFIER | c.154+42988T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775443 | ||||||
| chr4:147775516
|
T | C | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 30 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.154+43061T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775516 | ||||||
| chr4:147775676
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154+43221A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775676 | ||||||
| chr4:147775742
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+43287G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775742 | ||||||
| chr4:147775753
|
C | T | 1 | a0001c0005t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+43298C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775753 | ||||||
| chr4:147775766
|
T | C | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 30 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.154+43311T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775766 | ||||||
| chr4:147775781
|
G | A | 3 | a0001c0001t0001g0083a0003c0007t0001g0079a0003c0007t0001g0082 | 3 | HG01891.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.154+43326G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775781 | ||||||
| chr4:147775861
|
A | G | 2 | a0001c0004t0001g0105a0004c0010t0001g0048 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.154+43406A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147775861 | ||||||
| chr4:147776114
|
C | T | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 30 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.154+43659C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147776114 | ||||||
| chr4:147776115
|
T | G | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 30 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.154+43660T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147776115 | ||||||
| chr4:147776166
|
T | A | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.154+43711T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147776166 | ||||||
| chr4:147776265
|
G | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+43810G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147776265 | ||||||
| chr4:147776302
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154+43847C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147776302 | ||||||
| chr4:147776675
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+44220C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147776675 | ||||||
| chr4:147776849
|
C | T | 1 | a0001c0009t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.154+44394C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147776849 | ||||||
| chr4:147777003
|
A | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154+44548A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147777003 | ||||||
| chr4:147777074
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+44619T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147777074 | ||||||
| chr4:147777214
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(45): Show | 48 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.154+44759C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147777214 | ||||||
| chr4:147777282
|
G | A | 34 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(31): Show | 34 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.154+44827G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147777282 | ||||||
| chr4:147777351
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+44896C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147777351 | ||||||
| chr4:147777352
|
G | A | 34 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(31): Show | 34 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.154+44897G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147777352 | ||||||
| chr4:147777627
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(6): Show | 9 | HG01243.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-45100G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147777627 | ||||||
| chr4:147777708
|
G | T | 1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.155-45019G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147777708 | ||||||
| chr4:147777784
|
C | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.155-44943C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147777784 | ||||||
| chr4:147777917
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.155-44810T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147777917 | ||||||
| chr4:147777942
|
C | T | 1 | a0001c0006t0001g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.155-44785C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147777942 | ||||||
| chr4:147778057
|
T | C | 1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.155-44670T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147778057 | ||||||
| chr4:147778126
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0091 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.155-44601G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147778126 | ||||||
| chr4:147778392
|
C | T | 12 | a0001c0001t0001g0047a0001c0001t0001g0088a0001c0001t0001g0099others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.155-44335C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147778392 | ||||||
| chr4:147778590
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.155-44137C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147778590 | ||||||
| chr4:147778758
|
C | T | 4 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(1): Show | 4 | HG02258.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-43969C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147778758 | ||||||
| chr4:147778877
|
T | C | 2 | a0001c0001t0001g0014a0002c0003t0001g0009 | 2 | HG01169.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.155-43850T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147778877 | ||||||
| chr4:147778888
|
GACTTAA | G | 8 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-43834_155-4382 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147778888 | |||||
| chr4:147779185
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.155-43542C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147779185 | ||||||
| chr4:147779221
|
G | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0097a0001c0002t0001g0072others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-43506G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147779221 | ||||||
| chr4:147779473
|
AG | A | 8 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-43248delG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147779473 | |||||
| chr4:147779637
|
G | A | 6 | a0001c0001t0001g0046a0001c0001t0001g0097a0001c0002t0001g0072others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-43090G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147779637 | ||||||
| chr4:147779703
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155-43024A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147779703 | ||||||
| chr4:147779873
|
A | C | 11 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0097others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-42854A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147779873 | ||||||
| chr4:147779946
|
C | A | 4 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-42781C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147779946 | ||||||
| chr4:147780132
|
T | C | 1 | a0001c0006t0001g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.155-42595T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147780132 | ||||||
| chr4:147780209
|
C | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0091 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.155-42518C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147780209 | ||||||
| chr4:147780269
|
G | T | 4 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-42458G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147780269 | ||||||
| chr4:147780376
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.155-42351A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147780376 | ||||||
| chr4:147780560
|
G | GA | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(92): Show | 95 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.155-42160dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147780560 | |||||
| chr4:147780938
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-41789C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147780938 | ||||||
| chr4:147780964
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.155-41763C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147780964 | ||||||
| chr4:147781115
|
T | G | 3 | a0001c0001t0001g0083a0003c0007t0001g0079a0003c0007t0001g0082 | 3 | HG01891.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.155-41612T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147781115 | ||||||
| chr4:147781155
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.155-41572G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147781155 | ||||||
| chr4:147781201
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.155-41526T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147781201 | ||||||
| chr4:147781234
|
C | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0106a0001c0004t0001g0105others(1): Show | 4 | HG02572.hp2 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-41493C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147781234 | ||||||
| chr4:147781242
|
G | A | 1 | a0001c0002t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.155-41485G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147781242 | ||||||
| chr4:147781450
|
C | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0094 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.155-41277C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147781450 | ||||||
| chr4:147781474
|
T | C | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-41253T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147781474 | ||||||
| chr4:147781560
|
G | T | 1 | a0001c0001t0001g0015 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.155-41167G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147781560 | ||||||
| chr4:147781681
|
C | CT | 6 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0046others(3): Show | 6 | HG01169.hp1 HG01243.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-41030dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147781681 | |||||
| chr4:147781681
|
C | CTT | 43 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0041others(40): Show | 43 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.155-41031_155-4103 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147781681 | |||||
| chr4:147781733
|
A | T | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.155-40994A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147781733 | ||||||
| chr4:147781841
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-40886C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147781841 | ||||||
| chr4:147781977
|
T | TA | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-40749dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147781977 | |||||
| chr4:147782032
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0097a0001c0005t0001g0098others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-40695G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147782032 | ||||||
| chr4:147782280
|
G | A | 2 | a0001c0002t0001g0072a0001c0002t0001g0078 | 2 | HG02738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.155-40447G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147782280 | ||||||
| chr4:147782407
|
G | A | 19 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0046others(16): Show | 19 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.155-40320G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147782407 | ||||||
| chr4:147782478
|
G | A | 1 | a0001c0002t0001g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.155-40249G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147782478 | ||||||
| chr4:147782489
|
A | G | 2 | a0001c0002t0001g0090a0001c0011t0001g0092 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.155-40238A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147782489 | ||||||
| chr4:147782619
|
G | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0106a0001c0004t0001g0045others(2): Show | 5 | HG02572.hp2 HG02896.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-40108G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147782619 | ||||||
| chr4:147782687
|
A | T | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.155-40040A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147782687 | ||||||
| chr4:147782781
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.155-39946A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147782781 | ||||||
| chr4:147782926
|
A | G | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.155-39801A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147782926 | ||||||
| chr4:147782964
|
A | G | 35 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0035others(32): Show | 35 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.155-39763A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147782964 | ||||||
| chr4:147782998
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.155-39729T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147782998 | ||||||
| chr4:147783145
|
T | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(67): Show | 70 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.155-39582T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783145 | ||||||
| chr4:147783173
|
A | G | 1 | a0001c0002t0001g0029 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.155-39554A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783173 | ||||||
| chr4:147783176
|
CATTAA | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0036others(3): Show | 6 | HG01070.hp1 HG01243.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-39546_155-3954 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783176 | |||||
| chr4:147783205
|
A | AACACATT others(28): Show |
2 | a0001c0001t0003g0087a0001c0011t0001g0092 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.155-39418_155-3938 others(39): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783205 | |||||
| chr4:147783309
|
ACACACAT others(28): Show |
A | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.155-39245_155-3921 others(39): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783309 | |||||
| chr4:147783309
|
ACACACAT others(63): Show |
A | 3 | a0001c0001t0001g0083a0003c0007t0001g0079a0003c0007t0001g0082 | 3 | HG01891.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.155-39280_155-3921 others(74): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783309 | |||||
| chr4:147783344
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-39383G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783344 | ||||||
| chr4:147783375
|
T | C | 5 | a0001c0001t0001g0047a0001c0001t0001g0106a0001c0004t0001g0045others(2): Show | 5 | HG02572.hp2 HG02896.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-39352T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783375 | ||||||
| chr4:147783410
|
T | C | 5 | a0001c0001t0001g0047a0001c0001t0001g0106a0001c0004t0001g0045others(2): Show | 5 | HG02572.hp2 HG02896.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-39317T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783410 | ||||||
| chr4:147783482
|
T | G | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-39245T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783482 | ||||||
| chr4:147783484
|
G | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-39243G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783484 | ||||||
| chr4:147783499
|
T | C | 1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.155-39228T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783499 | ||||||
| chr4:147783517
|
G | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0046others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.155-39210G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783517 | ||||||
| chr4:147783519
|
A | G | 15 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0046others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.155-39208A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783519 | ||||||
| chr4:147783533
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.155-39194A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783533 | ||||||
| chr4:147783538
|
T | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-39189T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783538 | ||||||
| chr4:147783553
|
AAC | A | 3 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.155-39168_155-3916 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783553 | |||||
| chr4:147783555
|
C | CACACATT others(26): Show |
1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-39060_155-3902 others(37): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783555 | |||||
| chr4:147783555
|
CACACATT others(59): Show |
C | 3 | a0001c0001t0001g0106a0001c0004t0001g0105a0004c0010t0001g0048 | 3 | HG02572.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.155-39093_155-3902 others(70): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783555 | |||||
| chr4:147783568
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0046others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.155-39159G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783568 | ||||||
| chr4:147783582
|
T | TTA | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-39142_155-3914 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783582 | |||||
| chr4:147783588
|
A | AAC | 7 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-39135_155-3913 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783588 | |||||
| chr4:147783588
|
A | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-39139A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783588 | ||||||
| chr4:147783601
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(2): Show | 5 | HG01169.hp2 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-39126G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783601 | ||||||
| chr4:147783621
|
A | AAC | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-39102_155-3910 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783621 | |||||
| chr4:147783634
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-39093G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783634 | ||||||
| chr4:147783700
|
A | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(60): Show | 63 | HG00558.hp1 HG00558.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.155-39027A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783700 | ||||||
| chr4:147783731
|
TTATGTAT others(154): Show |
T | 3 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.155-38992_155-3883 others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783731 | |||||
| chr4:147783733
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(46): Show | 49 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.155-38994A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783733 | ||||||
| chr4:147783753
|
AACACATT others(21): Show |
A | 15 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.155-38959_155-3893 others(32): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783753 | |||||
| chr4:147783753
|
AACACATT others(53): Show |
A | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38961_155-3890 others(64): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783753 | |||||
| chr4:147783764
|
T | TTGTG | 21 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0037others(18): Show | 21 | HG01261.hp2 HG01891.hp1 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.155-38962_155-3896 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783764 | |||||
| chr4:147783766
|
A | G | 1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.155-38961A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783766 | ||||||
| chr4:147783767
|
T | TGTATTG | 14 | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0001t0001g0047others(11): Show | 14 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.155-38960_155-3895 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783767 | ||||||
| chr4:147783769
|
A | G | 21 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0037others(18): Show | 21 | HG01261.hp2 HG01891.hp1 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.155-38958A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783769 | ||||||
| chr4:147783772
|
T | A | 13 | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0001t0001g0047others(10): Show | 13 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.155-38955T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783772 | ||||||
| chr4:147783772
|
T | TA | 21 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0037others(18): Show | 21 | HG01261.hp2 HG01891.hp1 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.155-38955_155-3895 others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783772 | ||||||
| chr4:147783773
|
T | A | 23 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0037others(20): Show | 23 | HG01261.hp2 HG01891.hp1 HG01993.hp1 others(20): Show |
intron_variant | MODIFIER | c.155-38954T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783773 | ||||||
| chr4:147783774
|
TA | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0001t0001g0047others(10): Show | 13 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.155-38952delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783774 | ||||||
| chr4:147783775
|
A | T | 21 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0037others(18): Show | 21 | HG01261.hp2 HG01891.hp1 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.155-38952A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783775 | ||||||
| chr4:147783778
|
T | G | 1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.155-38949T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783778 | ||||||
| chr4:147783780
|
A | G | 34 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0035others(31): Show | 34 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.155-38947A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783780 | ||||||
| chr4:147783781
|
C | A | 34 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0035others(31): Show | 34 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.155-38946C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783781 | ||||||
| chr4:147783781
|
C | CACATTAA others(24): Show |
1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.155-38943_155-3894 others(35): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783781 | |||||
| chr4:147783792
|
TTATG | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0001t0001g0047others(10): Show | 13 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.155-38931_155-3892 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783792 | |||||
| chr4:147783794
|
A | ATGTATTA others(25): Show |
4 | a0001c0001t0001g0038a0001c0001t0001g0070a0001c0001t0001g0077others(1): Show | 4 | HG00558.hp2 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38777_155-3874 others(36): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783794 | |||||
| chr4:147783794
|
ATGTATTA others(121): Show |
A | 4 | a0001c0001t0001g0046a0001c0001t0001g0089a0001c0002t0001g0072others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-38873_155-3874 others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783794 | |||||
| chr4:147783796
|
G | GTATTGTA others(22): Show |
8 | a0001c0001t0001g0035a0001c0001t0001g0061a0001c0001t0001g0062others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-38927_155-3892 others(33): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783796 | |||||
| chr4:147783796
|
G | GTATTGTA others(55): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0037 | 2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.155-38927_155-3892 others(66): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783796 | |||||
| chr4:147783801
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-38926A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783801 | ||||||
| chr4:147783804
|
T | TA | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-38923_155-3892 others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783804 | ||||||
| chr4:147783805
|
T | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-38922T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783805 | ||||||
| chr4:147783807
|
A | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-38920A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783807 | ||||||
| chr4:147783811
|
AAC | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0002t0001g0029others(1): Show | 4 | HG02056.hp2 HG02080.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-38910_155-3890 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783811 | |||||
| chr4:147783811
|
AACACACA others(27): Show |
A | 20 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-38910_155-3887 others(38): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783811 | |||||
| chr4:147783811
|
AACACACA others(59): Show |
A | 1 | a0001c0002t0001g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.155-38910_155-3884 others(70): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783811 | |||||
| chr4:147783812
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-38915A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783812 | ||||||
| chr4:147783813
|
C | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-38914C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783813 | ||||||
| chr4:147783824
|
TTGTG | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-38901_155-3889 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783824 | |||||
| chr4:147783826
|
G | A | 23 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0035others(20): Show | 23 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.155-38901G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783826 | ||||||
| chr4:147783833
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38894A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783833 | ||||||
| chr4:147783836
|
T | TA | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38891_155-3889 others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783836 | ||||||
| chr4:147783837
|
T | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38890T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783837 | ||||||
| chr4:147783839
|
A | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38888A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783839 | ||||||
| chr4:147783843
|
AAC | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0037others(4): Show | 7 | HG00558.hp1 HG01261.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-38878_155-3887 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783843 | |||||
| chr4:147783844
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38883A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783844 | ||||||
| chr4:147783845
|
C | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(2): Show | 5 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-38882C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783845 | ||||||
| chr4:147783858
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(28): Show | 31 | HG01070.hp2 HG01071.hp1 HG02080.hp1 others(28): Show |
intron_variant | MODIFIER | c.155-38869G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783858 | ||||||
| chr4:147783865
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38862A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783865 | ||||||
| chr4:147783868
|
T | TA | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38859_155-3885 others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783868 | ||||||
| chr4:147783869
|
T | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38858T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783869 | ||||||
| chr4:147783871
|
A | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38856A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783871 | ||||||
| chr4:147783875
|
AAC | A | 8 | a0001c0001t0001g0035a0001c0001t0001g0061a0001c0001t0001g0062others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-38846_155-3884 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783875 | |||||
| chr4:147783876
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38851A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783876 | ||||||
| chr4:147783877
|
C | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38850C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783877 | ||||||
| chr4:147783888
|
TTGTG | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38837_155-3883 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783888 | |||||
| chr4:147783907
|
AAC | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0041others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-38814_155-3881 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783907 | |||||
| chr4:147783922
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0097others(4): Show | 7 | HG02145.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-38805G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147783922 | ||||||
| chr4:147783924
|
GTATTATA others(30): Show |
G | 3 | a0001c0001t0001g0106a0001c0004t0001g0105a0004c0010t0001g0048 | 3 | HG02572.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.155-38798_155-3876 others(41): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783924 | |||||
| chr4:147783956
|
GTATTA | G | 10 | a0001c0001t0001g0047a0001c0001t0001g0088a0001c0001t0001g0099others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.155-38766_155-3876 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147783956 | |||||
| chr4:147784025
|
AAC | A | 2 | a0001c0002t0001g0072a0001c0002t0001g0078 | 2 | HG02738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.155-38696_155-3869 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784025 | |||||
| chr4:147784052
|
T | TTTTACAT others(24): Show |
1 | a0001c0001t0001g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.155-38613_155-3858 others(35): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784052 | |||||
| chr4:147784114
|
ATTTACAT others(24): Show |
A | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(82): Show | 85 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(82): Show |
intron_variant | MODIFIER | c.155-38520_155-3849 others(35): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784114 | |||||
| chr4:147784114
|
ATTTACAT others(55): Show |
A | 2 | a0001c0001t0001g0011a0001c0004t0001g0102 | 2 | HG03098.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.155-38551_155-3849 others(66): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784114 | |||||
| chr4:147784145
|
T | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0106others(4): Show | 7 | HG02572.hp2 HG03098.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-38582T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784145 | ||||||
| chr4:147784176
|
T | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0035others(31): Show | 34 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.155-38551T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784176 | ||||||
| chr4:147784476
|
TTA | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38241_155-3824 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784476 | |||||
| chr4:147784533
|
CAT | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(68): Show | 71 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.155-38189_155-3818 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784533 | |||||
| chr4:147784617
|
T | TAAATATA others(34): Show |
2 | a0001c0001t0001g0038a0002c0003t0001g0073 | 2 | HG02622.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.155-38054_155-3801 others(45): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784617 | |||||
| chr4:147784660
|
AATATATA others(4): Show |
A | 35 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0035others(32): Show | 35 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.155-38062_155-3805 others(15): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784660 | |||||
| chr4:147784660
|
AATATATA others(99): Show |
A | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.155-38066_155-3796 others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784660 | ||||||
| chr4:147784661
|
ATATATAT | A | 52 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(49): Show | 52 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.155-38054_155-3804 others(11): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784661 | |||||
| chr4:147784668
|
T | TTATAAAT others(20): Show |
4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-38055_155-3805 others(31): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784668 | |||||
| chr4:147784668
|
T | TTATAAAT others(54): Show |
1 | a0001c0001t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.155-38055_155-3805 others(65): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784668 | |||||
| chr4:147784668
|
T | TTATAAAT others(110): Show |
1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.155-38055_155-3805 others(121): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784668 | |||||
| chr4:147784679
|
A | G | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 30 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.155-38048A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784679 | ||||||
| chr4:147784704
|
ATATATTA others(50): Show |
A | 4 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0037others(1): Show | 4 | HG01993.hp1 HG02080.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-37977_155-3792 others(61): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784704 | |||||
| chr4:147784713
|
A | G | 24 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(21): Show | 24 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.155-38014A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784713 | ||||||
| chr4:147784716
|
TATA | T | 2 | a0001c0001t0001g0091a0001c0004t0001g0045 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.155-38007_155-3800 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784716 | |||||
| chr4:147784716
|
TATAATAT others(108): Show |
T | 2 | a0001c0001t0001g0034a0001c0002t0001g0029 | 2 | HG02056.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.155-38007_155-3789 others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784716 | |||||
| chr4:147784719
|
A | AAAAT | 3 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.155-38007_155-3800 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784719 | |||||
| chr4:147784721
|
T | A | 1 | a0001c0002t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.155-38006T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784721 | ||||||
| chr4:147784734
|
ATATATTA others(20): Show |
A | 17 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 17 | HG00558.hp1 HG01071.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.155-37977_155-3795 others(31): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784734 | |||||
| chr4:147784743
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0002g0023others(3): Show | 6 | HG01070.hp1 HG01243.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-37984A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784743 | ||||||
| chr4:147784746
|
T | TATA | 24 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0024others(21): Show | 24 | HG00558.hp2 HG01070.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.155-37980_155-3797 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784746 | |||||
| chr4:147784746
|
TATATATT others(23): Show |
T | 1 | a0001c0001t0001g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.155-37966_155-3793 others(34): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784746 | |||||
| chr4:147784746
|
TATATATT others(78): Show |
T | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.155-37966_155-3788 others(89): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784746 | |||||
| chr4:147784748
|
T | TAAA | 4 | a0001c0001t0001g0097a0001c0002t0001g0078a0001c0005t0001g0098others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-37978_155-3797 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784748 | |||||
| chr4:147784761
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(67): Show | 70 | HG00558.hp2 HG01070.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.155-37966G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784761 | ||||||
| chr4:147784763
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-37964A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784763 | ||||||
| chr4:147784770
|
A | G | 24 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(21): Show | 24 | HG00558.hp1 HG01071.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.155-37957A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784770 | ||||||
| chr4:147784771
|
AATATAAT | A | 2 | a0001c0002t0001g0090a0001c0011t0001g0092 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.155-37951_155-3794 others(11): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784771 | |||||
| chr4:147784773
|
TATA | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0088others(4): Show | 7 | HG01070.hp1 HG01884.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-37950_155-3794 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784773 | |||||
| chr4:147784775
|
TAATATAT others(48): Show |
T | 2 | a0001c0001t0001g0070a0001c0001t0001g0077 | 2 | HG00558.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.155-37920_155-3786 others(59): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784775 | |||||
| chr4:147784785
|
T | C | 11 | a0001c0001t0001g0035a0001c0001t0001g0053a0001c0001t0001g0054others(8): Show | 11 | HG01891.hp1 HG02080.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.155-37942T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784785 | ||||||
| chr4:147784799
|
T | A | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.155-37928T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784799 | ||||||
| chr4:147784800
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0037others(1): Show | 4 | HG01993.hp1 HG02080.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-37927A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784800 | ||||||
| chr4:147784800
|
AAATAT | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0053a0001c0001t0001g0056others(8): Show | 11 | HG02080.hp1 HG02280.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.155-37920_155-3791 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784800 | |||||
| chr4:147784803
|
TATA | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 28 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.155-37920_155-3791 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784803 | |||||
| chr4:147784805
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.155-37922T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784805 | ||||||
| chr4:147784805
|
T | TAATATAT others(18): Show |
17 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0049others(14): Show | 17 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.155-37913_155-3791 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784805 | |||||
| chr4:147784805
|
T | TAATATAT others(43): Show |
3 | a0001c0001t0001g0001a0001c0005t0001g0003a0001c0006t0001g0071 | 3 | HG02615.hp2 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.155-37913_155-3791 others(54): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784805 | |||||
| chr4:147784805
|
T | TAATATAT others(18): Show |
2 | a0001c0001t0001g0038a0001c0001t0001g0047 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.155-37840_155-3781 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784805 | |||||
| chr4:147784805
|
T | TAATATAT others(183): Show |
1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.155-37891_155-3789 others(194): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784805 | |||||
| chr4:147784805
|
T | TAATATAT others(178): Show |
1 | a0001c0009t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.155-37891_155-3789 others(189): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784805 | |||||
| chr4:147784805
|
T | TAATATAT others(73): Show |
1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.155-37891_155-3789 others(84): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784805 | |||||
| chr4:147784805
|
T | TATTATAA others(13): Show |
3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0069 | 3 | HG01891.hp1 NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.155-37921_155-3792 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784805 | |||||
| chr4:147784805
|
T | TATTATAA others(213): Show |
1 | a0001c0002t0001g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.155-37921_155-3792 others(224): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784805 | |||||
| chr4:147784805
|
T | TATTATAA others(238): Show |
1 | a0001c0001t0001g0004 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.155-37921_155-3792 others(249): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784805 | |||||
| chr4:147784805
|
T | TATTATAA others(263): Show |
1 | a0001c0001t0001g0006 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.155-37921_155-3792 others(274): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784805 | |||||
| chr4:147784805
|
TAATATAT others(18): Show |
T | 4 | a0001c0001t0001g0052a0001c0004t0001g0105a0001c0008t0001g0059others(1): Show | 4 | HG01261.hp1 HG02572.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-37840_155-3781 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784805 | |||||
| chr4:147784805
|
TAATATAT others(43): Show |
T | 2 | a0001c0001t0001g0088a0004c0010t0001g0048 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.155-37865_155-3781 others(54): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784805 | |||||
| chr4:147784806
|
A | AATATATT others(102): Show |
1 | a0001c0002t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.155-37890_155-3788 others(113): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784806 | |||||
| chr4:147784806
|
A | ATATTATA others(86): Show |
1 | a0001c0001t0001g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.155-37921_155-3792 others(97): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784806 | ||||||
| chr4:147784806
|
A | ATATTATA others(99): Show |
2 | a0001c0005t0001g0098a0002c0003t0001g0096 | 2 | HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.155-37921_155-3792 others(110): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784806 | ||||||
| chr4:147784806
|
A | ATATTATA others(15): Show |
1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.155-37921_155-3792 others(26): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784806 | ||||||
| chr4:147784815
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0061a0001c0005t0001g0074 | 3 | HG02145.hp2 HG02886.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.155-37912T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784815 | ||||||
| chr4:147784815
|
TA | T | 3 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.155-37908delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784815 | |||||
| chr4:147784830
|
A | AAATAT | 5 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0103others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-37895_155-3789 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784830 | |||||
| chr4:147784831
|
A | AAT | 25 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(22): Show | 25 | HG00558.hp1 HG01071.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.155-37891_155-3789 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784831 | |||||
| chr4:147784835
|
TATTATAA others(13): Show |
T | 2 | a0001c0001t0001g0099a0001c0011t0001g0092 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.155-37890_155-3787 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784835 | |||||
| chr4:147784856
|
A | AAT | 3 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0002t0001g0033 | 3 | HG01261.hp2 HG01993.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.155-37866_155-3786 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784856 | |||||
| chr4:147784905
|
AAATAT | A | 2 | a0001c0001t0001g0056a0001c0004t0001g0102 | 2 | HG02080.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.155-37815_155-3781 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784905 | |||||
| chr4:147784908
|
TATA | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0002t0001g0029others(1): Show | 4 | HG02056.hp2 HG02080.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-37815_155-3781 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784908 | |||||
| chr4:147784930
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005 | 3 | HG02572.hp1 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.155-37797G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784930 | ||||||
| chr4:147784934
|
T | TA | 2 | a0001c0001t0001g0018a0001c0001t0001g0037 | 2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.155-37789dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147784934 | |||||
| chr4:147784946
|
CAT | C | 2 | a0001c0001t0001g0047a0001c0004t0001g0045 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.155-37780_155-3777 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147784946 | ||||||
| chr4:147785001
|
T | C | 8 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-37726T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147785001 | ||||||
| chr4:147785058
|
A | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-37669A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147785058 | ||||||
| chr4:147785083
|
T | TA | 30 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.155-37627dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147785083 | |||||
| chr4:147785083
|
T | TAAA | 25 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(22): Show | 25 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.155-37629_155-3762 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147785083 | |||||
| chr4:147785083
|
T | TAAAA | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(4): Show | 7 | HG01071.hp2 HG01169.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-37630_155-3762 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147785083 | |||||
| chr4:147785406
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.155-37321T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147785406 | ||||||
| chr4:147785435
|
G | A | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-37292G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147785435 | ||||||
| chr4:147785592
|
T | G | 2 | a0001c0002t0001g0072a0001c0002t0001g0078 | 2 | HG02738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.155-37135T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147785592 | ||||||
| chr4:147785912
|
C | T | 1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.155-36815C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147785912 | ||||||
| chr4:147785994
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.155-36733C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147785994 | ||||||
| chr4:147786113
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(92): Show | 95 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.155-36614G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147786113 | ||||||
| chr4:147786183
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.155-36544A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147786183 | ||||||
| chr4:147786198
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(92): Show | 95 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.155-36529T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147786198 | ||||||
| chr4:147786220
|
C | T | 1 | a0001c0009t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.155-36507C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147786220 | ||||||
| chr4:147786382
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.155-36345A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147786382 | ||||||
| chr4:147786426
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-36301A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147786426 | ||||||
| chr4:147786930
|
C | A | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.155-35797C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147786930 | ||||||
| chr4:147786965
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.155-35762C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147786965 | ||||||
| chr4:147787101
|
A | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-35626A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147787101 | ||||||
| chr4:147787153
|
A | G | 1 | a0001c0002t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.155-35574A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147787153 | ||||||
| chr4:147787353
|
A | G | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.155-35374A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147787353 | ||||||
| chr4:147787452
|
C | CG | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(37): Show | 40 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.155-35273dupG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147787452 | |||||
| chr4:147787875
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(92): Show | 95 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.155-34852T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147787875 | ||||||
| chr4:147788002
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(92): Show | 95 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.155-34725G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147788002 | ||||||
| chr4:147788025
|
T | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0097a0001c0005t0001g0098others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-34702T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147788025 | ||||||
| chr4:147788038
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.155-34689C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147788038 | ||||||
| chr4:147788138
|
T | TG | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(92): Show | 95 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.155-34589_155-3458 others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147788138 | ||||||
| chr4:147788289
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.155-34438A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147788289 | ||||||
| chr4:147788458
|
A | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(47): Show | 50 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.155-34269A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147788458 | ||||||
| chr4:147788679
|
C | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-34048C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147788679 | ||||||
| chr4:147788914
|
G | T | 1 | a0001c0001t0001g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.155-33813G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147788914 | ||||||
| chr4:147789086
|
T | A | 3 | a0001c0001t0001g0088a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp1 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.155-33641T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147789086 | ||||||
| chr4:147789377
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.155-33350C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147789377 | ||||||
| chr4:147789414
|
T | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-33313T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147789414 | ||||||
| chr4:147789526
|
G | A | 2 | a0001c0004t0001g0105a0004c0010t0001g0048 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.155-33201G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147789526 | ||||||
| chr4:147789814
|
G | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(38): Show | 41 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.155-32913G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147789814 | ||||||
| chr4:147789821
|
A | G | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.155-32906A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147789821 | ||||||
| chr4:147789991
|
A | AT | 8 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0058others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.155-32711dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147789991 | |||||
| chr4:147789991
|
AT | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0046others(9): Show | 12 | HG00558.hp2 HG01167.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.155-32711delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147789991 | |||||
| chr4:147789991
|
ATTTTTTT others(2): Show |
A | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-32719_155-3271 others(13): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147789991 | |||||
| chr4:147789991
|
ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-32720_155-3271 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147789991 | |||||
| chr4:147790045
|
A | G | 5 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-32682A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147790045 | ||||||
| chr4:147790047
|
A | T | 3 | a0001c0001t0001g0106a0001c0004t0001g0105a0004c0010t0001g0048 | 3 | HG02572.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.155-32680A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147790047 | ||||||
| chr4:147790150
|
G | A | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.155-32577G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147790150 | ||||||
| chr4:147790417
|
T | C | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.155-32310T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147790417 | ||||||
| chr4:147790427
|
A | G | 5 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-32300A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147790427 | ||||||
| chr4:147790495
|
T | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-32232T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147790495 | ||||||
| chr4:147790547
|
C | T | 4 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(1): Show | 4 | HG02258.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-32180C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147790547 | ||||||
| chr4:147790685
|
A | G | 5 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-32042A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147790685 | ||||||
| chr4:147790768
|
T | G | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155-31959T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147790768 | ||||||
| chr4:147790984
|
T | C | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.155-31743T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147790984 | ||||||
| chr4:147791112
|
C | CT | 4 | a0001c0001t0001g0047a0001c0004t0001g0045a0001c0004t0001g0105others(1): Show | 4 | HG02572.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-31598dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147791112 | |||||
| chr4:147791112
|
CT | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0070a0001c0001t0001g0077others(6): Show | 9 | HG00558.hp1 HG00558.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.155-31598delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147791112 | |||||
| chr4:147791482
|
T | A | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-31245T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147791482 | ||||||
| chr4:147791521
|
CGT | C | 2 | a0001c0001t0001g0077a0001c0008t0001g0060 | 2 | HG00558.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.155-31194_155-3119 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147791521 | |||||
| chr4:147791533
|
T | C | 2 | a0001c0001t0001g0070a0001c0008t0001g0059 | 2 | HG03471.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.155-31194T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147791533 | ||||||
| chr4:147791543
|
T | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-31184T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147791543 | ||||||
| chr4:147791546
|
G | A | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.155-31181G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147791546 | ||||||
| chr4:147791556
|
G | GTA | 4 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-31159_155-3115 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147791556 | |||||
| chr4:147791569
|
TTTTG | T | 2 | a0001c0001t0001g0002a0001c0009t0001g0007 | 2 | HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.155-31138_155-3113 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147791569 | |||||
| chr4:147791804
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-30923C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147791804 | ||||||
| chr4:147792016
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(38): Show | 41 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.155-30711C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147792016 | ||||||
| chr4:147792357
|
A | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-30370A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147792357 | ||||||
| chr4:147792560
|
T | G | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.155-30167T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147792560 | ||||||
| chr4:147792615
|
T | G | 1 | a0001c0001t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.155-30112T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147792615 | ||||||
| chr4:147792971
|
C | G | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.155-29756C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147792971 | ||||||
| chr4:147792990
|
T | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-29737T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147792990 | ||||||
| chr4:147792998
|
T | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-29729T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147792998 | ||||||
| chr4:147793005
|
A | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(38): Show | 41 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.155-29722A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793005 | ||||||
| chr4:147793125
|
G | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0106a0001c0004t0001g0045others(2): Show | 5 | HG02572.hp2 HG02896.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-29602G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793125 | ||||||
| chr4:147793138
|
G | GA | 3 | a0001c0001t0001g0088a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp1 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.155-29582dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147793138 | |||||
| chr4:147793158
|
G | T | 1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.155-29569G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793158 | ||||||
| chr4:147793238
|
A | G | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.155-29489A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793238 | ||||||
| chr4:147793305
|
CAT | C | 2 | a0001c0001t0001g0047a0001c0004t0001g0045 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.155-29407_155-2940 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147793305 | |||||
| chr4:147793307
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-29420T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793307 | ||||||
| chr4:147793319
|
TA | T | 2 | a0001c0001t0001g0106a0004c0010t0001g0048 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.155-29407delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793319 | ||||||
| chr4:147793320
|
AT | A | 48 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(45): Show | 48 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.155-29394delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147793320 | |||||
| chr4:147793321
|
T | TA | 3 | a0001c0001t0001g0044a0001c0001t0002g0031a0001c0002t0001g0072 | 3 | HG03239.hp1 HG03492.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.155-29406_155-2940 others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793321 | ||||||
| chr4:147793321
|
T | TATA | 2 | a0001c0002t0001g0090a0001c0011t0001g0092 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.155-29406_155-2940 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793321 | ||||||
| chr4:147793322
|
T | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(39): Show | 42 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.155-29405T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793322 | ||||||
| chr4:147793323
|
T | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0070others(5): Show | 8 | HG00558.hp2 HG01167.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-29404T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793323 | ||||||
| chr4:147793324
|
T | A | 2 | a0001c0001t0001g0088a0001c0004t0001g0102 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.155-29403T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793324 | ||||||
| chr4:147793325
|
T | A | 6 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0002t0001g0090others(3): Show | 6 | HG00558.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-29402T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793325 | ||||||
| chr4:147793327
|
T | A | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.155-29400T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793327 | ||||||
| chr4:147793383
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(7): Show | 10 | HG01071.hp2 HG01169.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.155-29344G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793383 | ||||||
| chr4:147793409
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.155-29318G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793409 | ||||||
| chr4:147793651
|
G | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-29076G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793651 | ||||||
| chr4:147793714
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.155-29013C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793714 | ||||||
| chr4:147793776
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0097a0001c0002t0001g0072others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-28951C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793776 | ||||||
| chr4:147793784
|
C | A | 5 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-28943C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793784 | ||||||
| chr4:147793895
|
T | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-28832T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147793895 | ||||||
| chr4:147794515
|
A | T | 5 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-28212A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147794515 | ||||||
| chr4:147794535
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.155-28192C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147794535 | ||||||
| chr4:147794646
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(38): Show | 41 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.155-28081T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147794646 | ||||||
| chr4:147794817
|
A | G | 3 | a0001c0001t0001g0106a0001c0004t0001g0105a0004c0010t0001g0048 | 3 | HG02572.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.155-27910A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147794817 | ||||||
| chr4:147794836
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.155-27891G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147794836 | ||||||
| chr4:147795003
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.155-27724T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147795003 | ||||||
| chr4:147795153
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.155-27574G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147795153 | ||||||
| chr4:147795216
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.155-27511G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147795216 | ||||||
| chr4:147795256
|
T | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0097a0001c0005t0001g0098others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-27471T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147795256 | ||||||
| chr4:147795339
|
G | A | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.155-27388G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147795339 | ||||||
| chr4:147795555
|
G | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-27172G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147795555 | ||||||
| chr4:147795608
|
G | A | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG02258.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-27119G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147795608 | ||||||
| chr4:147795700
|
AT | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-27014delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147795700 | |||||
| chr4:147795734
|
G | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-26993G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147795734 | ||||||
| chr4:147795819
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.155-26908C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147795819 | ||||||
| chr4:147795929
|
G | A | 1 | a0001c0002t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.155-26798G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147795929 | ||||||
| chr4:147795973
|
A | C | 1 | a0001c0002t0001g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.155-26754A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147795973 | ||||||
| chr4:147796073
|
A | C | 1 | a0001c0002t0001g0029 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.155-26654A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147796073 | ||||||
| chr4:147796089
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.155-26638T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147796089 | ||||||
| chr4:147796440
|
G | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-26287G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147796440 | ||||||
| chr4:147796580
|
A | C | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.155-26147A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147796580 | ||||||
| chr4:147796611
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-26116C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147796611 | ||||||
| chr4:147796686
|
C | T | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.155-26041C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147796686 | ||||||
| chr4:147796727
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0081 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.155-26000G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147796727 | ||||||
| chr4:147797375
|
T | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0001t0002g0031 | 3 | HG00558.hp1 HG03239.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.155-25352T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147797375 | ||||||
| chr4:147797522
|
C | A | 1 | a0001c0001t0001g0010 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.155-25205C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147797522 | ||||||
| chr4:147797647
|
G | A | 3 | a0001c0001t0001g0088a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp1 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.155-25080G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147797647 | ||||||
| chr4:147797673
|
A | T | 33 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(30): Show | 33 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.155-25054A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147797673 | ||||||
| chr4:147797882
|
A | T | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.155-24845A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147797882 | ||||||
| chr4:147798137
|
CT | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0035others(34): Show | 37 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.155-24578delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798137 | |||||
| chr4:147798253
|
C | T | 2 | a0001c0002t0001g0072a0001c0002t0001g0078 | 2 | HG02738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.155-24474C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798253 | ||||||
| chr4:147798308
|
C | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(40): Show | 43 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.155-24419C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798308 | ||||||
| chr4:147798436
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.155-24291T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798436 | ||||||
| chr4:147798496
|
A | C | 3 | a0001c0001t0001g0088a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp1 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.155-24231A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798496 | ||||||
| chr4:147798608
|
C | T | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.155-24119C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798608 | ||||||
| chr4:147798721
|
GACACTCT others(7): Show |
G | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.155-24005_155-2399 others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798721 | ||||||
| chr4:147798722
|
A | ACTCTCTC others(7): Show |
1 | a0001c0005t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.155-24004_155-2400 others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798722 | |||||
| chr4:147798722
|
ACACT | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0002t0001g0005 | 3 | HG02895.hp1 HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.155-24003_155-2400 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798722 | |||||
| chr4:147798722
|
ACACTCTC others(1): Show |
A | 4 | a0001c0001t0001g0069a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-24003_155-2399 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798722 | |||||
| chr4:147798722
|
ACACTCTC others(5): Show |
A | 1 | a0001c0001t0001g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.155-24003_155-2399 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798722 | |||||
| chr4:147798722
|
ACACTCTC others(9): Show |
A | 1 | a0001c0009t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.155-24003_155-2398 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798722 | |||||
| chr4:147798722
|
ACACTCTC others(13): Show |
A | 1 | a0001c0006t0001g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.155-24003_155-2398 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798722 | |||||
| chr4:147798724
|
A | ACTCTCTC others(1): Show |
2 | a0003c0007t0001g0079a0003c0007t0001g0082 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.155-23952_155-2394 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798724 | |||||
| chr4:147798724
|
A | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0050others(26): Show | 29 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.155-24003A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798724 | ||||||
| chr4:147798724
|
ACTCTCTC others(5): Show |
A | 4 | a0001c0001t0001g0052a0001c0001t0001g0091a0001c0001t0003g0087others(1): Show | 4 | HG01261.hp1 HG02109.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-23956_155-2394 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798724 | |||||
| chr4:147798724
|
ACTCTCTC others(9): Show |
A | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.155-23960_155-2394 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798724 | |||||
| chr4:147798724
|
ACTCTCTC others(11): Show |
A | 1 | a0001c0001t0001g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.155-23962_155-2394 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798724 | |||||
| chr4:147798726
|
T | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.155-24001T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798726 | ||||||
| chr4:147798734
|
T | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.155-23993T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798734 | ||||||
| chr4:147798743
|
C | T | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.155-23984C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798743 | ||||||
| chr4:147798749
|
CTCTCTCT others(29): Show |
C | 1 | a0001c0001t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.155-23976_155-2394 others(40): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798749 | |||||
| chr4:147798749
|
CTCTCTCT others(35): Show |
C | 2 | a0001c0001t0001g0046a0001c0005t0001g0098 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.155-23976_155-2393 others(46): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798749 | |||||
| chr4:147798749
|
CTCTCTCT others(41): Show |
C | 1 | a0001c0001t0001g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.155-23976_155-2392 others(52): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798749 | |||||
| chr4:147798751
|
CTCTCTCT others(35): Show |
C | 2 | a0001c0001t0001g0097a0002c0003t0001g0096 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.155-23974_155-2393 others(46): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798751 | |||||
| chr4:147798753
|
CTCTCTCT others(29): Show |
C | 4 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0044others(1): Show | 4 | HG02080.hp2 HG04184.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-23972_155-2393 others(40): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798753 | |||||
| chr4:147798755
|
CTCTCTCT others(25): Show |
C | 2 | a0001c0001t0001g0036a0001c0001t0002g0023 | 2 | HG01070.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.155-23970_155-2393 others(36): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798755 | |||||
| chr4:147798755
|
CTCTCTCT others(27): Show |
C | 4 | a0001c0001t0001g0037a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 4 | HG01993.hp1 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-23970_155-2393 others(38): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798755 | |||||
| chr4:147798755
|
CTCTCTCT others(29): Show |
C | 5 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0022others(2): Show | 5 | HG01167.hp2 HG01993.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-23970_155-2393 others(40): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798755 | |||||
| chr4:147798755
|
CTCTCTCT others(33): Show |
C | 2 | a0001c0001t0001g0011a0002c0003t0001g0009 | 2 | HG01169.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.155-23970_155-2393 others(44): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798755 | |||||
| chr4:147798757
|
CTCTCTCT others(27): Show |
C | 2 | a0001c0001t0001g0018a0001c0001t0002g0031 | 2 | HG01261.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.155-23968_155-2393 others(38): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798757 | |||||
| chr4:147798757
|
CTCTCTCT others(29): Show |
C | 3 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0034 | 3 | HG02056.hp2 NA18983.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.155-23968_155-2393 others(40): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798757 | |||||
| chr4:147798759
|
CTCTCTCT others(27): Show |
C | 1 | a0001c0002t0001g0029 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.155-23966_155-2393 others(38): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798759 | |||||
| chr4:147798759
|
CTCTCTCT others(29): Show |
C | 4 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0002t0001g0013others(1): Show | 4 | HG01243.hp1 HG03710.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-23966_155-2393 others(40): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798759 | |||||
| chr4:147798761
|
CTCTCTCT others(29): Show |
C | 2 | a0001c0001t0001g0025a0001c0001t0001g0058 | 2 | HG00558.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.155-23964_155-2392 others(40): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798761 | |||||
| chr4:147798763
|
CTCTCTCT others(17): Show |
C | 1 | a0001c0008t0001g0060 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.155-23962_155-2393 others(28): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798763 | |||||
| chr4:147798763
|
CTCTCTCT others(29): Show |
C | 1 | a0001c0001t0001g0028 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.155-23962_155-2392 others(40): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798763 | |||||
| chr4:147798765
|
C | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0065a0001c0001t0001g0068others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-23962C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798765 | ||||||
| chr4:147798765
|
C | CTATATAT others(5): Show |
1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-23961_155-2396 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798765 | |||||
| chr4:147798765
|
C | CTATATAT others(7): Show |
1 | a0001c0001t0001g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.155-23961_155-2396 others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798765 | |||||
| chr4:147798765
|
CTCTCTCT others(17): Show |
C | 1 | a0001c0008t0001g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.155-23960_155-2393 others(28): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798765 | |||||
| chr4:147798765
|
CTCTCTCT others(19): Show |
C | 2 | a0001c0001t0001g0081a0001c0002t0001g0078 | 2 | HG02738.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.155-23960_155-2393 others(30): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798765 | |||||
| chr4:147798765
|
CTCTCTCT others(21): Show |
C | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.155-23960_155-2393 others(32): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798765 | |||||
| chr4:147798765
|
CTCTCTCT others(23): Show |
C | 1 | a0001c0001t0001g0056 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.155-23960_155-2393 others(34): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798765 | |||||
| chr4:147798766
|
T | C | 1 | a0001c0009t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.155-23961T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798766 | ||||||
| chr4:147798767
|
C | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0051others(5): Show | 8 | HG02280.hp2 HG02622.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.155-23960C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798767 | ||||||
| chr4:147798767
|
C | CTATATAT others(5): Show |
1 | a0001c0001t0001g0050 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.155-23959_155-2395 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798767 | |||||
| chr4:147798769
|
C | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0050others(7): Show | 10 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.155-23958C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798769 | ||||||
| chr4:147798769
|
CTCTCTCT others(9): Show |
C | 1 | a0001c0006t0001g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.155-23956_155-2394 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798769 | |||||
| chr4:147798771
|
C | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0038others(9): Show | 12 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.155-23956C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798771 | ||||||
| chr4:147798771
|
C | CTATATAT others(9): Show |
1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.155-23955_155-2395 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798771 | |||||
| chr4:147798773
|
C | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0038others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.155-23954C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798773 | ||||||
| chr4:147798773
|
CTCTCTCT others(7): Show |
C | 1 | a0001c0001t0001g0070 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.155-23952_155-2393 others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798773 | |||||
| chr4:147798775
|
C | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0035others(14): Show | 17 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.155-23952C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798775 | ||||||
| chr4:147798775
|
CTCTCTCT others(3): Show |
C | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.155-23950_155-2394 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798775 | |||||
| chr4:147798775
|
CTCTCTCT others(11): Show |
C | 1 | a0001c0001t0001g0055 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.155-23950_155-2393 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798775 | |||||
| chr4:147798777
|
C | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(17): Show | 20 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.155-23950C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798777 | ||||||
| chr4:147798777
|
C | CTATATA | 2 | a0001c0001t0001g0061a0001c0001t0001g0088 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.155-23949_155-2394 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798777 | |||||
| chr4:147798777
|
CTCTCTAT others(3): Show |
C | 1 | a0001c0001t0001g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.155-23948_155-2393 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798777 | |||||
| chr4:147798777
|
CTCTCTAT others(11): Show |
C | 1 | a0001c0001t0001g0054 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.155-23948_155-2393 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798777 | |||||
| chr4:147798779
|
C | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(25): Show | 28 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.155-23948C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798779 | ||||||
| chr4:147798779
|
C | CTATATAT others(5): Show |
1 | a0001c0001t0001g0053 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.155-23947_155-2394 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798779 | |||||
| chr4:147798779
|
C | CTATATAT others(19): Show |
1 | a0001c0001t0001g0047 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.155-23947_155-2394 others(30): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798779 | |||||
| chr4:147798781
|
C | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(31): Show | 34 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.155-23946C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798781 | ||||||
| chr4:147798781
|
C | CTATATAT others(3): Show |
1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.155-23919_155-2391 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798781 | |||||
| chr4:147798781
|
C | CTATATAT others(5): Show |
2 | a0001c0001t0001g0080a0002c0003t0001g0064 | 2 | HG02886.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.155-23921_155-2391 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798781 | |||||
| chr4:147798781
|
C | CTATATAT others(17): Show |
1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.155-23933_155-2391 others(28): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798781 | |||||
| chr4:147798781
|
C | CTCTCTAT others(3): Show |
1 | a0001c0002t0001g0066 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.155-23945_155-2394 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798781 | |||||
| chr4:147798781
|
C | CTCTCTCT others(21): Show |
1 | a0001c0001t0001g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.155-23945_155-2394 others(32): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798781 | |||||
| chr4:147798781
|
C | CTCTCTCT others(3): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.155-23945_155-2394 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798781 | |||||
| chr4:147798781
|
C | CTCTCTCT others(15): Show |
1 | a0001c0005t0001g0003 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.155-23945_155-2394 others(26): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798781 | |||||
| chr4:147798781
|
C | CTCTCTCT others(19): Show |
1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.155-23945_155-2394 others(30): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798781 | |||||
| chr4:147798781
|
C | CTCTCTCT others(9): Show |
1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.155-23945_155-2394 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798781 | |||||
| chr4:147798781
|
CTATATA | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0043 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.155-23915_155-2391 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147798781 | |||||
| chr4:147798783
|
A | C | 5 | a0001c0004t0001g0105a0001c0005t0001g0074a0003c0007t0001g0079others(2): Show | 5 | HG01891.hp2 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-23944A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798783 | ||||||
| chr4:147798785
|
A | C | 6 | a0001c0001t0001g0083a0001c0004t0001g0105a0001c0005t0001g0074others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-23942A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798785 | ||||||
| chr4:147798787
|
A | C | 3 | a0001c0005t0001g0074a0003c0007t0001g0082a0004c0010t0001g0048 | 3 | HG02886.hp1 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.155-23940A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798787 | ||||||
| chr4:147798789
|
A | C | 3 | a0001c0005t0001g0074a0003c0007t0001g0082a0004c0010t0001g0048 | 3 | HG02886.hp1 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.155-23938A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798789 | ||||||
| chr4:147798830
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(51): Show | 54 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.155-23897C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798830 | ||||||
| chr4:147798889
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.155-23838A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147798889 | ||||||
| chr4:147799223
|
C | T | 3 | a0001c0001t0001g0106a0001c0004t0001g0105a0004c0010t0001g0048 | 3 | HG02572.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.155-23504C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147799223 | ||||||
| chr4:147799428
|
A | G | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 31 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.155-23299A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147799428 | ||||||
| chr4:147799515
|
C | T | 3 | a0001c0001t0001g0088a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp1 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.155-23212C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147799515 | ||||||
| chr4:147799807
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.155-22920G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147799807 | ||||||
| chr4:147800304
|
C | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(44): Show | 47 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.155-22423C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147800304 | ||||||
| chr4:147800550
|
C | G | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.155-22177C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147800550 | ||||||
| chr4:147800737
|
G | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0097a0001c0005t0001g0098others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-21990G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147800737 | ||||||
| chr4:147800774
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.155-21953G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147800774 | ||||||
| chr4:147800793
|
G | A | 3 | a0001c0001t0001g0097a0001c0005t0001g0098a0002c0003t0001g0096 | 3 | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.155-21934G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147800793 | ||||||
| chr4:147800932
|
A | G | 33 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(30): Show | 33 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.155-21795A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147800932 | ||||||
| chr4:147801157
|
A | G | 1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.155-21570A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147801157 | ||||||
| chr4:147801436
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.155-21291A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147801436 | ||||||
| chr4:147801581
|
C | A | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-21146C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147801581 | ||||||
| chr4:147802324
|
A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 96 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.155-20403A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147802324 | ||||||
| chr4:147802995
|
T | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0035others(34): Show | 37 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.155-19732T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147802995 | ||||||
| chr4:147803015
|
CT | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(40): Show | 43 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.155-19701delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147803015 | |||||
| chr4:147803200
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.155-19527G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147803200 | ||||||
| chr4:147803309
|
T | C | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-19418T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147803309 | ||||||
| chr4:147803401
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.155-19326A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147803401 | ||||||
| chr4:147803449
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.155-19278T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147803449 | ||||||
| chr4:147803487
|
A | G | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 31 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.155-19240A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147803487 | ||||||
| chr4:147803641
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.155-19086G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147803641 | ||||||
| chr4:147803678
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.155-19049G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147803678 | ||||||
| chr4:147803796
|
A | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-18931A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147803796 | ||||||
| chr4:147803872
|
G | A | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.155-18855G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147803872 | ||||||
| chr4:147803937
|
G | T | 1 | a0001c0002t0001g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.155-18790G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147803937 | ||||||
| chr4:147803955
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(45): Show | 48 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.155-18772A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147803955 | ||||||
| chr4:147803994
|
GT | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0043a0001c0001t0001g0070others(8): Show | 11 | HG00558.hp2 HG02080.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.155-18717delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147803994 | |||||
| chr4:147804066
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.155-18661C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147804066 | ||||||
| chr4:147804161
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.155-18566C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147804161 | ||||||
| chr4:147804755
|
T | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-17972T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147804755 | ||||||
| chr4:147804782
|
G | A | 3 | a0001c0001t0001g0106a0001c0004t0001g0105a0004c0010t0001g0048 | 3 | HG02572.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.155-17945G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147804782 | ||||||
| chr4:147804817
|
T | A | 3 | a0001c0001t0001g0088a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp1 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.155-17910T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147804817 | ||||||
| chr4:147805125
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.155-17602T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147805125 | ||||||
| chr4:147805220
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(44): Show | 47 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.155-17507A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147805220 | ||||||
| chr4:147805283
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.155-17444G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147805283 | ||||||
| chr4:147805362
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-17365C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147805362 | ||||||
| chr4:147805496
|
A | G | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0008t0001g0059others(1): Show | 4 | HG00558.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-17231A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147805496 | ||||||
| chr4:147805857
|
T | A | 15 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0052others(12): Show | 15 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.155-16870T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147805857 | ||||||
| chr4:147806009
|
A | G | 3 | a0001c0001t0001g0088a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp1 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.155-16718A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147806009 | ||||||
| chr4:147806103
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(45): Show | 48 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.155-16624A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147806103 | ||||||
| chr4:147806198
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.155-16529C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147806198 | ||||||
| chr4:147806204
|
G | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0035others(34): Show | 37 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.155-16523G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147806204 | ||||||
| chr4:147806972
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0037others(2): Show | 5 | HG00558.hp1 HG01261.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-15755C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147806972 | ||||||
| chr4:147806973
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0002t0001g0029others(1): Show | 4 | HG02056.hp2 HG02080.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-15754G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147806973 | ||||||
| chr4:147807072
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0077 | 2 | HG00558.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.155-15655G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147807072 | ||||||
| chr4:147807119
|
G | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(39): Show | 42 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.155-15608G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147807119 | ||||||
| chr4:147807186
|
AC | A | 4 | a0001c0001t0001g0047a0001c0001t0001g0094a0001c0004t0001g0045others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-15535delC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147807186 | |||||
| chr4:147807901
|
G | A | 3 | a0001c0001t0001g0081a0001c0004t0001g0105a0004c0010t0001g0048 | 3 | HG02572.hp2 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.155-14826G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147807901 | ||||||
| chr4:147808043
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.155-14684A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147808043 | ||||||
| chr4:147808110
|
T | G | 1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.155-14617T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147808110 | ||||||
| chr4:147808186
|
G | A | 2 | a0001c0002t0001g0090a0001c0011t0001g0092 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.155-14541G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147808186 | ||||||
| chr4:147808771
|
C | G | 2 | a0001c0008t0001g0059a0001c0008t0001g0060 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.155-13956C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147808771 | ||||||
| chr4:147808816
|
C | T | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.155-13911C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147808816 | ||||||
| chr4:147809302
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(100): Show | 103 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(100): Show |
intron_variant | MODIFIER | c.155-13425G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147809302 | ||||||
| chr4:147809355
|
G | A | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-13372G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147809355 | ||||||
| chr4:147809371
|
T | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-13356T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147809371 | ||||||
| chr4:147809490
|
A | T | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(35): Show | 38 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.155-13237A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147809490 | ||||||
| chr4:147809581
|
A | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.155-13146A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147809581 | ||||||
| chr4:147809648
|
T | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-13079T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147809648 | ||||||
| chr4:147809674
|
C | T | 26 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 26 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.155-13053C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147809674 | ||||||
| chr4:147810093
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-12634C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147810093 | ||||||
| chr4:147810706
|
G | T | 2 | a0001c0008t0001g0059a0001c0008t0001g0060 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.155-12021G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147810706 | ||||||
| chr4:147810833
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(70): Show | 73 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.155-11894T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147810833 | ||||||
| chr4:147810833
|
T | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-11894T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147810833 | ||||||
| chr4:147810842
|
C | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.155-11885C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147810842 | ||||||
| chr4:147811138
|
T | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.155-11589T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147811138 | ||||||
| chr4:147811583
|
CT | C | 25 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(22): Show | 25 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.155-11137delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147811583 | |||||
| chr4:147811590
|
T | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0052others(8): Show | 11 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.155-11137T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147811590 | ||||||
| chr4:147811590
|
TA | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0077others(6): Show | 9 | HG00558.hp2 HG02572.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.155-11125delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147811590 | |||||
| chr4:147811596
|
A | C | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.155-11131A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147811596 | ||||||
| chr4:147811602
|
A | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-11125A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147811602 | ||||||
| chr4:147811603
|
C | A | 1 | a0001c0001t0001g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.155-11124C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147811603 | ||||||
| chr4:147811764
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.155-10963C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147811764 | ||||||
| chr4:147811768
|
T | G | 1 | a0001c0005t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.155-10959T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147811768 | ||||||
| chr4:147811805
|
A | C | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.155-10922A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147811805 | ||||||
| chr4:147811973
|
G | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(30): Show | 33 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.155-10754G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147811973 | ||||||
| chr4:147812139
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-10588G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147812139 | ||||||
| chr4:147812252
|
C | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(29): Show | 32 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.155-10475C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147812252 | ||||||
| chr4:147812575
|
C | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(29): Show | 32 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.155-10152C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147812575 | ||||||
| chr4:147812601
|
T | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(29): Show | 32 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.155-10126T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147812601 | ||||||
| chr4:147812613
|
T | G | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.155-10114T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147812613 | ||||||
| chr4:147813257
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(100): Show | 103 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(100): Show |
intron_variant | MODIFIER | c.155-9470T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147813257 | ||||||
| chr4:147813476
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(44): Show | 47 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.155-9251A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147813476 | ||||||
| chr4:147813749
|
A | T | 3 | a0001c0001t0001g0088a0001c0004t0001g0105a0004c0010t0001g0048 | 3 | HG01884.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.155-8978A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147813749 | ||||||
| chr4:147813828
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(29): Show | 32 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.155-8899A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147813828 | ||||||
| chr4:147814206
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.155-8521G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147814206 | ||||||
| chr4:147814224
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.155-8503A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147814224 | ||||||
| chr4:147814291
|
CT | C | 15 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0061others(12): Show | 15 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.155-8423delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147814291 | |||||
| chr4:147814427
|
T | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(70): Show | 73 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.155-8300T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147814427 | ||||||
| chr4:147814493
|
C | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(29): Show | 32 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.155-8234C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147814493 | ||||||
| chr4:147814576
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.155-8151G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147814576 | ||||||
| chr4:147814713
|
A | G | 7 | a0001c0001t0001g0052a0001c0001t0001g0075a0001c0001t0001g0083others(4): Show | 7 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-8014A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147814713 | ||||||
| chr4:147814817
|
G | A | 2 | a0001c0002t0001g0072a0001c0002t0001g0078 | 2 | HG02738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.155-7910G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147814817 | ||||||
| chr4:147814995
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.155-7732G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147814995 | ||||||
| chr4:147815270
|
T | C | 11 | a0001c0001t0001g0035a0001c0001t0001g0061a0001c0001t0001g0062others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-7457T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147815270 | ||||||
| chr4:147815732
|
GT | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(100): Show | 103 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(100): Show |
intron_variant | MODIFIER | c.155-6992delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147815732 | |||||
| chr4:147815756
|
C | T | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.155-6971C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147815756 | ||||||
| chr4:147815833
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.155-6894G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147815833 | ||||||
| chr4:147815858
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0041others(9): Show | 12 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.155-6869A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147815858 | ||||||
| chr4:147815932
|
G | T | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.155-6795G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147815932 | ||||||
| chr4:147815993
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(100): Show | 103 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(100): Show |
intron_variant | MODIFIER | c.155-6734A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147815993 | ||||||
| chr4:147816099
|
T | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-6628T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147816099 | ||||||
| chr4:147816539
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(100): Show | 103 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(100): Show |
intron_variant | MODIFIER | c.155-6188T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147816539 | ||||||
| chr4:147816629
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(86): Show | 89 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(86): Show |
intron_variant | MODIFIER | c.155-6098T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147816629 | ||||||
| chr4:147816780
|
G | T | 8 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-5947G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147816780 | ||||||
| chr4:147817183
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0077 | 2 | HG00558.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.155-5544C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147817183 | ||||||
| chr4:147817299
|
G | C | 4 | a0001c0001t0001g0050a0001c0004t0001g0045a0001c0005t0001g0074others(1): Show | 4 | HG02886.hp1 HG02976.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-5428G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147817299 | ||||||
| chr4:147817388
|
T | C | 2 | a0001c0001t0001g0089a0001c0002t0001g0090 | 2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.155-5339T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147817388 | ||||||
| chr4:147817556
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0035others(13): Show | 16 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.155-5171C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147817556 | ||||||
| chr4:147817590
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.155-5137C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147817590 | ||||||
| chr4:147818164
|
C | CT | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(2): Show | 5 | HG02572.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-4549dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147818164 | |||||
| chr4:147818164
|
CT | C | 4 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0101others(1): Show | 4 | HG01070.hp1 HG01167.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-4549delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147818164 | |||||
| chr4:147818454
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(64): Show | 67 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(64): Show |
intron_variant | MODIFIER | c.155-4273C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147818454 | ||||||
| chr4:147818509
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.155-4218T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147818509 | ||||||
| chr4:147818565
|
CA | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(55): Show | 58 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.155-4142delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147818565 | |||||
| chr4:147818582
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.155-4145A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147818582 | ||||||
| chr4:147818863
|
G | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005 | 3 | HG02572.hp1 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.155-3864G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147818863 | ||||||
| chr4:147818963
|
T | C | 6 | a0001c0001t0001g0050a0001c0001t0001g0089a0001c0001t0001g0091others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-3764T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147818963 | ||||||
| chr4:147818974
|
C | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.155-3753C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147818974 | ||||||
| chr4:147819029
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.155-3698G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147819029 | ||||||
| chr4:147819068
|
A | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.155-3659A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147819068 | ||||||
| chr4:147819649
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.155-3078C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147819649 | ||||||
| chr4:147819814
|
C | A | 32 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0037others(29): Show | 32 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.155-2913C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147819814 | ||||||
| chr4:147820007
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(51): Show | 54 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.155-2720G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147820007 | ||||||
| chr4:147820168
|
A | G | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.155-2559A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147820168 | ||||||
| chr4:147820322
|
C | G | 18 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0035others(15): Show | 18 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.155-2405C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147820322 | ||||||
| chr4:147820388
|
C | T | 4 | a0001c0001t0001g0083a0002c0003t0001g0096a0003c0007t0001g0079others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-2339C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147820388 | ||||||
| chr4:147820446
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0076 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.155-2281C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147820446 | ||||||
| chr4:147820451
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.155-2276A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147820451 | ||||||
| chr4:147820580
|
G | GT | 12 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0047others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.155-2117dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147820580 | |||||
| chr4:147820580
|
G | GTT | 4 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 4 | HG02109.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-2118_155-2117d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147820580 | |||||
| chr4:147820580
|
GT | G | 8 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0001t0001g0101others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.155-2117delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147820580 | |||||
| chr4:147820580
|
GTT | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0035others(12): Show | 15 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.155-2118_155-2117d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147820580 | |||||
| chr4:147820580
|
GTTT | G | 18 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0038others(15): Show | 18 | HG00558.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.155-2119_155-2117d others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147820580 | |||||
| chr4:147820580
|
GTTTT | G | 22 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.155-2120_155-2117d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147820580 | |||||
| chr4:147820580
|
GTTTTT | G | 8 | a0001c0001t0001g0052a0001c0001t0001g0075a0001c0001t0003g0087others(5): Show | 8 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-2121_155-2117d others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147820580 | |||||
| chr4:147820701
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.155-2026G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147820701 | ||||||
| chr4:147820793
|
G | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005 | 3 | HG02572.hp1 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.155-1934G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147820793 | ||||||
| chr4:147820885
|
T | A | 2 | a0001c0001t0001g0097a0001c0005t0001g0098 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.155-1842T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147820885 | ||||||
| chr4:147820957
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(64): Show | 67 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(64): Show |
intron_variant | MODIFIER | c.155-1770T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147820957 | ||||||
| chr4:147821163
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 75 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.155-1564G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147821163 | ||||||
| chr4:147821172
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.155-1555G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147821172 | ||||||
| chr4:147821230
|
GCA | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0093 | 3 | HG02258.hp1 HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.155-1494_155-1493d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 147821230 | |||||
| chr4:147821273
|
C | T | 5 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(2): Show | 5 | HG02258.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-1454C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147821273 | ||||||
| chr4:147821303
|
T | A | 5 | a0001c0001t0001g0081a0001c0002t0001g0072a0001c0004t0001g0105others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-1424T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147821303 | ||||||
| chr4:147821422
|
A | G | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.155-1305A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147821422 | ||||||
| chr4:147821772
|
G | A | 4 | a0001c0002t0001g0072a0001c0004t0001g0105a0001c0011t0001g0092others(1): Show | 4 | HG02451.hp2 HG02572.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-955G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147821772 | ||||||
| chr4:147821777
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.155-950C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147821777 | ||||||
| chr4:147821806
|
C | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(70): Show | 73 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.155-921C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147821806 | ||||||
| chr4:147821931
|
C | A | 6 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-796C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147821931 | ||||||
| chr4:147822122
|
A | T | 2 | a0001c0002t0001g0090a0001c0004t0001g0102 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.155-605A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | 147822122 | ||||||
| chr4:147823168
|
G | A | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.312+211G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147823168 | ||||||
| chr4:147823996
|
T | G | 1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.312+1039T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147823996 | ||||||
| chr4:147824232
|
G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0095 | 3 | HG02055.hp2 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.312+1275G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147824232 | ||||||
| chr4:147824321
|
C | CA | 23 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0044others(20): Show | 23 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.312+1377dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147824321 | |||||
| chr4:147824352
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.312+1395A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147824352 | ||||||
| chr4:147824385
|
G | A | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.312+1428G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147824385 | ||||||
| chr4:147824445
|
C | G | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.312+1488C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147824445 | ||||||
| chr4:147824576
|
G | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.312+1619G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147824576 | ||||||
| chr4:147824636
|
AC | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0076 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.312+1680delC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147824636 | ||||||
| chr4:147824981
|
T | G | 6 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+2024T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147824981 | ||||||
| chr4:147825149
|
T | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(26): Show | 29 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.312+2192T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147825149 | ||||||
| chr4:147825187
|
CCT | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.312+2233_312+2234d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147825187 | |||||
| chr4:147825279
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.312+2322G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147825279 | ||||||
| chr4:147825425
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0076 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.312+2468C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147825425 | ||||||
| chr4:147825446
|
C | CA | 25 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(22): Show | 25 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.312+2501dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147825446 | |||||
| chr4:147825810
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 84 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.312+2853C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147825810 | ||||||
| chr4:147826064
|
C | T | 2 | a0001c0002t0001g0090a0001c0004t0001g0102 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.312+3107C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147826064 | ||||||
| chr4:147826210
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.312+3253T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147826210 | ||||||
| chr4:147826313
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(81): Show | 84 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.312+3356G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147826313 | ||||||
| chr4:147826664
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0077 | 2 | HG00558.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.312+3707C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147826664 | ||||||
| chr4:147826679
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0086 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.312+3722C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147826679 | ||||||
| chr4:147826681
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(35): Show | 38 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.312+3724C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147826681 | ||||||
| chr4:147827178
|
CT | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(36): Show | 39 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.312+4235delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147827178 | |||||
| chr4:147827207
|
G | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(25): Show | 28 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.312+4250G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147827207 | ||||||
| chr4:147827521
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.312+4564G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147827521 | ||||||
| chr4:147827751
|
G | A | 2 | a0001c0002t0001g0090a0001c0004t0001g0102 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.312+4794G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147827751 | ||||||
| chr4:147827928
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(40): Show | 43 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.312+4971C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147827928 | ||||||
| chr4:147828526
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.312+5569T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147828526 | ||||||
| chr4:147828557
|
C | T | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.312+5600C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147828557 | ||||||
| chr4:147828807
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.312+5850G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147828807 | ||||||
| chr4:147828860
|
C | A | 1 | a0002c0003t0001g0096 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.312+5903C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147828860 | ||||||
| chr4:147828880
|
G | GT | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(78): Show | 81 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.312+5937dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147828880 | |||||
| chr4:147829044
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.312+6087A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147829044 | ||||||
| chr4:147829055
|
A | AT | 4 | a0001c0001t0001g0038a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+6112dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147829055 | |||||
| chr4:147829055
|
AT | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(77): Show | 80 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.312+6112delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147829055 | |||||
| chr4:147829211
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.312+6254C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147829211 | ||||||
| chr4:147829234
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.312+6277A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147829234 | ||||||
| chr4:147829423
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(36): Show | 39 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.312+6466G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147829423 | ||||||
| chr4:147829435
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.312+6478C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147829435 | ||||||
| chr4:147829478
|
C | T | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(34): Show | 37 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.312+6521C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147829478 | ||||||
| chr4:147829762
|
T | G | 1 | a0001c0001t0001g0053 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.312+6805T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147829762 | ||||||
| chr4:147829767
|
G | A | 1 | a0003c0007t0001g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.312+6810G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147829767 | ||||||
| chr4:147829955
|
G | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.312+6998G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147829955 | ||||||
| chr4:147830006
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+7049G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147830006 | ||||||
| chr4:147830079
|
G | A | 34 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(31): Show | 34 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.312+7122G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147830079 | ||||||
| chr4:147830239
|
C | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 81 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.312+7282C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147830239 | ||||||
| chr4:147830275
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.312+7318A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147830275 | ||||||
| chr4:147830322
|
C | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0043others(11): Show | 14 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.312+7365C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147830322 | ||||||
| chr4:147830427
|
G | A | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.312+7470G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147830427 | ||||||
| chr4:147830445
|
A | G | 4 | a0001c0001t0001g0050a0001c0001t0001g0091a0001c0004t0001g0045others(1): Show | 4 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+7488A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147830445 | ||||||
| chr4:147830481
|
C | T | 1 | a0001c0001t0001g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.312+7524C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147830481 | ||||||
| chr4:147830512
|
C | CT | 7 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0089others(4): Show | 7 | HG01243.hp2 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.312+7578dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147830512 | |||||
| chr4:147830512
|
C | CTTTT | 30 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(27): Show | 30 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.312+7575_312+7578d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147830512 | |||||
| chr4:147830512
|
C | CTTTTT | 7 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0061others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.312+7574_312+7578d others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147830512 | |||||
| chr4:147830512
|
CTTTTTT | C | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(34): Show | 37 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.312+7573_312+7578d others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147830512 | |||||
| chr4:147830767
|
G | A | 2 | a0001c0002t0001g0033a0002c0003t0001g0073 | 2 | HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.312+7810G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147830767 | ||||||
| chr4:147830891
|
G | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(35): Show | 38 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.312+7934G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147830891 | ||||||
| chr4:147831208
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 81 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.312+8251A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147831208 | ||||||
| chr4:147831759
|
G | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0097a0001c0005t0001g0098others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+8802G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147831759 | ||||||
| chr4:147831905
|
A | C | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.312+8948A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147831905 | ||||||
| chr4:147832082
|
C | T | 34 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(31): Show | 34 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.312+9125C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147832082 | ||||||
| chr4:147832084
|
C | T | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(34): Show | 37 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.312+9127C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147832084 | ||||||
| chr4:147832159
|
A | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(31): Show | 34 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.312+9202A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147832159 | ||||||
| chr4:147832201
|
G | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(31): Show | 34 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.312+9244G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147832201 | ||||||
| chr4:147832356
|
TA | T | 6 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0055others(3): Show | 6 | HG01884.hp2 HG01993.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+9404delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147832356 | |||||
| chr4:147832357
|
A | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 75 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.312+9400A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147832357 | ||||||
| chr4:147832361
|
A | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0093 | 2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+9404A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147832361 | ||||||
| chr4:147832419
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 77 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.312+9462T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147832419 | ||||||
| chr4:147832422
|
G | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(25): Show | 28 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.312+9465G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147832422 | ||||||
| chr4:147832577
|
G | A | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.312+9620G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147832577 | ||||||
| chr4:147832646
|
C | CAAAAAAA others(1): Show |
9 | a0001c0001t0001g0055a0001c0001t0001g0075a0001c0001t0001g0076others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.312+9700_312+9707d others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147832646 | |||||
| chr4:147832646
|
C | CAAAAAAA others(2): Show |
55 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(52): Show | 55 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.312+9699_312+9707d others(11): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147832646 | |||||
| chr4:147832646
|
C | CAAAAAAA others(3): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0026others(10): Show | 13 | HG01261.hp1 HG01261.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.312+9698_312+9707d others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147832646 | |||||
| chr4:147832646
|
C | CAAAAAAA others(7): Show |
1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.312+9694_312+9707d others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147832646 | |||||
| chr4:147832691
|
G | A | 2 | a0001c0002t0001g0072a0004c0010t0001g0048 | 2 | HG03492.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.312+9734G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147832691 | ||||||
| chr4:147832707
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.312+9750A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147832707 | ||||||
| chr4:147832792
|
A | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(31): Show | 34 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.312+9835A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147832792 | ||||||
| chr4:147833089
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+10132G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147833089 | ||||||
| chr4:147833161
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.312+10204G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147833161 | ||||||
| chr4:147833493
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.312+10536G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147833493 | ||||||
| chr4:147833494
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.312+10537C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147833494 | ||||||
| chr4:147833703
|
TGCTAAGT others(5): Show |
T | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.312+10751_312+1076 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147833703 | |||||
| chr4:147833742
|
T | A | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.312+10785T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147833742 | ||||||
| chr4:147833750
|
G | T | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.312+10793G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147833750 | ||||||
| chr4:147833802
|
G | GAT | 3 | a0001c0008t0001g0059a0001c0008t0001g0060a0001c0009t0001g0008 | 3 | HG03098.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.312+10854_312+1085 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147833802 | |||||
| chr4:147833807
|
A | G | 6 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0068others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.312+10850A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147833807 | ||||||
| chr4:147833825
|
A | G | 2 | a0001c0002t0001g0090a0001c0004t0001g0102 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.312+10868A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147833825 | ||||||
| chr4:147834376
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(26): Show | 29 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.312+11419C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147834376 | ||||||
| chr4:147834420
|
T | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(26): Show | 29 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.312+11463T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147834420 | ||||||
| chr4:147834449
|
T | A | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.312+11492T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147834449 | ||||||
| chr4:147834565
|
G | T | 39 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(36): Show | 39 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.312+11608G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147834565 | ||||||
| chr4:147834589
|
G | T | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.312+11632G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147834589 | ||||||
| chr4:147834633
|
T | C | 6 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+11676T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147834633 | ||||||
| chr4:147834692
|
ACACCCAC others(15): Show |
A | 6 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+11743_312+1176 others(26): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147834692 | |||||
| chr4:147834722
|
T | C | 6 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+11765T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147834722 | ||||||
| chr4:147834966
|
C | A | 10 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.312+12009C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147834966 | ||||||
| chr4:147834988
|
GGTACTTA others(5): Show |
G | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.312+12034_312+1204 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147834988 | |||||
| chr4:147835103
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.313-12048T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147835103 | ||||||
| chr4:147835133
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.313-12018C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147835133 | ||||||
| chr4:147835137
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.313-12014C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147835137 | ||||||
| chr4:147835146
|
A | T | 1 | a0001c0001t0001g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.313-12005A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147835146 | ||||||
| chr4:147835196
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-11955G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147835196 | ||||||
| chr4:147835405
|
C | T | 1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313-11746C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147835405 | ||||||
| chr4:147835433
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.313-11718C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147835433 | ||||||
| chr4:147835521
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.313-11630G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147835521 | ||||||
| chr4:147835613
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.313-11538A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147835613 | ||||||
| chr4:147835792
|
A | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(81): Show | 84 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.313-11359A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147835792 | ||||||
| chr4:147836183
|
G | A | 8 | a0001c0001t0001g0038a0001c0001t0001g0075a0001c0001t0001g0076others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.313-10968G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147836183 | ||||||
| chr4:147836194
|
A | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-10957A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147836194 | ||||||
| chr4:147836208
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0044 | 2 | HG00558.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.313-10943G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147836208 | ||||||
| chr4:147836226
|
T | C | 6 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-10925T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147836226 | ||||||
| chr4:147836240
|
T | A | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.313-10911T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147836240 | ||||||
| chr4:147836315
|
A | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0002t0001g0019others(1): Show | 4 | HG01167.hp2 HG02165.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-10836A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147836315 | ||||||
| chr4:147836383
|
T | C | 1 | a0001c0002t0001g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.313-10768T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147836383 | ||||||
| chr4:147836455
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.313-10696C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147836455 | ||||||
| chr4:147836530
|
C | T | 2 | a0001c0001t0001g0050a0001c0005t0001g0074 | 2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.313-10621C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147836530 | ||||||
| chr4:147836608
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-10543G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147836608 | ||||||
| chr4:147836654
|
C | CT | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.313-10496dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147836654 | |||||
| chr4:147836793
|
G | T | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.313-10358G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147836793 | ||||||
| chr4:147836978
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.313-10173G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147836978 | ||||||
| chr4:147837247
|
A | G | 4 | a0001c0001t0001g0038a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-9904A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147837247 | ||||||
| chr4:147837404
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.313-9747A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147837404 | ||||||
| chr4:147837643
|
G | GT | 6 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0002t0001g0005others(3): Show | 6 | HG02572.hp1 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.313-9489dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837643 | |||||
| chr4:147837643
|
G | GTTTTT | 4 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0004t0001g0102others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-9493_313-9489d others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837643 | |||||
| chr4:147837643
|
G | GTTTTTT | 27 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0025others(24): Show | 27 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.313-9494_313-9489d others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837643 | |||||
| chr4:147837643
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0001g0052a0001c0002t0001g0072 | 2 | HG01261.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.313-9498_313-9489d others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837643 | |||||
| chr4:147837643
|
G | GTTTTTTT others(5): Show |
1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.313-9500_313-9489d others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837643 | |||||
| chr4:147837643
|
G | GTTTTTTT others(9): Show |
4 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(1): Show | 4 | HG02258.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-9504_313-9489d others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837643 | |||||
| chr4:147837643
|
G | GTTTTTTT others(10): Show |
1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.313-9505_313-9489d others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837643 | |||||
| chr4:147837643
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0017 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.313-9506_313-9489d others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837643 | |||||
| chr4:147837643
|
G | GTTTTTTT others(13): Show |
3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.313-9489_313-9488i others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837643 | |||||
| chr4:147837649
|
T | TTTTTTTT others(12): Show |
4 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0077others(1): Show | 4 | HG00558.hp2 HG01070.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-9489_313-9488i others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837649 | |||||
| chr4:147837650
|
T | TTTTTTTT others(11): Show |
1 | a0001c0002t0001g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.313-9494_313-9493i others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837650 | |||||
| chr4:147837650
|
T | TTTTTTTT others(10): Show |
1 | a0001c0001t0001g0028 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.313-9489_313-9488i others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837650 | |||||
| chr4:147837650
|
T | TTTTTTTT others(11): Show |
21 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(18): Show | 21 | HG01169.hp2 HG01243.hp1 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.313-9489_313-9488i others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837650 | |||||
| chr4:147837650
|
T | TTTTTTTT others(12): Show |
5 | a0001c0001t0001g0058a0001c0001t0001g0083a0001c0001t0003g0087others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-9489_313-9488i others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147837650 | |||||
| chr4:147837675
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.313-9476T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147837675 | ||||||
| chr4:147837710
|
G | C | 1 | a0001c0001t0002g0023 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.313-9441G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147837710 | ||||||
| chr4:147838307
|
A | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-8844A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147838307 | ||||||
| chr4:147838314
|
T | G | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.313-8837T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147838314 | ||||||
| chr4:147838362
|
T | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(33): Show | 36 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.313-8789T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147838362 | ||||||
| chr4:147838402
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.313-8749C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147838402 | ||||||
| chr4:147838473
|
T | TA | 44 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(41): Show | 44 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.313-8668dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147838473 | |||||
| chr4:147838473
|
TA | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(32): Show | 35 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.313-8668delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147838473 | |||||
| chr4:147838482
|
A | C | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.313-8669A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147838482 | ||||||
| chr4:147838484
|
C | A | 1 | a0001c0001t0002g0023 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.313-8667C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147838484 | ||||||
| chr4:147838527
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 81 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.313-8624C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147838527 | ||||||
| chr4:147838545
|
CT | C | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.313-8605delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147838545 | ||||||
| chr4:147838548
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.313-8603T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147838548 | ||||||
| chr4:147838927
|
G | A | 45 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(42): Show | 45 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.313-8224G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147838927 | ||||||
| chr4:147838946
|
G | A | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.313-8205G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147838946 | ||||||
| chr4:147839092
|
G | GTATC | 5 | a0001c0001t0001g0053a0001c0001t0001g0086a0001c0002t0001g0033others(2): Show | 5 | HG02886.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-8009_313-8006d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839092 | |||||
| chr4:147839092
|
GTATC | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(27): Show | 30 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.313-8009_313-8006d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839092 | |||||
| chr4:147839092
|
GTATCTAT others(1): Show |
G | 11 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.313-8013_313-8006d others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839092 | |||||
| chr4:147839092
|
GTATCTAT others(5): Show |
G | 1 | a0001c0001t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.313-8017_313-8006d others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839092 | |||||
| chr4:147839092
|
GTATCTAT others(9): Show |
G | 2 | a0001c0001t0001g0038a0001c0001t0001g0093 | 2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.313-8021_313-8006d others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839092 | |||||
| chr4:147839114
|
A | ATCTG | 3 | a0001c0002t0001g0090a0001c0004t0001g0102a0001c0006t0001g0071 | 3 | HG01884.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.313-8034_313-8033i others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839114 | |||||
| chr4:147839118
|
A | G | 7 | a0001c0001t0001g0041a0001c0002t0001g0090a0001c0004t0001g0102others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.313-8033A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147839118 | ||||||
| chr4:147839122
|
A | G | 8 | a0001c0001t0001g0041a0001c0002t0001g0090a0001c0004t0001g0102others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-8029A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147839122 | ||||||
| chr4:147839126
|
A | G | 8 | a0001c0001t0001g0041a0001c0002t0001g0090a0001c0004t0001g0102others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-8025A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147839126 | ||||||
| chr4:147839130
|
A | G | 8 | a0001c0001t0001g0041a0001c0002t0001g0090a0001c0004t0001g0102others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-8021A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147839130 | ||||||
| chr4:147839134
|
A | G | 8 | a0001c0001t0001g0041a0001c0002t0001g0090a0001c0004t0001g0102others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-8017A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147839134 | ||||||
| chr4:147839138
|
A | ATCTG | 3 | a0001c0001t0001g0046a0001c0002t0001g0029a0004c0010t0001g0048 | 3 | HG02109.hp2 NA18906.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.313-8010_313-8009i others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839138 | |||||
| chr4:147839138
|
A | G | 9 | a0001c0001t0001g0041a0001c0002t0001g0021a0001c0002t0001g0090others(6): Show | 9 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.313-8013A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147839138 | ||||||
| chr4:147839138
|
ATCTATCT others(1): Show |
A | 4 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0063others(1): Show | 4 | HG01261.hp2 HG01993.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-8009_313-8002d others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839138 | |||||
| chr4:147839138
|
ATCTATCT others(5): Show |
A | 2 | a0001c0001t0001g0052a0001c0002t0001g0072 | 2 | HG01261.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.313-8009_313-7998d others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839138 | |||||
| chr4:147839142
|
A | ATCTATCT others(1): Show |
2 | a0001c0001t0001g0015a0001c0001t0001g0070 | 2 | NA19012.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.313-8006_313-8005i others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839142 | |||||
| chr4:147839142
|
A | ATCTG | 14 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0030others(11): Show | 14 | HG00558.hp2 HG01169.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.313-7997_313-7994d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839142 | |||||
| chr4:147839142
|
A | ATCTGTCT others(1): Show |
2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.313-8001_313-7994d others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839142 | |||||
| chr4:147839142
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(29): Show | 32 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.313-8009A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147839142 | ||||||
| chr4:147839142
|
ATCTG | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0061 | 2 | HG02145.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.313-7997_313-7994d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147839142 | |||||
| chr4:147839146
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA18995.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.313-8005G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147839146 | ||||||
| chr4:147839158
|
A | G | 2 | a0001c0001t0001g0052a0001c0002t0001g0072 | 2 | HG01261.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.313-7993A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147839158 | ||||||
| chr4:147839270
|
A | C | 2 | a0001c0001t0001g0052a0001c0002t0001g0072 | 2 | HG01261.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.313-7881A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147839270 | ||||||
| chr4:147839513
|
C | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0043 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.313-7638C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147839513 | ||||||
| chr4:147840406
|
C | G | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.313-6745C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147840406 | ||||||
| chr4:147840563
|
G | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(35): Show | 38 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.313-6588G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147840563 | ||||||
| chr4:147840946
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(54): Show | 57 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.313-6205T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147840946 | ||||||
| chr4:147840976
|
T | G | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.313-6175T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147840976 | ||||||
| chr4:147841543
|
T | A | 1 | a0001c0001t0002g0031 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.313-5608T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147841543 | ||||||
| chr4:147841868
|
A | G | 8 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0083others(5): Show | 8 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-5283A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147841868 | ||||||
| chr4:147841873
|
C | T | 2 | a0001c0002t0001g0090a0001c0004t0001g0102 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.313-5278C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147841873 | ||||||
| chr4:147841950
|
C | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0083others(5): Show | 8 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-5201C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147841950 | ||||||
| chr4:147842536
|
C | T | 25 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(22): Show | 25 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.313-4615C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147842536 | ||||||
| chr4:147842552
|
T | A | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.313-4599T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147842552 | ||||||
| chr4:147842852
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.313-4299G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147842852 | ||||||
| chr4:147843066
|
A | G | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.313-4085A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147843066 | ||||||
| chr4:147843101
|
G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(56): Show | 59 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.313-4050G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147843101 | ||||||
| chr4:147843456
|
TA | T | 16 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0038others(13): Show | 16 | HG01243.hp2 HG01891.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.313-3694delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147843456 | ||||||
| chr4:147843462
|
T | C | 6 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-3689T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147843462 | ||||||
| chr4:147843517
|
TTTTTTC | T | 11 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0046others(8): Show | 11 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.313-3612_313-3607d others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 147843517 | |||||
| chr4:147843803
|
T | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(32): Show | 35 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.313-3348T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147843803 | ||||||
| chr4:147843835
|
C | T | 6 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0081others(3): Show | 6 | HG01243.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-3316C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147843835 | ||||||
| chr4:147843872
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.313-3279C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147843872 | ||||||
| chr4:147843999
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313-3152G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147843999 | ||||||
| chr4:147844111
|
G | T | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.313-3040G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147844111 | ||||||
| chr4:147844325
|
C | G | 35 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(32): Show | 35 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.313-2826C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147844325 | ||||||
| chr4:147844479
|
C | G | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.313-2672C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147844479 | ||||||
| chr4:147844696
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.313-2455A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147844696 | ||||||
| chr4:147844843
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.313-2308C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147844843 | ||||||
| chr4:147844982
|
C | T | 17 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0038others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.313-2169C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147844982 | ||||||
| chr4:147845154
|
C | T | 2 | a0001c0001t0001g0052a0001c0002t0001g0072 | 2 | HG01261.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.313-1997C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147845154 | ||||||
| chr4:147845258
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.313-1893G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147845258 | ||||||
| chr4:147845317
|
A | C | 11 | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0001t0001g0062others(8): Show | 11 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.313-1834A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147845317 | ||||||
| chr4:147845480
|
A | T | 17 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0038others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.313-1671A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147845480 | ||||||
| chr4:147845641
|
C | T | 1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313-1510C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147845641 | ||||||
| chr4:147846262
|
C | T | 17 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0038others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.313-889C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147846262 | ||||||
| chr4:147846332
|
A | C | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.313-819A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147846332 | ||||||
| chr4:147846356
|
C | T | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.313-795C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147846356 | ||||||
| chr4:147846357
|
G | A | 17 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0038others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.313-794G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147846357 | ||||||
| chr4:147846401
|
A | G | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.313-750A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147846401 | ||||||
| chr4:147846490
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-661A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147846490 | ||||||
| chr4:147847081
|
A | G | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-70A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | chr4 | 147847081 | ||||||
| chr4:147847510
|
A | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0046others(8): Show | 11 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.384+288A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147847510 | ||||||
| chr4:147847541
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0089 | 3 | HG01243.hp2 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.384+319G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147847541 | ||||||
| chr4:147847767
|
G | T | 2 | a0001c0001t0001g0052a0001c0002t0001g0072 | 2 | HG01261.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.384+545G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147847767 | ||||||
| chr4:147847826
|
G | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(31): Show | 34 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.384+604G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147847826 | ||||||
| chr4:147847872
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.384+650T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147847872 | ||||||
| chr4:147847923
|
C | T | 11 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0046others(8): Show | 11 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.384+701C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147847923 | ||||||
| chr4:147847969
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.384+747C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147847969 | ||||||
| chr4:147848048
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.384+826T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147848048 | ||||||
| chr4:147848091
|
G | GT | 68 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(65): Show | 68 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.384+882dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 147848091 | |||||
| chr4:147848147
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0044 | 2 | HG00558.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.384+925A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147848147 | ||||||
| chr4:147848311
|
G | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0005t0001g0003 | 3 | HG02976.hp2 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.384+1089G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147848311 | ||||||
| chr4:147848451
|
G | A | 17 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0038others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.384+1229G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147848451 | ||||||
| chr4:147848567
|
T | C | 1 | a0001c0005t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.384+1345T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147848567 | ||||||
| chr4:147848642
|
C | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.384+1420C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147848642 | ||||||
| chr4:147848722
|
A | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(31): Show | 34 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.384+1500A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147848722 | ||||||
| chr4:147848916
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.384+1694C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147848916 | ||||||
| chr4:147849088
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.384+1866A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147849088 | ||||||
| chr4:147849204
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(83): Show | 86 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.384+1982T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147849204 | ||||||
| chr4:147849236
|
CTT | C | 16 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0038others(13): Show | 16 | HG01243.hp2 HG01891.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.384+2029_384+2030d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 147849236 | |||||
| chr4:147849380
|
G | A | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.384+2158G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147849380 | ||||||
| chr4:147849511
|
A | G | 27 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 27 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.384+2289A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147849511 | ||||||
| chr4:147849656
|
G | A | 1 | a0001c0002t0001g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.384+2434G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147849656 | ||||||
| chr4:147849753
|
T | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0089 | 3 | HG01243.hp2 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.384+2531T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147849753 | ||||||
| chr4:147849977
|
A | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0046others(8): Show | 11 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.384+2755A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147849977 | ||||||
| chr4:147850019
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 28 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.384+2797C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147850019 | ||||||
| chr4:147850035
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.384+2813A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147850035 | ||||||
| chr4:147850228
|
A | G | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.384+3006A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147850228 | ||||||
| chr4:147850390
|
C | G | 1 | a0001c0001t0001g0015 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.384+3168C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147850390 | ||||||
| chr4:147850490
|
G | A | 1 | a0001c0006t0001g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.384+3268G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147850490 | ||||||
| chr4:147850512
|
C | T | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.384+3290C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147850512 | ||||||
| chr4:147850529
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.384+3307G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147850529 | ||||||
| chr4:147850639
|
G | A | 17 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0038others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.384+3417G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147850639 | ||||||
| chr4:147850673
|
G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 28 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.384+3451G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147850673 | ||||||
| chr4:147850684
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0089 | 3 | HG01243.hp2 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.384+3462C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147850684 | ||||||
| chr4:147851074
|
G | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0046others(8): Show | 11 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.384+3852G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147851074 | ||||||
| chr4:147851255
|
AT | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.384+4048delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 147851255 | |||||
| chr4:147851271
|
A | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0089 | 3 | HG01243.hp2 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.384+4049A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147851271 | ||||||
| chr4:147851307
|
A | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(81): Show | 84 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.384+4085A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147851307 | ||||||
| chr4:147851401
|
G | C | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.384+4179G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147851401 | ||||||
| chr4:147851530
|
A | G | 27 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 27 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.384+4308A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147851530 | ||||||
| chr4:147851708
|
T | C | 11 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0046others(8): Show | 11 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.384+4486T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147851708 | ||||||
| chr4:147851714
|
C | T | 6 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.384+4492C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147851714 | ||||||
| chr4:147851974
|
C | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0046others(8): Show | 11 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.384+4752C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147851974 | ||||||
| chr4:147852665
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.385-4888G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147852665 | ||||||
| chr4:147852716
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.385-4837T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147852716 | ||||||
| chr4:147852725
|
TTTTTTA | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0004t0001g0045others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-4827_385-4822d others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147852725 | ||||||
| chr4:147852726
|
TTTTTA | T | 9 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0081others(6): Show | 9 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.385-4826_385-4822d others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147852726 | ||||||
| chr4:147852728
|
TTTA | T | 13 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0046others(10): Show | 13 | HG00558.hp2 HG01070.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.385-4824_385-4822d others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147852728 | ||||||
| chr4:147852729
|
TTA | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 51 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.385-4823_385-4822d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147852729 | ||||||
| chr4:147852730
|
TA | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-4819delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 147852730 | |||||
| chr4:147852918
|
C | G | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.385-4635C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147852918 | ||||||
| chr4:147853092
|
A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(83): Show | 86 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.385-4461A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147853092 | ||||||
| chr4:147853541
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.385-4012G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147853541 | ||||||
| chr4:147853634
|
C | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(31): Show | 34 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.385-3919C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147853634 | ||||||
| chr4:147853740
|
A | AT | 34 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(31): Show | 34 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.385-3803dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 147853740 | |||||
| chr4:147853740
|
AT | A | 24 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0038others(21): Show | 24 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.385-3803delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 147853740 | |||||
| chr4:147853893
|
G | T | 17 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0038others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.385-3660G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147853893 | ||||||
| chr4:147853942
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.385-3611A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147853942 | ||||||
| chr4:147854001
|
A | G | 1 | a0001c0005t0001g0003 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.385-3552A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147854001 | ||||||
| chr4:147854048
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.385-3505G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147854048 | ||||||
| chr4:147854228
|
T | C | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.385-3325T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147854228 | ||||||
| chr4:147854237
|
T | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(31): Show | 34 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.385-3316T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147854237 | ||||||
| chr4:147854354
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.385-3199G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147854354 | ||||||
| chr4:147854408
|
T | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(66): Show | 69 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.385-3145T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147854408 | ||||||
| chr4:147854583
|
T | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0046others(8): Show | 11 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.385-2970T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147854583 | ||||||
| chr4:147854818
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0089 | 3 | HG01243.hp2 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.385-2735C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147854818 | ||||||
| chr4:147854986
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(66): Show | 69 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.385-2567C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147854986 | ||||||
| chr4:147854994
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.385-2559A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147854994 | ||||||
| chr4:147855013
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.385-2540G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147855013 | ||||||
| chr4:147855047
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.385-2506G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147855047 | ||||||
| chr4:147855190
|
CAG | C | 7 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0067others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-2361_385-2360d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 147855190 | |||||
| chr4:147855221
|
A | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(31): Show | 34 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.385-2332A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147855221 | ||||||
| chr4:147855257
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.385-2296C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147855257 | ||||||
| chr4:147855302
|
A | G | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(35): Show | 38 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.385-2251A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147855302 | ||||||
| chr4:147855414
|
A | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0089 | 3 | HG01243.hp2 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.385-2139A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147855414 | ||||||
| chr4:147855415
|
CTA | C | 7 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.385-2136_385-2135d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 147855415 | |||||
| chr4:147855442
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.385-2111G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147855442 | ||||||
| chr4:147855682
|
G | GT | 20 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0030others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.385-1849dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 147855682 | |||||
| chr4:147855682
|
GT | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0049others(8): Show | 11 | HG00558.hp2 HG01070.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-1849delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 147855682 | |||||
| chr4:147855685
|
T | G | 3 | a0001c0001t0001g0020a0001c0002t0001g0019a0002c0003t0001g0032 | 3 | HG02165.hp1 HG03239.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.385-1868T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147855685 | ||||||
| chr4:147855990
|
G | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0002t0001g0029 | 3 | HG02056.hp2 HG02080.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.385-1563G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147855990 | ||||||
| chr4:147856175
|
A | G | 47 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(44): Show | 47 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.385-1378A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147856175 | ||||||
| chr4:147856361
|
C | T | 1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.385-1192C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147856361 | ||||||
| chr4:147856362
|
G | A | 4 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-1191G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147856362 | ||||||
| chr4:147856374
|
A | G | 7 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.385-1179A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147856374 | ||||||
| chr4:147856430
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0037 | 2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.385-1123C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147856430 | ||||||
| chr4:147856433
|
G | A | 1 | a0002c0003t0001g0009 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.385-1120G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147856433 | ||||||
| chr4:147856435
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 75 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.385-1118C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147856435 | ||||||
| chr4:147856727
|
G | A | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.385-826G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147856727 | ||||||
| chr4:147857020
|
C | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0046others(8): Show | 11 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.385-533C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147857020 | ||||||
| chr4:147857110
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 28 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.385-443C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147857110 | ||||||
| chr4:147857143
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.385-410G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147857143 | ||||||
| chr4:147857231
|
G | T | 11 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0046others(8): Show | 11 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.385-322G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147857231 | ||||||
| chr4:147857268
|
G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(83): Show | 86 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.385-285G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | chr4 | 147857268 | ||||||
| chr4:147857534
|
G | GT | 32 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(29): Show | 32 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
splice_region_variant&intron_variant | LOW | c.385-9dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 147857534 | |||||
| chr4:147857816
|
CAAG | C | 7 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+165_486+167del others(3): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 147857816 | |||||
| chr4:147857963
|
C | CA | 3 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0089 | 3 | HG01243.hp2 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.486+311dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 147857963 | |||||
| chr4:147858039
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(36): Show | 39 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.486+385G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147858039 | ||||||
| chr4:147858168
|
ATTTATAT | A | 8 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0067others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+520_486+526del others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 147858168 | |||||
| chr4:147858339
|
T | A | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.486+685T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147858339 | ||||||
| chr4:147858343
|
AT | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(37): Show | 40 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.486+698delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 147858343 | |||||
| chr4:147858397
|
G | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(47): Show | 50 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.486+743G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147858397 | ||||||
| chr4:147858742
|
C | T | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.486+1088C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147858742 | ||||||
| chr4:147858823
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(36): Show | 39 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.486+1169G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147858823 | ||||||
| chr4:147859273
|
CT | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(44): Show | 47 | HG00558.hp1 HG01071.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.486+1635delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 147859273 | |||||
| chr4:147859352
|
A | C | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.486+1698A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147859352 | ||||||
| chr4:147859511
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.486+1857C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147859511 | ||||||
| chr4:147859578
|
T | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.486+1924T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147859578 | ||||||
| chr4:147859979
|
A | C | 27 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 27 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.486+2325A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147859979 | ||||||
| chr4:147860045
|
G | A | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.486+2391G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860045 | ||||||
| chr4:147860143
|
T | C | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.486+2489T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860143 | ||||||
| chr4:147860180
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0015 | 2 | HG02056.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.486+2526C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860180 | ||||||
| chr4:147860217
|
T | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0002t0001g0029 | 3 | HG02056.hp2 HG02080.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.486+2563T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860217 | ||||||
| chr4:147860258
|
C | T | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.486+2604C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860258 | ||||||
| chr4:147860320
|
C | T | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.486+2666C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860320 | ||||||
| chr4:147860420
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0037 | 2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.486+2766C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860420 | ||||||
| chr4:147860435
|
A | AAAAAC | 5 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0049others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+2811_486+2815d others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 147860435 | |||||
| chr4:147860435
|
AAAAAC | A | 2 | a0001c0002t0001g0033a0002c0003t0001g0073 | 2 | HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.486+2811_486+2815d others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 147860435 | |||||
| chr4:147860435
|
AAAAACAA others(3): Show |
A | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.486+2806_486+2815d others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 147860435 | |||||
| chr4:147860495
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(83): Show | 86 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.486+2841T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860495 | ||||||
| chr4:147860528
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0047 | 2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.486+2874C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860528 | ||||||
| chr4:147860589
|
A | G | 7 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+2935A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860589 | ||||||
| chr4:147860737
|
A | C | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.486+3083A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860737 | ||||||
| chr4:147860825
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0091 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.486+3171T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860825 | ||||||
| chr4:147860852
|
G | T | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.486+3198G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860852 | ||||||
| chr4:147860865
|
G | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0046others(8): Show | 11 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.486+3211G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860865 | ||||||
| chr4:147860913
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 73 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.486+3259G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860913 | ||||||
| chr4:147860961
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.486+3307G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860961 | ||||||
| chr4:147860971
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0076 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.486+3317C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147860971 | ||||||
| chr4:147861058
|
T | C | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.486+3404T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861058 | ||||||
| chr4:147861141
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.486+3487C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861141 | ||||||
| chr4:147861298
|
G | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0093 | 2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.487-3548G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861298 | ||||||
| chr4:147861318
|
C | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0083others(5): Show | 8 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-3528C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861318 | ||||||
| chr4:147861415
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0047 | 2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.487-3431C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861415 | ||||||
| chr4:147861419
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.487-3427G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861419 | ||||||
| chr4:147861441
|
C | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0083others(5): Show | 8 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-3405C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861441 | ||||||
| chr4:147861582
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.487-3264G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861582 | ||||||
| chr4:147861683
|
C | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(81): Show | 84 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.487-3163C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861683 | ||||||
| chr4:147861708
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.487-3138G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861708 | ||||||
| chr4:147861740
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.487-3106T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861740 | ||||||
| chr4:147861977
|
C | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 77 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.487-2869C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861977 | ||||||
| chr4:147861995
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0086 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.487-2851C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147861995 | ||||||
| chr4:147862057
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.487-2789G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862057 | ||||||
| chr4:147862084
|
C | G | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.487-2762C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862084 | ||||||
| chr4:147862231
|
T | A | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.487-2615T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862231 | ||||||
| chr4:147862251
|
G | A | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.487-2595G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862251 | ||||||
| chr4:147862360
|
C | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.487-2486C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862360 | ||||||
| chr4:147862438
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.487-2408C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862438 | ||||||
| chr4:147862505
|
T | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0002t0001g0013 | 3 | HG00558.hp1 NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.487-2341T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862505 | ||||||
| chr4:147862507
|
C | T | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.487-2339C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862507 | ||||||
| chr4:147862677
|
A | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0076others(1): Show | 4 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-2169A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862677 | ||||||
| chr4:147862680
|
T | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.487-2166T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862680 | ||||||
| chr4:147862730
|
G | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0076others(1): Show | 4 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-2116G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862730 | ||||||
| chr4:147862822
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0076 | 3 | HG02258.hp1 HG02622.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.487-2024C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862822 | ||||||
| chr4:147862860
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.487-1986A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147862860 | ||||||
| chr4:147863239
|
C | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.487-1607C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147863239 | ||||||
| chr4:147863329
|
G | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(32): Show | 35 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.487-1517G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147863329 | ||||||
| chr4:147863345
|
A | G | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.487-1501A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147863345 | ||||||
| chr4:147863400
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.487-1446T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147863400 | ||||||
| chr4:147863500
|
C | T | 7 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-1346C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147863500 | ||||||
| chr4:147863639
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.487-1207T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147863639 | ||||||
| chr4:147863740
|
A | G | 2 | a0001c0002t0001g0033a0002c0003t0001g0073 | 2 | HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.487-1106A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147863740 | ||||||
| chr4:147864062
|
ATT | A | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.487-780_487-779del others(2): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 147864062 | |||||
| chr4:147864249
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.487-597C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147864249 | ||||||
| chr4:147864275
|
C | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(43): Show | 46 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.487-571C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147864275 | ||||||
| chr4:147864302
|
C | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0083others(5): Show | 8 | HG01891.hp2 HG02056.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-544C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147864302 | ||||||
| chr4:147864360
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.487-486T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147864360 | ||||||
| chr4:147864527
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0038others(4): Show | 7 | HG01243.hp2 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.487-319G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147864527 | ||||||
| chr4:147864577
|
G | A | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.487-269G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 5/22 | chr4 | 147864577 | ||||||
| chr4:147865126
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0006t0001g0040others(4): Show | 7 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.597+170C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 6/22 | chr4 | 147865126 | ||||||
| chr4:147865419
|
G | T | 2 | a0003c0007t0001g0079a0003c0007t0001g0082 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.597+463G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 6/22 | chr4 | 147865419 | ||||||
| chr4:147865579
|
CA | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(41): Show | 44 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.597+630delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr4 | 147865579 | |||||
| chr4:147865589
|
CTG | C | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.597+634_597+635del others(2): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 6/22 | chr4 | 147865589 | ||||||
| chr4:147865674
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.597+718T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 6/22 | chr4 | 147865674 | ||||||
| chr4:147865755
|
T | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0038others(4): Show | 7 | HG01243.hp2 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.597+799T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 6/22 | chr4 | 147865755 | ||||||
| chr4:147866045
|
C | T | 34 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(31): Show | 34 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.598-667C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 6/22 | chr4 | 147866045 | ||||||
| chr4:147866124
|
G | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.598-588G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 6/22 | chr4 | 147866124 | ||||||
| chr4:147866518
|
G | A | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.598-194G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 6/22 | chr4 | 147866518 | ||||||
| chr4:147867587
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0038others(4): Show | 7 | HG01243.hp2 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.702+771C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147867587 | ||||||
| chr4:147867841
|
G | A | 3 | a0001c0001t0001g0081a0001c0004t0001g0045a0001c0004t0001g0105 | 3 | HG02572.hp2 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.702+1025G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147867841 | ||||||
| chr4:147867842
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0081others(4): Show | 7 | HG02056.hp2 HG02080.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+1026C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147867842 | ||||||
| chr4:147867863
|
CA | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0012others(38): Show | 41 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.702+1070delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147867863 | |||||
| chr4:147867863
|
CAA | C | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0015others(32): Show | 35 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.702+1069_702+1070d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147867863 | |||||
| chr4:147867863
|
CAAA | C | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.702+1068_702+1070d others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147867863 | |||||
| chr4:147867926
|
CT | C | 20 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0052others(17): Show | 20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.702+1124delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147867926 | |||||
| chr4:147867926
|
CTT | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(63): Show | 66 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.702+1123_702+1124d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147867926 | |||||
| chr4:147867990
|
A | G | 35 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(32): Show | 35 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.702+1174A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147867990 | ||||||
| chr4:147868093
|
T | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0097a0001c0005t0001g0098others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.702+1277T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147868093 | ||||||
| chr4:147868243
|
G | GT | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(36): Show | 39 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.702+1438dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147868243 | |||||
| chr4:147868263
|
G | A | 3 | a0001c0001t0001g0081a0001c0004t0001g0045a0001c0004t0001g0105 | 3 | HG02572.hp2 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.702+1447G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147868263 | ||||||
| chr4:147868349
|
GC | G | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0053others(5): Show | 8 | HG01261.hp2 HG01884.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.702+1535delC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147868349 | |||||
| chr4:147868391
|
C | T | 47 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(44): Show | 47 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.702+1575C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147868391 | ||||||
| chr4:147868786
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.702+1970C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147868786 | ||||||
| chr4:147868917
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.702+2101C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147868917 | ||||||
| chr4:147869222
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(32): Show | 35 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.702+2406C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147869222 | ||||||
| chr4:147869236
|
C | T | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.702+2420C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147869236 | ||||||
| chr4:147869355
|
G | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(25): Show | 28 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.702+2539G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147869355 | ||||||
| chr4:147869497
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.702+2681A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147869497 | ||||||
| chr4:147869582
|
GA | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(28): Show | 31 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.702+2777delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147869582 | |||||
| chr4:147869716
|
A | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(25): Show | 28 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.702+2900A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147869716 | ||||||
| chr4:147869995
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.702+3179A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147869995 | ||||||
| chr4:147869996
|
G | GTT | 28 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 28 | HG00558.hp2 HG01071.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.702+3182_702+3183d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147869996 | |||||
| chr4:147869996
|
G | GTTTT | 10 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0083others(7): Show | 10 | HG01891.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.702+3183_702+3184i others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147869996 | |||||
| chr4:147869996
|
G | GTTTTTT | 6 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(3): Show | 6 | HG01261.hp1 HG02056.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+3183_702+3184i others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147869996 | |||||
| chr4:147869998
|
T | TTTG | 2 | a0001c0005t0001g0003a0001c0008t0001g0060 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.702+3183_702+3184i others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147869998 | |||||
| chr4:147869998
|
T | TTTTG | 4 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0080others(1): Show | 4 | HG02615.hp1 HG02886.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+3183_702+3184i others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147869998 | |||||
| chr4:147869998
|
T | TTTTTTTT others(1): Show |
12 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0075others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.702+3183_702+3184i others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147869998 | |||||
| chr4:147869998
|
T | TTTTTTTT others(3): Show |
3 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0104 | 3 | HG02109.hp2 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.702+3183_702+3184i others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147869998 | |||||
| chr4:147869998
|
T | TTTTTTTT others(5): Show |
1 | a0001c0001t0001g0103 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.702+3183_702+3184i others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147869998 | |||||
| chr4:147869998
|
TTG | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0002g0023 | 3 | HG01070.hp1 HG02896.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.702+3228_702+3229d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147869998 | |||||
| chr4:147869998
|
TTGTG | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG02895.hp2 HG03209.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+3226_702+3229d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147869998 | |||||
| chr4:147869998
|
TTGTGTG | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0024others(7): Show | 10 | HG01243.hp2 HG01261.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.702+3224_702+3229d others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147869998 | |||||
| chr4:147870000
|
G | C | 12 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0075others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.702+3184G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870000 | ||||||
| chr4:147870000
|
G | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 51 | HG00558.hp1 HG00558.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.702+3184G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870000 | ||||||
| chr4:147870002
|
G | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(3): Show | 6 | HG01261.hp1 HG02056.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+3186G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870002 | ||||||
| chr4:147870002
|
G | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(41): Show | 44 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.702+3186G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870002 | ||||||
| chr4:147870004
|
G | C | 10 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0083others(7): Show | 10 | HG01891.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.702+3188G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870004 | ||||||
| chr4:147870004
|
G | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0025others(23): Show | 26 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.702+3188G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870004 | ||||||
| chr4:147870006
|
G | C | 21 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(18): Show | 21 | HG00558.hp2 HG01071.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.702+3190G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870006 | ||||||
| chr4:147870006
|
G | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0024others(13): Show | 16 | HG01070.hp1 HG01243.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.702+3190G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870006 | ||||||
| chr4:147870008
|
G | C | 20 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0025others(17): Show | 20 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.702+3192G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870008 | ||||||
| chr4:147870008
|
G | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0024others(12): Show | 15 | HG01243.hp2 HG01261.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3192G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870008 | ||||||
| chr4:147870010
|
G | C | 2 | a0001c0001t0001g0058a0001c0001t0002g0023 | 2 | HG01070.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.702+3194G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870010 | ||||||
| chr4:147870010
|
G | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0024others(8): Show | 11 | HG01243.hp2 HG01261.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.702+3194G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870010 | ||||||
| chr4:147870012
|
G | C | 4 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG02895.hp2 HG03209.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+3196G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870012 | ||||||
| chr4:147870012
|
G | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.702+3196G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870012 | ||||||
| chr4:147870014
|
G | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0024others(7): Show | 10 | HG01243.hp2 HG01261.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.702+3198G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870014 | ||||||
| chr4:147870016
|
G | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.702+3200G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870016 | ||||||
| chr4:147870062
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.702+3246T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870062 | ||||||
| chr4:147870137
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(2): Show | 5 | HG02056.hp2 HG02080.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+3321G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870137 | ||||||
| chr4:147870174
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(47): Show | 50 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.702+3358T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870174 | ||||||
| chr4:147870190
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.702+3374T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870190 | ||||||
| chr4:147870221
|
G | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(32): Show | 35 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.702+3405G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870221 | ||||||
| chr4:147870360
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0077 | 2 | HG00558.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.702+3544C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870360 | ||||||
| chr4:147870367
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.702+3551A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870367 | ||||||
| chr4:147870535
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.702+3719A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870535 | ||||||
| chr4:147870556
|
G | A | 14 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0061others(11): Show | 14 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.702+3740G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870556 | ||||||
| chr4:147870562
|
CT | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 64 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.702+3761delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870562 | |||||
| chr4:147870562
|
CTTT | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(24): Show | 27 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.702+3759_702+3761d others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870562 | |||||
| chr4:147870801
|
G | T | 1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.702+3985G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870801 | ||||||
| chr4:147870848
|
T | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(32): Show | 35 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.702+4032T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870848 | ||||||
| chr4:147870928
|
C | CTG | 9 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0020others(6): Show | 9 | HG01261.hp1 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.703-4047_703-4046d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870928 | |||||
| chr4:147870928
|
C | CTGTG | 13 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0051others(10): Show | 13 | HG02055.hp2 HG02145.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-4049_703-4046d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870928 | |||||
| chr4:147870928
|
C | CTGTGTG | 4 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0001t0003g0087others(1): Show | 4 | HG02080.hp2 HG02818.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-4051_703-4046d others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870928 | |||||
| chr4:147870928
|
CTG | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0080others(2): Show | 5 | HG01993.hp2 HG02165.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-4047_703-4046d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870928 | |||||
| chr4:147870928
|
CTGTG | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0046others(7): Show | 10 | HG00558.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.703-4049_703-4046d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870928 | |||||
| chr4:147870928
|
CTGTGTG | C | 2 | a0001c0001t0001g0081a0001c0004t0001g0102 | 2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.703-4051_703-4046d others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870928 | |||||
| chr4:147870928
|
CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0001g0010 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.703-4055_703-4046d others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870928 | |||||
| chr4:147870928
|
CTGTGTGT others(7): Show |
C | 12 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(9): Show | 12 | HG01169.hp1 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.703-4059_703-4046d others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870928 | |||||
| chr4:147870928
|
CTGTGTGT others(9): Show |
C | 29 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0024others(26): Show | 29 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.703-4061_703-4046d others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870928 | |||||
| chr4:147870928
|
CTGTGTGT others(11): Show |
C | 5 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0047others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-4063_703-4046d others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870928 | |||||
| chr4:147870928
|
CTGTGTGT others(13): Show |
C | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.703-4065_703-4046d others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147870928 | |||||
| chr4:147870944
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.703-4077G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870944 | ||||||
| chr4:147870946
|
G | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0024others(26): Show | 29 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.703-4075G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870946 | ||||||
| chr4:147870948
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0002t0001g0090others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-4073G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870948 | ||||||
| chr4:147870975
|
T | TG | 3 | a0001c0001t0001g0058a0001c0002t0001g0078a0001c0006t0001g0042 | 3 | HG02258.hp2 HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.703-4046_703-4045i others(3): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870975 | ||||||
| chr4:147870990
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(40): Show | 43 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.703-4031T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147870990 | ||||||
| chr4:147871109
|
G | A | 1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.703-3912G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147871109 | ||||||
| chr4:147871160
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.703-3861G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147871160 | ||||||
| chr4:147871455
|
A | C | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.703-3566A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147871455 | ||||||
| chr4:147871701
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0047 | 2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.703-3320G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147871701 | ||||||
| chr4:147871820
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.703-3201G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147871820 | ||||||
| chr4:147871845
|
A | G | 3 | a0001c0001t0001g0081a0001c0004t0001g0045a0001c0004t0001g0105 | 3 | HG02572.hp2 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.703-3176A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147871845 | ||||||
| chr4:147871916
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(35): Show | 38 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.703-3105T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147871916 | ||||||
| chr4:147871985
|
C | T | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.703-3036C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147871985 | ||||||
| chr4:147872023
|
G | T | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.703-2998G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147872023 | ||||||
| chr4:147872095
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(32): Show | 35 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.703-2926C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147872095 | ||||||
| chr4:147872099
|
C | CA | 13 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0052others(10): Show | 13 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.703-2901dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147872099 | |||||
| chr4:147872099
|
C | CAA | 9 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0061others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.703-2902_703-2901d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147872099 | |||||
| chr4:147872099
|
C | CAAA | 4 | a0001c0001t0001g0081a0001c0004t0001g0045a0001c0004t0001g0105others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-2903_703-2901d others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147872099 | |||||
| chr4:147872099
|
CAA | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0038others(4): Show | 7 | HG01243.hp2 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.703-2902_703-2901d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147872099 | |||||
| chr4:147872099
|
CAAAAAAA | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(25): Show | 28 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.703-2907_703-2901d others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147872099 | |||||
| chr4:147872164
|
G | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0076 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.703-2857G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147872164 | ||||||
| chr4:147872453
|
A | G | 7 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0006t0001g0040others(4): Show | 7 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-2568A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147872453 | ||||||
| chr4:147872569
|
C | T | 1 | a0001c0005t0001g0003 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.703-2452C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147872569 | ||||||
| chr4:147872648
|
G | A | 2 | a0001c0002t0001g0033a0002c0003t0001g0073 | 2 | HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.703-2373G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147872648 | ||||||
| chr4:147873177
|
C | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(44): Show | 47 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.703-1844C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873177 | ||||||
| chr4:147873189
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.703-1832A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873189 | ||||||
| chr4:147873431
|
A | G | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.703-1590A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873431 | ||||||
| chr4:147873546
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(40): Show | 43 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.703-1475T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873546 | ||||||
| chr4:147873645
|
A | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(31): Show | 34 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.703-1376A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873645 | ||||||
| chr4:147873681
|
A | AAC | 3 | a0001c0001t0001g0054a0001c0001t0001g0091a0001c0004t0001g0105 | 3 | HG02109.hp1 HG02572.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.703-1299_703-1298d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | AACAC | 4 | a0001c0001t0001g0014a0001c0001t0001g0047a0001c0001t0001g0062others(1): Show | 4 | HG02896.hp2 HG03209.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-1301_703-1298d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | AACACACA others(1): Show |
5 | a0001c0001t0001g0026a0001c0001t0001g0063a0001c0001t0001g0070others(2): Show | 5 | HG00558.hp2 HG02055.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.703-1305_703-1298d others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | AACACACA others(3): Show |
10 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0036others(7): Show | 10 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.703-1307_703-1298d others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | AACACACA others(5): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0058others(5): Show | 8 | HG01169.hp2 HG02080.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.703-1309_703-1298d others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | AACACACA others(7): Show |
6 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0001g0049others(3): Show | 6 | HG02109.hp2 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-1311_703-1298d others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | AACACACA others(9): Show |
7 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0076others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-1313_703-1298d others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | AACACACA others(11): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0002g0023others(3): Show | 6 | HG01070.hp1 HG02080.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-1315_703-1298d others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | AACACACA others(13): Show |
2 | a0001c0002t0001g0033a0004c0010t0001g0048 | 2 | HG04184.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.703-1317_703-1298d others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | AACACACA others(15): Show |
3 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0103 | 3 | HG01993.hp2 HG02451.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.703-1319_703-1298d others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | AACACACA others(17): Show |
6 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0002t0001g0016others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-1321_703-1298d others(26): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | AACACACA others(19): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0002t0001g0021 | 3 | HG01071.hp2 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.703-1323_703-1298d others(28): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | AACACACA others(21): Show |
1 | a0001c0001t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.703-1325_703-1298d others(30): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
A | ACACACAC others(4): Show |
2 | a0001c0001t0001g0052a0001c0001t0001g0083 | 2 | HG01261.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.703-1340_703-1339i others(13): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873681 | ||||||
| chr4:147873681
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.703-1340_703-1339i others(17): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873681 | ||||||
| chr4:147873681
|
A | ACACACAC others(10): Show |
1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.703-1340_703-1339i others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873681 | ||||||
| chr4:147873681
|
AAC | A | 13 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0037others(10): Show | 13 | HG01261.hp2 HG01884.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.703-1299_703-1298d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873681
|
AACAC | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0002t0001g0066 | 3 | HG02818.hp2 HG02896.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.703-1301_703-1298d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873681 | |||||
| chr4:147873728
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.703-1293G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873728 | ||||||
| chr4:147873738
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.703-1283A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873738 | ||||||
| chr4:147873806
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.703-1215T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873806 | ||||||
| chr4:147873875
|
TA | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0034others(26): Show | 29 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.703-1132delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147873875 | |||||
| chr4:147873888
|
A | AG | 12 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.703-1133_703-1132i others(3): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873888 | ||||||
| chr4:147873888
|
A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(47): Show | 50 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.703-1133A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873888 | ||||||
| chr4:147873889
|
A | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(60): Show | 63 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.703-1132A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873889 | ||||||
| chr4:147873936
|
G | A | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.703-1085G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147873936 | ||||||
| chr4:147874036
|
C | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.703-985C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147874036 | ||||||
| chr4:147874357
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.703-664G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147874357 | ||||||
| chr4:147874365
|
C | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0036 | 2 | HG02080.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.703-656C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147874365 | ||||||
| chr4:147874456
|
A | AT | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.703-557dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 147874456 | |||||
| chr4:147874630
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0006t0001g0040others(4): Show | 7 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-391C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147874630 | ||||||
| chr4:147874696
|
C | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0099others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.703-325C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147874696 | ||||||
| chr4:147874704
|
T | G | 7 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0006t0001g0040others(4): Show | 7 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-317T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147874704 | ||||||
| chr4:147874706
|
A | G | 34 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(31): Show | 34 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.703-315A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147874706 | ||||||
| chr4:147874738
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.703-283T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147874738 | ||||||
| chr4:147874905
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.703-116A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | chr4 | 147874905 | ||||||
| chr4:147875313
|
C | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(54): Show | 57 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.832+163C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147875313 | ||||||
| chr4:147875682
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.832+532G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147875682 | ||||||
| chr4:147876013
|
T | G | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+863T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147876013 | ||||||
| chr4:147876086
|
C | T | 3 | a0001c0004t0001g0045a0001c0004t0001g0102a0001c0004t0001g0105 | 3 | HG02572.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.832+936C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147876086 | ||||||
| chr4:147876163
|
G | T | 1 | a0002c0003t0001g0009 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.832+1013G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147876163 | ||||||
| chr4:147876369
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.832+1219G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147876369 | ||||||
| chr4:147876486
|
G | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(21): Show | 24 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.832+1336G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147876486 | ||||||
| chr4:147876511
|
T | G | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 31 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.832+1361T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147876511 | ||||||
| chr4:147876520
|
G | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(35): Show | 38 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.832+1370G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147876520 | ||||||
| chr4:147876638
|
T | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+1488T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147876638 | ||||||
| chr4:147876656
|
T | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+1506T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147876656 | ||||||
| chr4:147876823
|
C | A | 1 | a0002c0003t0001g0009 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.832+1673C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147876823 | ||||||
| chr4:147876907
|
A | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+1757A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147876907 | ||||||
| chr4:147876939
|
A | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.832+1789A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147876939 | ||||||
| chr4:147877177
|
C | G | 3 | a0001c0004t0001g0045a0001c0004t0001g0102a0001c0004t0001g0105 | 3 | HG02572.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.832+2027C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147877177 | ||||||
| chr4:147877264
|
AT | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.833-1960delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147877264 | |||||
| chr4:147877322
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(34): Show | 37 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.833-1910A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147877322 | ||||||
| chr4:147877517
|
G | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0006t0001g0040others(4): Show | 7 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.833-1715G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147877517 | ||||||
| chr4:147877764
|
T | TG | 10 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0075others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.833-1464dupG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147877764 | |||||
| chr4:147877774
|
T | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(24): Show | 27 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.833-1458T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147877774 | ||||||
| chr4:147877779
|
C | G | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.833-1453C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147877779 | ||||||
| chr4:147877819
|
C | CTTT | 5 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0006t0001g0040others(2): Show | 5 | HG01261.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.833-1400_833-1398d others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147877819 | |||||
| chr4:147877819
|
C | CTTTTTTT | 5 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0099others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.833-1404_833-1398d others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147877819 | |||||
| chr4:147877819
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0050a0001c0001t0001g0063a0001c0001t0001g0083others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.833-1405_833-1398d others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147877819 | |||||
| chr4:147877819
|
C | CTTTTTTT others(2): Show |
29 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(26): Show | 29 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.833-1406_833-1398d others(11): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147877819 | |||||
| chr4:147877819
|
C | CTTTTTTT others(3): Show |
7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0046others(4): Show | 7 | HG01261.hp2 HG02109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.833-1407_833-1398d others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147877819 | |||||
| chr4:147877819
|
C | CTTTTTTT others(8): Show |
1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.833-1412_833-1398d others(17): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147877819 | |||||
| chr4:147877819
|
C | CTTTTTTT others(11): Show |
1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.833-1398_833-1397i others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147877819 | |||||
| chr4:147877819
|
C | CTTTTTTT others(13): Show |
1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.833-1398_833-1397i others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147877819 | |||||
| chr4:147877989
|
G | A | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.833-1243G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147877989 | ||||||
| chr4:147878051
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.833-1181C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147878051 | ||||||
| chr4:147878155
|
G | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0099others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.833-1077G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147878155 | ||||||
| chr4:147878220
|
C | T | 3 | a0001c0004t0001g0045a0001c0004t0001g0102a0001c0004t0001g0105 | 3 | HG02572.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.833-1012C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147878220 | ||||||
| chr4:147878242
|
C | T | 3 | a0001c0004t0001g0045a0001c0004t0001g0102a0001c0004t0001g0105 | 3 | HG02572.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.833-990C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147878242 | ||||||
| chr4:147878243
|
G | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.833-989G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147878243 | ||||||
| chr4:147878296
|
A | T | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.833-936A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147878296 | ||||||
| chr4:147878440
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0089 | 3 | HG01243.hp2 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.833-792G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147878440 | ||||||
| chr4:147878462
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(46): Show | 49 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.833-770A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147878462 | ||||||
| chr4:147878490
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.833-742A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147878490 | ||||||
| chr4:147878521
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(50): Show | 53 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.833-711T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147878521 | ||||||
| chr4:147878770
|
T | C | 1 | a0001c0001t0001g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.833-462T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147878770 | ||||||
| chr4:147878774
|
C | CT | 40 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0014others(37): Show | 40 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.833-438dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147878774 | |||||
| chr4:147878774
|
C | CTT | 10 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0055others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.833-439_833-438dup others(2): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147878774 | |||||
| chr4:147878774
|
CT | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0091others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.833-438delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 147878774 | |||||
| chr4:147878966
|
T | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0037 | 2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.833-266T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147878966 | ||||||
| chr4:147879060
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.833-172G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147879060 | ||||||
| chr4:147879065
|
C | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-167C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147879065 | ||||||
| chr4:147879148
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.833-84A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | chr4 | 147879148 | ||||||
| chr4:147879961
|
C | T | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+623C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | chr4 | 147879961 | ||||||
| chr4:147880341
|
A | G | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.939+1003A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | chr4 | 147880341 | ||||||
| chr4:147880370
|
A | G | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+1032A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | chr4 | 147880370 | ||||||
| chr4:147880372
|
A | G | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.939+1034A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | chr4 | 147880372 | ||||||
| chr4:147880396
|
T | A | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.939+1058T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | chr4 | 147880396 | ||||||
| chr4:147880555
|
A | G | 5 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0099others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.939+1217A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | chr4 | 147880555 | ||||||
| chr4:147880706
|
TAAGTA | T | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.940-1128_940-1124d others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 147880706 | |||||
| chr4:147880908
|
TA | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.940-922delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 147880908 | |||||
| chr4:147881071
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(50): Show | 53 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.940-767T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | chr4 | 147881071 | ||||||
| chr4:147881268
|
CA | C | 13 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0075others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.940-556delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | 147881268 | |||||
| chr4:147881403
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(50): Show | 53 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.940-435T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | chr4 | 147881403 | ||||||
| chr4:147881492
|
T | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(50): Show | 53 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.940-346T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | chr4 | 147881492 | ||||||
| chr4:147881608
|
A | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(50): Show | 53 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.940-230A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | chr4 | 147881608 | ||||||
| chr4:147881622
|
A | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(50): Show | 53 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.940-216A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 9/22 | chr4 | 147881622 | ||||||
| chr4:147881950
|
T | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(36): Show | 39 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1034+18T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147881950 | ||||||
| chr4:147882154
|
G | C | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1034+222G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147882154 | ||||||
| chr4:147882179
|
G | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1034+247G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147882179 | ||||||
| chr4:147882184
|
C | T | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1034+252C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147882184 | ||||||
| chr4:147882304
|
G | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1034+372G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147882304 | ||||||
| chr4:147882462
|
C | CA | 37 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(34): Show | 37 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1034+544dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147882462 | |||||
| chr4:147882462
|
C | CAA | 28 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(25): Show | 28 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1034+543_1034+544d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147882462 | |||||
| chr4:147882462
|
C | CAAA | 12 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0034others(9): Show | 12 | HG01261.hp1 HG02056.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.1034+542_1034+544d others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147882462 | |||||
| chr4:147882462
|
CA | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1034+544delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147882462 | |||||
| chr4:147882537
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1034+605C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147882537 | ||||||
| chr4:147882591
|
T | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0006t0001g0040others(4): Show | 7 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1034+659T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147882591 | ||||||
| chr4:147882641
|
T | C | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(34): Show | 37 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1034+709T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147882641 | ||||||
| chr4:147882688
|
G | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(38): Show | 41 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1034+756G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147882688 | ||||||
| chr4:147883035
|
C | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1034+1103C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147883035 | ||||||
| chr4:147883233
|
G | A | 1 | a0002c0003t0001g0009 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1034+1301G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147883233 | ||||||
| chr4:147883320
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1034+1388C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147883320 | ||||||
| chr4:147883376
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1034+1444G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147883376 | ||||||
| chr4:147883444
|
G | A | 13 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0050others(10): Show | 13 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1034+1512G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147883444 | ||||||
| chr4:147883665
|
T | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.1034+1733T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147883665 | ||||||
| chr4:147883946
|
T | C | 15 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0049others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1034+2014T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147883946 | ||||||
| chr4:147884081
|
G | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(1): Show | 4 | HG02056.hp2 HG02080.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1034+2149G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147884081 | ||||||
| chr4:147884211
|
G | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.1034+2279G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147884211 | ||||||
| chr4:147884703
|
TG | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0006t0001g0040others(4): Show | 7 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1034+2772delG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147884703 | ||||||
| chr4:147884828
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0095 | 2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1034+2896A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147884828 | ||||||
| chr4:147884897
|
A | G | 10 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0075others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1034+2965A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147884897 | ||||||
| chr4:147885152
|
A | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1034+3220A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147885152 | ||||||
| chr4:147885236
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1034+3304G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147885236 | ||||||
| chr4:147885331
|
C | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1034+3399C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147885331 | ||||||
| chr4:147885713
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0094 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1034+3781C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147885713 | ||||||
| chr4:147885749
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1034+3817T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147885749 | ||||||
| chr4:147885776
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1034+3844A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147885776 | ||||||
| chr4:147885849
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(79): Show | 82 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.1034+3917C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147885849 | ||||||
| chr4:147885884
|
A | G | 1 | a0001c0001t0001g0015 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1034+3952A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147885884 | ||||||
| chr4:147885964
|
C | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1034+4032C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147885964 | ||||||
| chr4:147886132
|
C | T | 16 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0049others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1034+4200C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886132 | ||||||
| chr4:147886217
|
A | G | 2 | a0001c0001t0001g0034a0001c0002t0001g0029 | 2 | HG02056.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1034+4285A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886217 | ||||||
| chr4:147886296
|
G | C | 6 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1034+4364G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886296 | ||||||
| chr4:147886305
|
T | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.1034+4373T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886305 | ||||||
| chr4:147886429
|
T | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(26): Show | 29 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1034+4497T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886429 | ||||||
| chr4:147886518
|
A | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1034+4586A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886518 | ||||||
| chr4:147886550
|
A | G | 14 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0075others(11): Show | 14 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1034+4618A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886550 | ||||||
| chr4:147886587
|
C | T | 16 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0049others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1034+4655C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886587 | ||||||
| chr4:147886590
|
C | T | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1034+4658C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886590 | ||||||
| chr4:147886669
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1034+4737G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886669 | ||||||
| chr4:147886700
|
T | C | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1034+4768T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886700 | ||||||
| chr4:147886792
|
A | G | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1034+4860A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886792 | ||||||
| chr4:147886834
|
C | G | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1034+4902C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147886834 | ||||||
| chr4:147887050
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0094 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1034+5118C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887050 | ||||||
| chr4:147887199
|
G | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.1034+5267G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887199 | ||||||
| chr4:147887211
|
A | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1034+5279A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887211 | ||||||
| chr4:147887217
|
C | G | 1 | a0001c0001t0001g0006 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1034+5285C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887217 | ||||||
| chr4:147887243
|
C | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(71): Show | 74 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.1034+5311C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887243 | ||||||
| chr4:147887245
|
C | A | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1034+5313C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887245 | ||||||
| chr4:147887442
|
T | TA | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(67): Show | 70 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.1034+5517dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147887442 | |||||
| chr4:147887442
|
T | TAA | 4 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(1): Show | 4 | HG02258.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1034+5516_1034+551 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147887442 | |||||
| chr4:147887473
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1034+5541A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887473 | ||||||
| chr4:147887550
|
A | G | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1034+5618A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887550 | ||||||
| chr4:147887552
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.1034+5620C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887552 | ||||||
| chr4:147887590
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1034+5658G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887590 | ||||||
| chr4:147887604
|
G | A | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1034+5672G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887604 | ||||||
| chr4:147887734
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(1): Show | 4 | HG02056.hp2 HG02080.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1034+5802C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887734 | ||||||
| chr4:147887841
|
G | A | 2 | a0001c0001t0001g0049a0001c0002t0001g0005 | 2 | HG02895.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1034+5909G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147887841 | ||||||
| chr4:147887861
|
C | CA | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1034+5943dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147887861 | |||||
| chr4:147887861
|
CA | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(4): Show | 7 | HG01070.hp1 HG02109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1034+5943delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147887861 | |||||
| chr4:147888048
|
A | G | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1034+6116A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147888048 | ||||||
| chr4:147888224
|
A | G | 5 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0099others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1034+6292A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147888224 | ||||||
| chr4:147888257
|
A | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1034+6325A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147888257 | ||||||
| chr4:147888334
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1034+6402A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147888334 | ||||||
| chr4:147888444
|
C | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1034+6512C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147888444 | ||||||
| chr4:147888493
|
A | G | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1034+6561A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147888493 | ||||||
| chr4:147888530
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1034+6598C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147888530 | ||||||
| chr4:147888764
|
T | A | 6 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1034+6832T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147888764 | ||||||
| chr4:147889089
|
C | T | 2 | a0001c0001t0001g0024a0002c0003t0001g0073 | 2 | NA18612.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1034+7157C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147889089 | ||||||
| chr4:147889109
|
A | G | 24 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(21): Show | 24 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1034+7177A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147889109 | ||||||
| chr4:147889356
|
A | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0057others(2): Show | 5 | HG00558.hp2 HG01167.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1034+7424A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147889356 | ||||||
| chr4:147889502
|
A | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1034+7570A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147889502 | ||||||
| chr4:147889667
|
GTCT | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1034+7740_1034+774 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147889667 | |||||
| chr4:147889865
|
A | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1034+7933A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147889865 | ||||||
| chr4:147889895
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1034+7963C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147889895 | ||||||
| chr4:147889925
|
T | C | 5 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0099others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1034+7993T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147889925 | ||||||
| chr4:147889970
|
C | T | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1034+8038C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147889970 | ||||||
| chr4:147889987
|
C | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1034+8055C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147889987 | ||||||
| chr4:147889989
|
T | A | 1 | a0001c0002t0001g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1034+8057T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147889989 | ||||||
| chr4:147890154
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1034+8222C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147890154 | ||||||
| chr4:147890168
|
G | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0002t0001g0013 | 3 | HG00558.hp1 NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1034+8236G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147890168 | ||||||
| chr4:147890293
|
TTTGA | T | 36 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1034+8364_1034+836 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147890293 | |||||
| chr4:147890381
|
A | T | 2 | a0001c0001t0001g0049a0001c0002t0001g0005 | 2 | HG02895.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1034+8449A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147890381 | ||||||
| chr4:147890496
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(63): Show | 66 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1034+8564C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147890496 | ||||||
| chr4:147890569
|
A | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1034+8637A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147890569 | ||||||
| chr4:147890602
|
G | A | 5 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0099others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1034+8670G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147890602 | ||||||
| chr4:147890693
|
G | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0056 | 2 | HG02056.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1034+8761G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147890693 | ||||||
| chr4:147890719
|
C | T | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1034+8787C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147890719 | ||||||
| chr4:147890752
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1034+8820G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147890752 | ||||||
| chr4:147890803
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.1034+8871A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147890803 | ||||||
| chr4:147890846
|
A | C | 1 | a0001c0001t0002g0031 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1034+8914A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147890846 | ||||||
| chr4:147891050
|
C | A | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1034+9118C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147891050 | ||||||
| chr4:147891214
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.1034+9282A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147891214 | ||||||
| chr4:147891478
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(1): Show | 4 | HG02056.hp2 HG02080.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1034+9546G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147891478 | ||||||
| chr4:147891518
|
G | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(24): Show | 27 | HG00558.hp1 HG01261.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1034+9586G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147891518 | ||||||
| chr4:147891956
|
AC | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0037others(7): Show | 10 | HG01261.hp2 HG01884.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1034+10031delC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147891956 | |||||
| chr4:147892109
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1034+10177C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147892109 | ||||||
| chr4:147892187
|
AGAG | A | 10 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0075others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1034+10261_1034+10 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147892187 | |||||
| chr4:147892222
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1034+10290C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147892222 | ||||||
| chr4:147892573
|
GGGGAGTG others(11): Show |
G | 61 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(58): Show | 61 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.1034+10662_1034+10 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147892573 | |||||
| chr4:147892688
|
G | T | 3 | a0001c0001t0001g0091a0001c0004t0001g0045a0001c0004t0001g0105 | 3 | HG02109.hp1 HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1034+10756G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147892688 | ||||||
| chr4:147892774
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1034+10842C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147892774 | ||||||
| chr4:147892775
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1034+10843G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147892775 | ||||||
| chr4:147893059
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1034+11127G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893059 | ||||||
| chr4:147893063
|
A | AC | 9 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1034+11131_1034+11 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893063 | ||||||
| chr4:147893064
|
T | C | 50 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(47): Show | 50 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.1034+11132T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893064 | ||||||
| chr4:147893190
|
C | T | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1034+11258C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893190 | ||||||
| chr4:147893248
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1034+11316G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893248 | ||||||
| chr4:147893271
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1034+11339T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893271 | ||||||
| chr4:147893353
|
C | T | 4 | a0001c0001t0001g0083a0002c0003t0001g0096a0003c0007t0001g0079others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1034+11421C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893353 | ||||||
| chr4:147893442
|
T | C | 14 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0049others(11): Show | 14 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1034+11510T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893442 | ||||||
| chr4:147893458
|
A | C | 13 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0049others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1034+11526A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893458 | ||||||
| chr4:147893703
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1034+11771G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893703 | ||||||
| chr4:147893844
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0044 | 2 | HG00558.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1034+11912G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893844 | ||||||
| chr4:147893877
|
T | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(23): Show | 26 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1034+11945T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893877 | ||||||
| chr4:147893928
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0094 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1034+11996G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147893928 | ||||||
| chr4:147894140
|
TG | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.1034+12211delG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147894140 | |||||
| chr4:147894437
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1035-12201T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147894437 | ||||||
| chr4:147894460
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(26): Show | 29 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1035-12178C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147894460 | ||||||
| chr4:147894606
|
A | AT | 14 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0049others(11): Show | 14 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1035-12024dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147894606 | |||||
| chr4:147894801
|
T | G | 2 | a0001c0001t0001g0097a0001c0005t0001g0098 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1035-11837T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147894801 | ||||||
| chr4:147894870
|
T | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(26): Show | 29 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1035-11768T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147894870 | ||||||
| chr4:147894939
|
T | C | 45 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(42): Show | 45 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.1035-11699T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147894939 | ||||||
| chr4:147895130
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1035-11508G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147895130 | ||||||
| chr4:147895512
|
C | CA | 52 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(49): Show | 52 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.1035-11103dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147895512 | |||||
| chr4:147895512
|
CA | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0089others(1): Show | 4 | HG01243.hp2 HG01993.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1035-11103delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147895512 | |||||
| chr4:147895562
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1035-11076G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147895562 | ||||||
| chr4:147895626
|
C | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1035-11012C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147895626 | ||||||
| chr4:147895685
|
C | CA | 4 | a0001c0001t0001g0070a0001c0004t0001g0045a0001c0004t0001g0105others(1): Show | 4 | HG01169.hp2 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1035-10939dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147895685 | |||||
| chr4:147895685
|
CA | C | 6 | a0001c0001t0001g0046a0001c0001t0001g0084a0001c0001t0001g0091others(3): Show | 6 | HG01070.hp2 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1035-10939delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147895685 | |||||
| chr4:147895866
|
T | C | 51 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(48): Show | 51 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.1035-10772T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147895866 | ||||||
| chr4:147895929
|
A | C | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1035-10709A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147895929 | ||||||
| chr4:147896253
|
C | G | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1035-10385C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147896253 | ||||||
| chr4:147896299
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(23): Show | 26 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1035-10339G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147896299 | ||||||
| chr4:147896401
|
T | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1035-10237T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147896401 | ||||||
| chr4:147896404
|
A | G | 1 | a0001c0009t0001g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1035-10234A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147896404 | ||||||
| chr4:147896677
|
A | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0099others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-9961A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147896677 | ||||||
| chr4:147896849
|
C | T | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1035-9789C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147896849 | ||||||
| chr4:147896850
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1035-9788G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147896850 | ||||||
| chr4:147896875
|
A | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1035-9763A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147896875 | ||||||
| chr4:147897426
|
G | A | 55 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(52): Show | 55 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.1035-9212G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147897426 | ||||||
| chr4:147897448
|
T | G | 1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1035-9190T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147897448 | ||||||
| chr4:147897601
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0047 | 2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1035-9037C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147897601 | ||||||
| chr4:147897841
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1035-8797G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147897841 | ||||||
| chr4:147897857
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1035-8781A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147897857 | ||||||
| chr4:147897860
|
T | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(27): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1035-8778T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147897860 | ||||||
| chr4:147897947
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0086 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1035-8691G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147897947 | ||||||
| chr4:147898183
|
A | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.1035-8455A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898183 | ||||||
| chr4:147898184
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.1035-8454G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898184 | ||||||
| chr4:147898186
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.1035-8452C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898186 | ||||||
| chr4:147898187
|
T | TTGA | 48 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.1035-8451_1035-845 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898187 | ||||||
| chr4:147898204
|
A | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(27): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1035-8434A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898204 | ||||||
| chr4:147898332
|
A | G | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1035-8306A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898332 | ||||||
| chr4:147898344
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1035-8294C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898344 | ||||||
| chr4:147898602
|
C | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0103others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1035-8036C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898602 | ||||||
| chr4:147898772
|
C | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.1035-7866C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898772 | ||||||
| chr4:147898840
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1035-7798A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898840 | ||||||
| chr4:147898867
|
TAAACC | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0099others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-7769_1035-776 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147898867 | |||||
| chr4:147898913
|
C | G | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1035-7725C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898913 | ||||||
| chr4:147898964
|
C | G | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1035-7674C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898964 | ||||||
| chr4:147898965
|
T | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.1035-7673T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147898965 | ||||||
| chr4:147899050
|
G | C | 2 | a0001c0001t0001g0028a0001c0001t0002g0023 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1035-7588G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147899050 | ||||||
| chr4:147899108
|
C | T | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1035-7530C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147899108 | ||||||
| chr4:147899152
|
C | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 25 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1035-7486C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147899152 | ||||||
| chr4:147899328
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(1): Show | 4 | HG02056.hp2 HG02080.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1035-7310C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147899328 | ||||||
| chr4:147899329
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1035-7309G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147899329 | ||||||
| chr4:147899332
|
T | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0006t0001g0040others(4): Show | 7 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1035-7306T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147899332 | ||||||
| chr4:147899339
|
GTGTGTC | G | 5 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0099others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-7281_1035-727 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147899339 | |||||
| chr4:147899365
|
C | G | 10 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0075others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1035-7273C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147899365 | ||||||
| chr4:147899427
|
T | C | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-7211T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147899427 | ||||||
| chr4:147899481
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.1035-7157G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147899481 | ||||||
| chr4:147899722
|
G | GA | 48 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.1035-6910dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147899722 | |||||
| chr4:147899876
|
GT | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(44): Show | 47 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.1035-6747delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147899876 | |||||
| chr4:147899985
|
A | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(27): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1035-6653A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147899985 | ||||||
| chr4:147900045
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0077 | 2 | HG00558.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1035-6593G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147900045 | ||||||
| chr4:147900132
|
T | C | 1 | a0001c0001t0001g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1035-6506T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147900132 | ||||||
| chr4:147900469
|
C | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 40 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.1035-6169C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147900469 | ||||||
| chr4:147900654
|
A | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0076 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1035-5984A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147900654 | ||||||
| chr4:147900819
|
T | TCAA | 27 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1035-5795_1035-579 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147900819 | |||||
| chr4:147900819
|
T | TCAACAA | 3 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0081 | 3 | HG01243.hp1 HG02056.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1035-5798_1035-579 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147900819 | |||||
| chr4:147900831
|
A | G | 45 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(42): Show | 45 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1035-5807A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147900831 | ||||||
| chr4:147900846
|
C | T | 8 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0003g0087others(5): Show | 8 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1035-5792C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147900846 | ||||||
| chr4:147901061
|
A | G | 4 | a0001c0001t0001g0093a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1035-5577A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901061 | ||||||
| chr4:147901133
|
A | G | 8 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1035-5505A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901133 | ||||||
| chr4:147901185
|
T | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(79): Show | 82 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.1035-5453T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901185 | ||||||
| chr4:147901237
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1035-5401C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901237 | ||||||
| chr4:147901252
|
A | G | 8 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0003g0087others(5): Show | 8 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1035-5386A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901252 | ||||||
| chr4:147901376
|
G | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0003g0087others(5): Show | 8 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1035-5262G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901376 | ||||||
| chr4:147901395
|
C | T | 41 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(38): Show | 41 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1035-5243C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901395 | ||||||
| chr4:147901429
|
A | G | 4 | a0001c0001t0001g0093a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1035-5209A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901429 | ||||||
| chr4:147901458
|
A | G | 8 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0003g0087others(5): Show | 8 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1035-5180A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901458 | ||||||
| chr4:147901559
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1035-5079A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901559 | ||||||
| chr4:147901632
|
C | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(79): Show | 82 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.1035-5006C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901632 | ||||||
| chr4:147901766
|
G | A | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1035-4872G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901766 | ||||||
| chr4:147901963
|
C | T | 8 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0003g0087others(5): Show | 8 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1035-4675C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147901963 | ||||||
| chr4:147902073
|
A | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 26 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1035-4565A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147902073 | ||||||
| chr4:147902485
|
T | C | 8 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0003g0087others(5): Show | 8 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1035-4153T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147902485 | ||||||
| chr4:147902494
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 26 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1035-4144G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147902494 | ||||||
| chr4:147902633
|
C | T | 8 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0003g0087others(5): Show | 8 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1035-4005C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147902633 | ||||||
| chr4:147902911
|
T | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(89): Show | 92 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(89): Show |
intron_variant | MODIFIER | c.1035-3727T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147902911 | ||||||
| chr4:147902924
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1035-3714C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147902924 | ||||||
| chr4:147903161
|
G | T | 16 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0052others(13): Show | 16 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1035-3477G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147903161 | ||||||
| chr4:147903165
|
T | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(30): Show | 33 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1035-3473T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147903165 | ||||||
| chr4:147903197
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1035-3441G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147903197 | ||||||
| chr4:147903309
|
T | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(27): Show | 30 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1035-3329T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147903309 | ||||||
| chr4:147903319
|
A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(83): Show | 86 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.1035-3319A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147903319 | ||||||
| chr4:147903364
|
G | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(75): Show | 78 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(75): Show |
intron_variant | MODIFIER | c.1035-3274G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147903364 | ||||||
| chr4:147903580
|
C | A | 32 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(29): Show | 32 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1035-3058C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147903580 | ||||||
| chr4:147903679
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1035-2959A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147903679 | ||||||
| chr4:147903817
|
A | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1035-2821A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147903817 | ||||||
| chr4:147903954
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1035-2684G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147903954 | ||||||
| chr4:147904301
|
A | G | 1 | a0002c0003t0001g0009 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1035-2337A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147904301 | ||||||
| chr4:147904339
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1035-2299G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147904339 | ||||||
| chr4:147904432
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1035-2206T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147904432 | ||||||
| chr4:147904550
|
A | G | 1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1035-2088A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147904550 | ||||||
| chr4:147904600
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0063 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1035-2038A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147904600 | ||||||
| chr4:147904650
|
G | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(39): Show | 42 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.1035-1988G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147904650 | ||||||
| chr4:147904801
|
C | G | 4 | a0001c0001t0001g0041a0001c0006t0001g0040a0001c0006t0001g0042others(1): Show | 4 | HG02258.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1035-1837C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147904801 | ||||||
| chr4:147904890
|
T | C | 16 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0052others(13): Show | 16 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1035-1748T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147904890 | ||||||
| chr4:147905058
|
T | G | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1035-1580T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905058 | ||||||
| chr4:147905076
|
G | A | 16 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0052others(13): Show | 16 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1035-1562G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905076 | ||||||
| chr4:147905111
|
C | G | 1 | a0001c0001t0001g0056 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1035-1527C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905111 | ||||||
| chr4:147905140
|
T | A | 16 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0052others(13): Show | 16 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1035-1498T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905140 | ||||||
| chr4:147905176
|
G | A | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1035-1462G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905176 | ||||||
| chr4:147905229
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1035-1409C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905229 | ||||||
| chr4:147905314
|
A | C | 16 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0052others(13): Show | 16 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1035-1324A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905314 | ||||||
| chr4:147905314
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1035-1324A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905314 | ||||||
| chr4:147905454
|
C | T | 16 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0052others(13): Show | 16 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1035-1184C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905454 | ||||||
| chr4:147905466
|
A | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 43 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.1035-1172A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905466 | ||||||
| chr4:147905529
|
G | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-1109G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905529 | ||||||
| chr4:147905543
|
A | C | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-1095A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905543 | ||||||
| chr4:147905550
|
C | T | 16 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0049others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1035-1088C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905550 | ||||||
| chr4:147905554
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1035-1084G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905554 | ||||||
| chr4:147905640
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1035-998G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905640 | ||||||
| chr4:147905676
|
A | G | 15 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0052others(12): Show | 15 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1035-962A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905676 | ||||||
| chr4:147905709
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1035-929G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905709 | ||||||
| chr4:147905759
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 26 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1035-879G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905759 | ||||||
| chr4:147905841
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1035-797G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905841 | ||||||
| chr4:147905897
|
C | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(39): Show | 42 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.1035-741C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147905897 | ||||||
| chr4:147906037
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.1035-601A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147906037 | ||||||
| chr4:147906216
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(39): Show | 42 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.1035-422A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147906216 | ||||||
| chr4:147906235
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1035-403C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147906235 | ||||||
| chr4:147906257
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(39): Show | 42 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.1035-381A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147906257 | ||||||
| chr4:147906546
|
T | TA | 42 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(39): Show | 42 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.1035-82dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 147906546 | |||||
| chr4:147906596
|
A | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 26 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1035-42A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | 147906596 | ||||||
| chr4:147906782
|
T | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(30): Show | 33 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1116+63T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147906782 | ||||||
| chr4:147906822
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(39): Show | 42 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.1116+103A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147906822 | ||||||
| chr4:147906883
|
A | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 26 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1116+164A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147906883 | ||||||
| chr4:147906908
|
G | A | 2 | a0001c0001t0001g0034a0001c0002t0001g0029 | 2 | HG02056.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1116+189G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147906908 | ||||||
| chr4:147906979
|
A | G | 16 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0052others(13): Show | 16 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1116+260A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147906979 | ||||||
| chr4:147907315
|
G | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0024others(21): Show | 24 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1116+596G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147907315 | ||||||
| chr4:147907389
|
A | G | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1116+670A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147907389 | ||||||
| chr4:147907482
|
G | A | 36 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(33): Show | 36 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1116+763G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147907482 | ||||||
| chr4:147907690
|
T | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 25 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1116+971T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147907690 | ||||||
| chr4:147907771
|
C | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(60): Show | 63 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1116+1052C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147907771 | ||||||
| chr4:147907969
|
A | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1116+1250A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147907969 | ||||||
| chr4:147908024
|
A | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1116+1305A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147908024 | ||||||
| chr4:147908369
|
G | T | 16 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0052others(13): Show | 16 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1117-1363G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147908369 | ||||||
| chr4:147908503
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1117-1229G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147908503 | ||||||
| chr4:147908803
|
A | C | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1117-929A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147908803 | ||||||
| chr4:147909102
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.1117-630T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147909102 | ||||||
| chr4:147909321
|
C | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0015others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1117-411C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147909321 | ||||||
| chr4:147909366
|
C | A | 4 | a0001c0001t0001g0093a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1117-366C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147909366 | ||||||
| chr4:147909387
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117-345G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147909387 | ||||||
| chr4:147909508
|
C | A | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1117-224C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 11/22 | chr4 | 147909508 | ||||||
| chr4:147909919
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1162+142A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147909919 | ||||||
| chr4:147909924
|
A | G | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1162+147A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147909924 | ||||||
| chr4:147910016
|
C | CT | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1162+248dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147910016 | |||||
| chr4:147910303
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0076 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1162+526G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147910303 | ||||||
| chr4:147910348
|
C | CA | 31 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(28): Show | 31 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1162+584dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147910348 | |||||
| chr4:147910348
|
CA | C | 10 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(7): Show | 10 | HG01169.hp2 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1162+584delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147910348 | |||||
| chr4:147910348
|
CAA | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0006t0001g0040others(4): Show | 7 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1162+583_1162+584d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147910348 | |||||
| chr4:147910492
|
G | T | 8 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+715G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147910492 | ||||||
| chr4:147910640
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(28): Show | 31 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1162+863G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147910640 | ||||||
| chr4:147911002
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0076 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1162+1225C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911002 | ||||||
| chr4:147911099
|
C | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 26 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1162+1322C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911099 | ||||||
| chr4:147911111
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1162+1334T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911111 | ||||||
| chr4:147911128
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 90 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.1162+1351G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911128 | ||||||
| chr4:147911198
|
A | ACCACTGC | 27 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1162+1425_1162+143 others(11): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147911198 | |||||
| chr4:147911420
|
G | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0091 | 3 | HG02109.hp1 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1162+1643G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911420 | ||||||
| chr4:147911424
|
G | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0006t0001g0040others(4): Show | 7 | HG01261.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1162+1647G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911424 | ||||||
| chr4:147911481
|
A | G | 4 | a0001c0001t0001g0093a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-1593A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911481 | ||||||
| chr4:147911493
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1163-1581A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911493 | ||||||
| chr4:147911545
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1163-1529G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911545 | ||||||
| chr4:147911547
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1163-1527A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911547 | ||||||
| chr4:147911569
|
A | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0051others(3): Show | 6 | HG02055.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1163-1505A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911569 | ||||||
| chr4:147911583
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(52): Show | 55 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.1163-1491T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911583 | ||||||
| chr4:147911594
|
C | G | 15 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0050others(12): Show | 15 | HG01891.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1163-1480C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911594 | ||||||
| chr4:147911595
|
T | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1163-1479T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911595 | ||||||
| chr4:147911608
|
C | T | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1163-1466C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911608 | ||||||
| chr4:147911609
|
A | G | 2 | a0001c0001t0001g0093a0001c0002t0001g0090 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1163-1465A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911609 | ||||||
| chr4:147911613
|
T | C | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1163-1461T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911613 | ||||||
| chr4:147911642
|
GT | G | 8 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0063others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1163-1431delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911642 | ||||||
| chr4:147911643
|
T | TG | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(69): Show | 72 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(69): Show |
intron_variant | MODIFIER | c.1163-1430dupG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147911643 | |||||
| chr4:147911651
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(48): Show | 51 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(48): Show |
intron_variant | MODIFIER | c.1163-1423C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911651 | ||||||
| chr4:147911652
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0093 | 2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1163-1422G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911652 | ||||||
| chr4:147911653
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0047others(3): Show | 6 | HG02258.hp2 HG02896.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1163-1421C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911653 | ||||||
| chr4:147911654
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1163-1420G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911654 | ||||||
| chr4:147911696
|
C | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0036 | 2 | HG02080.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1163-1378C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911696 | ||||||
| chr4:147911937
|
GT | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(72): Show | 75 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.1163-1125delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147911937 | |||||
| chr4:147911992
|
C | CAT | 7 | a0001c0002t0001g0013a0001c0004t0001g0045a0001c0005t0001g0074others(4): Show | 7 | HG02258.hp2 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1163-1081_1163-108 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147911992 | |||||
| chr4:147911992
|
C | CATAT | 8 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0036others(5): Show | 8 | HG02080.hp2 HG02895.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1163-1081_1163-108 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147911992 | |||||
| chr4:147911993
|
A | ATATATG | 10 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0043others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.1163-1081_1163-108 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911993 | ||||||
| chr4:147911993
|
A | ATATATGT others(1): Show |
5 | a0001c0001t0001g0035a0001c0001t0001g0062a0001c0001t0001g0069others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-1081_1163-108 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911993 | ||||||
| chr4:147911993
|
A | ATATATGT others(3): Show |
2 | a0001c0002t0001g0021a0001c0002t0001g0072 | 2 | HG02165.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1163-1081_1163-108 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911993 | ||||||
| chr4:147911993
|
A | ATATATGT others(5): Show |
2 | a0001c0001t0001g0025a0001c0001t0001g0106 | 2 | HG00558.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1163-1081_1163-108 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911993 | ||||||
| chr4:147911993
|
ACGTG | A | 5 | a0001c0001t0001g0083a0001c0011t0001g0092a0002c0003t0001g0096others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1163-1080_1163-107 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911993 | ||||||
| chr4:147911994
|
C | CGT | 4 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0008t0001g0059others(1): Show | 4 | HG01884.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-1035_1163-103 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147911994 | |||||
| chr4:147911994
|
C | T | 45 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0025others(42): Show | 45 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1163-1080C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911994 | ||||||
| chr4:147911994
|
CGT | C | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0097 | 3 | HG02145.hp1 NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1163-1035_1163-103 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147911994 | |||||
| chr4:147911994
|
CGTGT | C | 7 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0051others(4): Show | 7 | HG01993.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1163-1037_1163-103 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147911994 | |||||
| chr4:147911994
|
CGTGTGTG others(1): Show |
C | 9 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0022others(6): Show | 9 | HG01243.hp2 HG01261.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1163-1041_1163-103 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147911994 | |||||
| chr4:147911994
|
CGTGTGTG others(3): Show |
C | 9 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0026others(6): Show | 9 | HG00558.hp2 HG01070.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1163-1043_1163-103 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147911994 | |||||
| chr4:147911994
|
CGTGTGTG others(5): Show |
C | 13 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0015others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1163-1045_1163-103 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147911994 | |||||
| chr4:147911994
|
CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0001g0028a0001c0002t0001g0016 | 2 | HG01071.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1163-1047_1163-103 others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147911994 | |||||
| chr4:147911995
|
G | A | 16 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0061others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1163-1079G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911995 | ||||||
| chr4:147911997
|
G | A | 5 | a0001c0001t0001g0093a0001c0001t0001g0099a0001c0001t0001g0100others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1163-1077G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911997 | ||||||
| chr4:147911999
|
G | A | 5 | a0001c0001t0001g0083a0001c0011t0001g0092a0002c0003t0001g0096others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1163-1075G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147911999 | ||||||
| chr4:147912037
|
G | A | 4 | a0001c0001t0001g0093a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-1037G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147912037 | ||||||
| chr4:147912039
|
G | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0025others(31): Show | 34 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1163-1035G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147912039 | ||||||
| chr4:147912157
|
G | A | 49 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0025others(46): Show | 49 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.1163-917G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147912157 | ||||||
| chr4:147912548
|
A | AAT | 2 | a0001c0001t0001g0080a0003c0007t0001g0079 | 2 | HG01891.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1163-476_1163-475d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AAT | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0095 | 2 | HG02055.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1163-476_1163-475d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AATAT | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0053others(2): Show | 5 | HG02818.hp2 HG02896.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-478_1163-475d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AATATAT | A | 4 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0061others(1): Show | 4 | HG02145.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-480_1163-475d others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AATATATA others(1): Show |
A | 5 | a0001c0001t0001g0049a0001c0001t0001g0063a0001c0001t0001g0104others(2): Show | 5 | HG02280.hp1 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-482_1163-475d others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AATATATA others(3): Show |
A | 3 | a0001c0001t0001g0006a0001c0005t0001g0003a0004c0010t0001g0048 | 3 | HG02895.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1163-484_1163-475d others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AATATATA others(5): Show |
A | 37 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(34): Show | 37 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1163-486_1163-475d others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AATATATA others(7): Show |
A | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0088others(3): Show | 6 | HG01884.hp1 HG01993.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1163-488_1163-475d others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AATATATA others(11): Show |
A | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1163-492_1163-475d others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AATATATA others(13): Show |
A | 4 | a0001c0001t0001g0081a0001c0001t0001g0091a0001c0002t0001g0090others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-494_1163-475d others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AATATATA others(15): Show |
A | 4 | a0001c0001t0003g0087a0001c0002t0001g0021a0001c0002t0001g0072others(1): Show | 4 | HG02165.hp2 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-496_1163-475d others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AATATATA others(17): Show |
A | 28 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0025others(25): Show | 28 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1163-498_1163-475d others(26): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AATATATA others(19): Show |
A | 1 | a0001c0009t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1163-500_1163-475d others(28): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912548
|
AATATATA others(27): Show |
A | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1163-508_1163-475d others(36): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912548 | |||||
| chr4:147912566
|
T | G | 32 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(29): Show | 32 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1163-508T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147912566 | ||||||
| chr4:147912568
|
T | G | 2 | a0001c0001t0001g0038a0001c0002t0001g0016 | 2 | HG02622.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1163-506T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147912568 | ||||||
| chr4:147912574
|
T | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0091a0001c0002t0001g0090 | 3 | HG01884.hp2 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1163-500T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147912574 | ||||||
| chr4:147912576
|
T | G | 5 | a0001c0001t0001g0081a0001c0001t0003g0087a0001c0002t0001g0021others(2): Show | 5 | HG02165.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-498T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147912576 | ||||||
| chr4:147912578
|
T | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(54): Show | 57 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.1163-496T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147912578 | ||||||
| chr4:147912580
|
T | G | 2 | a0001c0002t0001g0016a0001c0009t0001g0008 | 2 | HG03225.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1163-494T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147912580 | ||||||
| chr4:147912588
|
T | G | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1163-486T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147912588 | ||||||
| chr4:147912645
|
C | CT | 28 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(25): Show | 28 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1163-404dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912645 | |||||
| chr4:147912645
|
C | CTT | 10 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1163-405_1163-404d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912645 | |||||
| chr4:147912645
|
CT | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0061others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1163-404delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912645 | |||||
| chr4:147912645
|
CTTT | C | 31 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0034others(28): Show | 31 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1163-406_1163-404d others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 147912645 | |||||
| chr4:147912705
|
G | C | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1163-369G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | 147912705 | ||||||
| chr4:147913239
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1228+100C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147913239 | ||||||
| chr4:147913857
|
T | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0077 | 2 | HG00558.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1228+718T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147913857 | ||||||
| chr4:147913890
|
C | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1228+751C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147913890 | ||||||
| chr4:147913962
|
G | C | 2 | a0001c0001t0001g0097a0001c0005t0001g0098 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1228+823G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147913962 | ||||||
| chr4:147914138
|
C | T | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1228+999C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147914138 | ||||||
| chr4:147914181
|
A | C | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1228+1042A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147914181 | ||||||
| chr4:147914344
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1228+1205C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147914344 | ||||||
| chr4:147914379
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(37): Show | 40 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1228+1240A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147914379 | ||||||
| chr4:147914389
|
ACT | A | 3 | a0001c0008t0001g0059a0001c0008t0001g0060a0001c0009t0001g0008 | 3 | HG03098.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1228+1253_1228+125 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147914389 | |||||
| chr4:147914420
|
G | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(85): Show | 88 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.1228+1281G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147914420 | ||||||
| chr4:147914503
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1228+1364A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147914503 | ||||||
| chr4:147914543
|
G | C | 2 | a0001c0001t0001g0093a0001c0002t0001g0090 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1228+1404G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147914543 | ||||||
| chr4:147914556
|
TC | T | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0015others(32): Show | 35 | HG00558.hp2 HG01070.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1228+1429delC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147914556 | |||||
| chr4:147914556
|
TCC | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(50): Show | 53 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1228+1428_1228+142 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147914556 | |||||
| chr4:147914568
|
C | T | 40 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 40 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.1228+1429C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147914568 | ||||||
| chr4:147914592
|
A | AT | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(86): Show | 89 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(86): Show |
intron_variant | MODIFIER | c.1228+1458dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147914592 | |||||
| chr4:147914607
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0047 | 2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1228+1468G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147914607 | ||||||
| chr4:147914800
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1228+1661T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147914800 | ||||||
| chr4:147914816
|
T | C | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1228+1677T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147914816 | ||||||
| chr4:147915020
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1228+1881C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147915020 | ||||||
| chr4:147915050
|
A | T | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1228+1911A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147915050 | ||||||
| chr4:147915562
|
A | C | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1228+2423A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147915562 | ||||||
| chr4:147915628
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1228+2489T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147915628 | ||||||
| chr4:147915675
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1228+2536A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147915675 | ||||||
| chr4:147915946
|
T | A | 3 | a0001c0001t0001g0093a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1228+2807T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147915946 | ||||||
| chr4:147915952
|
T | A | 1 | a0001c0001t0001g0055 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1228+2813T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147915952 | ||||||
| chr4:147915953
|
A | T | 37 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0025others(34): Show | 37 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1228+2814A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147915953 | ||||||
| chr4:147916014
|
C | T | 4 | a0001c0002t0001g0072a0001c0006t0001g0040a0001c0006t0001g0042others(1): Show | 4 | HG02258.hp2 HG02922.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228+2875C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147916014 | ||||||
| chr4:147916191
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(39): Show | 42 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.1228+3052C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147916191 | ||||||
| chr4:147916238
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1228+3099G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147916238 | ||||||
| chr4:147916276
|
A | T | 1 | a0001c0001t0001g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1228+3137A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147916276 | ||||||
| chr4:147916903
|
C | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(42): Show | 45 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1228+3764C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147916903 | ||||||
| chr4:147916978
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1228+3839G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147916978 | ||||||
| chr4:147917101
|
T | A | 1 | a0001c0001t0001g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1228+3962T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147917101 | ||||||
| chr4:147917134
|
A | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.1228+3995A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147917134 | ||||||
| chr4:147917248
|
A | G | 3 | a0001c0001t0001g0093a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1228+4109A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147917248 | ||||||
| chr4:147917287
|
T | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1228+4148T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147917287 | ||||||
| chr4:147917490
|
G | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(39): Show | 42 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1228+4351G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147917490 | ||||||
| chr4:147917839
|
G | GTCTT | 43 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(40): Show | 43 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1228+4701_1228+470 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147917839 | |||||
| chr4:147917850
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1228+4711G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147917850 | ||||||
| chr4:147917858
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1228+4719T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147917858 | ||||||
| chr4:147917868
|
C | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(40): Show | 43 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1228+4729C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147917868 | ||||||
| chr4:147918036
|
C | A | 1 | a0001c0009t0001g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1228+4897C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918036 | ||||||
| chr4:147918112
|
ATAATT | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1228+4977_1228+498 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147918112 | |||||
| chr4:147918133
|
A | AT | 8 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0026others(5): Show | 8 | HG02055.hp1 HG02056.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1228+5014dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147918133 | |||||
| chr4:147918133
|
A | ATTTTT | 7 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0004t0001g0045others(4): Show | 7 | HG02572.hp2 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1228+5010_1228+501 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147918133 | |||||
| chr4:147918133
|
A | ATTTTTT | 27 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0030others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1228+5009_1228+501 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147918133 | |||||
| chr4:147918133
|
A | ATTTTTTT | 5 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0004t0001g0102others(2): Show | 5 | HG00558.hp1 HG02056.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228+5008_1228+501 others(11): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147918133 | |||||
| chr4:147918133
|
AT | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0052others(6): Show | 9 | HG01167.hp2 HG01261.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1228+5014delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147918133 | |||||
| chr4:147918190
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0094 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1228+5051C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918190 | ||||||
| chr4:147918204
|
C | T | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1228+5065C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918204 | ||||||
| chr4:147918220
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1228+5081C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918220 | ||||||
| chr4:147918290
|
G | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(88): Show | 91 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(88): Show |
intron_variant | MODIFIER | c.1228+5151G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918290 | ||||||
| chr4:147918311
|
A | G | 3 | a0001c0001t0001g0093a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1228+5172A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918311 | ||||||
| chr4:147918335
|
C | A | 2 | a0001c0001t0001g0093a0001c0002t0001g0090 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1228+5196C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918335 | ||||||
| chr4:147918386
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1228+5247C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918386 | ||||||
| chr4:147918559
|
G | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(40): Show | 43 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1228+5420G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918559 | ||||||
| chr4:147918566
|
G | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(35): Show | 38 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1228+5427G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918566 | ||||||
| chr4:147918594
|
C | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(34): Show | 37 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.1228+5455C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918594 | ||||||
| chr4:147918604
|
G | T | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1228+5465G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918604 | ||||||
| chr4:147918678
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1228+5539G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147918678 | ||||||
| chr4:147919266
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(36): Show | 39 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.1228+6127G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147919266 | ||||||
| chr4:147919397
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1228+6258G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147919397 | ||||||
| chr4:147919526
|
C | T | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1228+6387C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147919526 | ||||||
| chr4:147919567
|
AT | A | 30 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(27): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1228+6437delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147919567 | |||||
| chr4:147919593
|
G | T | 13 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0052others(10): Show | 13 | HG01261.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1228+6454G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147919593 | ||||||
| chr4:147920122
|
AACAAC | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(39): Show | 42 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1228+6985_1228+698 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147920122 | |||||
| chr4:147920124
|
C | T | 3 | a0001c0001t0001g0093a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1228+6985C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147920124 | ||||||
| chr4:147920233
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1228+7094A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147920233 | ||||||
| chr4:147920297
|
A | ATCCCAGC others(297): Show |
1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1228+7189_1228+719 others(308): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147920297 | |||||
| chr4:147920297
|
A | ATCCCAGC others(297): Show |
6 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0088others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1228+7189_1228+719 others(308): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147920297 | |||||
| chr4:147920297
|
A | ATCCCAGC others(297): Show |
3 | a0001c0001t0001g0093a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1228+7189_1228+719 others(308): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147920297 | |||||
| chr4:147920297
|
A | ATCCCAGC others(297): Show |
35 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(32): Show | 35 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1228+7189_1228+719 others(308): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147920297 | |||||
| chr4:147920463
|
T | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(42): Show | 45 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1228+7324T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147920463 | ||||||
| chr4:147920479
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1228+7340A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147920479 | ||||||
| chr4:147920641
|
T | TA | 35 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 35 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1228+7503dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147920641 | |||||
| chr4:147920857
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1228+7718A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147920857 | ||||||
| chr4:147921082
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1228+7943A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147921082 | ||||||
| chr4:147921144
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1228+8005T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147921144 | ||||||
| chr4:147921157
|
G | A | 1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1228+8018G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147921157 | ||||||
| chr4:147921484
|
C | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(90): Show | 93 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.1228+8345C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147921484 | ||||||
| chr4:147921536
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1228+8397C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147921536 | ||||||
| chr4:147921558
|
CAGAG | C | 9 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0061others(6): Show | 9 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1228+8422_1228+842 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147921558 | |||||
| chr4:147921665
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1228+8526A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147921665 | ||||||
| chr4:147921741
|
C | T | 2 | a0001c0001t0001g0093a0001c0002t0001g0090 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1228+8602C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147921741 | ||||||
| chr4:147921752
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(42): Show | 45 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1228+8613G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147921752 | ||||||
| chr4:147921994
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(42): Show | 45 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1228+8855T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147921994 | ||||||
| chr4:147922390
|
TA | T | 11 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0062others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228+9265delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147922390 | |||||
| chr4:147922472
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0088 | 2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1228+9333G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147922472 | ||||||
| chr4:147922666
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1228+9527C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147922666 | ||||||
| chr4:147922667
|
G | A | 2 | a0001c0001t0001g0093a0001c0002t0001g0090 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1228+9528G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147922667 | ||||||
| chr4:147922687
|
C | CAA | 38 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(35): Show | 38 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.1228+9568_1228+956 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147922687 | |||||
| chr4:147922687
|
C | CAAA | 4 | a0001c0001t0001g0025a0001c0002t0001g0021a0001c0006t0001g0040others(1): Show | 4 | HG00558.hp1 HG02165.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228+9567_1228+956 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147922687 | |||||
| chr4:147922687
|
CA | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 28 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1228+9569delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147922687 | |||||
| chr4:147922709
|
T | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1228+9570T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147922709 | ||||||
| chr4:147922767
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(39): Show | 42 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1228+9628A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147922767 | ||||||
| chr4:147922932
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(42): Show | 45 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1228+9793A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147922932 | ||||||
| chr4:147923075
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(42): Show | 45 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1228+9936G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147923075 | ||||||
| chr4:147923265
|
G | C | 3 | a0001c0001t0001g0088a0001c0004t0001g0045a0001c0004t0001g0105 | 3 | HG01884.hp1 HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1228+10126G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147923265 | ||||||
| chr4:147923696
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(40): Show | 43 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1228+10557C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147923696 | ||||||
| chr4:147923858
|
T | G | 3 | a0001c0001t0001g0093a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1228+10719T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147923858 | ||||||
| chr4:147924039
|
A | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1228+10900A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147924039 | ||||||
| chr4:147924122
|
T | C | 1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1228+10983T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147924122 | ||||||
| chr4:147924249
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(36): Show | 39 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1228+11110G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147924249 | ||||||
| chr4:147924747
|
C | CA | 43 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(40): Show | 43 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1228+11608_1228+11 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147924747 | ||||||
| chr4:147924800
|
C | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1228+11661C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147924800 | ||||||
| chr4:147924971
|
AT | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(40): Show | 43 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1228+11845delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147924971 | |||||
| chr4:147924983
|
T | A | 3 | a0001c0001t0001g0006a0001c0005t0001g0003a0001c0011t0001g0092 | 3 | HG02451.hp2 HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1228+11844T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147924983 | ||||||
| chr4:147924984
|
T | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(39): Show | 42 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1228+11845T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147924984 | ||||||
| chr4:147924984
|
TA | T | 2 | a0001c0004t0001g0045a0001c0004t0001g0105 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1228+11849delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147924984 | |||||
| chr4:147924985
|
A | T | 6 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0099others(3): Show | 6 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228+11846A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147924985 | ||||||
| chr4:147925242
|
A | G | 3 | a0001c0001t0001g0093a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1228+12103A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147925242 | ||||||
| chr4:147925266
|
G | T | 3 | a0001c0001t0001g0093a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1228+12127G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147925266 | ||||||
| chr4:147925320
|
C | T | 1 | a0001c0002t0001g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1228+12181C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147925320 | ||||||
| chr4:147925398
|
C | T | 13 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0052others(10): Show | 13 | HG01261.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1228+12259C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147925398 | ||||||
| chr4:147925431
|
T | TC | 43 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(40): Show | 43 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1228+12292_1228+12 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147925431 | ||||||
| chr4:147925490
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1228+12351T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147925490 | ||||||
| chr4:147925524
|
C | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(40): Show | 43 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1228+12385C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147925524 | ||||||
| chr4:147926168
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1228+13029C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147926168 | ||||||
| chr4:147926433
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(92): Show | 95 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.1228+13294A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147926433 | ||||||
| chr4:147926448
|
A | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(40): Show | 43 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1228+13309A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147926448 | ||||||
| chr4:147926767
|
A | G | 2 | a0001c0001t0001g0093a0001c0002t0001g0090 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1229-13058A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147926767 | ||||||
| chr4:147926767
|
A | T | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1229-13058A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147926767 | ||||||
| chr4:147926844
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1229-12981G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147926844 | ||||||
| chr4:147926849
|
A | G | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1229-12976A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147926849 | ||||||
| chr4:147926941
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(36): Show | 39 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1229-12884A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147926941 | ||||||
| chr4:147927001
|
C | T | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1229-12824C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147927001 | ||||||
| chr4:147927132
|
T | G | 14 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0038others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1229-12693T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147927132 | ||||||
| chr4:147927371
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1229-12454C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147927371 | ||||||
| chr4:147927680
|
T | C | 1 | a0002c0003t0001g0009 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1229-12145T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147927680 | ||||||
| chr4:147927691
|
C | T | 1 | a0001c0002t0001g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1229-12134C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147927691 | ||||||
| chr4:147927734
|
T | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(47): Show | 50 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.1229-12091T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147927734 | ||||||
| chr4:147927756
|
C | G | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1229-12069C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147927756 | ||||||
| chr4:147927905
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1229-11920G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147927905 | ||||||
| chr4:147927977
|
G | A | 7 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1229-11848G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147927977 | ||||||
| chr4:147928018
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1229-11807G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147928018 | ||||||
| chr4:147928251
|
G | C | 7 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1229-11574G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147928251 | ||||||
| chr4:147929001
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1229-10824G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147929001 | ||||||
| chr4:147929287
|
A | G | 1 | a0001c0006t0001g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1229-10538A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147929287 | ||||||
| chr4:147929415
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0094 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1229-10410A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147929415 | ||||||
| chr4:147929571
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1229-10254A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147929571 | ||||||
| chr4:147929741
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1229-10084C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147929741 | ||||||
| chr4:147929816
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(36): Show | 39 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1229-10009A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147929816 | ||||||
| chr4:147929880
|
C | T | 2 | a0001c0001t0001g0093a0001c0011t0001g0092 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1229-9945C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147929880 | ||||||
| chr4:147929959
|
A | G | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1229-9866A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147929959 | ||||||
| chr4:147929976
|
A | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(47): Show | 50 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.1229-9849A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147929976 | ||||||
| chr4:147930022
|
A | G | 2 | a0001c0001t0001g0093a0001c0011t0001g0092 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1229-9803A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930022 | ||||||
| chr4:147930045
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(36): Show | 39 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1229-9780G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930045 | ||||||
| chr4:147930113
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1229-9712C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930113 | ||||||
| chr4:147930136
|
C | G | 7 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1229-9689C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930136 | ||||||
| chr4:147930217
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1229-9608A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930217 | ||||||
| chr4:147930296
|
G | A | 7 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1229-9529G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930296 | ||||||
| chr4:147930305
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(83): Show | 86 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.1229-9520T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930305 | ||||||
| chr4:147930394
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(90): Show | 93 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.1229-9431A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930394 | ||||||
| chr4:147930466
|
G | A | 13 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0052others(10): Show | 13 | HG01261.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1229-9359G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930466 | ||||||
| chr4:147930488
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1229-9337T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930488 | ||||||
| chr4:147930597
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(90): Show | 93 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.1229-9228G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930597 | ||||||
| chr4:147930644
|
G | A | 9 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0061others(6): Show | 9 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1229-9181G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930644 | ||||||
| chr4:147930960
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1229-8865C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147930960 | ||||||
| chr4:147931003
|
G | A | 3 | a0001c0001t0001g0093a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1229-8822G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147931003 | ||||||
| chr4:147931128
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1229-8697G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147931128 | ||||||
| chr4:147931154
|
T | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1229-8671T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147931154 | ||||||
| chr4:147931313
|
GA | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(90): Show | 93 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.1229-8498delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147931313 | |||||
| chr4:147931781
|
C | T | 7 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1229-8044C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147931781 | ||||||
| chr4:147932204
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1229-7621G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147932204 | ||||||
| chr4:147932620
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1229-7205G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147932620 | ||||||
| chr4:147932654
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1229-7171C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147932654 | ||||||
| chr4:147932728
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(82): Show | 85 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(82): Show |
intron_variant | MODIFIER | c.1229-7097G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147932728 | ||||||
| chr4:147932791
|
C | A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1229-7034C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147932791 | ||||||
| chr4:147932815
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1229-7010A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147932815 | ||||||
| chr4:147932910
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0015 | 2 | NA18612.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1229-6915A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147932910 | ||||||
| chr4:147933223
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0044 | 2 | HG00558.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1229-6602G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147933223 | ||||||
| chr4:147933249
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0047 | 2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1229-6576G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147933249 | ||||||
| chr4:147933322
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1229-6503A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147933322 | ||||||
| chr4:147933423
|
CTG | C | 3 | a0001c0001t0001g0093a0001c0002t0001g0090a0001c0011t0001g0092 | 3 | HG01884.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1229-6399_1229-639 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147933423 | |||||
| chr4:147933560
|
A | C | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1229-6265A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147933560 | ||||||
| chr4:147933716
|
A | G | 1 | a0001c0001t0001g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1229-6109A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147933716 | ||||||
| chr4:147934206
|
A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(83): Show | 86 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.1229-5619A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147934206 | ||||||
| chr4:147934273
|
C | T | 1 | a0001c0009t0001g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1229-5552C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147934273 | ||||||
| chr4:147934352
|
G | T | 1 | a0001c0002t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1229-5473G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147934352 | ||||||
| chr4:147934665
|
G | A | 2 | a0001c0001t0003g0087a0001c0011t0001g0092 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1229-5160G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147934665 | ||||||
| chr4:147934788
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1229-5037C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147934788 | ||||||
| chr4:147934882
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1229-4943A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147934882 | ||||||
| chr4:147934906
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(85): Show | 88 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.1229-4919G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147934906 | ||||||
| chr4:147935156
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(91): Show | 94 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(91): Show |
intron_variant | MODIFIER | c.1229-4669T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147935156 | ||||||
| chr4:147935214
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1229-4611C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147935214 | ||||||
| chr4:147935343
|
AAGAT | A | 2 | a0001c0001t0001g0006a0001c0005t0001g0003 | 2 | HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1229-4478_1229-447 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147935343 | |||||
| chr4:147935609
|
G | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(85): Show | 88 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.1229-4216G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147935609 | ||||||
| chr4:147935802
|
C | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 35 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1229-4023C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147935802 | ||||||
| chr4:147936184
|
A | G | 2 | a0001c0001t0003g0087a0001c0011t0001g0092 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1229-3641A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147936184 | ||||||
| chr4:147936301
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1229-3524G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147936301 | ||||||
| chr4:147936317
|
C | CT | 53 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 53 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.1229-3486dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147936317 | |||||
| chr4:147936317
|
CT | C | 5 | a0001c0001t0001g0088a0001c0002t0001g0072a0001c0004t0001g0102others(2): Show | 5 | HG01884.hp1 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1229-3486delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147936317 | |||||
| chr4:147936317
|
CTTT | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(1): Show | 4 | HG02056.hp2 HG02080.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1229-3488_1229-348 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147936317 | |||||
| chr4:147936344
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(91): Show | 94 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(91): Show |
intron_variant | MODIFIER | c.1229-3481T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147936344 | ||||||
| chr4:147936369
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(92): Show | 95 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.1229-3456T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147936369 | ||||||
| chr4:147936421
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1229-3404C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147936421 | ||||||
| chr4:147936482
|
C | T | 1 | a0001c0009t0001g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1229-3343C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147936482 | ||||||
| chr4:147936498
|
T | A | 6 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0099others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1229-3327T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147936498 | ||||||
| chr4:147936625
|
G | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0081others(1): Show | 4 | HG02055.hp2 HG02818.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1229-3200G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147936625 | ||||||
| chr4:147936683
|
T | C | 6 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0099others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1229-3142T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147936683 | ||||||
| chr4:147936856
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(92): Show | 95 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.1229-2969G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147936856 | ||||||
| chr4:147936946
|
A | G | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1229-2879A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147936946 | ||||||
| chr4:147936949
|
T | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(27): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1229-2876T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147936949 | ||||||
| chr4:147937138
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(92): Show | 95 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.1229-2687T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147937138 | ||||||
| chr4:147937236
|
CCTCT | C | 6 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0099others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1229-2584_1229-258 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 147937236 | |||||
| chr4:147937256
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(56): Show | 59 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.1229-2569A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147937256 | ||||||
| chr4:147937445
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1229-2380G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147937445 | ||||||
| chr4:147937466
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1229-2359G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147937466 | ||||||
| chr4:147937469
|
A | G | 2 | a0001c0001t0001g0006a0001c0005t0001g0003 | 2 | HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1229-2356A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147937469 | ||||||
| chr4:147937583
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1229-2242G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147937583 | ||||||
| chr4:147937601
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(56): Show | 59 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.1229-2224A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147937601 | ||||||
| chr4:147937838
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1229-1987G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147937838 | ||||||
| chr4:147938049
|
A | G | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1229-1776A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147938049 | ||||||
| chr4:147938194
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1229-1631C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147938194 | ||||||
| chr4:147938807
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1229-1018G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147938807 | ||||||
| chr4:147938823
|
C | G | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1229-1002C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147938823 | ||||||
| chr4:147938851
|
A | C | 1 | a0001c0001t0001g0025 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1229-974A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147938851 | ||||||
| chr4:147938918
|
G | T | 1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1229-907G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147938918 | ||||||
| chr4:147939405
|
G | A | 36 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(33): Show | 36 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1229-420G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147939405 | ||||||
| chr4:147939445
|
C | T | 2 | a0001c0001t0003g0087a0001c0011t0001g0092 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1229-380C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147939445 | ||||||
| chr4:147939734
|
G | A | 2 | a0001c0001t0003g0087a0001c0011t0001g0092 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1229-91G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | chr4 | 147939734 | ||||||
| chr4:147940686
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(35): Show | 38 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1303+787A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147940686 | ||||||
| chr4:147941355
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1303+1456G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147941355 | ||||||
| chr4:147941475
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0005t0001g0098 | 3 | HG02145.hp1 HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1303+1576G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147941475 | ||||||
| chr4:147941989
|
G | A | 2 | a0001c0001t0003g0087a0001c0011t0001g0092 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1303+2090G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147941989 | ||||||
| chr4:147941990
|
T | G | 1 | a0001c0002t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1303+2091T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147941990 | ||||||
| chr4:147942320
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1303+2421A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147942320 | ||||||
| chr4:147942583
|
G | A | 6 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303+2684G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147942583 | ||||||
| chr4:147942828
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1303+2929C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147942828 | ||||||
| chr4:147943071
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1303+3172G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147943071 | ||||||
| chr4:147943230
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(2): Show | 5 | HG02056.hp2 HG02080.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1303+3331G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147943230 | ||||||
| chr4:147943357
|
T | C | 7 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0099others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1304-3260T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147943357 | ||||||
| chr4:147943658
|
C | T | 1 | a0001c0009t0001g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1304-2959C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147943658 | ||||||
| chr4:147943659
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(101): Show | 104 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(101): Show |
intron_variant | MODIFIER | c.1304-2958A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147943659 | ||||||
| chr4:147944111
|
A | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1304-2506A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147944111 | ||||||
| chr4:147944129
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1304-2488A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147944129 | ||||||
| chr4:147944331
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1304-2286A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147944331 | ||||||
| chr4:147944449
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1304-2168C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147944449 | ||||||
| chr4:147944500
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(6): Show | 9 | HG01993.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1304-2117C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147944500 | ||||||
| chr4:147944581
|
A | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(48): Show | 51 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.1304-2036A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147944581 | ||||||
| chr4:147945091
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.1304-1526A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147945091 | ||||||
| chr4:147945375
|
G | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(36): Show | 39 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1304-1242G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147945375 | ||||||
| chr4:147945432
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1304-1185G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147945432 | ||||||
| chr4:147945437
|
T | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(36): Show | 39 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1304-1180T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147945437 | ||||||
| chr4:147946112
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0002t0001g0019others(1): Show | 4 | HG02165.hp1 HG03239.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304-505C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147946112 | ||||||
| chr4:147946166
|
A | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304-451A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 14/22 | chr4 | 147946166 | ||||||
| chr4:147946946
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1391+242G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147946946 | ||||||
| chr4:147946975
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1391+271A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147946975 | ||||||
| chr4:147947227
|
C | CT | 6 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0053others(3): Show | 6 | HG01993.hp1 HG02896.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.1391+543dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147947227 | |||||
| chr4:147947227
|
CT | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0025others(35): Show | 38 | HG00558.hp1 HG00558.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1391+543delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147947227 | |||||
| chr4:147947227
|
CTT | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0065others(2): Show | 5 | HG01070.hp2 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1391+542_1391+543d others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147947227 | |||||
| chr4:147947287
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1391+583G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147947287 | ||||||
| chr4:147947888
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1391+1184C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147947888 | ||||||
| chr4:147947943
|
G | GT | 8 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0047others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1391+1255dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147947943 | |||||
| chr4:147947943
|
G | GTT | 7 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0053others(4): Show | 7 | HG01993.hp1 HG02895.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1391+1254_1391+125 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147947943 | |||||
| chr4:147947943
|
GT | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(28): Show | 31 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1391+1255delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147947943 | |||||
| chr4:147948059
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1391+1355G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147948059 | ||||||
| chr4:147948101
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1391+1397C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147948101 | ||||||
| chr4:147948314
|
AAGTC | A | 3 | a0001c0001t0001g0093a0001c0001t0003g0087a0001c0011t0001g0092 | 3 | HG02451.hp2 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1391+1616_1391+161 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147948314 | |||||
| chr4:147948361
|
C | A | 2 | a0001c0001t0003g0087a0001c0011t0001g0092 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1391+1657C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147948361 | ||||||
| chr4:147948804
|
GA | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0047a0001c0001t0001g0088others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1391+2113delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147948804 | |||||
| chr4:147948805
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1391+2101A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147948805 | ||||||
| chr4:147948849
|
G | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(89): Show | 92 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(89): Show |
intron_variant | MODIFIER | c.1391+2145G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147948849 | ||||||
| chr4:147948965
|
C | CA | 4 | a0001c0001t0001g0034a0001c0001t0001g0058a0001c0001t0001g0091others(1): Show | 4 | HG02056.hp2 HG02109.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1391+2274dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147948965 | |||||
| chr4:147948979
|
C | CA | 10 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0037others(7): Show | 10 | HG01993.hp1 HG02895.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1391+2282dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147948979 | |||||
| chr4:147948987
|
C | A | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1391+2283C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147948987 | ||||||
| chr4:147949232
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1391+2528T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147949232 | ||||||
| chr4:147949260
|
T | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(89): Show | 92 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(89): Show |
intron_variant | MODIFIER | c.1391+2556T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147949260 | ||||||
| chr4:147949640
|
T | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(37): Show | 40 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1391+2936T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147949640 | ||||||
| chr4:147949842
|
C | CT | 38 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(35): Show | 38 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1391+3144dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147949842 | |||||
| chr4:147949881
|
T | G | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1391+3177T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147949881 | ||||||
| chr4:147949981
|
C | T | 2 | a0001c0001t0001g0088a0001c0002t0001g0090 | 2 | HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1391+3277C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147949981 | ||||||
| chr4:147950754
|
AATG | A | 4 | a0001c0001t0001g0083a0002c0003t0001g0096a0003c0007t0001g0079others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1391+4053_1391+405 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147950754 | |||||
| chr4:147950896
|
C | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0037others(7): Show | 10 | HG01993.hp1 HG02895.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1391+4192C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147950896 | ||||||
| chr4:147950942
|
A | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 67 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.1391+4238A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147950942 | ||||||
| chr4:147951045
|
A | G | 2 | a0001c0001t0001g0088a0001c0002t0001g0090 | 2 | HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1392-4271A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147951045 | ||||||
| chr4:147951173
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1392-4143T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147951173 | ||||||
| chr4:147951341
|
C | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0030others(18): Show | 21 | HG02056.hp2 HG02080.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1392-3975C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147951341 | ||||||
| chr4:147951403
|
AT | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(47): Show | 50 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1392-3898delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147951403 | |||||
| chr4:147951608
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1392-3708T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147951608 | ||||||
| chr4:147951658
|
G | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(42): Show | 45 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.1392-3658G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147951658 | ||||||
| chr4:147951681
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1392-3635C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147951681 | ||||||
| chr4:147951716
|
G | A | 10 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0061others(7): Show | 10 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1392-3600G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147951716 | ||||||
| chr4:147951792
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 99 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.1392-3524C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147951792 | ||||||
| chr4:147951830
|
A | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.1392-3486A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147951830 | ||||||
| chr4:147952387
|
G | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(47): Show | 50 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1392-2929G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147952387 | ||||||
| chr4:147952430
|
A | G | 6 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0002t0001g0072others(3): Show | 6 | HG02886.hp2 HG03098.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1392-2886A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147952430 | ||||||
| chr4:147952451
|
G | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(100): Show | 103 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(100): Show |
intron_variant | MODIFIER | c.1392-2865G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147952451 | ||||||
| chr4:147952912
|
T | C | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1392-2404T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147952912 | ||||||
| chr4:147952991
|
C | T | 1 | a0001c0005t0001g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1392-2325C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147952991 | ||||||
| chr4:147953034
|
T | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0095 | 3 | HG02055.hp2 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1392-2282T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147953034 | ||||||
| chr4:147953065
|
G | A | 4 | a0001c0006t0001g0040a0001c0006t0001g0042a0001c0006t0001g0071others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1392-2251G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147953065 | ||||||
| chr4:147953200
|
A | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(51): Show | 54 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.1392-2116A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147953200 | ||||||
| chr4:147953639
|
CTCTTT | C | 54 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(51): Show | 54 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.1392-1675_1392-167 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147953639 | |||||
| chr4:147953698
|
A | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1392-1618A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147953698 | ||||||
| chr4:147954151
|
A | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(63): Show | 66 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1392-1165A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147954151 | ||||||
| chr4:147954278
|
G | A | 1 | a0001c0002t0001g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1392-1038G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147954278 | ||||||
| chr4:147954290
|
T | G | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1392-1026T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147954290 | ||||||
| chr4:147954371
|
C | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1392-945C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147954371 | ||||||
| chr4:147954514
|
AT | A | 4 | a0001c0006t0001g0040a0001c0006t0001g0042a0001c0006t0001g0071others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1392-792delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 147954514 | |||||
| chr4:147954942
|
A | G | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1392-374A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147954942 | ||||||
| chr4:147955068
|
T | C | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1392-248T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147955068 | ||||||
| chr4:147955217
|
TTAAG | T | 2 | a0001c0002t0001g0090a0001c0004t0001g0105 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1392-98_1392-95del others(4): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | 147955217 | ||||||
| chr4:147955394
|
A | G | 3 | a0001c0008t0001g0059a0001c0008t0001g0060a0001c0009t0001g0008 | 3 | HG03098.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1450+20A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147955394 | ||||||
| chr4:147955544
|
G | A | 1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1450+170G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147955544 | ||||||
| chr4:147955618
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1450+244A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147955618 | ||||||
| chr4:147955708
|
A | G | 6 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0002t0001g0072others(3): Show | 6 | HG02886.hp2 HG03098.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1450+334A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147955708 | ||||||
| chr4:147955797
|
A | G | 1 | a0001c0009t0001g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1450+423A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147955797 | ||||||
| chr4:147955828
|
A | G | 14 | a0001c0001t0001g0022a0001c0001t0001g0050a0001c0001t0001g0052others(11): Show | 14 | HG01261.hp1 HG01891.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.1450+454A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147955828 | ||||||
| chr4:147956349
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1450+975C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147956349 | ||||||
| chr4:147956737
|
GT | G | 5 | a0001c0002t0001g0033a0001c0006t0001g0040a0001c0006t0001g0042others(2): Show | 5 | HG02258.hp2 HG02922.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1450+1374delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr4 | 147956737 | |||||
| chr4:147956750
|
CT | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.1450+1387delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr4 | 147956750 | |||||
| chr4:147956840
|
A | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(4): Show | 7 | HG01993.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1450+1466A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147956840 | ||||||
| chr4:147956856
|
C | T | 1 | a0001c0002t0001g0029 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1450+1482C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147956856 | ||||||
| chr4:147956863
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1450+1489T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147956863 | ||||||
| chr4:147957040
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0030others(22): Show | 25 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1450+1666G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147957040 | ||||||
| chr4:147957182
|
A | T | 1 | a0001c0005t0001g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1450+1808A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147957182 | ||||||
| chr4:147957199
|
G | A | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1450+1825G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147957199 | ||||||
| chr4:147957671
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0095 | 3 | HG02055.hp2 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1450+2297A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147957671 | ||||||
| chr4:147958301
|
G | T | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1450+2927G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147958301 | ||||||
| chr4:147958358
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1450+2984G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147958358 | ||||||
| chr4:147958383
|
TC | T | 11 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0061others(8): Show | 11 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1450+3011delC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr4 | 147958383 | |||||
| chr4:147958432
|
T | C | 11 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0061others(8): Show | 11 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1450+3058T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147958432 | ||||||
| chr4:147958531
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1450+3157G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147958531 | ||||||
| chr4:147958649
|
T | C | 2 | a0001c0002t0001g0090a0001c0004t0001g0105 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1450+3275T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147958649 | ||||||
| chr4:147959198
|
G | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.1450+3824G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147959198 | ||||||
| chr4:147959241
|
T | G | 14 | a0001c0001t0001g0022a0001c0001t0001g0050a0001c0001t0001g0052others(11): Show | 14 | HG01261.hp1 HG01891.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.1450+3867T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147959241 | ||||||
| chr4:147959516
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1450+4142G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147959516 | ||||||
| chr4:147959523
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(48): Show | 51 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.1450+4149C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147959523 | ||||||
| chr4:147959697
|
G | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0050a0001c0001t0001g0052others(11): Show | 14 | HG01261.hp1 HG01891.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.1450+4323G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147959697 | ||||||
| chr4:147959726
|
C | G | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(1): Show | 4 | HG02056.hp2 HG02080.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450+4352C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147959726 | ||||||
| chr4:147959747
|
A | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(48): Show | 51 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.1450+4373A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147959747 | ||||||
| chr4:147960196
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1450+4822T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147960196 | ||||||
| chr4:147961086
|
G | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0030others(20): Show | 23 | HG01167.hp1 HG01169.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.1451-3938G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147961086 | ||||||
| chr4:147961296
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(1): Show | 4 | HG02056.hp2 HG02080.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1451-3728G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147961296 | ||||||
| chr4:147961359
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1451-3665C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147961359 | ||||||
| chr4:147961861
|
T | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(51): Show | 54 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(51): Show |
intron_variant | MODIFIER | c.1451-3163T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147961861 | ||||||
| chr4:147961867
|
C | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0097a0001c0005t0001g0098 | 3 | HG02145.hp1 HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1451-3157C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147961867 | ||||||
| chr4:147961999
|
G | A | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1451-3025G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147961999 | ||||||
| chr4:147962037
|
A | T | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1451-2987A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147962037 | ||||||
| chr4:147962298
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0063 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1451-2726C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147962298 | ||||||
| chr4:147962321
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1451-2703A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147962321 | ||||||
| chr4:147962331
|
A | G | 2 | a0001c0002t0001g0090a0001c0004t0001g0105 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1451-2693A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147962331 | ||||||
| chr4:147962443
|
G | C | 1 | a0001c0001t0001g0015 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1451-2581G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147962443 | ||||||
| chr4:147962765
|
G | T | 1 | a0001c0001t0001g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1451-2259G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147962765 | ||||||
| chr4:147962791
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1451-2233G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147962791 | ||||||
| chr4:147962821
|
A | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0006t0001g0040others(3): Show | 6 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1451-2203A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147962821 | ||||||
| chr4:147962936
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(40): Show | 43 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.1451-2088T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147962936 | ||||||
| chr4:147963032
|
C | G | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1451-1992C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147963032 | ||||||
| chr4:147963038
|
C | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0030others(21): Show | 24 | HG01167.hp1 HG01169.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1451-1986C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147963038 | ||||||
| chr4:147963332
|
C | T | 7 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0091others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1451-1692C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147963332 | ||||||
| chr4:147963844
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1451-1180C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147963844 | ||||||
| chr4:147964131
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1451-893A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147964131 | ||||||
| chr4:147964217
|
T | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1451-807T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147964217 | ||||||
| chr4:147964306
|
T | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0091others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1451-718T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147964306 | ||||||
| chr4:147964446
|
T | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0091others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1451-578T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147964446 | ||||||
| chr4:147964719
|
A | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(40): Show | 43 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.1451-305A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 16/22 | chr4 | 147964719 | ||||||
| chr4:147965218
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1556+89A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 17/22 | chr4 | 147965218 | ||||||
| chr4:147965520
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(26): Show | 29 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(26): Show |
intron_variant | MODIFIER | c.1556+391C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 17/22 | chr4 | 147965520 | ||||||
| chr4:147965544
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(40): Show | 43 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.1556+415C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 17/22 | chr4 | 147965544 | ||||||
| chr4:147965882
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(4): Show | 7 | HG01993.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1556+753G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 17/22 | chr4 | 147965882 | ||||||
| chr4:147965962
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1557-718T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 17/22 | chr4 | 147965962 | ||||||
| chr4:147966060
|
A | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(4): Show | 7 | HG01993.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1557-620A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 17/22 | chr4 | 147966060 | ||||||
| chr4:147966163
|
T | C | 18 | a0001c0001t0001g0022a0001c0001t0001g0050a0001c0001t0001g0052others(15): Show | 18 | HG01261.hp1 HG01891.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.1557-517T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 17/22 | chr4 | 147966163 | ||||||
| chr4:147966397
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1557-283T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 17/22 | chr4 | 147966397 | ||||||
| chr4:147966960
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(48): Show | 51 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(48): Show |
intron_variant | MODIFIER | c.1716+121G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147966960 | ||||||
| chr4:147967222
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1716+383A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147967222 | ||||||
| chr4:147967259
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1716+420G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147967259 | ||||||
| chr4:147967340
|
G | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0030others(34): Show | 37 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(34): Show |
intron_variant | MODIFIER | c.1716+501G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147967340 | ||||||
| chr4:147967513
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(51): Show | 54 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(51): Show |
intron_variant | MODIFIER | c.1716+674T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147967513 | ||||||
| chr4:147967533
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0086 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1716+694G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147967533 | ||||||
| chr4:147967686
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(6): Show | 9 | HG01993.hp1 HG02738.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1716+847A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147967686 | ||||||
| chr4:147967717
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0003g0087a0001c0002t0001g0090others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716+878A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147967717 | ||||||
| chr4:147967939
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1716+1100C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147967939 | ||||||
| chr4:147968182
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1716+1343G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147968182 | ||||||
| chr4:147968560
|
C | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0030others(34): Show | 37 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(34): Show |
intron_variant | MODIFIER | c.1716+1721C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147968560 | ||||||
| chr4:147968717
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(51): Show | 54 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(51): Show |
intron_variant | MODIFIER | c.1716+1878A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147968717 | ||||||
| chr4:147968729
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1716+1890T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147968729 | ||||||
| chr4:147968868
|
C | G | 3 | a0001c0001t0001g0047a0001c0001t0001g0097a0001c0005t0001g0098 | 3 | HG02145.hp1 HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1716+2029C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147968868 | ||||||
| chr4:147968919
|
C | T | 10 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0061others(7): Show | 10 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1716+2080C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147968919 | ||||||
| chr4:147969082
|
A | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+2243A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147969082 | ||||||
| chr4:147969324
|
C | CT | 4 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0055others(1): Show | 4 | HG02622.hp1 HG04184.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+2506dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147969324 | |||||
| chr4:147969324
|
CT | C | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0001t0001g0095others(1): Show | 4 | HG00558.hp2 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716+2506delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147969324 | |||||
| chr4:147969324
|
CTT | C | 18 | a0001c0001t0001g0022a0001c0001t0001g0050a0001c0001t0001g0052others(15): Show | 18 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1716+2505_1716+250 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147969324 | |||||
| chr4:147969345
|
T | G | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1716+2506T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147969345 | ||||||
| chr4:147969345
|
T | TTG | 24 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0036others(21): Show | 24 | HG01167.hp1 HG01169.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.1716+2506_1716+250 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147969345 | ||||||
| chr4:147969345
|
T | TTTTG | 8 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(5): Show | 8 | HG01993.hp1 HG02738.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1716+2506_1716+250 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147969345 | ||||||
| chr4:147969394
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 102 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(99): Show |
intron_variant | MODIFIER | c.1716+2555T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147969394 | ||||||
| chr4:147969780
|
G | A | 2 | a0001c0002t0001g0090a0001c0004t0001g0105 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1716+2941G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147969780 | ||||||
| chr4:147969791
|
A | C | 4 | a0001c0001t0001g0088a0001c0001t0003g0087a0001c0002t0001g0090others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716+2952A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147969791 | ||||||
| chr4:147969876
|
C | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0030others(34): Show | 37 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(34): Show |
intron_variant | MODIFIER | c.1716+3037C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147969876 | ||||||
| chr4:147970064
|
G | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1716+3225G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147970064 | ||||||
| chr4:147970220
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1716+3381C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147970220 | ||||||
| chr4:147970267
|
T | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0076others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716+3428T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147970267 | ||||||
| chr4:147970425
|
C | T | 2 | a0001c0002t0001g0090a0001c0004t0001g0105 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1716+3586C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147970425 | ||||||
| chr4:147970684
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1716+3845G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147970684 | ||||||
| chr4:147970742
|
G | A | 10 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0061others(7): Show | 10 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1716+3903G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147970742 | ||||||
| chr4:147970858
|
C | T | 6 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0002t0001g0072others(3): Show | 6 | HG02886.hp2 HG03098.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1716+4019C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147970858 | ||||||
| chr4:147970917
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(53): Show | 56 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(53): Show |
intron_variant | MODIFIER | c.1716+4078A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147970917 | ||||||
| chr4:147970927
|
A | G | 3 | a0001c0001t0001g0014a0001c0002t0001g0090a0001c0004t0001g0105 | 3 | HG01884.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1716+4088A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147970927 | ||||||
| chr4:147970941
|
G | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(37): Show | 40 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(37): Show |
intron_variant | MODIFIER | c.1716+4102G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147970941 | ||||||
| chr4:147971093
|
CA | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(33): Show | 36 | HG01169.hp1 HG01261.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.1716+4276delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147971093 | |||||
| chr4:147971093
|
CAA | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0034others(4): Show | 7 | HG01993.hp2 HG02056.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1716+4275_1716+427 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147971093 | |||||
| chr4:147971879
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+5040C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147971879 | ||||||
| chr4:147971954
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+5115G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147971954 | ||||||
| chr4:147972053
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1716+5214G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147972053 | ||||||
| chr4:147972177
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1716+5338C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147972177 | ||||||
| chr4:147972352
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(36): Show | 39 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(36): Show |
intron_variant | MODIFIER | c.1716+5513G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147972352 | ||||||
| chr4:147972361
|
T | C | 10 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0061others(7): Show | 10 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1716+5522T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147972361 | ||||||
| chr4:147972508
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1716+5669C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147972508 | ||||||
| chr4:147972634
|
A | G | 3 | a0001c0001t0001g0014a0001c0002t0001g0090a0001c0004t0001g0105 | 3 | HG01884.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1716+5795A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147972634 | ||||||
| chr4:147972652
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+5813G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147972652 | ||||||
| chr4:147972669
|
C | T | 34 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0030others(31): Show | 34 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(31): Show |
intron_variant | MODIFIER | c.1716+5830C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147972669 | ||||||
| chr4:147972698
|
A | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0089a0001c0001t0001g0094 | 3 | HG01243.hp2 HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1716+5859A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147972698 | ||||||
| chr4:147972759
|
C | CT | 8 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(5): Show | 8 | HG01993.hp1 HG02738.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1716+5932dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147972759 | |||||
| chr4:147972989
|
A | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0034others(23): Show | 26 | HG01167.hp1 HG01169.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.1716+6150A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147972989 | ||||||
| chr4:147972994
|
A | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0030others(33): Show | 36 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(33): Show |
intron_variant | MODIFIER | c.1716+6155A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147972994 | ||||||
| chr4:147973077
|
A | T | 10 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0061others(7): Show | 10 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1716+6238A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147973077 | ||||||
| chr4:147973123
|
C | T | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1716+6284C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147973123 | ||||||
| chr4:147973199
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1716+6360C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147973199 | ||||||
| chr4:147973402
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(36): Show | 39 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(36): Show |
intron_variant | MODIFIER | c.1716+6563G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147973402 | ||||||
| chr4:147973437
|
C | T | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1716+6598C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147973437 | ||||||
| chr4:147973757
|
T | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0030others(31): Show | 34 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(31): Show |
intron_variant | MODIFIER | c.1716+6918T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147973757 | ||||||
| chr4:147973816
|
C | G | 3 | a0001c0001t0001g0070a0001c0001t0001g0077a0002c0003t0001g0009 | 3 | HG00558.hp2 HG01169.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1716+6977C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147973816 | ||||||
| chr4:147974430
|
A | T | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1716+7591A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147974430 | ||||||
| chr4:147974432
|
A | T | 3 | a0001c0001t0001g0014a0001c0002t0001g0090a0001c0004t0001g0105 | 3 | HG01884.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1716+7593A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147974432 | ||||||
| chr4:147974557
|
A | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(36): Show | 39 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(36): Show |
intron_variant | MODIFIER | c.1716+7718A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147974557 | ||||||
| chr4:147974633
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+7794T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147974633 | ||||||
| chr4:147974663
|
G | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(5): Show | 8 | HG01993.hp1 HG02738.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1716+7824G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147974663 | ||||||
| chr4:147974705
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1716+7866T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147974705 | ||||||
| chr4:147974812
|
C | A | 3 | a0001c0001t0001g0014a0001c0002t0001g0090a0001c0004t0001g0105 | 3 | HG01884.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1716+7973C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147974812 | ||||||
| chr4:147974825
|
A | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1716+7986A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147974825 | ||||||
| chr4:147974873
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1716+8034G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147974873 | ||||||
| chr4:147975223
|
A | T | 1 | a0001c0001t0001g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1716+8384A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147975223 | ||||||
| chr4:147975464
|
A | C | 1 | a0001c0002t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1716+8625A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147975464 | ||||||
| chr4:147975764
|
A | T | 1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1716+8925A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147975764 | ||||||
| chr4:147975879
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(53): Show | 56 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(53): Show |
intron_variant | MODIFIER | c.1716+9040C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147975879 | ||||||
| chr4:147976202
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1716+9363C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147976202 | ||||||
| chr4:147976247
|
C | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0065others(1): Show | 4 | HG02895.hp2 HG02896.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+9408C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147976247 | ||||||
| chr4:147976455
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1716+9616A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147976455 | ||||||
| chr4:147976541
|
G | GT | 34 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0034others(31): Show | 34 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(31): Show |
intron_variant | MODIFIER | c.1716+9717dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147976541 | |||||
| chr4:147976541
|
GT | G | 18 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(15): Show | 18 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1716+9717delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147976541 | |||||
| chr4:147976569
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1716+9730A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147976569 | ||||||
| chr4:147976730
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1716+9891A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147976730 | ||||||
| chr4:147976920
|
A | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0034others(31): Show | 34 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(31): Show |
intron_variant | MODIFIER | c.1716+10081A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147976920 | ||||||
| chr4:147977097
|
G | C | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1716+10258G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147977097 | ||||||
| chr4:147977237
|
A | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(53): Show | 56 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(53): Show |
intron_variant | MODIFIER | c.1716+10398A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147977237 | ||||||
| chr4:147977243
|
C | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(16): Show | 19 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1716+10404C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147977243 | ||||||
| chr4:147977307
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1716+10468C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147977307 | ||||||
| chr4:147977593
|
A | G | 7 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1716+10754A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147977593 | ||||||
| chr4:147977719
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(78): Show | 81 | HG00558.hp2 HG01071.hp2 HG01167.hp1 others(78): Show |
intron_variant | MODIFIER | c.1716+10880A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147977719 | ||||||
| chr4:147977931
|
A | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(64): Show | 67 | HG00558.hp2 HG01071.hp2 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.1716+11092A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147977931 | ||||||
| chr4:147978856
|
G | A | 4 | a0001c0006t0001g0040a0001c0006t0001g0042a0001c0006t0001g0071others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+12017G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147978856 | ||||||
| chr4:147978960
|
T | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(27): Show | 30 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1716+12121T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147978960 | ||||||
| chr4:147979653
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1716+12814T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147979653 | ||||||
| chr4:147979840
|
G | A | 19 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(16): Show | 19 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1716+13001G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147979840 | ||||||
| chr4:147979893
|
C | T | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1716+13054C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147979893 | ||||||
| chr4:147980042
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1716+13203G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147980042 | ||||||
| chr4:147980216
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(6): Show | 9 | HG01993.hp1 HG02738.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1716+13377T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147980216 | ||||||
| chr4:147980393
|
G | C | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1716+13554G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147980393 | ||||||
| chr4:147981205
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(8): Show | 11 | HG01993.hp1 HG02109.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1716+14366C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147981205 | ||||||
| chr4:147981313
|
C | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(6): Show | 9 | HG01993.hp1 HG02738.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1716+14474C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147981313 | ||||||
| chr4:147981415
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(8): Show | 11 | HG01993.hp1 HG02109.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1716+14576G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147981415 | ||||||
| chr4:147981754
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1716+14915C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147981754 | ||||||
| chr4:147981821
|
C | CT | 24 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(21): Show | 24 | HG01167.hp1 HG01169.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1716+14990dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147981821 | |||||
| chr4:147981944
|
CAGGGGCG others(3): Show |
C | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+15106_1716+15 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147981944 | ||||||
| chr4:147982052
|
C | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(16): Show | 19 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1716+15213C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147982052 | ||||||
| chr4:147982116
|
C | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(8): Show | 11 | HG01993.hp1 HG02109.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1716+15277C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147982116 | ||||||
| chr4:147982237
|
G | T | 22 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(19): Show | 22 | HG00558.hp2 HG01071.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1716+15398G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147982237 | ||||||
| chr4:147982260
|
A | C | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1716+15421A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147982260 | ||||||
| chr4:147982317
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1716+15478G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147982317 | ||||||
| chr4:147982351
|
T | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(8): Show | 11 | HG01993.hp1 HG02109.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1716+15512T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147982351 | ||||||
| chr4:147982365
|
C | CT | 14 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0050others(11): Show | 14 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1716+15542dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147982365 | |||||
| chr4:147982365
|
CT | C | 45 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0018others(42): Show | 45 | HG01071.hp2 HG01167.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.1716+15542delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147982365 | |||||
| chr4:147982369
|
T | C | 2 | a0001c0001t0001g0094a0001c0004t0001g0045 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1716+15530T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147982369 | ||||||
| chr4:147982546
|
C | CT | 23 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(20): Show | 23 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1716+15732dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147982546 | |||||
| chr4:147982546
|
C | CTT | 11 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0057others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1716+15731_1716+15 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147982546 | |||||
| chr4:147982546
|
C | CTTTT | 18 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(15): Show | 18 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1716+15729_1716+15 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147982546 | |||||
| chr4:147982546
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+15707C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147982546 | ||||||
| chr4:147982891
|
C | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(16): Show | 19 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1716+16052C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147982891 | ||||||
| chr4:147983124
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1716+16285C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147983124 | ||||||
| chr4:147983183
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1716+16344C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147983183 | ||||||
| chr4:147983187
|
G | GT | 23 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(20): Show | 23 | HG00558.hp2 HG01071.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1716+16364dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147983187 | |||||
| chr4:147983187
|
GT | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(16): Show | 19 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1716+16364delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147983187 | |||||
| chr4:147983193
|
T | TG | 11 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(8): Show | 11 | HG01993.hp1 HG02109.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1716+16354_1716+16 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147983193 | ||||||
| chr4:147983368
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1716+16529G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147983368 | ||||||
| chr4:147983394
|
C | A | 1 | a0001c0002t0001g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1716+16555C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147983394 | ||||||
| chr4:147983503
|
C | CT | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(26): Show | 29 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1716+16677dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147983503 | |||||
| chr4:147983607
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1716+16768A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147983607 | ||||||
| chr4:147983691
|
G | T | 1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1716+16852G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147983691 | ||||||
| chr4:147983767
|
A | G | 1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1716+16928A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147983767 | ||||||
| chr4:147983805
|
T | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0041others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1716+16966T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147983805 | ||||||
| chr4:147983980
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1716+17141T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147983980 | ||||||
| chr4:147984203
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1716+17364G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147984203 | ||||||
| chr4:147984337
|
C | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(27): Show | 30 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1716+17498C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147984337 | ||||||
| chr4:147984637
|
C | T | 1 | a0001c0005t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1716+17798C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147984637 | ||||||
| chr4:147984733
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1716+17894A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147984733 | ||||||
| chr4:147984772
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(1): Show | 4 | HG02056.hp2 HG02080.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716+17933C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147984772 | ||||||
| chr4:147984796
|
A | C | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1716+17957A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147984796 | ||||||
| chr4:147984869
|
C | T | 4 | a0001c0001t0001g0083a0002c0003t0001g0096a0003c0007t0001g0079others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+18030C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147984869 | ||||||
| chr4:147984941
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(8): Show | 11 | HG01993.hp1 HG02109.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1716+18102C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147984941 | ||||||
| chr4:147985055
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+18216A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147985055 | ||||||
| chr4:147985089
|
G | GGT | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+18250_1716+18 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147985089 | ||||||
| chr4:147985122
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1716+18283G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147985122 | ||||||
| chr4:147985178
|
G | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0052others(8): Show | 11 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1716+18339G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147985178 | ||||||
| chr4:147985281
|
G | C | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1716+18442G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147985281 | ||||||
| chr4:147985302
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(8): Show | 11 | HG01993.hp1 HG02109.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1716+18463A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147985302 | ||||||
| chr4:147985478
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1716+18639A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147985478 | ||||||
| chr4:147985511
|
GA | G | 3 | a0001c0006t0001g0040a0001c0006t0001g0042a0004c0010t0001g0048 | 3 | HG02258.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1716+18673delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147985511 | ||||||
| chr4:147985882
|
G | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0052others(8): Show | 11 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1716+19043G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147985882 | ||||||
| chr4:147985930
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1716+19091C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147985930 | ||||||
| chr4:147985963
|
TCTC | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0037others(11): Show | 14 | HG01884.hp2 HG01993.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1716+19128_1716+19 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147985963 | |||||
| chr4:147986194
|
A | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1716+19355A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147986194 | ||||||
| chr4:147986462
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0052others(8): Show | 11 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1716+19623C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147986462 | ||||||
| chr4:147986524
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1716+19685C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147986524 | ||||||
| chr4:147986531
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1716+19692C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147986531 | ||||||
| chr4:147986600
|
A | G | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1716+19761A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147986600 | ||||||
| chr4:147986738
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1716+19899G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147986738 | ||||||
| chr4:147986759
|
G | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(6): Show | 9 | HG01993.hp1 HG02738.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1716+19920G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147986759 | ||||||
| chr4:147987050
|
G | A | 2 | a0001c0001t0001g0006a0001c0005t0001g0003 | 2 | HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1716+20211G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147987050 | ||||||
| chr4:147987220
|
A | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1716+20381A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147987220 | ||||||
| chr4:147987274
|
A | G | 17 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(14): Show | 17 | HG02056.hp2 HG02080.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1716+20435A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147987274 | ||||||
| chr4:147987428
|
C | A | 3 | a0001c0001t0001g0014a0001c0002t0001g0090a0001c0004t0001g0105 | 3 | HG01884.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1716+20589C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147987428 | ||||||
| chr4:147987570
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1716+20731G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147987570 | ||||||
| chr4:147988007
|
G | A | 1 | a0001c0005t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1716+21168G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147988007 | ||||||
| chr4:147988167
|
CGT | C | 24 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(21): Show | 24 | HG01167.hp1 HG01169.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1716+21335_1716+21 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147988167 | |||||
| chr4:147988172
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+21333G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147988172 | ||||||
| chr4:147988172
|
G | T | 3 | a0001c0006t0001g0040a0001c0006t0001g0042a0004c0010t0001g0048 | 3 | HG02258.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1716+21333G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147988172 | ||||||
| chr4:147988271
|
T | C | 3 | a0001c0001t0001g0014a0001c0002t0001g0090a0001c0004t0001g0105 | 3 | HG01884.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1716+21432T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147988271 | ||||||
| chr4:147988353
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1716+21514A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147988353 | ||||||
| chr4:147988355
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(8): Show | 11 | HG01993.hp1 HG02109.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1716+21516A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147988355 | ||||||
| chr4:147988434
|
G | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0050others(13): Show | 16 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1716+21595G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147988434 | ||||||
| chr4:147988437
|
C | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(76): Show | 79 | HG00558.hp2 HG01071.hp2 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.1716+21598C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147988437 | ||||||
| chr4:147988512
|
T | A | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1716+21673T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147988512 | ||||||
| chr4:147988760
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+21921C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147988760 | ||||||
| chr4:147988991
|
C | T | 3 | a0001c0008t0001g0059a0001c0008t0001g0060a0001c0009t0001g0008 | 3 | HG03098.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1716+22152C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147988991 | ||||||
| chr4:147989081
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1716+22242A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989081 | ||||||
| chr4:147989182
|
C | G | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+22343C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989182 | ||||||
| chr4:147989210
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1716+22371G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989210 | ||||||
| chr4:147989274
|
C | T | 3 | a0001c0001t0001g0014a0001c0002t0001g0090a0001c0004t0001g0105 | 3 | HG01884.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1716+22435C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989274 | ||||||
| chr4:147989382
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1716+22543C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989382 | ||||||
| chr4:147989405
|
C | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0088others(5): Show | 8 | HG01884.hp1 HG01993.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1716+22566C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989405 | ||||||
| chr4:147989437
|
C | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(28): Show | 31 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1716+22598C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989437 | ||||||
| chr4:147989439
|
G | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(27): Show | 30 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1716+22600G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989439 | ||||||
| chr4:147989581
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+22742C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989581 | ||||||
| chr4:147989583
|
A | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0054 | 2 | NA19064.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1716+22744A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989583 | ||||||
| chr4:147989604
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1716+22765G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989604 | ||||||
| chr4:147989737
|
C | A | 1 | a0001c0006t0001g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1716+22898C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989737 | ||||||
| chr4:147989808
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1716+22969G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989808 | ||||||
| chr4:147989949
|
G | T | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1716+23110G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147989949 | ||||||
| chr4:147990119
|
G | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(25): Show | 28 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1716+23280G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147990119 | ||||||
| chr4:147990174
|
A | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+23335A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147990174 | ||||||
| chr4:147990333
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0052others(8): Show | 11 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1716+23494G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147990333 | ||||||
| chr4:147990427
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0015 | 2 | NA18612.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1716+23588A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147990427 | ||||||
| chr4:147990820
|
C | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(26): Show | 29 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1716+23981C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147990820 | ||||||
| chr4:147990869
|
G | A | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1716+24030G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147990869 | ||||||
| chr4:147990880
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(6): Show | 9 | HG01993.hp1 HG02738.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1716+24041G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147990880 | ||||||
| chr4:147991145
|
T | TA | 9 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(6): Show | 9 | HG01993.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1716+24321dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147991145 | |||||
| chr4:147991145
|
T | TAA | 4 | a0001c0001t0001g0014a0001c0001t0001g0057a0001c0002t0001g0090others(1): Show | 4 | HG01884.hp2 HG02572.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+24320_1716+24 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147991145 | |||||
| chr4:147991157
|
A | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+24318A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991157 | ||||||
| chr4:147991160
|
AT | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0094a0002c0003t0001g0073 | 3 | HG02280.hp2 HG02615.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1716+24322delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991160 | ||||||
| chr4:147991161
|
T | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(21): Show | 24 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1716+24322T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991161 | ||||||
| chr4:147991165
|
T | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(24): Show | 27 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1716+24326T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991165 | ||||||
| chr4:147991218
|
GT | G | 2 | a0001c0001t0001g0049a0001c0002t0001g0005 | 2 | HG02895.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1716+24380delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991218 | ||||||
| chr4:147991398
|
G | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(21): Show | 24 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1716+24559G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991398 | ||||||
| chr4:147991447
|
C | T | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1716+24608C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991447 | ||||||
| chr4:147991508
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1716+24669A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991508 | ||||||
| chr4:147991551
|
C | A | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1716+24712C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991551 | ||||||
| chr4:147991567
|
T | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(21): Show | 24 | HG01261.hp1 HG01891.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.1716+24728T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991567 | ||||||
| chr4:147991618
|
A | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0052others(8): Show | 11 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1716+24779A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991618 | ||||||
| chr4:147991682
|
G | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(24): Show | 27 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1716+24843G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991682 | ||||||
| chr4:147991752
|
G | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+24913G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991752 | ||||||
| chr4:147991911
|
C | G | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1716+25072C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991911 | ||||||
| chr4:147991988
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1716+25149A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147991988 | ||||||
| chr4:147992000
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1716+25161A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147992000 | ||||||
| chr4:147992261
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1716+25422C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147992261 | ||||||
| chr4:147992429
|
G | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(24): Show | 27 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.1716+25590G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147992429 | ||||||
| chr4:147992444
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(23): Show | 26 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1716+25605G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147992444 | ||||||
| chr4:147992526
|
C | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1716+25687C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147992526 | ||||||
| chr4:147992563
|
C | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0003g0087others(2): Show | 5 | HG01884.hp1 HG01993.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1716+25724C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147992563 | ||||||
| chr4:147992587
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1716+25748A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147992587 | ||||||
| chr4:147992705
|
C | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(24): Show | 27 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.1716+25866C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147992705 | ||||||
| chr4:147993206
|
C | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(24): Show | 27 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.1716+26367C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147993206 | ||||||
| chr4:147993423
|
G | C | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1716+26584G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147993423 | ||||||
| chr4:147993921
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+27082C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147993921 | ||||||
| chr4:147993952
|
A | G | 22 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(19): Show | 22 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1716+27113A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147993952 | ||||||
| chr4:147994392
|
T | TG | 6 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1716+27555dupG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147994392 | |||||
| chr4:147994593
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0003g0087others(2): Show | 5 | HG01884.hp1 HG01993.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1716+27754A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147994593 | ||||||
| chr4:147994841
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1716+28002C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147994841 | ||||||
| chr4:147995032
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0052others(9): Show | 12 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1716+28193A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995032 | ||||||
| chr4:147995134
|
C | A | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1717-28129C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995134 | ||||||
| chr4:147995225
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1717-28038T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995225 | ||||||
| chr4:147995286
|
G | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-27977G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995286 | ||||||
| chr4:147995433
|
G | A | 17 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0034others(14): Show | 17 | HG02056.hp2 HG02080.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1717-27830G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995433 | ||||||
| chr4:147995488
|
C | T | 2 | a0001c0005t0001g0074a0001c0005t0001g0098 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1717-27775C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995488 | ||||||
| chr4:147995489
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1717-27774G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995489 | ||||||
| chr4:147995497
|
T | A | 1 | a0001c0009t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1717-27766T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995497 | ||||||
| chr4:147995651
|
G | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(6): Show | 9 | HG01993.hp1 HG02738.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1717-27612G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995651 | ||||||
| chr4:147995795
|
C | T | 20 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0034others(17): Show | 20 | HG02056.hp2 HG02080.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1717-27468C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995795 | ||||||
| chr4:147995796
|
G | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-27467G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995796 | ||||||
| chr4:147995800
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0077 | 2 | HG00558.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1717-27463T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995800 | ||||||
| chr4:147995817
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1717-27446C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147995817 | ||||||
| chr4:147996080
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1717-27183A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147996080 | ||||||
| chr4:147996107
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0086 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1717-27156G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147996107 | ||||||
| chr4:147996109
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-27154A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147996109 | ||||||
| chr4:147996158
|
C | T | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1717-27105C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147996158 | ||||||
| chr4:147996213
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-27050A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147996213 | ||||||
| chr4:147996282
|
C | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-26981C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147996282 | ||||||
| chr4:147996283
|
G | A | 3 | a0001c0008t0001g0059a0001c0008t0001g0060a0001c0009t0001g0008 | 3 | HG03098.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1717-26980G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147996283 | ||||||
| chr4:147996339
|
A | G | 18 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0050others(15): Show | 18 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.1717-26924A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147996339 | ||||||
| chr4:147996576
|
C | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0003g0087others(2): Show | 5 | HG01884.hp1 HG01993.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1717-26687C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147996576 | ||||||
| chr4:147996747
|
G | T | 2 | a0001c0005t0001g0074a0001c0005t0001g0098 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1717-26516G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147996747 | ||||||
| chr4:147997265
|
A | G | 1 | a0001c0001t0002g0023 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1717-25998A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147997265 | ||||||
| chr4:147997741
|
G | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0053others(5): Show | 8 | HG01993.hp1 HG02738.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1717-25522G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147997741 | ||||||
| chr4:147997876
|
A | T | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1717-25387A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147997876 | ||||||
| chr4:147998208
|
T | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0053others(5): Show | 8 | HG01993.hp1 HG02738.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1717-25055T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147998208 | ||||||
| chr4:147998595
|
G | C | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1717-24668G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147998595 | ||||||
| chr4:147998693
|
G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(10): Show | 13 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1717-24570G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147998693 | ||||||
| chr4:147998766
|
C | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1717-24497C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147998766 | ||||||
| chr4:147998778
|
C | T | 2 | a0001c0001t0001g0006a0001c0005t0001g0003 | 2 | HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1717-24485C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147998778 | ||||||
| chr4:147998826
|
T | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0053others(5): Show | 8 | HG01993.hp1 HG02738.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1717-24437T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147998826 | ||||||
| chr4:147998938
|
G | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-24325G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147998938 | ||||||
| chr4:147999007
|
T | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-24256T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147999007 | ||||||
| chr4:147999027
|
C | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0086 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1717-24236C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147999027 | ||||||
| chr4:147999195
|
A | C | 1 | a0001c0001t0002g0023 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1717-24068A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147999195 | ||||||
| chr4:147999217
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1717-24046G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147999217 | ||||||
| chr4:147999468
|
C | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0089others(1): Show | 4 | HG01243.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-23795C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147999468 | ||||||
| chr4:147999469
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(78): Show | 81 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.1717-23794A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147999469 | ||||||
| chr4:147999532
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1717-23731G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147999532 | ||||||
| chr4:147999611
|
C | A | 2 | a0001c0005t0001g0074a0001c0005t0001g0098 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1717-23652C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147999611 | ||||||
| chr4:147999857
|
C | T | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1717-23406C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147999857 | ||||||
| chr4:147999926
|
GT | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(31): Show | 34 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.1717-23322delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 147999926 | |||||
| chr4:147999941
|
T | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0044a0001c0001t0001g0051others(2): Show | 5 | HG02055.hp2 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1717-23322T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147999941 | ||||||
| chr4:147999972
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(74): Show | 77 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.1717-23291A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 147999972 | ||||||
| chr4:148000033
|
G | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-23230G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148000033 | ||||||
| chr4:148000109
|
T | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(10): Show | 13 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1717-23154T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148000109 | ||||||
| chr4:148000208
|
G | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-23055G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148000208 | ||||||
| chr4:148000215
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-23048A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148000215 | ||||||
| chr4:148000415
|
A | T | 3 | a0001c0001t0001g0022a0001c0002t0001g0033a0002c0003t0001g0073 | 3 | HG01993.hp2 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1717-22848A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148000415 | ||||||
| chr4:148000707
|
T | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1717-22556T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148000707 | ||||||
| chr4:148000727
|
T | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0065 | 2 | HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1717-22536T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148000727 | ||||||
| chr4:148000754
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1717-22509G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148000754 | ||||||
| chr4:148000757
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0104 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1717-22506C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148000757 | ||||||
| chr4:148000766
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1717-22497A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148000766 | ||||||
| chr4:148000953
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1717-22310G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148000953 | ||||||
| chr4:148001009
|
T | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1717-22254T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001009 | ||||||
| chr4:148001192
|
T | G | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1717-22071T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001192 | ||||||
| chr4:148001218
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(73): Show | 76 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(73): Show |
intron_variant | MODIFIER | c.1717-22045C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001218 | ||||||
| chr4:148001294
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1717-21969C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001294 | ||||||
| chr4:148001395
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1717-21868G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001395 | ||||||
| chr4:148001444
|
T | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-21819T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001444 | ||||||
| chr4:148001522
|
G | A | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1717-21741G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001522 | ||||||
| chr4:148001539
|
T | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(10): Show | 13 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1717-21724T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001539 | ||||||
| chr4:148001547
|
T | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(10): Show | 13 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1717-21716T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001547 | ||||||
| chr4:148001599
|
C | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-21664C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001599 | ||||||
| chr4:148001648
|
T | TC | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(74): Show | 77 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.1717-21614dupC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148001648 | |||||
| chr4:148001696
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1717-21567A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001696 | ||||||
| chr4:148001793
|
C | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0062a0001c0001t0001g0097others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-21470C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001793 | ||||||
| chr4:148001913
|
C | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.1717-21350C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148001913 | ||||||
| chr4:148002387
|
C | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(31): Show | 34 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.1717-20876C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148002387 | ||||||
| chr4:148002419
|
T | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-20844T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148002419 | ||||||
| chr4:148002518
|
A | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0049others(16): Show | 19 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1717-20745A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148002518 | ||||||
| chr4:148002563
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1717-20700G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148002563 | ||||||
| chr4:148002625
|
TC | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0086 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1717-20636delC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148002625 | |||||
| chr4:148002648
|
GT | G | 2 | a0001c0005t0001g0074a0001c0005t0001g0098 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1717-20614delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148002648 | ||||||
| chr4:148002683
|
T | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(24): Show | 27 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.1717-20580T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148002683 | ||||||
| chr4:148002763
|
T | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-20500T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148002763 | ||||||
| chr4:148002809
|
T | A | 1 | a0001c0001t0001g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1717-20454T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148002809 | ||||||
| chr4:148002828
|
T | C | 1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1717-20435T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148002828 | ||||||
| chr4:148002918
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-20345A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148002918 | ||||||
| chr4:148003023
|
A | T | 24 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(21): Show | 24 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1717-20240A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148003023 | ||||||
| chr4:148003110
|
C | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-20153C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148003110 | ||||||
| chr4:148003219
|
T | G | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1717-20044T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148003219 | ||||||
| chr4:148003393
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1717-19870C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148003393 | ||||||
| chr4:148003442
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(74): Show | 77 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.1717-19821G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148003442 | ||||||
| chr4:148003453
|
T | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-19810T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148003453 | ||||||
| chr4:148003614
|
T | G | 2 | a0001c0005t0001g0074a0001c0005t0001g0098 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1717-19649T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148003614 | ||||||
| chr4:148003893
|
T | TCTAAGCC others(123): Show |
2 | a0001c0001t0001g0061a0001c0001t0001g0063 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1717-19370_1717-19 others(136): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148003893 | ||||||
| chr4:148003893
|
T | TCTAAGCC others(123): Show |
30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.1717-19370_1717-19 others(136): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148003893 | ||||||
| chr4:148003894
|
G | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-19369G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148003894 | ||||||
| chr4:148003947
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1717-19316A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148003947 | ||||||
| chr4:148003954
|
G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0050others(10): Show | 13 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1717-19309G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148003954 | ||||||
| chr4:148004137
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1717-19126G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148004137 | ||||||
| chr4:148004205
|
A | T | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1717-19058A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148004205 | ||||||
| chr4:148004206
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1717-19057C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148004206 | ||||||
| chr4:148004212
|
C | T | 1 | a0001c0002t0001g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1717-19051C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148004212 | ||||||
| chr4:148004365
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1717-18898T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148004365 | ||||||
| chr4:148004529
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-18734A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148004529 | ||||||
| chr4:148004638
|
G | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(73): Show | 76 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(73): Show |
intron_variant | MODIFIER | c.1717-18625G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148004638 | ||||||
| chr4:148004664
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1717-18599G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148004664 | ||||||
| chr4:148004914
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1717-18349G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148004914 | ||||||
| chr4:148004932
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0077 | 2 | HG00558.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1717-18331C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148004932 | ||||||
| chr4:148004948
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1717-18315T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148004948 | ||||||
| chr4:148005054
|
A | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1717-18209A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148005054 | ||||||
| chr4:148005306
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-17957A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148005306 | ||||||
| chr4:148005323
|
G | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-17940G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148005323 | ||||||
| chr4:148005327
|
A | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-17936A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148005327 | ||||||
| chr4:148005435
|
A | G | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1717-17828A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148005435 | ||||||
| chr4:148005505
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0017 | 2 | HG01167.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1717-17758C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148005505 | ||||||
| chr4:148005671
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-17592A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148005671 | ||||||
| chr4:148005734
|
TTCTC | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0034others(4): Show | 7 | HG02056.hp2 HG02080.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1717-17527_1717-17 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148005734 | |||||
| chr4:148005929
|
C | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1717-17334C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148005929 | ||||||
| chr4:148005942
|
C | A | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1717-17321C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148005942 | ||||||
| chr4:148005958
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1717-17305A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148005958 | ||||||
| chr4:148006163
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0003g0087 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1717-17100A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148006163 | ||||||
| chr4:148006200
|
A | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0053others(5): Show | 8 | HG01993.hp1 HG02738.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1717-17063A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148006200 | ||||||
| chr4:148006337
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1717-16926C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148006337 | ||||||
| chr4:148006348
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0052others(9): Show | 12 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1717-16915C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148006348 | ||||||
| chr4:148006448
|
C | A | 3 | a0001c0001t0001g0014a0001c0005t0001g0074a0001c0005t0001g0098 | 3 | HG02615.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1717-16815C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148006448 | ||||||
| chr4:148006512
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1717-16751A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148006512 | ||||||
| chr4:148006640
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1717-16623A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148006640 | ||||||
| chr4:148006689
|
A | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(28): Show | 31 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.1717-16574A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148006689 | ||||||
| chr4:148006785
|
A | T | 2 | a0001c0005t0001g0074a0001c0005t0001g0098 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1717-16478A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148006785 | ||||||
| chr4:148006851
|
A | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(77): Show | 80 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.1717-16412A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148006851 | ||||||
| chr4:148006869
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1717-16394C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148006869 | ||||||
| chr4:148007026
|
T | C | 3 | a0001c0008t0001g0059a0001c0008t0001g0060a0001c0009t0001g0008 | 3 | HG03098.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1717-16237T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007026 | ||||||
| chr4:148007062
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(62): Show | 65 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.1717-16201G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007062 | ||||||
| chr4:148007221
|
G | A | 34 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0018others(31): Show | 34 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1717-16042G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007221 | ||||||
| chr4:148007241
|
T | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0015others(50): Show | 53 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.1717-16022T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007241 | ||||||
| chr4:148007322
|
G | C | 1 | a0002c0003t0001g0096 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1717-15941G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007322 | ||||||
| chr4:148007363
|
A | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0004t0001g0045 | 3 | HG02145.hp2 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1717-15900A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007363 | ||||||
| chr4:148007422
|
G | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0006t0001g0042 | 3 | HG02145.hp2 HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1717-15841G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007422 | ||||||
| chr4:148007535
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1717-15728G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007535 | ||||||
| chr4:148007568
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0070others(1): Show | 4 | HG00558.hp2 HG01993.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-15695G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007568 | ||||||
| chr4:148007650
|
A | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(72): Show | 75 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.1717-15613A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007650 | ||||||
| chr4:148007821
|
T | C | 4 | a0001c0001t0001g0047a0001c0001t0001g0081a0001c0001t0001g0097others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-15442T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007821 | ||||||
| chr4:148007847
|
T | G | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1717-15416T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007847 | ||||||
| chr4:148007888
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1717-15375C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007888 | ||||||
| chr4:148007889
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0051 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1717-15374G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007889 | ||||||
| chr4:148007902
|
G | A | 4 | a0001c0001t0001g0047a0001c0001t0001g0081a0001c0001t0001g0097others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-15361G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148007902 | ||||||
| chr4:148008371
|
A | G | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1717-14892A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148008371 | ||||||
| chr4:148008473
|
G | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1717-14790G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148008473 | ||||||
| chr4:148008518
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0051 | 3 | HG02109.hp2 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1717-14745G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148008518 | ||||||
| chr4:148008610
|
C | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(59): Show | 62 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.1717-14653C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148008610 | ||||||
| chr4:148008831
|
G | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0046others(6): Show | 9 | HG01243.hp2 HG02109.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1717-14432G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148008831 | ||||||
| chr4:148008849
|
A | G | 1 | a0001c0001t0001g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1717-14414A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148008849 | ||||||
| chr4:148008991
|
A | G | 8 | a0001c0001t0001g0014a0001c0001t0001g0067a0001c0001t0001g0068others(5): Show | 8 | HG01243.hp2 HG02886.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1717-14272A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148008991 | ||||||
| chr4:148009137
|
C | CT | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0062others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1717-14114dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148009137 | |||||
| chr4:148009167
|
T | G | 2 | a0001c0001t0001g0088a0001c0002t0001g0090 | 2 | HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1717-14096T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148009167 | ||||||
| chr4:148009339
|
C | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0024others(5): Show | 8 | HG02056.hp1 HG02165.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.1717-13924C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148009339 | ||||||
| chr4:148009418
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1717-13845C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148009418 | ||||||
| chr4:148009518
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1717-13745T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148009518 | ||||||
| chr4:148009629
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1717-13634A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148009629 | ||||||
| chr4:148009691
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(19): Show | 22 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1717-13572G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148009691 | ||||||
| chr4:148009964
|
T | C | 21 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(18): Show | 21 | HG00558.hp1 HG01071.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1717-13299T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148009964 | ||||||
| chr4:148010302
|
C | T | 1 | a0002c0003t0001g0009 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1717-12961C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148010302 | ||||||
| chr4:148010460
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1717-12803C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148010460 | ||||||
| chr4:148010708
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0043a0001c0001t0001g0106 | 3 | HG01993.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1717-12555G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148010708 | ||||||
| chr4:148010955
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1717-12308A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148010955 | ||||||
| chr4:148011169
|
A | G | 1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1717-12094A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148011169 | ||||||
| chr4:148011377
|
G | A | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1717-11886G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148011377 | ||||||
| chr4:148011692
|
G | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(40): Show | 43 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.1717-11571G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148011692 | ||||||
| chr4:148011791
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1717-11472A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148011791 | ||||||
| chr4:148012401
|
T | C | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1717-10862T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148012401 | ||||||
| chr4:148012585
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(23): Show | 26 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1717-10678G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148012585 | ||||||
| chr4:148012924
|
G | GT | 16 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104others(13): Show | 16 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1717-10323dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148012924 | |||||
| chr4:148012924
|
G | GTT | 9 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0049others(6): Show | 9 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1717-10324_1717-10 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148012924 | |||||
| chr4:148012924
|
G | GTTT | 16 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0052others(13): Show | 16 | HG00558.hp2 HG01169.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1717-10325_1717-10 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148012924 | |||||
| chr4:148013088
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1717-10175C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148013088 | ||||||
| chr4:148013505
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1717-9758G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148013505 | ||||||
| chr4:148013677
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0091others(2): Show | 5 | HG02109.hp1 HG02572.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1717-9586G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148013677 | ||||||
| chr4:148013858
|
ACT | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0062a0001c0001t0001g0083others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1717-9402_1717-940 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148013858 | |||||
| chr4:148014100
|
A | T | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1717-9163A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148014100 | ||||||
| chr4:148014496
|
C | T | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1717-8767C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148014496 | ||||||
| chr4:148014560
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1717-8703G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148014560 | ||||||
| chr4:148014746
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1717-8517A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148014746 | ||||||
| chr4:148014769
|
A | ACT | 26 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(23): Show | 26 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1717-8493_1717-849 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148014769 | |||||
| chr4:148015263
|
T | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(23): Show | 26 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1717-8000T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148015263 | ||||||
| chr4:148015300
|
A | G | 4 | a0001c0004t0001g0045a0001c0009t0001g0007a0001c0009t0001g0008others(1): Show | 4 | HG03225.hp2 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1717-7963A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148015300 | ||||||
| chr4:148015335
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(42): Show | 45 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.1717-7928T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148015335 | ||||||
| chr4:148015544
|
A | G | 1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1717-7719A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148015544 | ||||||
| chr4:148016079
|
C | T | 3 | a0001c0009t0001g0007a0001c0009t0001g0008a0004c0010t0001g0048 | 3 | HG03225.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1717-7184C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148016079 | ||||||
| chr4:148016280
|
G | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0041others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-6983G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148016280 | ||||||
| chr4:148016325
|
G | A | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1717-6938G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148016325 | ||||||
| chr4:148016386
|
C | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(23): Show | 26 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1717-6877C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148016386 | ||||||
| chr4:148016520
|
T | A | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1717-6743T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148016520 | ||||||
| chr4:148016541
|
G | GT | 5 | a0001c0001t0001g0014a0001c0001t0001g0080a0001c0001t0001g0089others(2): Show | 5 | HG01243.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1717-6715dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148016541 | |||||
| chr4:148016703
|
C | T | 2 | a0001c0001t0001g0091a0001c0004t0001g0105 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1717-6560C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148016703 | ||||||
| chr4:148016873
|
C | A | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1717-6390C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148016873 | ||||||
| chr4:148016983
|
T | TA | 7 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0053others(4): Show | 7 | HG02055.hp2 HG02056.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1717-6258dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148016983 | |||||
| chr4:148016983
|
TA | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0091a0001c0004t0001g0105others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-6258delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148016983 | |||||
| chr4:148017180
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(35): Show | 38 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.1717-6083T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148017180 | ||||||
| chr4:148017447
|
C | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(23): Show | 26 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1717-5816C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148017447 | ||||||
| chr4:148017652
|
C | CTA | 8 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0036others(5): Show | 8 | HG01070.hp2 HG01167.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1717-5581_1717-558 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017652 | |||||
| chr4:148017652
|
C | CTATA | 13 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0038others(10): Show | 13 | HG02056.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1717-5583_1717-558 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017652 | |||||
| chr4:148017652
|
C | CTATATA | 3 | a0001c0001t0001g0025a0001c0001t0001g0050a0002c0003t0001g0073 | 3 | HG00558.hp1 HG02976.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1717-5585_1717-558 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017652 | |||||
| chr4:148017652
|
C | CTATATAT others(1): Show |
3 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0002g0031 | 3 | HG02886.hp2 HG03195.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1717-5587_1717-558 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017652 | |||||
| chr4:148017652
|
C | CTATATAT others(3): Show |
2 | a0001c0001t0001g0018a0001c0004t0001g0105 | 2 | HG01261.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1717-5589_1717-558 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017652 | |||||
| chr4:148017652
|
C | CTATATAT others(5): Show |
2 | a0001c0001t0001g0022a0001c0002t0001g0033 | 2 | HG01993.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1717-5591_1717-558 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017652 | |||||
| chr4:148017652
|
C | CTATATAT others(11): Show |
1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1717-5597_1717-558 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017652 | |||||
| chr4:148017652
|
C | CTATATAT others(13): Show |
1 | a0001c0008t0001g0060 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1717-5599_1717-558 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017652 | |||||
| chr4:148017652
|
CTATA | C | 14 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0019others(11): Show | 14 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1717-5583_1717-558 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017652 | |||||
| chr4:148017652
|
CTATATAT others(9): Show |
C | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1717-5595_1717-558 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017652 | |||||
| chr4:148017652
|
CTATATAT others(11): Show |
C | 3 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104 | 3 | HG02896.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1717-5597_1717-558 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017652 | |||||
| chr4:148017678
|
A | G | 13 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0019others(10): Show | 13 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1717-5585A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148017678 | ||||||
| chr4:148017679
|
T | A | 13 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0019others(10): Show | 13 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1717-5584T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148017679 | ||||||
| chr4:148017680
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1717-5580_1717-557 others(34): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017680 | |||||
| chr4:148017680
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1717-5580_1717-557 others(30): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017680 | |||||
| chr4:148017680
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0051 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1717-5580_1717-557 others(28): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017680 | |||||
| chr4:148017680
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0006 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1717-5580_1717-557 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017680 | |||||
| chr4:148017680
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1717-5580_1717-557 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017680 | |||||
| chr4:148017680
|
A | ATATATAT others(7): Show |
3 | a0001c0001t0001g0049a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1717-5580_1717-557 others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017680 | |||||
| chr4:148017680
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1717-5580_1717-557 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017680 | |||||
| chr4:148017680
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1717-5580_1717-557 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017680 | |||||
| chr4:148017680
|
A | ATATATGA others(1): Show |
12 | a0001c0001t0001g0037a0001c0001t0001g0052a0001c0001t0001g0053others(9): Show | 12 | HG00558.hp2 HG01261.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1717-5580_1717-557 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017680 | |||||
| chr4:148017680
|
A | ATATGAG | 2 | a0001c0001t0001g0076a0001c0001t0001g0081 | 2 | HG02258.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1717-5579_1717-557 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017680 | |||||
| chr4:148017680
|
A | G | 14 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0019others(11): Show | 14 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1717-5583A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148017680 | ||||||
| chr4:148017682
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1717-5580_1717-557 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017682 | |||||
| chr4:148017682
|
A | ATG | 2 | a0001c0001t0001g0075a0001c0001t0001g0103 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1717-5573_1717-557 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148017682 | |||||
| chr4:148017682
|
A | G | 2 | a0001c0001t0001g0015a0002c0003t0001g0009 | 2 | HG01169.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1717-5581A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148017682 | ||||||
| chr4:148017684
|
G | A | 2 | a0001c0001t0001g0022a0001c0008t0001g0060 | 2 | HG01993.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1717-5579G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148017684 | ||||||
| chr4:148017729
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1717-5534T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148017729 | ||||||
| chr4:148017936
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1717-5327T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148017936 | ||||||
| chr4:148018320
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1717-4943A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148018320 | ||||||
| chr4:148018524
|
TC | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0095 | 2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1717-4738delC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148018524 | ||||||
| chr4:148018572
|
C | CA | 4 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0091others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1717-4676dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148018572 | |||||
| chr4:148018942
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(40): Show | 43 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.1717-4321T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148018942 | ||||||
| chr4:148019093
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1717-4170T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148019093 | ||||||
| chr4:148019392
|
C | T | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1717-3871C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148019392 | ||||||
| chr4:148019402
|
G | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0051others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1717-3861G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148019402 | ||||||
| chr4:148019418
|
T | C | 13 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0019others(10): Show | 13 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1717-3845T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148019418 | ||||||
| chr4:148019722
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1717-3541G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148019722 | ||||||
| chr4:148019830
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1717-3433A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148019830 | ||||||
| chr4:148020010
|
T | G | 1 | a0001c0001t0001g0015 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1717-3253T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148020010 | ||||||
| chr4:148020486
|
C | T | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1717-2777C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148020486 | ||||||
| chr4:148020539
|
G | GT | 24 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(21): Show | 24 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1717-2718dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | 148020539 | |||||
| chr4:148020545
|
TG | T | 9 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0019others(6): Show | 9 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1717-2717delG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148020545 | ||||||
| chr4:148020546
|
G | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(33): Show | 36 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.1717-2717G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148020546 | ||||||
| chr4:148020980
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1717-2283A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148020980 | ||||||
| chr4:148021762
|
G | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0062a0001c0001t0001g0083others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1717-1501G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148021762 | ||||||
| chr4:148021780
|
G | C | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1717-1483G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148021780 | ||||||
| chr4:148021884
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1717-1379T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148021884 | ||||||
| chr4:148022050
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(42): Show | 45 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.1717-1213A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148022050 | ||||||
| chr4:148022126
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0054 | 2 | NA19064.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1717-1137A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148022126 | ||||||
| chr4:148022207
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1717-1056G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148022207 | ||||||
| chr4:148022847
|
C | A | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1717-416C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | 148022847 | ||||||
| chr4:148023431
|
T | C | 1 | a0001c0006t0001g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1867+18T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148023431 | ||||||
| chr4:148023819
|
T | C | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1867+406T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148023819 | ||||||
| chr4:148023850
|
T | G | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1867+437T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148023850 | ||||||
| chr4:148023985
|
A | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(23): Show | 26 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1867+572A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148023985 | ||||||
| chr4:148023993
|
C | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0049others(18): Show | 21 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1867+580C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148023993 | ||||||
| chr4:148024136
|
T | G | 2 | a0001c0001t0001g0028a0001c0001t0002g0031 | 2 | HG01071.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1867+723T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148024136 | ||||||
| chr4:148024326
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1867+913T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148024326 | ||||||
| chr4:148025052
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104 | 3 | HG02896.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1867+1639G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148025052 | ||||||
| chr4:148025063
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1867+1650T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148025063 | ||||||
| chr4:148025282
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1867+1869A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148025282 | ||||||
| chr4:148025384
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1867+1971G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148025384 | ||||||
| chr4:148025498
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104 | 3 | HG02896.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1867+2085G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148025498 | ||||||
| chr4:148025539
|
G | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0052others(12): Show | 15 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1867+2126G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148025539 | ||||||
| chr4:148025697
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(42): Show | 45 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.1867+2284T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148025697 | ||||||
| chr4:148025864
|
T | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(42): Show | 45 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.1867+2451T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148025864 | ||||||
| chr4:148026090
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104 | 3 | HG02896.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1867+2677T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148026090 | ||||||
| chr4:148026372
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1867+2959C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148026372 | ||||||
| chr4:148026496
|
C | T | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1867+3083C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148026496 | ||||||
| chr4:148026692
|
T | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0094 | 2 | HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1867+3279T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148026692 | ||||||
| chr4:148026746
|
A | G | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1867+3333A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148026746 | ||||||
| chr4:148027049
|
C | A | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1867+3636C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148027049 | ||||||
| chr4:148027537
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0051others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1867+4124C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148027537 | ||||||
| chr4:148027696
|
A | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(23): Show | 26 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1867+4283A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148027696 | ||||||
| chr4:148028022
|
A | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(44): Show | 47 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(44): Show |
intron_variant | MODIFIER | c.1867+4609A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148028022 | ||||||
| chr4:148028132
|
G | T | 4 | a0001c0004t0001g0045a0001c0009t0001g0007a0001c0009t0001g0008others(1): Show | 4 | HG03225.hp2 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1867+4719G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148028132 | ||||||
| chr4:148028724
|
A | T | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1867+5311A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148028724 | ||||||
| chr4:148028841
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(26): Show | 29 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.1867+5428C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148028841 | ||||||
| chr4:148028860
|
A | G | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1867+5447A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148028860 | ||||||
| chr4:148029042
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(22): Show | 25 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1867+5629G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148029042 | ||||||
| chr4:148029109
|
G | A | 2 | a0001c0009t0001g0007a0001c0009t0001g0008 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1867+5696G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148029109 | ||||||
| chr4:148029261
|
C | T | 7 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0021others(4): Show | 7 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1867+5848C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148029261 | ||||||
| chr4:148029287
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104 | 3 | HG02896.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1867+5874G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148029287 | ||||||
| chr4:148029722
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(39): Show | 42 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1867+6309A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148029722 | ||||||
| chr4:148029923
|
G | A | 1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1867+6510G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148029923 | ||||||
| chr4:148029986
|
G | C | 1 | a0001c0002t0001g0066 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1867+6573G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148029986 | ||||||
| chr4:148029994
|
T | TC | 20 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0037others(17): Show | 20 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1867+6591dupC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148029994 | |||||
| chr4:148030263
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1867+6850C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148030263 | ||||||
| chr4:148030617
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0050 | 2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1867+7204C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148030617 | ||||||
| chr4:148030871
|
GA | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(26): Show | 29 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.1867+7469delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148030871 | |||||
| chr4:148031071
|
C | A | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1867+7658C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148031071 | ||||||
| chr4:148031602
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1867+8189G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148031602 | ||||||
| chr4:148031697
|
T | A | 1 | a0001c0004t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1867+8284T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148031697 | ||||||
| chr4:148031783
|
A | T | 1 | a0001c0001t0001g0010 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1867+8370A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148031783 | ||||||
| chr4:148031831
|
A | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(26): Show | 29 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.1867+8418A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148031831 | ||||||
| chr4:148031903
|
C | T | 1 | a0001c0002t0001g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1867+8490C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148031903 | ||||||
| chr4:148032096
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0086a0001c0004t0001g0102 | 3 | HG03098.hp2 HG03195.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1867+8683C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148032096 | ||||||
| chr4:148032221
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1867+8808C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148032221 | ||||||
| chr4:148032305
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1867+8892C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148032305 | ||||||
| chr4:148032327
|
TC | T | 13 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0035others(10): Show | 13 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1867+8933delC | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148032327 | |||||
| chr4:148032327
|
TCC | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0075others(5): Show | 8 | HG01071.hp1 HG01071.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.1867+8932_1867+893 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148032327 | |||||
| chr4:148032327
|
TCCC | T | 22 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(19): Show | 22 | HG01169.hp2 HG01243.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1867+8931_1867+893 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148032327 | |||||
| chr4:148032327
|
TCCCC | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0030others(10): Show | 13 | HG02056.hp1 HG02056.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.1867+8930_1867+893 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148032327 | |||||
| chr4:148032327
|
TCCCCC | T | 9 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0003g0087others(6): Show | 9 | HG01884.hp2 HG02818.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1867+8929_1867+893 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148032327 | |||||
| chr4:148032327
|
TCCCCCCC others(1): Show |
T | 20 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0049others(17): Show | 20 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1867+8926_1867+893 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148032327 | |||||
| chr4:148032338
|
C | G | 1 | a0001c0001t0001g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1867+8925C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148032338 | ||||||
| chr4:148032692
|
A | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0050 | 2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1867+9279A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148032692 | ||||||
| chr4:148032802
|
G | GT | 3 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104 | 3 | HG02896.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1867+9390dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148032802 | |||||
| chr4:148032813
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1867+9400A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148032813 | ||||||
| chr4:148032895
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104 | 3 | HG02896.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1867+9482T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148032895 | ||||||
| chr4:148033158
|
G | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(26): Show | 29 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.1867+9745G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148033158 | ||||||
| chr4:148033251
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1867+9838G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148033251 | ||||||
| chr4:148033618
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(26): Show | 29 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.1867+10205C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148033618 | ||||||
| chr4:148033647
|
A | C | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1867+10234A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148033647 | ||||||
| chr4:148033904
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104 | 3 | HG02896.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1867+10491C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148033904 | ||||||
| chr4:148034484
|
AT | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104others(1): Show | 4 | HG02896.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1867+11088delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148034484 | |||||
| chr4:148034596
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(40): Show | 43 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.1867+11183C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148034596 | ||||||
| chr4:148035550
|
A | T | 1 | a0001c0002t0001g0066 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1868-11342A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148035550 | ||||||
| chr4:148035670
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(41): Show | 44 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1868-11222A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148035670 | ||||||
| chr4:148036042
|
A | T | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1868-10850A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148036042 | ||||||
| chr4:148036066
|
C | CTG | 18 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0017others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1868-10788_1868-10 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148036066 | |||||
| chr4:148036066
|
C | CTGTG | 33 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0025others(30): Show | 33 | HG00558.hp1 HG00558.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1868-10790_1868-10 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148036066 | |||||
| chr4:148036066
|
C | CTGTGTG | 6 | a0001c0001t0001g0028a0001c0001t0001g0095a0001c0004t0001g0045others(3): Show | 6 | HG01071.hp2 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1868-10792_1868-10 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148036066 | |||||
| chr4:148036066
|
CTG | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0065others(4): Show | 7 | HG02109.hp1 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1868-10788_1868-10 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148036066 | |||||
| chr4:148036106
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0080a0001c0001t0001g0089others(2): Show | 5 | HG01243.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1868-10786A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148036106 | ||||||
| chr4:148036249
|
T | G | 1 | a0001c0001t0001g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1868-10643T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148036249 | ||||||
| chr4:148036402
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1868-10490G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148036402 | ||||||
| chr4:148036594
|
G | T | 2 | a0001c0001t0001g0091a0001c0004t0001g0105 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1868-10298G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148036594 | ||||||
| chr4:148037125
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1868-9767T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148037125 | ||||||
| chr4:148037674
|
A | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104 | 3 | HG02896.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1868-9218A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148037674 | ||||||
| chr4:148037833
|
C | CA | 6 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0083others(3): Show | 6 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1868-9044dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148037833 | |||||
| chr4:148037833
|
CA | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(25): Show | 28 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.1868-9044delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148037833 | |||||
| chr4:148037881
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1868-9011C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148037881 | ||||||
| chr4:148038103
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1868-8789G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148038103 | ||||||
| chr4:148038142
|
T | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0080a0001c0001t0001g0089others(2): Show | 5 | HG01243.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1868-8750T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148038142 | ||||||
| chr4:148038402
|
C | G | 13 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0019others(10): Show | 13 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1868-8490C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148038402 | ||||||
| chr4:148038480
|
A | T | 1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1868-8412A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148038480 | ||||||
| chr4:148038909
|
GT | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104others(1): Show | 4 | HG02896.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1868-7975delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148038909 | |||||
| chr4:148038938
|
G | GTTTTGAA others(12): Show |
30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(27): Show | 30 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.1868-7951_1868-793 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148038938 | |||||
| chr4:148039029
|
A | C | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1868-7863A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148039029 | ||||||
| chr4:148039368
|
A | AT | 5 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0075others(2): Show | 5 | HG02055.hp1 HG02165.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1868-7495dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148039368 | |||||
| chr4:148039368
|
A | ATT | 4 | a0001c0002t0001g0066a0001c0005t0001g0003a0001c0005t0001g0074others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1868-7496_1868-749 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148039368 | |||||
| chr4:148039368
|
A | ATTTTTTT others(5): Show |
2 | a0001c0002t0001g0072a0001c0004t0001g0045 | 2 | HG03471.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1868-7506_1868-749 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148039368 | |||||
| chr4:148039368
|
A | ATTTTTTT others(14): Show |
1 | a0001c0002t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1868-7515_1868-749 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148039368 | |||||
| chr4:148039368
|
A | ATTTTTTT others(15): Show |
1 | a0001c0002t0001g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1868-7516_1868-749 others(26): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148039368 | |||||
| chr4:148039368
|
A | ATTTTTTT others(19): Show |
1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1868-7520_1868-749 others(30): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148039368 | |||||
| chr4:148039368
|
A | ATTTTTTT others(25): Show |
1 | a0001c0002t0001g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1868-7495_1868-749 others(36): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148039368 | |||||
| chr4:148039368
|
AT | A | 9 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0067others(6): Show | 9 | HG00558.hp1 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1868-7495delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148039368 | |||||
| chr4:148039368
|
ATTTT | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0104others(1): Show | 4 | HG02922.hp1 HG03130.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1868-7498_1868-749 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148039368 | |||||
| chr4:148039368
|
ATTTTT | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0037others(3): Show | 6 | HG00558.hp2 HG01261.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1868-7499_1868-749 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148039368 | |||||
| chr4:148039368
|
ATTTTTT | A | 20 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0046others(17): Show | 20 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1868-7500_1868-749 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148039368 | |||||
| chr4:148039368
|
ATTTTTTT others(6): Show |
A | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1868-7507_1868-749 others(17): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148039368 | |||||
| chr4:148039488
|
C | T | 4 | a0001c0004t0001g0045a0001c0009t0001g0007a0001c0009t0001g0008others(1): Show | 4 | HG03225.hp2 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1868-7404C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148039488 | ||||||
| chr4:148039519
|
C | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(27): Show | 30 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.1868-7373C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148039519 | ||||||
| chr4:148039585
|
T | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(27): Show | 30 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.1868-7307T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148039585 | ||||||
| chr4:148040492
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1868-6400C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148040492 | ||||||
| chr4:148040577
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1868-6315G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148040577 | ||||||
| chr4:148040814
|
T | TG | 29 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0026others(26): Show | 29 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.1868-6070dupG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148040814 | |||||
| chr4:148040821
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1868-6071G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148040821 | ||||||
| chr4:148040871
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1868-6021G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148040871 | ||||||
| chr4:148040994
|
A | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(27): Show | 30 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.1868-5898A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148040994 | ||||||
| chr4:148042206
|
T | C | 1 | a0001c0002t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1868-4686T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148042206 | ||||||
| chr4:148042274
|
T | C | 2 | a0001c0009t0001g0007a0001c0009t0001g0008 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1868-4618T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148042274 | ||||||
| chr4:148042364
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104 | 3 | HG02896.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1868-4528T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148042364 | ||||||
| chr4:148042712
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1868-4180A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148042712 | ||||||
| chr4:148043215
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1868-3677G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043215 | ||||||
| chr4:148043600
|
G | T | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1868-3292G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043600 | ||||||
| chr4:148043605
|
C | T | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1868-3287C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043605 | ||||||
| chr4:148043606
|
C | A | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1868-3286C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043606 | ||||||
| chr4:148043608
|
C | A | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1868-3284C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043608 | ||||||
| chr4:148043610
|
C | A | 1 | a0002c0003t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1868-3282C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043610 | ||||||
| chr4:148043614
|
A | AAT | 6 | a0001c0001t0001g0043a0001c0001t0001g0058a0001c0004t0001g0102others(3): Show | 6 | HG02615.hp1 HG02886.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1868-3241_1868-324 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | AATAT | 4 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0097others(1): Show | 4 | HG02145.hp1 HG02896.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1868-3243_1868-324 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | AATATAT | 2 | a0001c0001t0001g0035a0002c0003t0001g0009 | 2 | HG01169.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1868-3245_1868-324 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | AATATATA others(1): Show |
3 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0086 | 3 | HG01891.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1868-3247_1868-324 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | AATATATA others(3): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0062a0001c0001t0002g0031 | 3 | HG02572.hp1 HG03209.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1868-3249_1868-324 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | AATATATA others(5): Show |
6 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0002t0001g0016others(3): Show | 6 | HG02738.hp1 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1868-3251_1868-324 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0068 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1868-3253_1868-324 others(18): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | AATATATA others(9): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0002t0001g0033 | 3 | HG04184.hp2 NA18995.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1868-3255_1868-324 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | AATATATA others(11): Show |
8 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0030others(5): Show | 8 | HG01243.hp1 HG02080.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1868-3257_1868-324 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | AATATATA others(13): Show |
6 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0055others(3): Show | 6 | HG01243.hp2 HG01261.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1868-3259_1868-324 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0010 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1868-3261_1868-324 others(26): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | AATATATA others(17): Show |
1 | a0001c0001t0001g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1868-3263_1868-324 others(28): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | AATATATA others(19): Show |
1 | a0001c0002t0001g0029 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1868-3265_1868-324 others(30): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0028 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1868-3278_1868-327 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043614 | ||||||
| chr4:148043614
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0012 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1868-3278_1868-327 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043614 | ||||||
| chr4:148043614
|
AAT | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0104others(3): Show | 6 | HG00558.hp1 HG01993.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.1868-3241_1868-324 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
AATAT | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0091a0001c0001t0001g0103 | 3 | HG02109.hp1 HG02451.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1868-3243_1868-324 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
AATATAT | A | 2 | a0001c0001t0001g0006a0001c0002t0001g0013 | 2 | HG02895.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1868-3245_1868-324 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
AATATATA others(1): Show |
A | 10 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0051others(7): Show | 10 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1868-3247_1868-324 others(12): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
AATATATA others(3): Show |
A | 14 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0037others(11): Show | 14 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1868-3249_1868-324 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
AATATATA others(5): Show |
A | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1868-3251_1868-324 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
AATATATA others(11): Show |
A | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1868-3257_1868-324 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
AATATATA others(13): Show |
A | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1868-3259_1868-324 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
AATATATA others(17): Show |
A | 8 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0021others(5): Show | 8 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1868-3263_1868-324 others(28): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043614
|
AATATATA others(19): Show |
A | 3 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0054 | 3 | NA18979.hp2 NA18983.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1868-3265_1868-324 others(30): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043614 | |||||
| chr4:148043652
|
T | TA | 3 | a0001c0001t0001g0028a0001c0001t0001g0084a0001c0001t0002g0023 | 3 | HG01070.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1868-3240_1868-323 others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043652 | ||||||
| chr4:148043652
|
T | TATATATA others(18): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0083 | 2 | HG02056.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1868-3240_1868-323 others(29): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043652 | ||||||
| chr4:148043654
|
T | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0084a0001c0001t0001g0085others(2): Show | 5 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1868-3238T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043654 | ||||||
| chr4:148043724
|
A | ATATATAT others(23): Show |
1 | a0001c0002t0001g0066 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1868-3138_1868-310 others(34): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043724 | |||||
| chr4:148043730
|
A | ATATGTGT others(11): Show |
1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1868-3145_1868-314 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043730 | |||||
| chr4:148043736
|
G | GTATATAT others(35): Show |
1 | a0001c0001t0001g0055 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1868-3138_1868-309 others(46): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043736 | |||||
| chr4:148043746
|
G | GTATA | 28 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0026others(25): Show | 28 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.1868-3142_1868-313 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043746 | |||||
| chr4:148043746
|
G | GTATATAT others(27): Show |
2 | a0001c0001t0001g0002a0001c0001t0001g0065 | 2 | HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1868-3128_1868-309 others(38): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043746 | |||||
| chr4:148043748
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1868-3144A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043748 | ||||||
| chr4:148043752
|
ATGTATAT others(5): Show |
A | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1868-3126_1868-311 others(16): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148043752 | |||||
| chr4:148043760
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1868-3132A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043760 | ||||||
| chr4:148043767
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1868-3125T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043767 | ||||||
| chr4:148043768
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1868-3124A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043768 | ||||||
| chr4:148043790
|
A | G | 11 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0016others(8): Show | 11 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1868-3102A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148043790 | ||||||
| chr4:148044006
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1868-2886G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148044006 | ||||||
| chr4:148044245
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1868-2647G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148044245 | ||||||
| chr4:148044299
|
C | T | 1 | a0001c0011t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1868-2593C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148044299 | ||||||
| chr4:148044301
|
G | T | 2 | a0001c0009t0001g0007a0001c0009t0001g0008 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1868-2591G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148044301 | ||||||
| chr4:148044896
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0104 | 3 | HG02896.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1868-1996T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148044896 | ||||||
| chr4:148044911
|
A | C | 1 | a0001c0001t0001g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1868-1981A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148044911 | ||||||
| chr4:148045403
|
T | A | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1868-1489T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148045403 | ||||||
| chr4:148045595
|
G | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0095 | 2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1868-1297G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148045595 | ||||||
| chr4:148045687
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1868-1205G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148045687 | ||||||
| chr4:148045738
|
C | CA | 4 | a0001c0001t0001g0052a0001c0001t0001g0063a0001c0004t0001g0105others(1): Show | 4 | HG01261.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1868-1127dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148045738 | |||||
| chr4:148045738
|
CA | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(52): Show | 55 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.1868-1127delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148045738 | |||||
| chr4:148045738
|
CAA | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0055a0001c0001t0001g0103others(1): Show | 4 | HG01993.hp2 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1868-1128_1868-112 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | 148045738 | |||||
| chr4:148045766
|
G | A | 1 | a0004c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1868-1126G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148045766 | ||||||
| chr4:148045920
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1868-972A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148045920 | ||||||
| chr4:148046611
|
G | A | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1868-281G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148046611 | ||||||
| chr4:148046621
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1868-271C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | chr4 | 148046621 | ||||||
| chr4:148047880
|
T | C | 7 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0021others(4): Show | 7 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.2027+829T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148047880 | ||||||
| chr4:148047948
|
A | G | 1 | a0001c0002t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2027+897A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148047948 | ||||||
| chr4:148048098
|
C | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0026others(23): Show | 26 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.2027+1047C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148048098 | ||||||
| chr4:148048305
|
T | C | 7 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0021others(4): Show | 7 | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.2027+1254T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148048305 | ||||||
| chr4:148048467
|
G | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0037others(19): Show | 22 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.2027+1416G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148048467 | ||||||
| chr4:148048468
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2027+1417A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148048468 | ||||||
| chr4:148048877
|
A | G | 4 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0008t0001g0059others(1): Show | 4 | HG01243.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2027+1826A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148048877 | ||||||
| chr4:148048930
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2027+1879G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148048930 | ||||||
| chr4:148048958
|
A | AT | 6 | a0001c0001t0001g0004a0001c0001t0001g0086a0001c0001t0001g0091others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2027+1923dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148048958 | |||||
| chr4:148048958
|
AT | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0061others(5): Show | 8 | HG01167.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2027+1923delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148048958 | |||||
| chr4:148049009
|
TA | T | 3 | a0001c0001t0001g0104a0001c0009t0001g0007a0001c0009t0001g0008 | 3 | HG03130.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2027+1959delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049009 | ||||||
| chr4:148049010
|
A | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.2027+1959A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049010 | ||||||
| chr4:148049050
|
C | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(15): Show | 18 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.2027+1999C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049050 | ||||||
| chr4:148049252
|
C | T | 11 | a0001c0001t0001g0037a0001c0001t0001g0104a0001c0002t0001g0005others(8): Show | 11 | HG01884.hp2 HG01993.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.2027+2201C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049252 | ||||||
| chr4:148049320
|
A | G | 12 | a0001c0001t0001g0037a0001c0001t0001g0104a0001c0002t0001g0005others(9): Show | 12 | HG01884.hp2 HG01993.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.2027+2269A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049320 | ||||||
| chr4:148049386
|
C | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.2027+2335C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049386 | ||||||
| chr4:148049448
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2027+2397C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049448 | ||||||
| chr4:148049636
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2027+2585G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049636 | ||||||
| chr4:148049795
|
G | GTTTT | 9 | a0001c0001t0001g0037a0001c0002t0001g0019a0001c0002t0001g0021others(6): Show | 9 | HG01884.hp2 HG01993.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.2027+2749_2027+275 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148049795 | |||||
| chr4:148049800
|
TTTTG | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0080a0001c0001t0001g0091others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2027+2769_2027+277 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148049800 | |||||
| chr4:148049824
|
T | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0095a0001c0001t0003g0087 | 3 | HG02055.hp2 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2027+2773T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049824 | ||||||
| chr4:148049832
|
T | TG | 10 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0058others(7): Show | 10 | HG01167.hp1 HG01261.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2027+2788dupG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148049832 | |||||
| chr4:148049833
|
GGGGGGGC | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(32): Show | 35 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.2027+2803_2027+280 others(11): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148049833 | |||||
| chr4:148049845
|
G | C | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2027+2794G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049845 | ||||||
| chr4:148049847
|
C | G | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2027+2796C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049847 | ||||||
| chr4:148049853
|
G | C | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2027+2802G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049853 | ||||||
| chr4:148049854
|
C | G | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2027+2803C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049854 | ||||||
| chr4:148049862
|
G | T | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2027+2811G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049862 | ||||||
| chr4:148049937
|
G | A | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2027+2886G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148049937 | ||||||
| chr4:148050080
|
T | A | 2 | a0001c0001t0001g0081a0001c0005t0001g0003 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2027+3029T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148050080 | ||||||
| chr4:148050264
|
G | T | 10 | a0001c0001t0001g0037a0001c0001t0001g0104a0001c0002t0001g0019others(7): Show | 10 | HG01884.hp2 HG01993.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.2027+3213G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148050264 | ||||||
| chr4:148050336
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2027+3285A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148050336 | ||||||
| chr4:148050365
|
C | CT | 7 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0051others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2027+3340dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148050365 | |||||
| chr4:148050365
|
CT | C | 43 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(40): Show | 43 | HG00558.hp2 HG01070.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.2027+3340delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148050365 | |||||
| chr4:148050391
|
T | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(1): Show | 4 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2027+3340T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148050391 | ||||||
| chr4:148050524
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2027+3473C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148050524 | ||||||
| chr4:148050563
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2027+3512C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148050563 | ||||||
| chr4:148050678
|
ATCT | A | 2 | a0001c0004t0001g0105a0002c0003t0001g0096 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2027+3632_2027+363 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148050678 | |||||
| chr4:148050827
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2027+3776A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148050827 | ||||||
| chr4:148050853
|
A | G | 1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2027+3802A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148050853 | ||||||
| chr4:148050942
|
G | C | 1 | a0001c0001t0002g0031 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2027+3891G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148050942 | ||||||
| chr4:148051462
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0051 | 3 | HG02109.hp2 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2027+4411A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148051462 | ||||||
| chr4:148051679
|
T | G | 5 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2027+4628T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148051679 | ||||||
| chr4:148052079
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.2027+5028T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148052079 | ||||||
| chr4:148052080
|
G | A | 10 | a0001c0001t0001g0037a0001c0001t0001g0104a0001c0002t0001g0019others(7): Show | 10 | HG01884.hp2 HG01993.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.2027+5029G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148052080 | ||||||
| chr4:148052157
|
A | C | 2 | a0001c0001t0001g0091a0004c0010t0001g0048 | 2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2027+5106A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148052157 | ||||||
| chr4:148052272
|
C | T | 7 | a0001c0001t0001g0037a0001c0002t0001g0019a0001c0002t0001g0021others(4): Show | 7 | HG01884.hp2 HG01993.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.2027+5221C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148052272 | ||||||
| chr4:148052279
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0051 | 3 | HG02109.hp2 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2027+5228A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148052279 | ||||||
| chr4:148052339
|
T | TA | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0036others(2): Show | 5 | HG01167.hp2 HG01261.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2027+5305dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148052339 | |||||
| chr4:148052339
|
T | TAA | 19 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(16): Show | 19 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.2027+5304_2027+530 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148052339 | |||||
| chr4:148052339
|
TA | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0069a0001c0001t0001g0091others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.2027+5305delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148052339 | |||||
| chr4:148052392
|
C | CT | 35 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(32): Show | 35 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2027+5361dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148052392 | |||||
| chr4:148052392
|
C | CTT | 7 | a0001c0001t0001g0044a0001c0001t0001g0053a0001c0001t0001g0055others(4): Show | 7 | HG02055.hp1 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2027+5360_2027+536 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148052392 | |||||
| chr4:148052392
|
C | CTTT | 6 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2027+5359_2027+536 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148052392 | |||||
| chr4:148052392
|
CT | C | 20 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(17): Show | 20 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.2027+5361delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148052392 | |||||
| chr4:148052392
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2027+5352_2027+536 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148052392 | |||||
| chr4:148052425
|
CA | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0065 | 2 | HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2027+5378delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148052425 | |||||
| chr4:148052676
|
G | A | 20 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(17): Show | 20 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.2027+5625G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148052676 | ||||||
| chr4:148052677
|
A | T | 1 | a0002c0003t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2027+5626A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148052677 | ||||||
| chr4:148053139
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0065 | 2 | HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2027+6088G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148053139 | ||||||
| chr4:148053195
|
T | A | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2027+6144T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148053195 | ||||||
| chr4:148053339
|
C | G | 5 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2027+6288C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148053339 | ||||||
| chr4:148053451
|
T | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(37): Show | 40 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.2027+6400T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148053451 | ||||||
| chr4:148053970
|
C | T | 1 | a0001c0006t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2027+6919C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148053970 | ||||||
| chr4:148054371
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2027+7320C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148054371 | ||||||
| chr4:148054484
|
G | A | 64 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0012others(61): Show | 64 | HG00558.hp2 HG01071.hp2 HG01167.hp1 others(61): Show |
intron_variant | MODIFIER | c.2027+7433G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148054484 | ||||||
| chr4:148054523
|
T | C | 5 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2027+7472T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148054523 | ||||||
| chr4:148054596
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2027+7545G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148054596 | ||||||
| chr4:148054840
|
G | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0052others(11): Show | 14 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.2027+7789G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148054840 | ||||||
| chr4:148054866
|
C | T | 3 | a0001c0001t0001g0104a0001c0009t0001g0007a0001c0009t0001g0008 | 3 | HG03130.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2027+7815C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148054866 | ||||||
| chr4:148055415
|
G | T | 33 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(30): Show | 33 | HG00558.hp2 HG01071.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.2028-7733G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148055415 | ||||||
| chr4:148055830
|
A | G | 57 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0012others(54): Show | 57 | HG00558.hp1 HG00558.hp2 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.2028-7318A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148055830 | ||||||
| chr4:148055865
|
G | A | 36 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(33): Show | 36 | HG00558.hp2 HG01071.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.2028-7283G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148055865 | ||||||
| chr4:148055902
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2028-7246G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148055902 | ||||||
| chr4:148055933
|
C | A | 3 | a0001c0001t0001g0104a0001c0009t0001g0007a0001c0009t0001g0008 | 3 | HG03130.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2028-7215C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148055933 | ||||||
| chr4:148056133
|
G | A | 33 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(30): Show | 33 | HG00558.hp2 HG01071.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.2028-7015G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148056133 | ||||||
| chr4:148056238
|
T | C | 63 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0012others(60): Show | 63 | HG00558.hp2 HG01071.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.2028-6910T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148056238 | ||||||
| chr4:148056400
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2028-6748T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148056400 | ||||||
| chr4:148056725
|
T | C | 5 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2028-6423T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148056725 | ||||||
| chr4:148057255
|
C | T | 32 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(29): Show | 32 | HG00558.hp2 HG01071.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2028-5893C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148057255 | ||||||
| chr4:148057322
|
C | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2028-5826C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148057322 | ||||||
| chr4:148057334
|
G | A | 2 | a0001c0004t0001g0105a0002c0003t0001g0096 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2028-5814G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148057334 | ||||||
| chr4:148058023
|
G | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 97 | HG00558.hp2 HG01070.hp1 HG01070.hp2 others(94): Show |
intron_variant | MODIFIER | c.2028-5125G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148058023 | ||||||
| chr4:148058151
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2028-4997A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148058151 | ||||||
| chr4:148058198
|
G | C | 6 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2028-4950G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148058198 | ||||||
| chr4:148058447
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2028-4701T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148058447 | ||||||
| chr4:148058473
|
C | G | 14 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0047others(11): Show | 14 | HG01070.hp1 HG01167.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2028-4675C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148058473 | ||||||
| chr4:148058549
|
T | C | 56 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(53): Show | 56 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.2028-4599T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148058549 | ||||||
| chr4:148058556
|
A | G | 8 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2028-4592A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148058556 | ||||||
| chr4:148058816
|
A | C | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2028-4332A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148058816 | ||||||
| chr4:148059023
|
C | T | 48 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(45): Show | 48 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.2028-4125C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148059023 | ||||||
| chr4:148059126
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2028-4022G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148059126 | ||||||
| chr4:148059215
|
G | T | 1 | a0001c0002t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2028-3933G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148059215 | ||||||
| chr4:148059521
|
A | AT | 69 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(66): Show | 69 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2028-3627_2028-362 others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148059521 | ||||||
| chr4:148059823
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2028-3325T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148059823 | ||||||
| chr4:148059973
|
T | TGA | 35 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(32): Show | 35 | HG00558.hp1 HG00558.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.2028-3155_2028-315 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148059973 | |||||
| chr4:148059973
|
T | TGAGA | 2 | a0001c0001t0001g0056a0001c0002t0001g0013 | 2 | HG02080.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2028-3157_2028-315 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148059973 | |||||
| chr4:148059993
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2028-3155A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148059993 | ||||||
| chr4:148060026
|
A | ATG | 2 | a0001c0001t0001g0046a0001c0001t0001g0051 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2028-3122_2028-312 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148060026 | ||||||
| chr4:148060027
|
C | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0051 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2028-3121C>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148060027 | ||||||
| chr4:148060027
|
C | CGA | 73 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0012others(70): Show | 73 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.2028-3112_2028-311 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148060027 | |||||
| chr4:148060085
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2028-3063T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148060085 | ||||||
| chr4:148060255
|
G | A | 69 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(66): Show | 69 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2028-2893G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148060255 | ||||||
| chr4:148060344
|
A | AC | 12 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0047others(9): Show | 12 | HG01070.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2028-2804_2028-280 others(5): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148060344 | ||||||
| chr4:148060345
|
G | C | 49 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(46): Show | 49 | HG00558.hp2 HG01071.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.2028-2803G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148060345 | ||||||
| chr4:148060345
|
G | GT | 10 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0046others(7): Show | 10 | HG01169.hp2 HG01261.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.2028-2782dupT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148060345 | |||||
| chr4:148060345
|
G | T | 12 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0047others(9): Show | 12 | HG01070.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2028-2803G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148060345 | ||||||
| chr4:148060346
|
T | C | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2028-2802T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148060346 | ||||||
| chr4:148060509
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2028-2639G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148060509 | ||||||
| chr4:148060643
|
T | A | 35 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(32): Show | 35 | HG00558.hp1 HG00558.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.2028-2505T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148060643 | ||||||
| chr4:148060935
|
T | A | 6 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2028-2213T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148060935 | ||||||
| chr4:148061070
|
C | T | 7 | a0001c0001t0001g0037a0001c0002t0001g0019a0001c0002t0001g0021others(4): Show | 7 | HG01884.hp2 HG01993.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.2028-2078C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148061070 | ||||||
| chr4:148061096
|
CT | C | 14 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0047others(11): Show | 14 | HG01070.hp1 HG01167.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2028-2040delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148061096 | |||||
| chr4:148061127
|
C | T | 62 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(59): Show | 62 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.2028-2021C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148061127 | ||||||
| chr4:148061408
|
G | A | 63 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(60): Show | 63 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.2028-1740G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148061408 | ||||||
| chr4:148061466
|
T | TAA | 8 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2028-1674_2028-167 others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148061466 | |||||
| chr4:148061613
|
GT | G | 54 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(51): Show | 54 | HG00558.hp2 HG01071.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.2028-1523delT | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 148061613 | |||||
| chr4:148061615
|
T | G | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2028-1533T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148061615 | ||||||
| chr4:148061755
|
G | C | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2028-1393G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148061755 | ||||||
| chr4:148061765
|
G | A | 33 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(30): Show | 33 | HG00558.hp2 HG01071.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.2028-1383G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148061765 | ||||||
| chr4:148061988
|
A | C | 26 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(23): Show | 26 | HG00558.hp2 HG01071.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.2028-1160A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148061988 | ||||||
| chr4:148062042
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 105 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.2028-1106G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148062042 | ||||||
| chr4:148062053
|
C | T | 33 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(30): Show | 33 | HG00558.hp2 HG01071.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.2028-1095C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148062053 | ||||||
| chr4:148062096
|
C | T | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2028-1052C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148062096 | ||||||
| chr4:148062164
|
G | A | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2028-984G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148062164 | ||||||
| chr4:148062186
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2028-962C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148062186 | ||||||
| chr4:148062225
|
A | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0047others(6): Show | 9 | HG01070.hp1 HG01167.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2028-923A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148062225 | ||||||
| chr4:148062280
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2028-868G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148062280 | ||||||
| chr4:148062317
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0026others(5): Show | 8 | HG00558.hp2 HG02056.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.2028-831G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148062317 | ||||||
| chr4:148062327
|
G | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0052others(11): Show | 14 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.2028-821G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148062327 | ||||||
| chr4:148062647
|
C | T | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2028-501C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148062647 | ||||||
| chr4:148062912
|
G | C | 6 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2028-236G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148062912 | ||||||
| chr4:148062931
|
G | C | 64 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(61): Show | 64 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.2028-217G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | chr4 | 148062931 | ||||||
| chr4:148063316
|
T | G | 1 | a0001c0001t0001g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2180+16T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 21/22 | chr4 | 148063316 | ||||||
| chr4:148063557
|
A | G | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2180+257A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 21/22 | chr4 | 148063557 | ||||||
| chr4:148063782
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2180+482C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 21/22 | chr4 | 148063782 | ||||||
| chr4:148063953
|
T | C | 65 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(62): Show | 65 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.2181-463T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 21/22 | chr4 | 148063953 | ||||||
| chr4:148063958
|
C | T | 36 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(33): Show | 36 | HG00558.hp2 HG01071.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.2181-458C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 21/22 | chr4 | 148063958 | ||||||
| chr4:148063959
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2181-457G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 21/22 | chr4 | 148063959 | ||||||
| chr4:148064170
|
G | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0063 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2181-246G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 21/22 | chr4 | 148064170 | ||||||
| chr4:148064235
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2181-181A>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 21/22 | chr4 | 148064235 | ||||||
| chr4:148064546
|
G | T | 1 | a0001c0008t0001g0060 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2272+39G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148064546 | ||||||
| chr4:148064569
|
T | C | 66 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(63): Show | 66 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.2272+62T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148064569 | ||||||
| chr4:148064647
|
T | TGCGTTAG others(23): Show |
11 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0047others(8): Show | 11 | HG01070.hp1 HG01167.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2272+143_2272+172d others(32): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 148064647 | |||||
| chr4:148064711
|
T | C | 72 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(69): Show | 72 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.2272+204T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148064711 | ||||||
| chr4:148064755
|
A | G | 66 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(63): Show | 66 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.2272+248A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148064755 | ||||||
| chr4:148064777
|
C | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0052others(11): Show | 14 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.2272+270C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148064777 | ||||||
| chr4:148064879
|
C | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0094others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2272+372C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148064879 | ||||||
| chr4:148065029
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2272+522C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148065029 | ||||||
| chr4:148065060
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2272+553A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148065060 | ||||||
| chr4:148065653
|
G | A | 58 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(55): Show | 58 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.2272+1146G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148065653 | ||||||
| chr4:148065673
|
C | T | 1 | a0001c0002t0001g0029 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2272+1166C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148065673 | ||||||
| chr4:148065842
|
A | G | 3 | a0001c0001t0001g0104a0001c0009t0001g0007a0001c0009t0001g0008 | 3 | HG03130.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2272+1335A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148065842 | ||||||
| chr4:148065910
|
C | T | 65 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(62): Show | 65 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.2272+1403C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148065910 | ||||||
| chr4:148065979
|
C | CAAA | 5 | a0001c0001t0001g0070a0001c0001t0002g0031a0001c0002t0001g0072others(2): Show | 5 | HG02738.hp2 HG03239.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2272+1487_2272+148 others(7): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 148065979 | |||||
| chr4:148065979
|
C | CAAAA | 34 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(31): Show | 34 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.2272+1486_2272+148 others(8): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 148065979 | |||||
| chr4:148065979
|
C | CAAAAA | 14 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0062others(11): Show | 14 | HG01243.hp2 HG02145.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.2272+1485_2272+148 others(9): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 148065979 | |||||
| chr4:148065979
|
C | CAAAAAA | 10 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0076others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2272+1484_2272+148 others(10): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 148065979 | |||||
| chr4:148065979
|
CA | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0051others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.2272+1489delA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 148065979 | |||||
| chr4:148066036
|
G | A | 65 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(62): Show | 65 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.2272+1529G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148066036 | ||||||
| chr4:148066144
|
T | G | 65 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(62): Show | 65 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.2272+1637T>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148066144 | ||||||
| chr4:148066156
|
G | A | 14 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0052others(11): Show | 14 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.2272+1649G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148066156 | ||||||
| chr4:148066279
|
A | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(33): Show | 36 | HG00558.hp1 HG00558.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.2272+1772A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148066279 | ||||||
| chr4:148066298
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2272+1791C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148066298 | ||||||
| chr4:148066702
|
A | G | 3 | a0001c0001t0001g0093a0001c0004t0001g0105a0002c0003t0001g0096 | 3 | HG02572.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2272+2195A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148066702 | ||||||
| chr4:148066821
|
T | C | 38 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(35): Show | 38 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.2272+2314T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148066821 | ||||||
| chr4:148066861
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2272+2354C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148066861 | ||||||
| chr4:148067008
|
T | C | 76 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0012others(73): Show | 76 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.2272+2501T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148067008 | ||||||
| chr4:148067039
|
G | A | 1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2272+2532G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148067039 | ||||||
| chr4:148067248
|
C | G | 68 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(65): Show | 68 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.2272+2741C>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148067248 | ||||||
| chr4:148067305
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2272+2798A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148067305 | ||||||
| chr4:148067353
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2272+2846G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148067353 | ||||||
| chr4:148067601
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2272+3094T>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148067601 | ||||||
| chr4:148067766
|
C | CG | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2272+3260dupG | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 148067766 | |||||
| chr4:148067767
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2272+3260G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148067767 | ||||||
| chr4:148068149
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2272+3642C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148068149 | ||||||
| chr4:148068226
|
G | A | 6 | a0001c0001t0001g0080a0001c0001t0001g0091a0001c0001t0001g0095others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2272+3719G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148068226 | ||||||
| chr4:148068353
|
C | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(49): Show | 52 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.2273-3640C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148068353 | ||||||
| chr4:148068383
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0005t0001g0074others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2273-3610C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148068383 | ||||||
| chr4:148068709
|
G | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0094 | 2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2273-3284G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148068709 | ||||||
| chr4:148068860
|
G | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0052others(5): Show | 8 | HG01261.hp1 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2273-3133G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148068860 | ||||||
| chr4:148069024
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0051others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2273-2969C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069024 | ||||||
| chr4:148069030
|
T | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0052others(5): Show | 8 | HG01261.hp1 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2273-2963T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069030 | ||||||
| chr4:148069087
|
T | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0051others(7): Show | 10 | HG02109.hp2 HG02572.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2273-2906T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069087 | ||||||
| chr4:148069125
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0005t0001g0074others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2273-2868C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069125 | ||||||
| chr4:148069209
|
C | T | 41 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(38): Show | 41 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.2273-2784C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069209 | ||||||
| chr4:148069212
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2273-2781C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069212 | ||||||
| chr4:148069213
|
G | A | 4 | a0001c0001t0001g0067a0001c0001t0001g0093a0001c0001t0001g0106others(1): Show | 4 | HG03041.hp2 HG03471.hp2 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.2273-2780G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069213 | ||||||
| chr4:148069278
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0005t0001g0074others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2273-2715G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069278 | ||||||
| chr4:148069423
|
G | A | 1 | a0002c0003t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2273-2570G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069423 | ||||||
| chr4:148069449
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2273-2544T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069449 | ||||||
| chr4:148069491
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0005t0001g0074others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2273-2502A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069491 | ||||||
| chr4:148069601
|
T | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0051others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2273-2392T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069601 | ||||||
| chr4:148069844
|
G | A | 42 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(39): Show | 42 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2273-2149G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148069844 | ||||||
| chr4:148070078
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2273-1915C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148070078 | ||||||
| chr4:148070189
|
C | T | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2273-1804C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148070189 | ||||||
| chr4:148070245
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2273-1748G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148070245 | ||||||
| chr4:148070281
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2273-1712C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148070281 | ||||||
| chr4:148070363
|
G | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(63): Show | 66 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.2273-1630G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148070363 | ||||||
| chr4:148070447
|
G | C | 1 | a0001c0001t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2273-1546G>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148070447 | ||||||
| chr4:148070742
|
G | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0053others(2): Show | 5 | HG01071.hp2 HG01169.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.2273-1251G>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148070742 | ||||||
| chr4:148070831
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0005t0001g0074others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2273-1162C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148070831 | ||||||
| chr4:148070999
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2273-994A>G | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148070999 | ||||||
| chr4:148071397
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2273-596C>T | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148071397 | ||||||
| chr4:148071479
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2273-514G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148071479 | ||||||
| chr4:148071488
|
T | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0088 | 2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2273-505T>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148071488 | ||||||
| chr4:148071638
|
C | CA | 40 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(37): Show | 40 | HG00558.hp1 HG00558.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.2273-346dupA | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 148071638 | |||||
| chr4:148071638
|
CAAAA | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0052a0001c0001t0001g0076others(4): Show | 7 | HG01261.hp1 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2273-349_2273-346d others(6): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 148071638 | |||||
| chr4:148071642
|
A | C | 1 | a0001c0004t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2273-351A>C | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148071642 | ||||||
| chr4:148071893
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0052others(10): Show | 13 | HG01261.hp1 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2273-100G>A | ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | chr4 | 148071893 |