| geneid | 50649 |
|---|---|
| ensemblid | ENSG00000136002.21 |
| hgncid | 684 |
| symbol | ARHGEF4 |
| name | Rho guanine nucleotide exchange factor 4 |
| refseq_nuc | NM_001367493.1 |
| refseq_prot | NP_001354422.1 |
| ensembl_nuc | ENST00000409359.7 |
| ensembl_prot | ENSP00000386794.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 130836914 |
| end | 131047253 |
| strand | + |
| ver | v1.2 |
| region | chr2:130836914-131047253 |
| region5000 | chr2:130831914-131052253 |
| regionname0 | ARHGEF4_chr2_130836914_131047253 |
| regionname5000 | ARHGEF4_chr2_130831914_131052253 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1876 | 58 | 17 | 9 | 18 | 2 | 12 | 9 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002 | 0/0 | 1876 | 13 | 8 | 0 | 3 | 0 | 2 | 2 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0003 | 0/0 | 1876 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0004 | 0/1 | 1876 | 9 | 1 | 0 | 2 | 0 | 5 | 2 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0005 | 0/0 | 1876 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0006 | 0/0 | 1876 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0007 | 0/0 | 1876 | 6 | 4 | 1 | 0 | 0 | 1 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0008 | 0/0 | 1876 | 5 | 0 | 4 | 0 | 0 | 1 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0009 | 0/0 | 1876 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0010 | 0/0 | 1876 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0011 | 0/0 | 1876 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0012 | 0/0 | 1876 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0013 | 0/0 | 1876 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0014 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0015 | 0/0 | 1876 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0016 | 1/0 | 1876 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0017 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0018 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0019 | 0/0 | 1876 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0020 | 0/0 | 1876 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0021 | 0/0 | 1876 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0022 | 0/0 | 1876 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0023 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0024 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0025 | 0/0 | 1876 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 5631 | 27 | 2 | 3 | 11 | 1 | 10 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0002 | 0/0 | 5631 | 12 | 0 | 2 | 7 | 1 | 2 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0003 | 0/0 | 5631 | 8 | 7 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0004 | 0/0 | 5631 | 7 | 1 | 0 | 1 | 0 | 5 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0005 | 0/0 | 5631 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0006 | 0/0 | 5631 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0007 | 0/0 | 5631 | 5 | 3 | 2 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0008 | 0/0 | 5631 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0009 | 0/0 | 5631 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0010 | 0/0 | 5631 | 4 | 0 | 0 | 3 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0011 | 0/0 | 5631 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0012 | 0/0 | 5631 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0013 | 0/0 | 5631 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0014 | 0/0 | 5631 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0015 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0016 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0017 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0018 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0019 | 0/0 | 5631 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0020 | 0/1 | 5631 | 2 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0021 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0022 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0023 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0024 | 0/0 | 5631 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0025 | 0/0 | 5631 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0026 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0027 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0028 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0029 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0030 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0031 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0032 | 0/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0033 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0034 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0035 | 0/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0036 | 0/0 | 5631 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0037 | 0/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0038 | 0/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0039 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0040 | 0/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0041 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0042 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0043 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0044 | 0/0 | 5631 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0045 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0046 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0047 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0048 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0049 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0050 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0051 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0052 | 1/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0053 | 0/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| c0054 | 0/0 | 5631 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| 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 | 1105 | 115 | 48 | 14 | 26 | 2 | 23 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| t0002 | 0/0 | 1105 | 8 | 7 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| t0003 | 0/0 | 1105 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| t0004 | 0/0 | 1106 | 6 | 4 | 2 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| t0005 | 0/0 | 1105 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| t0006 | 0/0 | 1105 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| t0007 | 0/0 | 1105 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| t0008 | 0/0 | 1105 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| t0009 | 0/0 | 1105 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| 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 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 5631 | 27 | 2 | 3 | 11 | 1 | 10 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0002 | 0/0 | 5631 | 12 | 0 | 2 | 7 | 1 | 2 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0007 | 0/0 | 5631 | 5 | 3 | 2 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0014 | 0/0 | 5631 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0015 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0018 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0025 | 0/0 | 5631 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0026 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0027 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0034 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0039 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0044 | 0/0 | 5631 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0045 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0010 | 0/0 | 5631 | 4 | 0 | 0 | 3 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0011 | 0/0 | 5631 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0028 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0040 | 0/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0041 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0042 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0048 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0003c0003 | 0/0 | 5631 | 8 | 7 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0003c0030 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0003c0031 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0004c0004 | 0/0 | 5631 | 7 | 1 | 0 | 1 | 0 | 5 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0004c0020 | 0/1 | 5631 | 2 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0005c0006 | 0/0 | 5631 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0005c0008 | 0/0 | 5631 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0006c0005 | 0/0 | 5631 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0006c0050 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0007c0013 | 0/0 | 5631 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0007c0017 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0007c0032 | 0/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0008c0012 | 0/0 | 5631 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0008c0053 | 0/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0009c0021 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0009c0046 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0009c0047 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0010c0009 | 0/0 | 5631 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0011c0022 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0011c0049 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0012c0019 | 0/0 | 5631 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0013c0016 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0014c0023 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0015c0054 | 0/0 | 5631 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0016c0052 | 1/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0017c0051 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0018c0043 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0019c0036 | 0/0 | 5631 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0020c0038 | 0/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0021c0037 | 0/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0022c0035 | 0/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0023c0029 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0024c0033 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0025c0024 | 0/0 | 5631 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6735 | 25 | 0 | 3 | 11 | 1 | 10 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0001t0002 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0001t0008 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0002t0001 | 0/0 | 6735 | 12 | 0 | 2 | 7 | 1 | 2 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0007t0004 | 0/0 | 6736 | 5 | 3 | 2 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0014t0001 | 0/0 | 6735 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0014t0002 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0015t0001 | 0/0 | 6735 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0018t0002 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0018t0005 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0025t0005 | 0/0 | 6735 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0026t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0027t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0034t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0039t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0044t0001 | 0/0 | 6735 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0001c0045t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0010t0001 | 0/0 | 6735 | 4 | 0 | 0 | 3 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0011t0001 | 0/0 | 6735 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0011t0005 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0028t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0040t0001 | 0/0 | 6735 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0041t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0042t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0002c0048t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0003c0003t0001 | 0/0 | 6735 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0003c0003t0002 | 0/0 | 6735 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0003c0003t0003 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0003c0030t0004 | 0/0 | 6736 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0003c0031t0006 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0004c0004t0001 | 0/0 | 6735 | 6 | 1 | 0 | 1 | 0 | 4 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0004c0004t0007 | 0/0 | 6735 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0004c0020t0001 | 0/1 | 6735 | 2 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0005c0006t0001 | 0/0 | 6735 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0005c0006t0002 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0005c0006t0003 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0005c0008t0001 | 0/0 | 6735 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0006c0005t0001 | 0/0 | 6735 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0006c0005t0003 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0006c0005t0005 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0006c0050t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0007c0013t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0007c0013t0002 | 0/0 | 6735 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0007c0013t0003 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0007c0017t0001 | 0/0 | 6735 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0007c0032t0001 | 0/0 | 6735 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0008c0012t0001 | 0/0 | 6735 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0008c0053t0001 | 0/0 | 6735 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0009c0021t0001 | 0/0 | 6735 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0009c0046t0009 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0009c0047t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0010c0009t0001 | 0/0 | 6735 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0011c0022t0001 | 0/0 | 6735 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0011c0049t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0012c0019t0001 | 0/0 | 6735 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0013c0016t0003 | 0/0 | 6735 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0014c0023t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0015c0054t0001 | 0/0 | 6735 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0016c0052t0001 | 1/0 | 6735 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0017c0051t0006 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0018c0043t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0019c0036t0001 | 0/0 | 6735 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0020c0038t0001 | 0/0 | 6735 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0021c0037t0001 | 0/0 | 6735 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0022c0035t0001 | 0/0 | 6735 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0023c0029t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0024c0033t0001 | 0/0 | 6735 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| a0025c0024t0001 | 0/0 | 6735 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | copy fasta | chr2 | 130831914 | 131052253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0007t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0007t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0007t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0007t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0007t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0014t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0014t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0014t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0015t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0015t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0018t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0018t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0025t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0026t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0027t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0034t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0039t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0044t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0001c0045t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0010t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0010t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0010t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0010t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0011t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0011t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0011t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0011t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0028t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0040t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0041t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0042t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0002c0048t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0003c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0003c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0003c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0003c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0003c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0003c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0003c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0003c0003t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0003c0030t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0003c0031t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0004c0004t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0004c0004t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0004c0004t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0004c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0004c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0004c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0004c0004t0007g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0004c0020t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0004c0020t0001g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0005c0006t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0005c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0005c0006t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0005c0006t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0005c0006t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0005c0008t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0005c0008t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0005c0008t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0005c0008t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0006c0005t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0006c0005t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0006c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0006c0005t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0006c0005t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0006c0005t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0006c0050t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0007c0013t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0007c0013t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0007c0013t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0007c0017t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0007c0017t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0007c0032t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0008c0012t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0008c0012t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0008c0012t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0008c0012t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0008c0053t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0009c0021t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0009c0021t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0009c0046t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0009c0047t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0010c0009t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0010c0009t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0010c0009t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0010c0009t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0011c0022t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0011c0022t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0011c0049t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0012c0019t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0012c0019t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0013c0016t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0013c0016t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0014c0023t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0015c0054t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0016c0052t0001g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0017c0051t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0018c0043t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0019c0036t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0020c0038t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0021c0037t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0022c0035t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0023c0029t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0024c0033t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| a0025c0024t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00621 | hp1 | a0002 | c0010 | t0001 | g0003 | EAS | CHS | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG00642 | hp2 | a0008 | c0012 | t0001 | g0082 | AMR | PUR | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG00735 | hp2 | a0025 | c0024 | t0001 | g0029 | AMR | PUR | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01081 | hp1 | a0008 | c0012 | t0001 | g0027 | AMR | PUR | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01109 | hp1 | a0008 | c0012 | t0001 | g0045 | AMR | PUR | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0030 | AMR | PUR | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01175 | hp1 | a0008 | c0012 | t0001 | g0026 | AMR | PUR | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01175 | hp2 | a0007 | c0013 | t0002 | g0095 | AMR | PUR | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01243 | hp1 | a0001 | c0025 | t0005 | g0067 | AMR | PUR | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01243 | hp2 | a0005 | c0008 | t0001 | g0007 | AMR | PUR | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01257 | hp1 | a0001 | c0044 | t0001 | g0011 | AMR | CLM | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01257 | hp2 | a0001 | c0007 | t0004 | g0090 | AMR | CLM | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01258 | hp1 | a0001 | c0007 | t0004 | g0092 | AMR | CLM | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01258 | hp2 | a0015 | c0054 | t0001 | g0061 | AMR | CLM | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0038 | EUR | IBS | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0048 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01884 | hp2 | a0002 | c0011 | t0001 | g0132 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PEL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02055 | hp1 | a0024 | c0033 | t0001 | g0021 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0062 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | KHV | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | CDX | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CDX | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02257 | hp1 | a0006 | c0050 | t0001 | g0142 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02257 | hp2 | a0005 | c0006 | t0002 | g0099 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02258 | hp1 | a0010 | c0009 | t0001 | g0138 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02258 | hp2 | a0011 | c0022 | t0001 | g0084 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02280 | hp1 | a0003 | c0003 | t0003 | g0112 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02280 | hp2 | a0004 | c0004 | t0001 | g0144 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02572 | hp1 | a0013 | c0016 | t0003 | g0001 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02572 | hp2 | a0005 | c0008 | t0001 | g0097 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02615 | hp1 | a0017 | c0051 | t0006 | g0069 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02615 | hp2 | a0003 | c0030 | t0004 | g0022 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02622 | hp1 | a0001 | c0007 | t0004 | g0093 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02622 | hp2 | a0003 | c0003 | t0002 | g0117 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02630 | hp1 | a0005 | c0008 | t0001 | g0098 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02630 | hp2 | a0002 | c0011 | t0001 | g0133 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02647 | hp1 | a0001 | c0007 | t0004 | g0089 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02647 | hp2 | a0001 | c0014 | t0002 | g0075 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02698 | hp1 | a0002 | c0040 | t0001 | g0044 | SAS | PJL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02717 | hp1 | a0010 | c0009 | t0001 | g0065 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02717 | hp2 | a0001 | c0014 | t0001 | g0120 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02723 | hp1 | a0009 | c0021 | t0001 | g0139 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02723 | hp2 | a0010 | c0009 | t0001 | g0068 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02818 | hp1 | a0006 | c0005 | t0005 | g0119 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02818 | hp2 | a0003 | c0003 | t0002 | g0118 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02886 | hp1 | a0010 | c0009 | t0001 | g0066 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02886 | hp2 | a0003 | c0003 | t0002 | g0116 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02895 | hp1 | a0007 | c0017 | t0001 | g0108 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02895 | hp2 | a0005 | c0006 | t0001 | g0100 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02896 | hp1 | a0001 | c0015 | t0001 | g0078 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02896 | hp2 | a0018 | c0043 | t0001 | g0131 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02897 | hp1 | a0001 | c0015 | t0001 | g0079 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02897 | hp2 | a0005 | c0006 | t0001 | g0102 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02922 | hp1 | a0005 | c0006 | t0003 | g0103 | AFR | ESN | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02922 | hp2 | a0001 | c0018 | t0002 | g0105 | AFR | ESN | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02965 | hp1 | a0011 | c0022 | t0001 | g0096 | AFR | ESN | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02965 | hp2 | a0007 | c0013 | t0003 | g0060 | AFR | ESN | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02970 | hp1 | a0001 | c0018 | t0005 | g0106 | AFR | ESN | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02970 | hp2 | a0009 | c0021 | t0001 | g0130 | AFR | ESN | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03017 | hp1 | a0008 | c0053 | t0001 | g0055 | SAS | PJL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03041 | hp1 | a0006 | c0005 | t0001 | g0104 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03041 | hp2 | a0002 | c0041 | t0001 | g0053 | AFR | GWD | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03098 | hp1 | a0001 | c0007 | t0004 | g0091 | AFR | MSL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03098 | hp2 | a0009 | c0046 | t0009 | g0076 | AFR | MSL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03130 | hp1 | a0023 | c0029 | t0001 | g0141 | AFR | ESN | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ESN | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03195 | hp1 | a0003 | c0003 | t0001 | g0071 | AFR | ESN | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03195 | hp2 | a0003 | c0031 | t0006 | g0037 | AFR | ESN | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03209 | hp1 | a0007 | c0013 | t0001 | g0059 | AFR | MSL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03209 | hp2 | a0001 | c0045 | t0001 | g0085 | AFR | MSL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03225 | hp1 | a0006 | c0005 | t0003 | g0140 | AFR | MSL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03225 | hp2 | a0005 | c0008 | t0001 | g0101 | AFR | MSL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03453 | hp1 | a0002 | c0028 | t0001 | g0073 | AFR | MSL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03453 | hp2 | a0001 | c0014 | t0001 | g0036 | AFR | MSL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03491 | hp1 | a0020 | c0038 | t0001 | g0032 | SAS | PJL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0081 | AFR | ESN | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03516 | hp2 | a0005 | c0006 | t0001 | g0052 | AFR | ESN | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03654 | hp2 | a0002 | c0010 | t0001 | g0051 | SAS | PJL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03942 | hp1 | a0007 | c0032 | t0001 | g0004 | SAS | BEB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03942 | hp2 | a0022 | c0035 | t0001 | g0121 | SAS | BEB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0041 | SAS | STU | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG04115 | hp2 | a0004 | c0004 | t0007 | g0006 | SAS | STU | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG04184 | hp2 | a0004 | c0004 | t0001 | g0018 | SAS | BEB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG04199 | hp2 | a0004 | c0004 | t0001 | g0005 | SAS | STU | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG04204 | hp2 | a0004 | c0004 | t0001 | g0008 | SAS | STU | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | CHB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18906 | hp1 | a0001 | c0027 | t0001 | g0107 | AFR | YRI | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18906 | hp2 | a0006 | c0005 | t0001 | g0072 | AFR | YRI | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18948 | hp1 | a0019 | c0036 | t0001 | g0049 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18948 | hp2 | a0004 | c0004 | t0001 | g0128 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18970 | hp1 | a0002 | c0010 | t0001 | g0047 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18970 | hp2 | a0004 | c0020 | t0001 | g0016 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18971 | hp2 | a0012 | c0019 | t0001 | g0129 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18990 | hp1 | a0012 | c0019 | t0001 | g0127 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18999 | hp1 | a0002 | c0010 | t0001 | g0136 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA19030 | hp1 | a0002 | c0048 | t0001 | g0070 | AFR | LWK | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA19030 | hp2 | a0001 | c0034 | t0001 | g0111 | AFR | LWK | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA19043 | hp1 | a0011 | c0049 | t0001 | g0056 | AFR | LWK | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA19043 | hp2 | a0002 | c0042 | t0001 | g0064 | AFR | LWK | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA19240 | hp1 | a0007 | c0017 | t0001 | g0109 | AFR | YRI | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA19240 | hp2 | a0006 | c0005 | t0001 | g0143 | AFR | YRI | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA20129 | hp1 | a0009 | c0047 | t0001 | g0110 | AFR | ASW | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA20129 | hp2 | a0002 | c0011 | t0005 | g0054 | AFR | ASW | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA20905 | hp1 | a0004 | c0004 | t0001 | g0125 | SAS | GIH | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| NA20905 | hp2 | a0021 | c0037 | t0001 | g0050 | SAS | GIH | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02486 | hp1 | a0001 | c0039 | t0001 | g0039 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02486 | hp2 | a0006 | c0005 | t0001 | g0094 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02559 | hp1 | a0001 | c0026 | t0001 | g0080 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG02559 | hp2 | a0013 | c0016 | t0003 | g0002 | AFR | ACB | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03471 | hp1 | a0014 | c0023 | t0001 | g0057 | AFR | MSL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| HG03471 | hp2 | a0002 | c0011 | t0001 | g0134 | AFR | MSL | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| homoSapiens_chm13v2 | hp1 | a0004 | c0020 | t0001 | g0028 | REF | REF | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| homoSapiens_grch38 | hp1 | a0016 | c0052 | t0001 | g0019 | REF | REF | ARHGEF4_chr2_130831914_131052253 | ARHGEF4 | chr2 | 130831914 | 131052253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:130914191
|
G | C | 1 | a0014 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.245G>C | p.Gly82Ala | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 285/6735 | 245/5631 | 82/1876 | chr2 | 130914191 | ||
| chr2:130914266
|
A | C | 1 | a0015 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.320A>C | p.Asp107Ala | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 360/6735 | 320/5631 | 107/1876 | chr2 | 130914266 | ||
| chr2:130914469
|
G | A | 1 | a0025 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.523G>A | p.Ala175Thr | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 563/6735 | 523/5631 | 175/1876 | chr2 | 130914469 | ||
| chr2:130914572
|
C | T | 2 | a0008a0025 | 6 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(3): Show |
missense_variant | MODERATE | c.626C>T | p.Ser209Phe | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 666/6735 | 626/5631 | 209/1876 | chr2 | 130914572 | ||
| chr2:130914698
|
T | C | 24 | a0001a0002a0003others(21): Show | 143 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(140): Show |
missense_variant | MODERATE | c.752T>C | p.Leu251Pro | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 792/6735 | 752/5631 | 251/1876 | chr2 | 130914698 | ||
| chr2:130914757
|
A | G | 1 | a0017 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.811A>G | p.Lys271Glu | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 851/6735 | 811/5631 | 271/1876 | chr2 | 130914757 | ||
| chr2:130915676
|
A | T | 1 | a0011 | 3 | HG02258.hp2 HG02965.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.1730A>T | p.Asn577Ile | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 1770/6735 | 1730/5631 | 577/1876 | chr2 | 130915676 | ||
| chr2:130915923
|
T | G | 6 | a0003a0007a0013others(3): Show | 21 | HG01109.hp2 HG01175.hp2 HG02055.hp1 others(18): Show |
missense_variant | MODERATE | c.1977T>G | p.Phe659Leu | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2017/6735 | 1977/5631 | 659/1876 | chr2 | 130915923 | ||
| chr2:130915955
|
C | G | 2 | a0002a0018 | 14 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(11): Show |
missense_variant | MODERATE | c.2009C>G | p.Thr670Ser | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2049/6735 | 2009/5631 | 670/1876 | chr2 | 130915955 | ||
| chr2:130916129
|
G | A | 4 | a0004a0009a0011others(1): Show | 18 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(15): Show |
missense_variant | MODERATE | c.2183G>A | p.Ser728Asn | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2223/6735 | 2183/5631 | 728/1876 | chr2 | 130916129 | ||
| chr2:130916134
|
G | C | 1 | a0006 | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
missense_variant | MODERATE | c.2188G>C | p.Glu730Gln | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2228/6735 | 2188/5631 | 730/1876 | chr2 | 130916134 | ||
| chr2:130916357
|
G | A | 1 | a0013 | 2 | HG02559.hp2 HG02572.hp1 |
missense_variant | MODERATE | c.2411G>A | p.Arg804Lys | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2451/6735 | 2411/5631 | 804/1876 | chr2 | 130916357 | ||
| chr2:130916360
|
C | A | 1 | a0017 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.2414C>A | p.Pro805His | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2454/6735 | 2414/5631 | 805/1876 | chr2 | 130916360 | ||
| chr2:130917239
|
G | A | 1 | a0023 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.3293G>A | p.Arg1098Lys | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 3333/6735 | 3293/5631 | 1098/1876 | chr2 | 130917239 | ||
| chr2:130917278
|
G | C | 1 | a0022 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.3332G>C | p.Arg1111Thr | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 3372/6735 | 3332/5631 | 1111/1876 | chr2 | 130917278 | ||
| chr2:130917297
|
G | A | 1 | a0003 | 10 | HG01109.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
missense_variant | MODERATE | c.3351G>A | p.Met1117Ile | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 3391/6735 | 3351/5631 | 1117/1876 | chr2 | 130917297 | ||
| chr2:130917452
|
G | A | 1 | a0005 | 9 | HG01243.hp2 HG02257.hp2 HG02572.hp2 others(6): Show |
missense_variant | MODERATE | c.3506G>A | p.Arg1169His | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 3546/6735 | 3506/5631 | 1169/1876 | chr2 | 130917452 | ||
| chr2:130931054
|
G | C | 1 | a0023 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.3655G>C | p.Asp1219His | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/14 | 3695/6735 | 3655/5631 | 1219/1876 | chr2 | 130931054 | ||
| chr2:130931210
|
G | A | 2 | a0004a0012 | 11 | HG02280.hp2 HG04115.hp2 HG04184.hp2 others(8): Show |
missense_variant | MODERATE | c.3811G>A | p.Val1271Ile | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/14 | 3851/6735 | 3811/5631 | 1271/1876 | chr2 | 130931210 | ||
| chr2:130946613
|
G | C | 1 | a0010 | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
missense_variant | MODERATE | c.3963G>C | p.Trp1321Cys | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/14 | 4003/6735 | 3963/5631 | 1321/1876 | chr2 | 130946613 | ||
| chr2:131040106
|
A | G | 1 | a0018 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.4396A>G | p.Ser1466Gly | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 7/14 | 4436/6735 | 4396/5631 | 1466/1876 | chr2 | 131040106 | ||
| chr2:131040301
|
G | A | 2 | a0012a0019 | 3 | NA18948.hp1 NA18971.hp2 NA18990.hp1 |
missense_variant | MODERATE | c.4523G>A | p.Ser1508Asn | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 8/14 | 4563/6735 | 4523/5631 | 1508/1876 | chr2 | 131040301 | ||
| chr2:131040316
|
G | T | 1 | a0020 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.4538G>T | p.Arg1513Leu | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 8/14 | 4578/6735 | 4538/5631 | 1513/1876 | chr2 | 131040316 | ||
| chr2:131043544
|
G | C | 1 | a0024 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.5118G>C | p.Met1706Ile | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 11/14 | 5158/6735 | 5118/5631 | 1706/1876 | chr2 | 131043544 | ||
| chr2:131046047
|
G | A | 1 | a0021 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.5489G>A | p.Arg1830Gln | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 14/14 | 5529/6735 | 5489/5631 | 1830/1876 | chr2 | 131046047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:130914528
|
T | C | 33 | a0001c0001a0001c0002a0001c0015others(30): Show | 98 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(95): Show |
synonymous_variant | LOW | c.582T>C | p.Pro194Pro | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 622/6735 | 582/5631 | 194/1876 | chr2 | 130914528 | ||
| chr2:130914816
|
G | A | 1 | a0001c0025 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.870G>A | p.Ser290Ser | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 910/6735 | 870/5631 | 290/1876 | chr2 | 130914816 | ||
| chr2:130915377
|
A | G | 18 | a0001c0001a0001c0002a0001c0034others(15): Show | 66 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(63): Show |
synonymous_variant | LOW | c.1431A>G | p.Gln477Gln | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 1471/6735 | 1431/5631 | 477/1876 | chr2 | 130915377 | ||
| chr2:130915650
|
C | T | 6 | a0002c0010a0002c0011a0002c0040others(3): Show | 12 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(9): Show |
synonymous_variant | LOW | c.1704C>T | p.Ala568Ala | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 1744/6735 | 1704/5631 | 568/1876 | chr2 | 130915650 | ||
| chr2:130915686
|
A | G | 1 | a0001c0039 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1740A>G | p.Glu580Glu | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 1780/6735 | 1740/5631 | 580/1876 | chr2 | 130915686 | ||
| chr2:130915743
|
C | T | 20 | a0001c0001a0001c0002a0001c0034others(17): Show | 68 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(65): Show |
synonymous_variant | LOW | c.1797C>T | p.Pro599Pro | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 1837/6735 | 1797/5631 | 599/1876 | chr2 | 130915743 | ||
| chr2:130915893
|
G | A | 1 | a0001c0034 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1947G>A | p.Gly649Gly | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 1987/6735 | 1947/5631 | 649/1876 | chr2 | 130915893 | ||
| chr2:130915959
|
C | A | 1 | a0001c0018 | 2 | HG02922.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.2013C>A | p.Gly671Gly | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2053/6735 | 2013/5631 | 671/1876 | chr2 | 130915959 | ||
| chr2:130916004
|
T | C | 6 | a0001c0018a0001c0044a0001c0045others(3): Show | 10 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(7): Show |
synonymous_variant | LOW | c.2058T>C | p.Gly686Gly | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2098/6735 | 2058/5631 | 686/1876 | chr2 | 130916004 | ||
| chr2:130916127
|
G | A | 1 | a0002c0048 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.2181G>A | p.Pro727Pro | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2221/6735 | 2181/5631 | 727/1876 | chr2 | 130916127 | ||
| chr2:130916247
|
C | T | 1 | a0001c0027 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.2301C>T | p.Pro767Pro | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2341/6735 | 2301/5631 | 767/1876 | chr2 | 130916247 | ||
| chr2:130916298
|
C | T | 6 | a0002c0010a0002c0011a0002c0040others(3): Show | 12 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(9): Show |
synonymous_variant | LOW | c.2352C>T | p.Gly784Gly | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2392/6735 | 2352/5631 | 784/1876 | chr2 | 130916298 | ||
| chr2:130916385
|
G | A | 1 | a0023c0029 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.2439G>A | p.Gly813Gly | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2479/6735 | 2439/5631 | 813/1876 | chr2 | 130916385 | ||
| chr2:130916712
|
A | G | 10 | a0001c0001a0001c0002a0001c0034others(7): Show | 47 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(44): Show |
synonymous_variant | LOW | c.2766A>G | p.Ser922Ser | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2806/6735 | 2766/5631 | 922/1876 | chr2 | 130916712 | ||
| chr2:130916898
|
C | T | 7 | a0002c0010a0002c0011a0002c0040others(4): Show | 13 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
synonymous_variant | LOW | c.2952C>T | p.Thr984Thr | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 2992/6735 | 2952/5631 | 984/1876 | chr2 | 130916898 | ||
| chr2:130916964
|
C | G | 4 | a0002c0011a0002c0041a0002c0042others(1): Show | 7 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
synonymous_variant | LOW | c.3018C>G | p.Pro1006Pro | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/14 | 3058/6735 | 3018/5631 | 1006/1876 | chr2 | 130916964 | ||
| chr2:130931014
|
G | A | 16 | a0002c0010a0002c0011a0002c0040others(13): Show | 39 | HG00621.hp1 HG01109.hp2 HG01884.hp2 others(36): Show |
synonymous_variant | LOW | c.3615G>A | p.Ala1205Ala | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/14 | 3655/6735 | 3615/5631 | 1205/1876 | chr2 | 130931014 | ||
| chr2:131038975
|
G | A | 3 | a0001c0007a0003c0030a0009c0046 | 7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
synonymous_variant | LOW | c.4248G>A | p.Glu1416Glu | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 6/14 | 4288/6735 | 4248/5631 | 1416/1876 | chr2 | 131038975 | ||
| chr2:131044472
|
C | T | 16 | a0001c0002a0001c0026a0001c0045others(13): Show | 32 | HG00642.hp1 HG01243.hp2 HG01515.hp2 others(29): Show |
synonymous_variant | LOW | c.5331C>T | p.Pro1777Pro | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 12/14 | 5371/6735 | 5331/5631 | 1777/1876 | chr2 | 131044472 | ||
| chr2:131046051
|
C | T | 2 | a0002c0042a0006c0050 | 2 | HG02257.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.5493C>T | p.Pro1831Pro | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 14/14 | 5533/6735 | 5493/5631 | 1831/1876 | chr2 | 131046051 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:131046443
|
C | T | 1 | a0009c0046t0009 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*254C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 14/14 | 254 | chr2 | 131046443 | |||||
| chr2:131046531
|
G | GT | 2 | a0001c0007t0004a0003c0030t0004 | 6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*343dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 14/14 | 344 | INFO_REALIGN_3_PRIME | chr2 | 131046531 | ||||
| chr2:131046609
|
A | G | 4 | a0001c0018t0005a0001c0025t0005a0002c0011t0005others(1): Show | 4 | HG01243.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*420A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 14/14 | 420 | chr2 | 131046609 | |||||
| chr2:131046837
|
G | A | 1 | a0004c0004t0007 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*648G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 14/14 | 648 | chr2 | 131046837 | |||||
| chr2:131046885
|
G | A | 6 | a0001c0001t0002a0001c0014t0002a0001c0018t0002others(3): Show | 8 | HG01175.hp2 HG02257.hp2 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*696G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 14/14 | 696 | chr2 | 131046885 | |||||
| chr2:131046974
|
T | C | 2 | a0003c0031t0006a0017c0051t0006 | 2 | HG02615.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*785T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 14/14 | 785 | chr2 | 131046974 | |||||
| chr2:131047076
|
G | A | 5 | a0003c0003t0003a0005c0006t0003a0006c0005t0003others(2): Show | 6 | HG02280.hp1 HG02559.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*887G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 14/14 | 887 | chr2 | 131047076 | |||||
| chr2:131047081
|
G | A | 1 | a0001c0001t0008 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*892G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 14/14 | 892 | chr2 | 131047081 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:130837028
|
C | G | 80 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0087others(77): Show | 80 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.39+36C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130837028 | ||||||
| chr2:130837169
|
G | C | 2 | a0013c0016t0003g0001a0013c0016t0003g0002 | 2 | HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.39+177G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130837169 | ||||||
| chr2:130837191
|
C | T | 33 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(30): Show | 33 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(30): Show |
intron_variant | MODIFIER | c.39+199C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130837191 | ||||||
| chr2:130837282
|
G | T | 4 | a0001c0034t0001g0111a0007c0017t0001g0108a0007c0017t0001g0109others(1): Show | 4 | HG02895.hp1 NA19030.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+290G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130837282 | ||||||
| chr2:130837301
|
C | G | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+309C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130837301 | ||||||
| chr2:130837359
|
C | T | 11 | a0001c0018t0002g0105a0001c0018t0005g0106a0005c0006t0001g0100others(8): Show | 11 | HG02257.hp2 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.39+367C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130837359 | ||||||
| chr2:130837385
|
A | C | 30 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0087others(27): Show | 30 | HG00642.hp2 HG00735.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.39+393A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130837385 | ||||||
| chr2:130837449
|
G | C | 33 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(30): Show | 33 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(30): Show |
intron_variant | MODIFIER | c.39+457G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130837449 | ||||||
| chr2:130837697
|
C | G | 2 | a0001c0014t0002g0075a0009c0046t0009g0076 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.39+705C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130837697 | ||||||
| chr2:130837747
|
C | G | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+755C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130837747 | ||||||
| chr2:130838000
|
G | A | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+1008G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838000 | ||||||
| chr2:130838089
|
G | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+1097G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838089 | ||||||
| chr2:130838159
|
C | G | 1 | a0002c0042t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.39+1167C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838159 | ||||||
| chr2:130838322
|
C | A | 1 | a0002c0010t0001g0003 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.39+1330C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838322 | ||||||
| chr2:130838328
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.39+1336G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838328 | ||||||
| chr2:130838330
|
G | A | 4 | a0001c0034t0001g0111a0007c0017t0001g0108a0007c0017t0001g0109others(1): Show | 4 | HG02895.hp1 NA19030.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+1338G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838330 | ||||||
| chr2:130838466
|
C | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+1474C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838466 | ||||||
| chr2:130838523
|
T | C | 26 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(23): Show | 26 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.39+1531T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838523 | ||||||
| chr2:130838649
|
G | C | 4 | a0001c0034t0001g0111a0007c0017t0001g0108a0007c0017t0001g0109others(1): Show | 4 | HG02895.hp1 NA19030.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+1657G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838649 | ||||||
| chr2:130838683
|
G | A | 1 | a0007c0032t0001g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.39+1691G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838683 | ||||||
| chr2:130838815
|
A | G | 1 | a0007c0032t0001g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.39+1823A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838815 | ||||||
| chr2:130838875
|
G | C | 1 | a0004c0004t0001g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.39+1883G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838875 | ||||||
| chr2:130838931
|
C | G | 19 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0087others(16): Show | 19 | HG00642.hp2 HG00735.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.39+1939C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838931 | ||||||
| chr2:130838958
|
C | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+1966C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838958 | ||||||
| chr2:130838960
|
G | A | 4 | a0001c0014t0002g0075a0003c0003t0001g0071a0006c0005t0001g0072others(1): Show | 4 | HG02647.hp2 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+1968G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130838960 | ||||||
| chr2:130839339
|
T | G | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.39+2347T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130839339 | ||||||
| chr2:130839466
|
G | C | 11 | a0001c0018t0002g0105a0001c0018t0005g0106a0005c0006t0001g0100others(8): Show | 11 | HG02257.hp2 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.39+2474G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130839466 | ||||||
| chr2:130839558
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.39+2566G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130839558 | ||||||
| chr2:130839584
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.39+2592C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130839584 | ||||||
| chr2:130839598
|
G | A | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+2606G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130839598 | ||||||
| chr2:130840062
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.39+3070A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130840062 | ||||||
| chr2:130840262
|
C | T | 1 | a0003c0003t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.39+3270C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130840262 | ||||||
| chr2:130840309
|
A | G | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+3317A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130840309 | ||||||
| chr2:130840336
|
G | C | 7 | a0004c0004t0001g0144a0006c0005t0001g0143a0006c0005t0003g0140others(4): Show | 7 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.39+3344G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130840336 | ||||||
| chr2:130840420
|
G | T | 1 | a0002c0010t0001g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.39+3428G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130840420 | ||||||
| chr2:130840434
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+3442G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130840434 | ||||||
| chr2:130840531
|
A | G | 6 | a0004c0004t0001g0144a0006c0005t0001g0143a0006c0005t0003g0140others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+3539A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130840531 | ||||||
| chr2:130840892
|
A | G | 1 | a0015c0054t0001g0061 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.39+3900A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130840892 | ||||||
| chr2:130841096
|
G | T | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+4104G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841096 | ||||||
| chr2:130841176
|
T | A | 1 | a0008c0012t0001g0082 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.39+4184T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841176 | ||||||
| chr2:130841203
|
T | C | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+4211T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841203 | ||||||
| chr2:130841281
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+4289G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841281 | ||||||
| chr2:130841344
|
A | G | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.39+4352A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841344 | ||||||
| chr2:130841371
|
C | CT | 12 | a0001c0018t0002g0105a0001c0018t0005g0106a0005c0006t0001g0100others(9): Show | 12 | HG01175.hp2 HG02257.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.39+4397dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130841371 | |||||
| chr2:130841371
|
CT | C | 8 | a0001c0025t0005g0067a0001c0027t0001g0107a0002c0048t0001g0070others(5): Show | 8 | HG01243.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.39+4397delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130841371 | |||||
| chr2:130841371
|
CTT | C | 37 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(34): Show | 37 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(34): Show |
intron_variant | MODIFIER | c.39+4396_39+4397del others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130841371 | |||||
| chr2:130841389
|
T | G | 45 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(42): Show | 45 | HG01081.hp2 HG01243.hp1 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.39+4397T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841389 | ||||||
| chr2:130841470
|
T | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+4478T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841470 | ||||||
| chr2:130841601
|
G | A | 1 | a0005c0008t0001g0007 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.39+4609G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841601 | ||||||
| chr2:130841640
|
G | C | 3 | a0001c0001t0001g0009a0001c0002t0001g0010a0004c0004t0001g0008 | 3 | HG00642.hp1 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.39+4648G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841640 | ||||||
| chr2:130841898
|
T | C | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+4906T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841898 | ||||||
| chr2:130841918
|
G | A | 1 | a0002c0010t0001g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.39+4926G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841918 | ||||||
| chr2:130841948
|
G | T | 11 | a0001c0018t0002g0105a0001c0018t0005g0106a0005c0006t0001g0100others(8): Show | 11 | HG02257.hp2 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.39+4956G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841948 | ||||||
| chr2:130841953
|
A | G | 8 | a0001c0025t0005g0067a0001c0027t0001g0107a0002c0028t0001g0073others(5): Show | 8 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.39+4961A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130841953 | ||||||
| chr2:130842418
|
G | A | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+5426G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130842418 | ||||||
| chr2:130842449
|
G | A | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+5457G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130842449 | ||||||
| chr2:130842473
|
A | G | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+5481A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130842473 | ||||||
| chr2:130842487
|
C | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+5495C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130842487 | ||||||
| chr2:130842499
|
C | T | 8 | a0001c0025t0005g0067a0001c0027t0001g0107a0002c0028t0001g0073others(5): Show | 8 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.39+5507C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130842499 | ||||||
| chr2:130842543
|
G | C | 1 | a0001c0044t0001g0011 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.39+5551G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130842543 | ||||||
| chr2:130842648
|
A | G | 5 | a0001c0034t0001g0111a0007c0017t0001g0108a0007c0017t0001g0109others(2): Show | 5 | HG02258.hp1 HG02895.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+5656A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130842648 | ||||||
| chr2:130842775
|
C | T | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+5783C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130842775 | ||||||
| chr2:130842882
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.39+5890G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130842882 | ||||||
| chr2:130842947
|
G | C | 4 | a0001c0034t0001g0111a0007c0017t0001g0108a0007c0017t0001g0109others(1): Show | 4 | HG02895.hp1 NA19030.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+5955G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130842947 | ||||||
| chr2:130842989
|
A | G | 1 | a0002c0010t0001g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.39+5997A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130842989 | ||||||
| chr2:130843005
|
G | A | 1 | a0001c0002t0001g0083 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.39+6013G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130843005 | ||||||
| chr2:130843412
|
G | A | 5 | a0001c0034t0001g0111a0007c0017t0001g0108a0007c0017t0001g0109others(2): Show | 5 | HG02258.hp1 HG02895.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+6420G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130843412 | ||||||
| chr2:130843520
|
C | A | 2 | a0001c0001t0001g0014a0001c0002t0001g0013 | 2 | HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.39+6528C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130843520 | ||||||
| chr2:130843638
|
C | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+6646C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130843638 | ||||||
| chr2:130843780
|
G | C | 11 | a0001c0018t0002g0105a0001c0018t0005g0106a0005c0006t0001g0100others(8): Show | 11 | HG02257.hp2 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.39+6788G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130843780 | ||||||
| chr2:130844171
|
G | T | 1 | a0015c0054t0001g0061 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.39+7179G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130844171 | ||||||
| chr2:130844177
|
C | T | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.39+7185C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130844177 | ||||||
| chr2:130844224
|
G | T | 11 | a0001c0018t0002g0105a0001c0018t0005g0106a0005c0006t0001g0100others(8): Show | 11 | HG02257.hp2 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.39+7232G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130844224 | ||||||
| chr2:130844289
|
C | T | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+7297C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130844289 | ||||||
| chr2:130844379
|
G | A | 5 | a0001c0034t0001g0111a0007c0017t0001g0108a0007c0017t0001g0109others(2): Show | 5 | HG02258.hp1 HG02895.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+7387G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130844379 | ||||||
| chr2:130844410
|
A | G | 40 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(37): Show | 40 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(37): Show |
intron_variant | MODIFIER | c.39+7418A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130844410 | ||||||
| chr2:130844485
|
C | T | 2 | a0001c0027t0001g0107a0002c0028t0001g0073 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.39+7493C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130844485 | ||||||
| chr2:130844750
|
G | A | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+7758G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130844750 | ||||||
| chr2:130845065
|
G | A | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.39+8073G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845065 | ||||||
| chr2:130845248
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0002t0001g0113 | 3 | HG01081.hp2 HG01975.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.39+8256G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845248 | ||||||
| chr2:130845262
|
G | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+8270G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845262 | ||||||
| chr2:130845276
|
T | C | 35 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(32): Show | 35 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.39+8284T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845276 | ||||||
| chr2:130845293
|
C | A | 1 | a0001c0002t0001g0113 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.39+8301C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845293 | ||||||
| chr2:130845312
|
C | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+8320C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845312 | ||||||
| chr2:130845365
|
A | G | 40 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(37): Show | 40 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(37): Show |
intron_variant | MODIFIER | c.39+8373A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845365 | ||||||
| chr2:130845653
|
T | C | 53 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(50): Show | 53 | HG01081.hp2 HG01175.hp2 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.39+8661T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845653 | ||||||
| chr2:130845667
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+8675G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845667 | ||||||
| chr2:130845734
|
T | A | 3 | a0001c0001t0001g0009a0001c0002t0001g0010a0004c0004t0001g0008 | 3 | HG00642.hp1 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.39+8742T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845734 | ||||||
| chr2:130845794
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.39+8802C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845794 | ||||||
| chr2:130845905
|
C | T | 2 | a0001c0027t0001g0107a0002c0028t0001g0073 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.39+8913C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845905 | ||||||
| chr2:130845992
|
C | G | 5 | a0001c0034t0001g0111a0007c0017t0001g0108a0007c0017t0001g0109others(2): Show | 5 | HG02258.hp2 HG02895.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+9000C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845992 | ||||||
| chr2:130845992
|
C | T | 1 | a0006c0005t0001g0094 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.39+9000C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130845992 | ||||||
| chr2:130846020
|
G | T | 2 | a0001c0001t0002g0058a0014c0023t0001g0057 | 2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.39+9028G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846020 | ||||||
| chr2:130846052
|
C | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+9060C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846052 | ||||||
| chr2:130846099
|
G | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+9107G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846099 | ||||||
| chr2:130846281
|
G | A | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.39+9289G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846281 | ||||||
| chr2:130846484
|
A | C | 53 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(50): Show | 53 | HG01081.hp2 HG01175.hp2 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.39+9492A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846484 | ||||||
| chr2:130846511
|
C | T | 32 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(29): Show | 32 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(29): Show |
intron_variant | MODIFIER | c.39+9519C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846511 | ||||||
| chr2:130846512
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0077 | 2 | NA18612.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.39+9520G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846512 | ||||||
| chr2:130846545
|
A | G | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+9553A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846545 | ||||||
| chr2:130846565
|
C | T | 2 | a0002c0028t0001g0073a0007c0013t0002g0095 | 2 | HG01175.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.39+9573C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846565 | ||||||
| chr2:130846628
|
A | G | 1 | a0003c0003t0003g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.39+9636A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846628 | ||||||
| chr2:130846804
|
G | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+9812G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846804 | ||||||
| chr2:130846810
|
G | C | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+9818G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846810 | ||||||
| chr2:130846832
|
T | G | 53 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(50): Show | 53 | HG01081.hp2 HG01175.hp2 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.39+9840T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846832 | ||||||
| chr2:130846928
|
G | A | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.39+9936G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130846928 | ||||||
| chr2:130847063
|
G | C | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+10071G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130847063 | ||||||
| chr2:130847091
|
C | T | 12 | a0001c0018t0002g0105a0001c0018t0005g0106a0005c0006t0001g0100others(9): Show | 12 | HG01175.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.39+10099C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130847091 | ||||||
| chr2:130847146
|
G | A | 6 | a0001c0034t0001g0111a0007c0017t0001g0108a0007c0017t0001g0109others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+10154G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130847146 | ||||||
| chr2:130847281
|
G | A | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+10289G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130847281 | ||||||
| chr2:130847598
|
T | C | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+10606T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130847598 | ||||||
| chr2:130847622
|
C | T | 11 | a0001c0034t0001g0111a0002c0011t0001g0132a0002c0011t0001g0133others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.39+10630C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130847622 | ||||||
| chr2:130847724
|
A | G | 17 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(14): Show | 17 | HG01257.hp2 HG01258.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.39+10732A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130847724 | ||||||
| chr2:130847808
|
C | T | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.39+10816C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130847808 | ||||||
| chr2:130847835
|
C | T | 6 | a0004c0004t0001g0144a0006c0005t0001g0143a0006c0005t0003g0140others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+10843C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130847835 | ||||||
| chr2:130847996
|
G | A | 2 | a0001c0027t0001g0107a0002c0048t0001g0070 | 2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.39+11004G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130847996 | ||||||
| chr2:130847997
|
C | T | 5 | a0001c0018t0002g0105a0001c0018t0005g0106a0001c0026t0001g0080others(2): Show | 5 | HG02280.hp1 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+11005C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130847997 | ||||||
| chr2:130848100
|
G | C | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+11108G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130848100 | ||||||
| chr2:130848131
|
G | A | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.39+11139G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130848131 | ||||||
| chr2:130848145
|
A | G | 134 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(131): Show | 134 | HG00621.hp1 HG00621.hp2 HG00642.hp2 others(131): Show |
intron_variant | MODIFIER | c.39+11153A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130848145 | ||||||
| chr2:130848152
|
A | G | 24 | a0001c0001t0001g0135a0001c0027t0001g0107a0001c0034t0001g0111others(21): Show | 24 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.39+11160A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130848152 | ||||||
| chr2:130848271
|
G | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+11279G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130848271 | ||||||
| chr2:130848285
|
T | C | 62 | a0001c0001t0001g0015a0001c0001t0001g0114a0001c0001t0001g0115others(59): Show | 62 | HG01081.hp2 HG01175.hp2 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.39+11293T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130848285 | ||||||
| chr2:130848372
|
A | G | 36 | a0001c0001t0001g0015a0001c0001t0001g0114a0001c0001t0001g0115others(33): Show | 36 | HG01081.hp2 HG01257.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.39+11380A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130848372 | ||||||
| chr2:130848421
|
G | A | 4 | a0001c0014t0001g0120a0006c0005t0005g0119a0007c0013t0002g0095others(1): Show | 4 | HG01175.hp2 HG02055.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+11429G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130848421 | ||||||
| chr2:130848444
|
G | A | 1 | a0005c0008t0001g0098 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.39+11452G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130848444 | ||||||
| chr2:130848516
|
C | A | 1 | a0001c0001t0001g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.39+11524C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130848516 | ||||||
| chr2:130848537
|
G | C | 1 | a0002c0010t0001g0003 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.39+11545G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130848537 | ||||||
| chr2:130849027
|
GGA | G | 30 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(27): Show | 30 | HG01081.hp2 HG01243.hp1 HG01975.hp2 others(27): Show |
intron_variant | MODIFIER | c.39+12039_39+12040d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130849027 | |||||
| chr2:130849196
|
C | T | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+12204C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849196 | ||||||
| chr2:130849217
|
G | A | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+12225G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849217 | ||||||
| chr2:130849234
|
G | C | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+12242G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849234 | ||||||
| chr2:130849277
|
A | G | 26 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(23): Show | 26 | HG01175.hp2 HG01243.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.39+12285A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849277 | ||||||
| chr2:130849402
|
G | A | 1 | a0001c0045t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.39+12410G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849402 | ||||||
| chr2:130849480
|
C | CT | 3 | a0010c0009t0001g0138a0013c0016t0003g0001a0013c0016t0003g0002 | 3 | HG02258.hp1 HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.39+12489dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130849480 | |||||
| chr2:130849553
|
C | T | 3 | a0010c0009t0001g0138a0013c0016t0003g0001a0013c0016t0003g0002 | 3 | HG02258.hp1 HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.39+12561C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849553 | ||||||
| chr2:130849556
|
T | TTCA | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+12564_39+12565i others(5): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849556 | ||||||
| chr2:130849591
|
C | T | 8 | a0001c0027t0001g0107a0004c0004t0001g0144a0006c0005t0001g0072others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.39+12599C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849591 | ||||||
| chr2:130849769
|
C | T | 63 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(60): Show | 63 | HG01081.hp2 HG01175.hp2 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.39+12777C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849769 | ||||||
| chr2:130849770
|
G | T | 1 | a0002c0011t0001g0134 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.39+12778G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849770 | ||||||
| chr2:130849838
|
T | C | 15 | a0001c0001t0001g0135a0001c0025t0005g0067a0002c0010t0001g0051others(12): Show | 15 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.39+12846T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849838 | ||||||
| chr2:130849886
|
C | T | 31 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(28): Show | 31 | HG01175.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+12894C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849886 | ||||||
| chr2:130849989
|
C | T | 32 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(29): Show | 32 | HG01175.hp2 HG01243.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.39+12997C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130849989 | ||||||
| chr2:130850123
|
G | A | 1 | a0001c0002t0001g0023 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.39+13131G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130850123 | ||||||
| chr2:130850180
|
T | C | 15 | a0001c0001t0001g0135a0001c0025t0005g0067a0002c0010t0001g0051others(12): Show | 15 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.39+13188T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130850180 | ||||||
| chr2:130850190
|
G | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+13198G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130850190 | ||||||
| chr2:130850207
|
G | A | 10 | a0001c0001t0001g0135a0002c0010t0001g0051a0002c0010t0001g0136others(7): Show | 10 | HG03041.hp2 HG03516.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+13215G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130850207 | ||||||
| chr2:130850302
|
A | G | 3 | a0011c0022t0001g0084a0011c0022t0001g0096a0011c0049t0001g0056 | 3 | HG02258.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.39+13310A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130850302 | ||||||
| chr2:130850311
|
A | G | 3 | a0010c0009t0001g0138a0013c0016t0003g0001a0013c0016t0003g0002 | 3 | HG02258.hp1 HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.39+13319A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130850311 | ||||||
| chr2:130850364
|
C | G | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+13372C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130850364 | ||||||
| chr2:130850447
|
G | A | 36 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(33): Show | 36 | HG01081.hp2 HG01175.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.39+13455G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130850447 | ||||||
| chr2:130850853
|
C | G | 4 | a0002c0028t0001g0073a0010c0009t0001g0138a0013c0016t0003g0001others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+13861C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130850853 | ||||||
| chr2:130850882
|
C | T | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+13890C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130850882 | ||||||
| chr2:130850990
|
G | A | 1 | a0006c0005t0003g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.39+13998G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130850990 | ||||||
| chr2:130851075
|
C | G | 32 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(29): Show | 32 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.39+14083C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851075 | ||||||
| chr2:130851095
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.39+14103G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851095 | ||||||
| chr2:130851183
|
C | A | 18 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(15): Show | 18 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.39+14191C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851183 | ||||||
| chr2:130851376
|
G | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.39+14384G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851376 | ||||||
| chr2:130851388
|
A | G | 128 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(125): Show | 128 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(125): Show |
intron_variant | MODIFIER | c.39+14396A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851388 | ||||||
| chr2:130851466
|
C | G | 1 | a0008c0053t0001g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.39+14474C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851466 | ||||||
| chr2:130851534
|
C | T | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+14542C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851534 | ||||||
| chr2:130851549
|
G | A | 4 | a0007c0013t0001g0059a0010c0009t0001g0138a0013c0016t0003g0001others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+14557G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851549 | ||||||
| chr2:130851683
|
C | T | 49 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(46): Show | 49 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.39+14691C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851683 | ||||||
| chr2:130851715
|
A | G | 18 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.39+14723A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851715 | ||||||
| chr2:130851762
|
A | C | 1 | a0001c0001t0008g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.39+14770A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851762 | ||||||
| chr2:130851846
|
G | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.39+14854G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851846 | ||||||
| chr2:130851966
|
A | C | 83 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(80): Show | 83 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(80): Show |
intron_variant | MODIFIER | c.39+14974A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130851966 | ||||||
| chr2:130852088
|
T | C | 2 | a0001c0001t0001g0086a0019c0036t0001g0049 | 2 | HG00735.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.39+15096T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130852088 | ||||||
| chr2:130852110
|
G | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+15118G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130852110 | ||||||
| chr2:130852139
|
A | G | 53 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(50): Show | 53 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.39+15147A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130852139 | ||||||
| chr2:130852284
|
G | T | 3 | a0011c0022t0001g0084a0011c0022t0001g0096a0011c0049t0001g0056 | 3 | HG02258.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.39+15292G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130852284 | ||||||
| chr2:130852467
|
C | T | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+15475C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130852467 | ||||||
| chr2:130852501
|
G | T | 49 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(46): Show | 49 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.39+15509G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130852501 | ||||||
| chr2:130852636
|
G | C | 2 | a0001c0001t0001g0015a0001c0002t0001g0031 | 2 | HG01975.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.39+15644G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130852636 | ||||||
| chr2:130852766
|
G | A | 1 | a0007c0013t0003g0060 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.39+15774G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130852766 | ||||||
| chr2:130852767
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+15775G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130852767 | ||||||
| chr2:130853028
|
G | C | 22 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(19): Show | 22 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.39+16036G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853028 | ||||||
| chr2:130853105
|
G | T | 16 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(13): Show | 16 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.39+16113G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853105 | ||||||
| chr2:130853133
|
G | T | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.39+16141G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853133 | ||||||
| chr2:130853142
|
C | G | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02647.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+16150C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853142 | ||||||
| chr2:130853170
|
A | C | 19 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(16): Show | 19 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.39+16178A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853170 | ||||||
| chr2:130853213
|
G | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+16221G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853213 | ||||||
| chr2:130853335
|
G | T | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.39+16343G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853335 | ||||||
| chr2:130853365
|
C | T | 1 | a0008c0012t0001g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.39+16373C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853365 | ||||||
| chr2:130853420
|
G | A | 1 | a0006c0005t0003g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.39+16428G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853420 | ||||||
| chr2:130853475
|
T | C | 52 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(49): Show | 52 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.39+16483T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853475 | ||||||
| chr2:130853535
|
G | C | 5 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(2): Show | 5 | HG01257.hp2 HG01258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+16543G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853535 | ||||||
| chr2:130853544
|
C | T | 6 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+16552C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853544 | ||||||
| chr2:130853545
|
A | G | 52 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(49): Show | 52 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.39+16553A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853545 | ||||||
| chr2:130853651
|
G | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.39+16659G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853651 | ||||||
| chr2:130853699
|
C | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+16707C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853699 | ||||||
| chr2:130853708
|
T | G | 2 | a0001c0001t0001g0025a0021c0037t0001g0050 | 2 | HG01515.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.39+16716T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853708 | ||||||
| chr2:130853759
|
T | G | 50 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(47): Show | 50 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.39+16767T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853759 | ||||||
| chr2:130853770
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+16778G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853770 | ||||||
| chr2:130853795
|
G | A | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02647.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+16803G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853795 | ||||||
| chr2:130853868
|
G | A | 22 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(19): Show | 22 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.39+16876G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130853868 | ||||||
| chr2:130854053
|
A | G | 1 | a0024c0033t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.39+17061A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130854053 | ||||||
| chr2:130854368
|
C | T | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+17376C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130854368 | ||||||
| chr2:130854381
|
G | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+17389G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130854381 | ||||||
| chr2:130854540
|
TC | T | 49 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(46): Show | 49 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.39+17549delC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130854540 | ||||||
| chr2:130854675
|
A | G | 50 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(47): Show | 50 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.39+17683A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130854675 | ||||||
| chr2:130854846
|
T | TTTTA | 46 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0017others(43): Show | 46 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.39+17894_39+17897d others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130854846 | |||||
| chr2:130854846
|
T | TTTTATTT others(1): Show |
27 | a0001c0001t0001g0015a0001c0001t0001g0033a0001c0001t0001g0035others(24): Show | 27 | HG01243.hp1 HG02080.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.39+17890_39+17897d others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130854846 | |||||
| chr2:130854846
|
T | TTTTATTT others(5): Show |
4 | a0001c0001t0001g0046a0001c0002t0001g0024a0001c0034t0001g0111others(1): Show | 4 | HG01258.hp2 NA18962.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+17886_39+17897d others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130854846 | |||||
| chr2:130854846
|
TTTTA | T | 2 | a0002c0028t0001g0073a0024c0033t0001g0021 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.39+17894_39+17897d others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130854846 | |||||
| chr2:130854846
|
TTTTATTT others(5): Show |
T | 55 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(52): Show | 55 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.39+17886_39+17897d others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130854846 | |||||
| chr2:130854873
|
T | A | 1 | a0007c0017t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.39+17881T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130854873 | ||||||
| chr2:130855040
|
A | AT | 25 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(22): Show | 25 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.39+18059dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130855040 | |||||
| chr2:130855066
|
G | C | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.39+18074G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130855066 | ||||||
| chr2:130855240
|
A | G | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02647.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+18248A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130855240 | ||||||
| chr2:130855279
|
TA | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0086a0008c0012t0001g0082others(1): Show | 4 | HG00642.hp2 HG00735.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+18288delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130855279 | ||||||
| chr2:130855392
|
T | C | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+18400T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130855392 | ||||||
| chr2:130855396
|
A | G | 1 | a0003c0003t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.39+18404A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130855396 | ||||||
| chr2:130855428
|
GAAGA | G | 2 | a0001c0001t0001g0043a0002c0040t0001g0044 | 2 | HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.39+18437_39+18440d others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130855428 | ||||||
| chr2:130855629
|
C | T | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+18637C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130855629 | ||||||
| chr2:130855753
|
G | A | 4 | a0007c0013t0001g0059a0010c0009t0001g0138a0013c0016t0003g0001others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+18761G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130855753 | ||||||
| chr2:130855852
|
CCAAT | C | 22 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0025t0005g0067others(19): Show | 22 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.39+18864_39+18867d others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130855852 | |||||
| chr2:130855865
|
A | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0137 | 2 | HG04184.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.39+18873A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130855865 | ||||||
| chr2:130855879
|
C | G | 13 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0034t0001g0111others(10): Show | 13 | HG03041.hp2 HG03516.hp2 HG03654.hp2 others(10): Show |
intron_variant | MODIFIER | c.39+18887C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130855879 | ||||||
| chr2:130855898
|
T | G | 6 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+18906T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130855898 | ||||||
| chr2:130856034
|
T | C | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+19042T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130856034 | ||||||
| chr2:130856061
|
G | C | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+19069G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130856061 | ||||||
| chr2:130856150
|
G | A | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+19158G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130856150 | ||||||
| chr2:130856197
|
G | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0137 | 2 | HG04184.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.39+19205G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130856197 | ||||||
| chr2:130856316
|
G | A | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+19324G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130856316 | ||||||
| chr2:130856389
|
A | C | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02647.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+19397A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130856389 | ||||||
| chr2:130856516
|
C | T | 1 | a0014c0023t0001g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.39+19524C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130856516 | ||||||
| chr2:130856707
|
G | A | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.39+19715G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130856707 | ||||||
| chr2:130856803
|
T | TA | 26 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0025t0005g0067others(23): Show | 26 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(23): Show |
intron_variant | MODIFIER | c.39+19820dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130856803 | |||||
| chr2:130856957
|
T | C | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.39+19965T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130856957 | ||||||
| chr2:130856958
|
C | A | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+19966C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130856958 | ||||||
| chr2:130856989
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+19997G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130856989 | ||||||
| chr2:130857040
|
G | A | 1 | a0004c0004t0001g0008 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.39+20048G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130857040 | ||||||
| chr2:130857100
|
C | T | 1 | a0009c0021t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.39+20108C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130857100 | ||||||
| chr2:130857149
|
A | G | 1 | a0003c0003t0001g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.39+20157A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130857149 | ||||||
| chr2:130857187
|
G | A | 1 | a0001c0002t0001g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.39+20195G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130857187 | ||||||
| chr2:130857213
|
CAGAGCGA others(3473): Show |
C | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+20224_39+23703d others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130857213 | |||||
| chr2:130857323
|
A | G | 1 | a0025c0024t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.39+20331A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130857323 | ||||||
| chr2:130857410
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.39+20418C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130857410 | ||||||
| chr2:130857451
|
G | A | 6 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+20459G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130857451 | ||||||
| chr2:130857512
|
C | T | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+20520C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130857512 | ||||||
| chr2:130857535
|
TA | T | 55 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(52): Show | 55 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.39+20564delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130857535 | |||||
| chr2:130857535
|
TAAAAAAA others(3472): Show |
T | 9 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+20563_39+24041d others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130857535 | |||||
| chr2:130857535
|
TAAAAAAA others(3474): Show |
T | 16 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(13): Show | 16 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.39+20561_39+24041d others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130857535 | |||||
| chr2:130857576
|
G | C | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+20584G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130857576 | ||||||
| chr2:130857650
|
C | A | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02647.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+20658C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130857650 | ||||||
| chr2:130857741
|
A | G | 1 | a0009c0021t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.39+20749A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130857741 | ||||||
| chr2:130857798
|
TTTTATTT others(3478): Show |
T | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02647.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+20818_39+24302d others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130857798 | |||||
| chr2:130857886
|
G | A | 4 | a0003c0003t0001g0071a0007c0017t0001g0109a0009c0021t0001g0130others(1): Show | 4 | HG02970.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+20894G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130857886 | ||||||
| chr2:130858033
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.39+21041G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130858033 | ||||||
| chr2:130858354
|
C | T | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+21362C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130858354 | ||||||
| chr2:130858481
|
A | T | 7 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.39+21489A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130858481 | ||||||
| chr2:130858703
|
G | T | 2 | a0001c0001t0001g0009a0004c0004t0001g0008 | 2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.39+21711G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130858703 | ||||||
| chr2:130859131
|
G | A | 1 | a0004c0004t0001g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.39+22139G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130859131 | ||||||
| chr2:130859252
|
A | G | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.39+22260A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130859252 | ||||||
| chr2:130859387
|
CA | C | 25 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(22): Show | 25 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.39+22409delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130859387 | |||||
| chr2:130859387
|
CAAAAAAA others(3470): Show |
C | 2 | a0001c0015t0001g0079a0003c0030t0004g0022 | 2 | HG02615.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.39+22409_39+25885d others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130859387 | |||||
| chr2:130859388
|
AAAAAAAA others(3469): Show |
A | 52 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(49): Show | 52 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.39+23651_39+27126d others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130859388 | |||||
| chr2:130859451
|
A | G | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+22459A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130859451 | ||||||
| chr2:130859583
|
AAAAAAAA others(3468): Show |
A | 9 | a0001c0001t0001g0123a0001c0025t0005g0067a0003c0003t0002g0116others(6): Show | 9 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.39+22606_39+26080d others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130859583 | |||||
| chr2:130860152
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.39+23160G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130860152 | ||||||
| chr2:130860398
|
G | A | 1 | a0001c0002t0001g0038 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.39+23406G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130860398 | ||||||
| chr2:130860578
|
C | T | 2 | a0001c0001t0001g0009a0004c0004t0001g0008 | 2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.39+23586C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130860578 | ||||||
| chr2:130860579
|
G | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+23587G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130860579 | ||||||
| chr2:130860801
|
A | G | 1 | a0025c0024t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.39+23809A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130860801 | ||||||
| chr2:130860820
|
T | G | 1 | a0001c0001t0008g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.39+23828T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130860820 | ||||||
| chr2:130860840
|
A | G | 1 | a0007c0013t0003g0060 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.39+23848A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130860840 | ||||||
| chr2:130860868
|
A | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+23876A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130860868 | ||||||
| chr2:130861012
|
G | GTTAAAAA others(3471): Show |
1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+24021_39+24022i others(3480): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130861012 | |||||
| chr2:130861022
|
A | G | 1 | a0001c0001t0008g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.39+24030A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130861022 | ||||||
| chr2:130861030
|
A | G | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+24038A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130861030 | ||||||
| chr2:130861134
|
C | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+24142C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130861134 | ||||||
| chr2:130861218
|
A | G | 1 | a0009c0021t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.39+24226A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130861218 | ||||||
| chr2:130861438
|
G | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+24446G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130861438 | ||||||
| chr2:130861574
|
G | C | 22 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(19): Show | 22 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.39+24582G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130861574 | ||||||
| chr2:130861742
|
T | A | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.39+24750T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130861742 | ||||||
| chr2:130862088
|
C | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+25096C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130862088 | ||||||
| chr2:130862366
|
T | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+25374T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130862366 | ||||||
| chr2:130862640
|
C | T | 25 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(22): Show | 25 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.39+25648C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130862640 | ||||||
| chr2:130862864
|
C | CA | 33 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(30): Show | 33 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.39+25885dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130862864 | |||||
| chr2:130862878
|
T | A | 2 | a0006c0050t0001g0142a0023c0029t0001g0141 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.39+25886T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130862878 | ||||||
| chr2:130863146
|
C | T | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.39+26154C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863146 | ||||||
| chr2:130863177
|
C | T | 16 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(13): Show | 16 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.39+26185C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863177 | ||||||
| chr2:130863216
|
A | C | 22 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0025t0005g0067others(19): Show | 22 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.39+26224A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863216 | ||||||
| chr2:130863239
|
C | T | 1 | a0002c0042t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.39+26247C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863239 | ||||||
| chr2:130863264
|
A | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+26272A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863264 | ||||||
| chr2:130863305
|
A | T | 22 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(19): Show | 22 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.39+26313A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863305 | ||||||
| chr2:130863340
|
A | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+26348A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863340 | ||||||
| chr2:130863485
|
A | G | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+26493A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863485 | ||||||
| chr2:130863692
|
T | G | 4 | a0007c0013t0001g0059a0010c0009t0001g0138a0013c0016t0003g0001others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+26700T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863692 | ||||||
| chr2:130863770
|
A | G | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+26778A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863770 | ||||||
| chr2:130863798
|
G | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(15): Show | 18 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.39+26806G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863798 | ||||||
| chr2:130863806
|
A | C | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+26814A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863806 | ||||||
| chr2:130863879
|
C | G | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+26887C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863879 | ||||||
| chr2:130863887
|
C | G | 19 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(16): Show | 19 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.39+26895C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863887 | ||||||
| chr2:130863967
|
G | A | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.39+26975G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130863967 | ||||||
| chr2:130864000
|
C | T | 1 | a0011c0022t0001g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.39+27008C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864000 | ||||||
| chr2:130864011
|
C | T | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02647.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+27019C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864011 | ||||||
| chr2:130864086
|
C | T | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+27094C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864086 | ||||||
| chr2:130864119
|
G | A | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.39+27127G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864119 | ||||||
| chr2:130864127
|
A | G | 2 | a0001c0001t0001g0014a0004c0004t0007g0006 | 2 | HG03831.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.39+27135A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864127 | ||||||
| chr2:130864134
|
C | T | 25 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(22): Show | 25 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.39+27142C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864134 | ||||||
| chr2:130864140
|
T | C | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.39+27148T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864140 | ||||||
| chr2:130864143
|
A | G | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.39+27151A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864143 | ||||||
| chr2:130864144
|
C | T | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.39+27152C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864144 | ||||||
| chr2:130864151
|
T | A | 35 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(32): Show | 35 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.39+27159T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864151 | ||||||
| chr2:130864165
|
G | A | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+27173G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864165 | ||||||
| chr2:130864181
|
C | CAAAG | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.39+27209_39+27212d others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130864181 | |||||
| chr2:130864181
|
CAAAG | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+27209_39+27212d others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130864181 | |||||
| chr2:130864205
|
A | G | 38 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0007t0004g0089others(35): Show | 38 | HG01243.hp1 HG01243.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.39+27213A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864205 | ||||||
| chr2:130864209
|
A | G | 1 | a0011c0049t0001g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.39+27217A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864209 | ||||||
| chr2:130864210
|
AAAAAG | A | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0134others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+27219_39+27223d others(7): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864210 | ||||||
| chr2:130864214
|
AG | A | 17 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(14): Show | 17 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.39+27224delG | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130864214 | |||||
| chr2:130864215
|
G | A | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(6): Show | 9 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+27223G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864215 | ||||||
| chr2:130864391
|
G | T | 6 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+27399G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864391 | ||||||
| chr2:130864407
|
G | A | 1 | a0007c0017t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.39+27415G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864407 | ||||||
| chr2:130864462
|
C | T | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.39+27470C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864462 | ||||||
| chr2:130864490
|
C | T | 1 | a0009c0021t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.39+27498C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864490 | ||||||
| chr2:130864642
|
G | T | 81 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(78): Show | 81 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.39+27650G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864642 | ||||||
| chr2:130864683
|
C | A | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.39+27691C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130864683 | ||||||
| chr2:130865028
|
A | C | 34 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(31): Show | 34 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.39+28036A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130865028 | ||||||
| chr2:130865029
|
G | A | 34 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(31): Show | 34 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.39+28037G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130865029 | ||||||
| chr2:130865057
|
T | C | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+28065T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130865057 | ||||||
| chr2:130865082
|
G | A | 59 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(56): Show | 59 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.39+28090G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130865082 | ||||||
| chr2:130865190
|
C | T | 1 | a0001c0002t0001g0083 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.39+28198C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130865190 | ||||||
| chr2:130865318
|
G | C | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+28326G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130865318 | ||||||
| chr2:130865342
|
A | C | 1 | a0001c0002t0001g0113 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.39+28350A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130865342 | ||||||
| chr2:130865369
|
G | A | 4 | a0001c0027t0001g0107a0011c0022t0001g0084a0011c0022t0001g0096others(1): Show | 4 | HG02258.hp2 HG02965.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+28377G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130865369 | ||||||
| chr2:130865593
|
A | C | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+28601A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130865593 | ||||||
| chr2:130865621
|
A | G | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02647.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+28629A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130865621 | ||||||
| chr2:130865646
|
C | T | 1 | a0009c0021t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.39+28654C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130865646 | ||||||
| chr2:130865704
|
T | TTTTG | 24 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(21): Show | 24 | HG01081.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.39+28736_39+28739d others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130865704 | |||||
| chr2:130865704
|
T | TTTTGTTT others(1): Show |
12 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0034t0001g0111others(9): Show | 12 | HG03041.hp2 HG03516.hp2 HG03942.hp1 others(9): Show |
intron_variant | MODIFIER | c.39+28732_39+28739d others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130865704 | |||||
| chr2:130865704
|
T | TTTTGTTT others(5): Show |
1 | a0002c0010t0001g0051 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.39+28728_39+28739d others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130865704 | |||||
| chr2:130865704
|
TTTTGTTT others(1): Show |
T | 16 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(13): Show | 16 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.39+28732_39+28739d others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130865704 | |||||
| chr2:130865801
|
C | A | 1 | a0007c0032t0001g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.39+28809C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130865801 | ||||||
| chr2:130866026
|
C | G | 3 | a0004c0004t0001g0128a0012c0019t0001g0127a0012c0019t0001g0129 | 3 | NA18948.hp2 NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.39+29034C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130866026 | ||||||
| chr2:130866070
|
C | T | 18 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0025t0005g0067others(15): Show | 18 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.39+29078C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130866070 | ||||||
| chr2:130866075
|
A | G | 7 | a0004c0004t0001g0144a0006c0005t0001g0072a0006c0005t0001g0143others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.39+29083A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130866075 | ||||||
| chr2:130866225
|
G | T | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+29233G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130866225 | ||||||
| chr2:130866289
|
C | T | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+29297C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130866289 | ||||||
| chr2:130866475
|
C | A | 1 | a0007c0017t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.39+29483C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130866475 | ||||||
| chr2:130866549
|
G | A | 13 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0034t0001g0111others(10): Show | 13 | HG03041.hp2 HG03516.hp2 HG03654.hp2 others(10): Show |
intron_variant | MODIFIER | c.39+29557G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130866549 | ||||||
| chr2:130866848
|
A | G | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+29856A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130866848 | ||||||
| chr2:130866937
|
A | T | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(28): Show | 31 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+29945A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130866937 | ||||||
| chr2:130867212
|
G | T | 1 | a0003c0003t0001g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.39+30220G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867212 | ||||||
| chr2:130867241
|
TA | T | 5 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(2): Show | 5 | HG01257.hp2 HG01258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+30250delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867241 | ||||||
| chr2:130867242
|
A | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0087others(38): Show | 41 | HG00642.hp2 HG01243.hp2 HG01515.hp1 others(38): Show |
intron_variant | MODIFIER | c.39+30250A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867242 | ||||||
| chr2:130867245
|
T | A | 27 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0040others(24): Show | 27 | HG00642.hp1 HG00735.hp1 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.39+30253T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867245 | ||||||
| chr2:130867248
|
T | A | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02647.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+30256T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867248 | ||||||
| chr2:130867348
|
C | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+30356C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867348 | ||||||
| chr2:130867483
|
G | A | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02647.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+30491G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867483 | ||||||
| chr2:130867527
|
T | C | 36 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(33): Show | 36 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.39+30535T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867527 | ||||||
| chr2:130867539
|
A | C | 2 | a0001c0002t0001g0023a0001c0002t0001g0024 | 2 | NA18612.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.39+30547A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867539 | ||||||
| chr2:130867546
|
A | G | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+30554A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867546 | ||||||
| chr2:130867722
|
A | G | 94 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(91): Show | 94 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(91): Show |
intron_variant | MODIFIER | c.39+30730A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867722 | ||||||
| chr2:130867802
|
C | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+30810C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867802 | ||||||
| chr2:130867891
|
G | T | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.39+30899G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867891 | ||||||
| chr2:130867928
|
T | C | 5 | a0001c0027t0001g0107a0009c0021t0001g0139a0011c0022t0001g0084others(2): Show | 5 | HG02258.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+30936T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867928 | ||||||
| chr2:130867935
|
T | C | 4 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+30943T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867935 | ||||||
| chr2:130867936
|
C | CT | 28 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(25): Show | 28 | HG01081.hp2 HG01243.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.39+30960dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130867936 | |||||
| chr2:130867936
|
C | T | 4 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+30944C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130867936 | ||||||
| chr2:130868146
|
C | T | 6 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+31154C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130868146 | ||||||
| chr2:130868470
|
C | T | 15 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(12): Show | 15 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+31478C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130868470 | ||||||
| chr2:130868602
|
C | T | 20 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0025t0005g0067others(17): Show | 20 | HG01243.hp1 HG02615.hp1 HG02698.hp1 others(17): Show |
intron_variant | MODIFIER | c.39+31610C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130868602 | ||||||
| chr2:130868769
|
A | G | 15 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(12): Show | 15 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+31777A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130868769 | ||||||
| chr2:130868787
|
C | A | 7 | a0004c0004t0001g0144a0006c0005t0001g0072a0006c0005t0001g0143others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.39+31795C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130868787 | ||||||
| chr2:130868791
|
C | T | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0034t0001g0111others(12): Show | 15 | HG02698.hp1 HG03041.hp2 HG03516.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+31799C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130868791 | ||||||
| chr2:130869008
|
C | G | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+32016C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130869008 | ||||||
| chr2:130869037
|
C | G | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+32045C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130869037 | ||||||
| chr2:130869223
|
G | A | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02647.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.39+32231G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130869223 | ||||||
| chr2:130869352
|
A | G | 15 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(12): Show | 15 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+32360A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130869352 | ||||||
| chr2:130869357
|
T | C | 5 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(2): Show | 5 | HG01257.hp2 HG01258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+32365T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130869357 | ||||||
| chr2:130869400
|
C | G | 7 | a0004c0004t0001g0144a0006c0005t0001g0072a0006c0005t0001g0143others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.39+32408C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130869400 | ||||||
| chr2:130869451
|
A | G | 7 | a0004c0004t0001g0144a0006c0005t0001g0072a0006c0005t0001g0143others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.39+32459A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130869451 | ||||||
| chr2:130869529
|
T | C | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+32537T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130869529 | ||||||
| chr2:130869722
|
C | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+32730C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130869722 | ||||||
| chr2:130869723
|
G | A | 1 | a0002c0011t0005g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.39+32731G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130869723 | ||||||
| chr2:130870067
|
C | T | 1 | a0001c0014t0001g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.39+33075C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130870067 | ||||||
| chr2:130870254
|
G | C | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0034t0001g0111others(12): Show | 15 | HG02698.hp1 HG03041.hp2 HG03516.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+33262G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130870254 | ||||||
| chr2:130870277
|
G | A | 6 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+33285G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130870277 | ||||||
| chr2:130870341
|
C | T | 1 | a0001c0002t0001g0013 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.39+33349C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130870341 | ||||||
| chr2:130870367
|
A | C | 1 | a0001c0007t0004g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.39+33375A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130870367 | ||||||
| chr2:130870517
|
G | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+33525G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130870517 | ||||||
| chr2:130870524
|
A | G | 15 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(12): Show | 15 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+33532A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130870524 | ||||||
| chr2:130870668
|
G | GGGGAA | 15 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(12): Show | 15 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+33682_39+33686d others(7): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130870668 | |||||
| chr2:130870685
|
T | G | 15 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(12): Show | 15 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+33693T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130870685 | ||||||
| chr2:130870781
|
G | C | 40 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(37): Show | 40 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.39+33789G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130870781 | ||||||
| chr2:130870970
|
C | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+33978C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130870970 | ||||||
| chr2:130871161
|
C | A | 3 | a0011c0022t0001g0084a0011c0022t0001g0096a0011c0049t0001g0056 | 3 | HG02258.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.39+34169C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130871161 | ||||||
| chr2:130871302
|
G | A | 53 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0007t0004g0089others(50): Show | 53 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.39+34310G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130871302 | ||||||
| chr2:130871419
|
C | T | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.39+34427C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130871419 | ||||||
| chr2:130871461
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+34469G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130871461 | ||||||
| chr2:130871502
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.39+34510C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130871502 | ||||||
| chr2:130871544
|
T | A | 20 | a0001c0001t0001g0135a0001c0025t0005g0067a0001c0034t0001g0111others(17): Show | 20 | HG01243.hp1 HG02615.hp1 HG02698.hp1 others(17): Show |
intron_variant | MODIFIER | c.39+34552T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130871544 | ||||||
| chr2:130871596
|
TAC | T | 95 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(92): Show | 95 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(92): Show |
intron_variant | MODIFIER | c.39+34619_39+34620d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130871596 | |||||
| chr2:130871633
|
G | GA | 15 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(12): Show | 15 | HG01081.hp2 HG01884.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+34649dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130871633 | |||||
| chr2:130871755
|
T | C | 1 | a0004c0004t0001g0008 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.39+34763T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130871755 | ||||||
| chr2:130871768
|
C | T | 1 | a0001c0045t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.39+34776C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130871768 | ||||||
| chr2:130871792
|
C | A | 16 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(13): Show | 16 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.39+34800C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130871792 | ||||||
| chr2:130871940
|
C | T | 4 | a0007c0013t0001g0059a0010c0009t0001g0138a0013c0016t0003g0001others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+34948C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130871940 | ||||||
| chr2:130872045
|
G | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+35053G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872045 | ||||||
| chr2:130872059
|
C | T | 19 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(16): Show | 19 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.39+35067C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872059 | ||||||
| chr2:130872141
|
T | G | 4 | a0001c0014t0001g0036a0007c0013t0001g0059a0013c0016t0003g0001others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+35149T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872141 | ||||||
| chr2:130872239
|
G | A | 1 | a0001c0034t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.39+35247G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872239 | ||||||
| chr2:130872260
|
G | A | 5 | a0001c0014t0001g0036a0007c0013t0001g0059a0010c0009t0001g0138others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+35268G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872260 | ||||||
| chr2:130872503
|
C | G | 32 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0086others(29): Show | 32 | HG00735.hp1 HG01515.hp1 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.39+35511C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872503 | ||||||
| chr2:130872522
|
G | A | 1 | a0005c0006t0003g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.39+35530G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872522 | ||||||
| chr2:130872576
|
A | G | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+35584A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872576 | ||||||
| chr2:130872606
|
T | C | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+35614T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872606 | ||||||
| chr2:130872620
|
A | G | 10 | a0001c0001t0001g0077a0001c0001t0001g0114a0001c0001t0001g0115others(7): Show | 10 | HG00642.hp2 HG01081.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+35628A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872620 | ||||||
| chr2:130872764
|
G | A | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.39+35772G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872764 | ||||||
| chr2:130872814
|
G | A | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+35822G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872814 | ||||||
| chr2:130872839
|
G | A | 10 | a0001c0001t0001g0025a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG00735.hp1 HG01515.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+35847G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872839 | ||||||
| chr2:130872934
|
C | T | 34 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0014t0002g0075others(31): Show | 34 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.39+35942C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130872934 | ||||||
| chr2:130872938
|
C | CTGGGGCA others(14): Show |
1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+35952_39+35972d others(23): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130872938 | |||||
| chr2:130873210
|
A | C | 15 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+36218A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130873210 | ||||||
| chr2:130873395
|
C | A | 4 | a0007c0013t0001g0059a0010c0009t0001g0138a0013c0016t0003g0001others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+36403C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130873395 | ||||||
| chr2:130873520
|
C | CAG | 89 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(86): Show | 89 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(86): Show |
intron_variant | MODIFIER | c.39+36529_39+36530d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130873520 | |||||
| chr2:130873587
|
C | CA | 61 | a0001c0001t0001g0135a0001c0015t0001g0078a0001c0015t0001g0079others(58): Show | 61 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.39+36609dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130873587 | |||||
| chr2:130873808
|
T | C | 1 | a0009c0021t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.39+36816T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130873808 | ||||||
| chr2:130873902
|
G | A | 1 | a0001c0026t0001g0080 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.39+36910G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130873902 | ||||||
| chr2:130873920
|
G | A | 1 | a0001c0044t0001g0011 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.39+36928G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130873920 | ||||||
| chr2:130873990
|
G | C | 2 | a0007c0013t0002g0095a0024c0033t0001g0021 | 2 | HG01175.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.39+36998G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130873990 | ||||||
| chr2:130874098
|
CT | C | 61 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0015t0001g0078others(58): Show | 61 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.39+37111delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130874098 | |||||
| chr2:130874174
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.39+37182C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130874174 | ||||||
| chr2:130874235
|
A | G | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+37243A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130874235 | ||||||
| chr2:130874290
|
A | G | 3 | a0011c0022t0001g0084a0011c0022t0001g0096a0011c0049t0001g0056 | 3 | HG02258.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.39+37298A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130874290 | ||||||
| chr2:130874461
|
C | A | 37 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(34): Show | 37 | HG01175.hp2 HG01243.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.39+37469C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130874461 | ||||||
| chr2:130874493
|
A | T | 3 | a0011c0022t0001g0084a0011c0022t0001g0096a0011c0049t0001g0056 | 3 | HG02258.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.39+37501A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130874493 | ||||||
| chr2:130874558
|
T | C | 24 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0025t0005g0067others(21): Show | 24 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.39+37566T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130874558 | ||||||
| chr2:130874757
|
C | T | 61 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0015t0001g0078others(58): Show | 61 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.39+37765C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130874757 | ||||||
| chr2:130874758
|
C | G | 61 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0015t0001g0078others(58): Show | 61 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.39+37766C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130874758 | ||||||
| chr2:130874869
|
T | C | 61 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0015t0001g0078others(58): Show | 61 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.39+37877T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130874869 | ||||||
| chr2:130874901
|
G | A | 1 | a0007c0032t0001g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.39+37909G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130874901 | ||||||
| chr2:130875198
|
C | T | 1 | a0025c0024t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.39+38206C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875198 | ||||||
| chr2:130875237
|
G | T | 24 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0025t0005g0067others(21): Show | 24 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.39+38245G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875237 | ||||||
| chr2:130875239
|
G | A | 8 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0025t0005g0067others(5): Show | 8 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.39+38247G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875239 | ||||||
| chr2:130875269
|
G | T | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+38277G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875269 | ||||||
| chr2:130875391
|
A | G | 2 | a0001c0002t0001g0023a0001c0002t0001g0024 | 2 | NA18612.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.39+38399A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875391 | ||||||
| chr2:130875464
|
A | G | 24 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0025t0005g0067others(21): Show | 24 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.39+38472A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875464 | ||||||
| chr2:130875640
|
C | T | 4 | a0003c0003t0001g0071a0007c0017t0001g0109a0009c0021t0001g0130others(1): Show | 4 | HG02970.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-38346C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875640 | ||||||
| chr2:130875668
|
C | T | 1 | a0007c0017t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.40-38318C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875668 | ||||||
| chr2:130875669
|
G | A | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.40-38317G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875669 | ||||||
| chr2:130875689
|
T | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-38297T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875689 | ||||||
| chr2:130875789
|
C | G | 23 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(20): Show | 23 | HG01175.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.40-38197C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875789 | ||||||
| chr2:130875921
|
G | T | 1 | a0001c0002t0001g0010 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.40-38065G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875921 | ||||||
| chr2:130875989
|
C | T | 4 | a0007c0013t0001g0059a0010c0009t0001g0138a0013c0016t0003g0001others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-37997C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130875989 | ||||||
| chr2:130876097
|
G | C | 32 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(29): Show | 32 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.40-37889G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130876097 | ||||||
| chr2:130876100
|
G | A | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.40-37886G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130876100 | ||||||
| chr2:130876272
|
G | C | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0034t0001g0111others(12): Show | 15 | HG02698.hp1 HG03041.hp2 HG03516.hp2 others(12): Show |
intron_variant | MODIFIER | c.40-37714G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130876272 | ||||||
| chr2:130876294
|
G | T | 15 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0034t0001g0111others(12): Show | 15 | HG02698.hp1 HG03041.hp2 HG03516.hp2 others(12): Show |
intron_variant | MODIFIER | c.40-37692G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130876294 | ||||||
| chr2:130876432
|
C | T | 9 | a0001c0025t0005g0067a0003c0003t0001g0071a0007c0017t0001g0109others(6): Show | 9 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.40-37554C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130876432 | ||||||
| chr2:130876455
|
G | A | 14 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(11): Show | 14 | HG00642.hp2 HG00735.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.40-37531G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130876455 | ||||||
| chr2:130876536
|
G | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-37450G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130876536 | ||||||
| chr2:130876582
|
C | T | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-37404C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130876582 | ||||||
| chr2:130876634
|
C | T | 1 | a0003c0003t0001g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40-37352C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130876634 | ||||||
| chr2:130876684
|
G | A | 19 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0034t0001g0111others(16): Show | 19 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.40-37302G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130876684 | ||||||
| chr2:130876756
|
A | G | 2 | a0008c0012t0001g0045a0009c0046t0009g0076 | 2 | HG01109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.40-37230A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130876756 | ||||||
| chr2:130876953
|
G | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.40-37033G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130876953 | ||||||
| chr2:130877054
|
C | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-36932C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130877054 | ||||||
| chr2:130877183
|
A | T | 46 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(43): Show | 46 | HG00642.hp2 HG00735.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.40-36803A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130877183 | ||||||
| chr2:130877185
|
A | G | 93 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(90): Show | 93 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.40-36801A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130877185 | ||||||
| chr2:130877306
|
T | C | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-36680T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130877306 | ||||||
| chr2:130877564
|
T | C | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-36422T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130877564 | ||||||
| chr2:130877581
|
C | T | 4 | a0007c0013t0001g0059a0010c0009t0001g0138a0013c0016t0003g0001others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-36405C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130877581 | ||||||
| chr2:130877594
|
G | C | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-36392G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130877594 | ||||||
| chr2:130877760
|
A | C | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-36226A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130877760 | ||||||
| chr2:130877795
|
T | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-36191T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130877795 | ||||||
| chr2:130877796
|
T | C | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-36190T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130877796 | ||||||
| chr2:130877827
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-36159A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130877827 | ||||||
| chr2:130877993
|
G | T | 1 | a0008c0053t0001g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.40-35993G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130877993 | ||||||
| chr2:130878071
|
C | G | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.40-35915C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878071 | ||||||
| chr2:130878072
|
A | G | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-35914A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878072 | ||||||
| chr2:130878157
|
T | G | 1 | a0004c0004t0001g0005 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.40-35829T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878157 | ||||||
| chr2:130878191
|
T | G | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-35795T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878191 | ||||||
| chr2:130878281
|
C | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-35705C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878281 | ||||||
| chr2:130878309
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-35677A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878309 | ||||||
| chr2:130878412
|
A | G | 3 | a0007c0013t0001g0059a0013c0016t0003g0001a0013c0016t0003g0002 | 3 | HG02559.hp2 HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.40-35574A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878412 | ||||||
| chr2:130878657
|
A | G | 6 | a0001c0025t0005g0067a0002c0028t0001g0073a0010c0009t0001g0065others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-35329A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878657 | ||||||
| chr2:130878823
|
G | A | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-35163G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878823 | ||||||
| chr2:130878828
|
C | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-35158C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878828 | ||||||
| chr2:130878874
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-35112A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878874 | ||||||
| chr2:130878888
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-35098A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878888 | ||||||
| chr2:130878921
|
G | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.40-35065G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130878921 | ||||||
| chr2:130879040
|
A | G | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-34946A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130879040 | ||||||
| chr2:130879055
|
G | T | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-34931G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130879055 | ||||||
| chr2:130879442
|
G | T | 2 | a0007c0013t0002g0095a0024c0033t0001g0021 | 2 | HG01175.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.40-34544G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130879442 | ||||||
| chr2:130879456
|
A | T | 1 | a0001c0001t0001g0126 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.40-34530A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130879456 | ||||||
| chr2:130879777
|
T | C | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-34209T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130879777 | ||||||
| chr2:130879780
|
A | AT | 14 | a0001c0014t0001g0120a0001c0015t0001g0078a0001c0015t0001g0079others(11): Show | 14 | HG01175.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.40-34198dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130879780 | |||||
| chr2:130879782
|
T | TA | 7 | a0004c0004t0001g0144a0006c0005t0001g0072a0006c0005t0001g0143others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-34204_40-34203i others(3): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130879782 | ||||||
| chr2:130879855
|
C | T | 7 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-34131C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130879855 | ||||||
| chr2:130880005
|
C | T | 2 | a0001c0001t0001g0025a0021c0037t0001g0050 | 2 | HG01515.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.40-33981C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880005 | ||||||
| chr2:130880017
|
G | A | 2 | a0006c0050t0001g0142a0023c0029t0001g0141 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.40-33969G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880017 | ||||||
| chr2:130880116
|
G | A | 72 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0077others(69): Show | 72 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.40-33870G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880116 | ||||||
| chr2:130880273
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.40-33713G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880273 | ||||||
| chr2:130880275
|
T | C | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-33711T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880275 | ||||||
| chr2:130880448
|
A | G | 64 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0077others(61): Show | 64 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.40-33538A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880448 | ||||||
| chr2:130880554
|
A | G | 17 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(14): Show | 17 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.40-33432A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880554 | ||||||
| chr2:130880584
|
C | T | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-33402C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880584 | ||||||
| chr2:130880735
|
A | G | 8 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-33251A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880735 | ||||||
| chr2:130880788
|
A | G | 3 | a0011c0022t0001g0084a0011c0022t0001g0096a0011c0049t0001g0056 | 3 | HG02258.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40-33198A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880788 | ||||||
| chr2:130880831
|
A | AT | 6 | a0001c0025t0005g0067a0002c0028t0001g0073a0010c0009t0001g0065others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-33139dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130880831 | |||||
| chr2:130880831
|
AT | A | 20 | a0001c0001t0001g0017a0001c0001t0001g0088a0001c0002t0001g0020others(17): Show | 20 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.40-33139delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130880831 | |||||
| chr2:130880868
|
G | A | 17 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(14): Show | 17 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.40-33118G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880868 | ||||||
| chr2:130880874
|
G | C | 8 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-33112G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880874 | ||||||
| chr2:130880939
|
C | T | 8 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-33047C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880939 | ||||||
| chr2:130880982
|
T | C | 8 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-33004T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880982 | ||||||
| chr2:130880993
|
G | T | 3 | a0007c0013t0001g0059a0013c0016t0003g0001a0013c0016t0003g0002 | 3 | HG02559.hp2 HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.40-32993G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130880993 | ||||||
| chr2:130881003
|
C | A | 8 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-32983C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881003 | ||||||
| chr2:130881030
|
TTTG | T | 3 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080 | 3 | HG02559.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40-32937_40-32935d others(5): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130881030 | |||||
| chr2:130881101
|
C | T | 1 | a0001c0002t0001g0013 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.40-32885C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881101 | ||||||
| chr2:130881110
|
A | G | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-32876A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881110 | ||||||
| chr2:130881153
|
C | T | 2 | a0007c0013t0002g0095a0024c0033t0001g0021 | 2 | HG01175.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.40-32833C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881153 | ||||||
| chr2:130881175
|
G | A | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.40-32811G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881175 | ||||||
| chr2:130881457
|
T | TA | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-32527dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130881457 | |||||
| chr2:130881495
|
AAGAGCGG others(8237): Show |
A | 1 | a0001c0014t0001g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.40-32488_40-24245d others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130881495 | |||||
| chr2:130881525
|
A | G | 4 | a0003c0003t0001g0071a0007c0017t0001g0109a0009c0021t0001g0130others(1): Show | 4 | HG02970.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-32461A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881525 | ||||||
| chr2:130881632
|
T | G | 4 | a0009c0021t0001g0139a0011c0022t0001g0084a0011c0022t0001g0096others(1): Show | 4 | HG02258.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-32354T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881632 | ||||||
| chr2:130881750
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(10): Show | 13 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.40-32236C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881750 | ||||||
| chr2:130881782
|
A | G | 71 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0077others(68): Show | 71 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.40-32204A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881782 | ||||||
| chr2:130881797
|
G | A | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-32189G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881797 | ||||||
| chr2:130881844
|
G | A | 2 | a0007c0013t0002g0095a0024c0033t0001g0021 | 2 | HG01175.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.40-32142G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881844 | ||||||
| chr2:130881879
|
C | T | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-32107C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881879 | ||||||
| chr2:130881919
|
T | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-32067T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130881919 | ||||||
| chr2:130882045
|
G | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-31941G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130882045 | ||||||
| chr2:130882046
|
C | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-31940C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130882046 | ||||||
| chr2:130882150
|
T | C | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-31836T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130882150 | ||||||
| chr2:130882154
|
G | A | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.40-31832G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130882154 | ||||||
| chr2:130882178
|
G | A | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.40-31808G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130882178 | ||||||
| chr2:130882261
|
G | A | 7 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-31725G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130882261 | ||||||
| chr2:130882428
|
C | T | 14 | a0002c0048t0001g0070a0004c0004t0001g0144a0006c0005t0001g0072others(11): Show | 14 | HG01175.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.40-31558C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130882428 | ||||||
| chr2:130882736
|
C | T | 4 | a0009c0021t0001g0139a0011c0022t0001g0084a0011c0022t0001g0096others(1): Show | 4 | HG02258.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-31250C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130882736 | ||||||
| chr2:130882767
|
A | T | 4 | a0003c0003t0001g0071a0007c0017t0001g0109a0009c0021t0001g0130others(1): Show | 4 | HG02970.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-31219A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130882767 | ||||||
| chr2:130882780
|
T | C | 1 | a0010c0009t0001g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.40-31206T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130882780 | ||||||
| chr2:130882791
|
G | A | 17 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(14): Show | 17 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.40-31195G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130882791 | ||||||
| chr2:130883139
|
G | A | 17 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(14): Show | 17 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.40-30847G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130883139 | ||||||
| chr2:130883174
|
G | T | 1 | a0004c0004t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.40-30812G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130883174 | ||||||
| chr2:130883266
|
G | C | 4 | a0003c0003t0001g0071a0007c0017t0001g0109a0009c0021t0001g0130others(1): Show | 4 | HG02970.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-30720G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130883266 | ||||||
| chr2:130883364
|
A | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-30622A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130883364 | ||||||
| chr2:130883898
|
A | G | 17 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(14): Show | 17 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.40-30088A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130883898 | ||||||
| chr2:130884090
|
T | C | 8 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-29896T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130884090 | ||||||
| chr2:130884231
|
T | TAC | 51 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0077others(48): Show | 51 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.40-29744_40-29743d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130884231 | |||||
| chr2:130884292
|
A | G | 17 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(14): Show | 17 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.40-29694A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130884292 | ||||||
| chr2:130884302
|
G | GCA | 4 | a0003c0003t0001g0071a0007c0017t0001g0109a0009c0021t0001g0130others(1): Show | 4 | HG02970.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-29668_40-29667d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130884302 | |||||
| chr2:130884318
|
A | C | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-29668A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130884318 | ||||||
| chr2:130884327
|
A | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-29659A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130884327 | ||||||
| chr2:130884548
|
C | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-29438C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130884548 | ||||||
| chr2:130884559
|
T | C | 2 | a0001c0001t0001g0025a0021c0037t0001g0050 | 2 | HG01515.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.40-29427T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130884559 | ||||||
| chr2:130884627
|
T | C | 71 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0077others(68): Show | 71 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.40-29359T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130884627 | ||||||
| chr2:130884727
|
G | C | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.40-29259G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130884727 | ||||||
| chr2:130884829
|
AT | A | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-29156delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130884829 | ||||||
| chr2:130884899
|
G | A | 24 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(21): Show | 24 | HG01081.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.40-29087G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130884899 | ||||||
| chr2:130884902
|
C | T | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-29084C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130884902 | ||||||
| chr2:130884906
|
C | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-29080C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130884906 | ||||||
| chr2:130885079
|
A | G | 17 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(14): Show | 17 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.40-28907A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885079 | ||||||
| chr2:130885194
|
G | A | 2 | a0001c0001t0001g0033a0020c0038t0001g0032 | 2 | HG03491.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.40-28792G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885194 | ||||||
| chr2:130885233
|
G | A | 1 | a0001c0001t0008g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.40-28753G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885233 | ||||||
| chr2:130885234
|
A | C | 1 | a0001c0001t0008g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.40-28752A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885234 | ||||||
| chr2:130885433
|
C | T | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-28553C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885433 | ||||||
| chr2:130885470
|
C | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-28516C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885470 | ||||||
| chr2:130885518
|
G | C | 20 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(17): Show | 20 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.40-28468G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885518 | ||||||
| chr2:130885522
|
G | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.40-28464G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885522 | ||||||
| chr2:130885543
|
A | G | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-28443A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885543 | ||||||
| chr2:130885564
|
C | CT | 9 | a0001c0001t0001g0009a0001c0001t0001g0046a0001c0034t0001g0111others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.40-28398dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130885564 | |||||
| chr2:130885564
|
CT | C | 44 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0114others(41): Show | 44 | HG01081.hp2 HG01175.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.40-28398delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130885564 | |||||
| chr2:130885564
|
CTT | C | 25 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(22): Show | 25 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.40-28399_40-28398d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130885564 | |||||
| chr2:130885591
|
A | T | 20 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0086others(17): Show | 20 | HG00642.hp2 HG00735.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.40-28395A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885591 | ||||||
| chr2:130885593
|
G | T | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-28393G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885593 | ||||||
| chr2:130885607
|
T | C | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.40-28379T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885607 | ||||||
| chr2:130885633
|
A | G | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-28353A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885633 | ||||||
| chr2:130885690
|
C | T | 35 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(32): Show | 35 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.40-28296C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885690 | ||||||
| chr2:130885726
|
T | C | 35 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(32): Show | 35 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.40-28260T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885726 | ||||||
| chr2:130885780
|
C | T | 35 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(32): Show | 35 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.40-28206C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885780 | ||||||
| chr2:130885889
|
A | T | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.40-28097A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130885889 | ||||||
| chr2:130886209
|
A | C | 35 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(32): Show | 35 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.40-27777A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886209 | ||||||
| chr2:130886251
|
T | C | 35 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(32): Show | 35 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.40-27735T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886251 | ||||||
| chr2:130886288
|
GT | G | 86 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(83): Show | 86 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.40-27689delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130886288 | |||||
| chr2:130886351
|
C | G | 6 | a0001c0025t0005g0067a0002c0028t0001g0073a0010c0009t0001g0065others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-27635C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886351 | ||||||
| chr2:130886364
|
A | AG | 3 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080 | 3 | HG02559.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40-27622_40-27621i others(3): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886364 | ||||||
| chr2:130886433
|
A | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-27553A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886433 | ||||||
| chr2:130886454
|
C | T | 1 | a0007c0013t0003g0060 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.40-27532C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886454 | ||||||
| chr2:130886497
|
G | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-27489G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886497 | ||||||
| chr2:130886546
|
T | C | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-27440T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886546 | ||||||
| chr2:130886554
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-27432A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886554 | ||||||
| chr2:130886570
|
A | G | 2 | a0002c0048t0001g0070a0017c0051t0006g0069 | 2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.40-27416A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886570 | ||||||
| chr2:130886573
|
T | C | 69 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(66): Show | 69 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.40-27413T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886573 | ||||||
| chr2:130886580
|
C | A | 1 | a0009c0021t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.40-27406C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886580 | ||||||
| chr2:130886599
|
G | T | 69 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(66): Show | 69 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.40-27387G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886599 | ||||||
| chr2:130886659
|
T | C | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-27327T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886659 | ||||||
| chr2:130886661
|
G | A | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-27325G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886661 | ||||||
| chr2:130886666
|
C | G | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-27320C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886666 | ||||||
| chr2:130886680
|
C | CA | 5 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(2): Show | 5 | HG01257.hp2 HG01258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-27291dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130886680 | |||||
| chr2:130886680
|
CA | C | 55 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(52): Show | 55 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.40-27291delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130886680 | |||||
| chr2:130886778
|
A | G | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-27208A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130886778 | ||||||
| chr2:130886839
|
A | AT | 11 | a0001c0025t0005g0067a0001c0045t0001g0085a0002c0011t0001g0132others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.40-27136dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130886839 | |||||
| chr2:130887020
|
A | G | 1 | a0006c0005t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.40-26966A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887020 | ||||||
| chr2:130887081
|
ATGT | A | 6 | a0001c0025t0005g0067a0002c0028t0001g0073a0010c0009t0001g0065others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-26900_40-26898d others(5): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130887081 | |||||
| chr2:130887169
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.40-26817C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887169 | ||||||
| chr2:130887273
|
A | T | 64 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(61): Show | 64 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.40-26713A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887273 | ||||||
| chr2:130887331
|
C | CA | 6 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.40-26645dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130887331 | |||||
| chr2:130887367
|
A | G | 86 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(83): Show | 86 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.40-26619A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887367 | ||||||
| chr2:130887393
|
G | A | 54 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(51): Show | 54 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.40-26593G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887393 | ||||||
| chr2:130887417
|
A | G | 86 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(83): Show | 86 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.40-26569A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887417 | ||||||
| chr2:130887551
|
G | A | 47 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(44): Show | 47 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.40-26435G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887551 | ||||||
| chr2:130887578
|
C | T | 47 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(44): Show | 47 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.40-26408C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887578 | ||||||
| chr2:130887625
|
T | A | 86 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(83): Show | 86 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.40-26361T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887625 | ||||||
| chr2:130887700
|
T | A | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-26286T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887700 | ||||||
| chr2:130887779
|
C | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-26207C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887779 | ||||||
| chr2:130887808
|
C | T | 1 | a0007c0017t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.40-26178C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887808 | ||||||
| chr2:130887857
|
C | T | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-26129C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887857 | ||||||
| chr2:130887901
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-26085A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130887901 | ||||||
| chr2:130888003
|
C | T | 47 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(44): Show | 47 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.40-25983C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888003 | ||||||
| chr2:130888077
|
A | G | 15 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.40-25909A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888077 | ||||||
| chr2:130888110
|
A | T | 47 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(44): Show | 47 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.40-25876A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888110 | ||||||
| chr2:130888135
|
G | A | 3 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080 | 3 | HG02559.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40-25851G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888135 | ||||||
| chr2:130888183
|
A | C | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-25803A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888183 | ||||||
| chr2:130888245
|
C | CG | 47 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(44): Show | 47 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.40-25738dupG | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130888245 | |||||
| chr2:130888340
|
A | G | 47 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(44): Show | 47 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.40-25646A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888340 | ||||||
| chr2:130888386
|
A | G | 86 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(83): Show | 86 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.40-25600A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888386 | ||||||
| chr2:130888401
|
T | A | 47 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(44): Show | 47 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.40-25585T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888401 | ||||||
| chr2:130888417
|
A | G | 52 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(49): Show | 52 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.40-25569A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888417 | ||||||
| chr2:130888440
|
C | T | 47 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(44): Show | 47 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.40-25546C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888440 | ||||||
| chr2:130888541
|
A | C | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-25445A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888541 | ||||||
| chr2:130888645
|
A | G | 47 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(44): Show | 47 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.40-25341A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888645 | ||||||
| chr2:130888662
|
G | A | 4 | a0003c0003t0001g0071a0007c0017t0001g0109a0009c0021t0001g0130others(1): Show | 4 | HG02970.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-25324G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888662 | ||||||
| chr2:130888737
|
A | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-25249A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888737 | ||||||
| chr2:130888818
|
C | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(38): Show | 41 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.40-25168C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888818 | ||||||
| chr2:130888854
|
A | C | 35 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(32): Show | 35 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.40-25132A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888854 | ||||||
| chr2:130888916
|
C | T | 1 | a0001c0014t0002g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.40-25070C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888916 | ||||||
| chr2:130888929
|
C | T | 7 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-25057C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888929 | ||||||
| chr2:130888962
|
G | A | 27 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(24): Show | 27 | HG01175.hp2 HG01243.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.40-25024G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130888962 | ||||||
| chr2:130889105
|
C | CA | 44 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.40-24868dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130889105 | |||||
| chr2:130889105
|
C | CAA | 7 | a0001c0001t0001g0087a0001c0025t0005g0067a0002c0028t0001g0073others(4): Show | 7 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-24869_40-24868d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130889105 | |||||
| chr2:130889305
|
C | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-24681C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130889305 | ||||||
| chr2:130889308
|
A | G | 86 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(83): Show | 86 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.40-24678A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130889308 | ||||||
| chr2:130889358
|
T | C | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-24628T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130889358 | ||||||
| chr2:130889778
|
C | T | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-24208C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130889778 | ||||||
| chr2:130889811
|
C | CA | 5 | a0001c0001t0001g0009a0001c0002t0001g0034a0004c0004t0001g0005others(2): Show | 5 | HG01175.hp1 HG02055.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-24154dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130889811 | |||||
| chr2:130889811
|
C | CAA | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-24155_40-24154d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130889811 | |||||
| chr2:130889811
|
C | CAAA | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0137others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-24156_40-24154d others(5): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130889811 | |||||
| chr2:130889811
|
C | CAAAA | 34 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(31): Show | 34 | HG00621.hp1 HG00642.hp2 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.40-24157_40-24154d others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130889811 | |||||
| chr2:130889848
|
C | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-24138C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130889848 | ||||||
| chr2:130889872
|
A | G | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-24114A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130889872 | ||||||
| chr2:130889901
|
C | T | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-24085C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130889901 | ||||||
| chr2:130889919
|
T | C | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.40-24067T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130889919 | ||||||
| chr2:130890077
|
A | G | 6 | a0001c0025t0005g0067a0002c0028t0001g0073a0010c0009t0001g0065others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-23909A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130890077 | ||||||
| chr2:130890288
|
A | C | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.40-23698A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130890288 | ||||||
| chr2:130890431
|
G | A | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-23555G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130890431 | ||||||
| chr2:130890508
|
G | A | 35 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(32): Show | 35 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.40-23478G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130890508 | ||||||
| chr2:130890560
|
T | TA | 20 | a0001c0014t0001g0120a0001c0027t0001g0107a0004c0004t0001g0144others(17): Show | 20 | HG01175.hp2 HG01243.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.40-23410dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130890560 | |||||
| chr2:130890560
|
T | TAA | 5 | a0005c0008t0001g0097a0011c0022t0001g0084a0011c0022t0001g0096others(2): Show | 5 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-23411_40-23410d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130890560 | |||||
| chr2:130890575
|
AAT | A | 6 | a0001c0025t0005g0067a0002c0028t0001g0073a0010c0009t0001g0065others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-23410_40-23409d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130890575 | ||||||
| chr2:130890576
|
AT | A | 39 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(36): Show | 39 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.40-23408delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130890576 | |||||
| chr2:130890577
|
T | A | 2 | a0001c0001t0001g0077a0001c0027t0001g0107 | 2 | NA18906.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.40-23409T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130890577 | ||||||
| chr2:130890626
|
T | C | 1 | a0004c0004t0001g0008 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.40-23360T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130890626 | ||||||
| chr2:130891167
|
G | T | 2 | a0007c0013t0002g0095a0024c0033t0001g0021 | 2 | HG01175.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.40-22819G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130891167 | ||||||
| chr2:130891315
|
G | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-22671G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130891315 | ||||||
| chr2:130891455
|
C | G | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.40-22531C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130891455 | ||||||
| chr2:130891759
|
A | G | 41 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(38): Show | 41 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.40-22227A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130891759 | ||||||
| chr2:130891886
|
G | A | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.40-22100G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130891886 | ||||||
| chr2:130892000
|
C | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-21986C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892000 | ||||||
| chr2:130892079
|
C | T | 1 | a0001c0002t0001g0023 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.40-21907C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892079 | ||||||
| chr2:130892188
|
C | G | 35 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0077others(32): Show | 35 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.40-21798C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892188 | ||||||
| chr2:130892243
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.40-21743G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892243 | ||||||
| chr2:130892268
|
G | A | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-21718G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892268 | ||||||
| chr2:130892306
|
C | T | 4 | a0003c0003t0001g0071a0007c0017t0001g0109a0009c0021t0001g0130others(1): Show | 4 | HG02970.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-21680C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892306 | ||||||
| chr2:130892345
|
T | G | 7 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-21641T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892345 | ||||||
| chr2:130892395
|
C | G | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.40-21591C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892395 | ||||||
| chr2:130892450
|
C | T | 29 | a0001c0014t0001g0120a0001c0015t0001g0078a0001c0015t0001g0079others(26): Show | 29 | HG01175.hp2 HG01243.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.40-21536C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892450 | ||||||
| chr2:130892465
|
A | G | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-21521A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892465 | ||||||
| chr2:130892491
|
A | C | 1 | a0025c0024t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.40-21495A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892491 | ||||||
| chr2:130892753
|
C | T | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-21233C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892753 | ||||||
| chr2:130892818
|
G | T | 1 | a0008c0053t0001g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.40-21168G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892818 | ||||||
| chr2:130892962
|
G | A | 41 | a0001c0014t0001g0120a0001c0014t0002g0075a0001c0015t0001g0078others(38): Show | 41 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.40-21024G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130892962 | ||||||
| chr2:130893036
|
T | A | 7 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-20950T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130893036 | ||||||
| chr2:130893039
|
G | A | 7 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-20947G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130893039 | ||||||
| chr2:130893041
|
C | G | 7 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-20945C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130893041 | ||||||
| chr2:130893153
|
G | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-20833G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130893153 | ||||||
| chr2:130893299
|
T | C | 1 | a0007c0017t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.40-20687T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130893299 | ||||||
| chr2:130893328
|
C | T | 36 | a0001c0014t0001g0120a0001c0014t0002g0075a0001c0015t0001g0078others(33): Show | 36 | HG01175.hp2 HG01243.hp2 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.40-20658C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130893328 | ||||||
| chr2:130893563
|
G | T | 1 | a0002c0042t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.40-20423G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130893563 | ||||||
| chr2:130893599
|
G | C | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-20387G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130893599 | ||||||
| chr2:130893619
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-20367G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130893619 | ||||||
| chr2:130894238
|
T | C | 7 | a0004c0004t0001g0144a0006c0005t0001g0072a0006c0005t0001g0143others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-19748T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130894238 | ||||||
| chr2:130894373
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(2): Show | 5 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-19613G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130894373 | ||||||
| chr2:130894408
|
A | G | 87 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(84): Show | 87 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.40-19578A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130894408 | ||||||
| chr2:130894551
|
G | A | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-19435G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130894551 | ||||||
| chr2:130894659
|
C | CT | 41 | a0001c0014t0001g0120a0001c0014t0002g0075a0001c0015t0001g0078others(38): Show | 41 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.40-19317dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130894659 | |||||
| chr2:130894791
|
G | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.40-19195G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130894791 | ||||||
| chr2:130894862
|
C | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-19124C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130894862 | ||||||
| chr2:130894875
|
T | C | 87 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(84): Show | 87 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.40-19111T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130894875 | ||||||
| chr2:130894942
|
C | T | 41 | a0001c0014t0001g0120a0001c0014t0002g0075a0001c0015t0001g0078others(38): Show | 41 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.40-19044C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130894942 | ||||||
| chr2:130894982
|
G | A | 1 | a0005c0008t0001g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.40-19004G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130894982 | ||||||
| chr2:130895125
|
G | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-18861G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130895125 | ||||||
| chr2:130895165
|
A | G | 7 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-18821A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130895165 | ||||||
| chr2:130895220
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01081.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.40-18766C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130895220 | ||||||
| chr2:130895612
|
A | G | 10 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-18374A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130895612 | ||||||
| chr2:130895657
|
C | T | 41 | a0001c0014t0001g0120a0001c0014t0002g0075a0001c0015t0001g0078others(38): Show | 41 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.40-18329C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130895657 | ||||||
| chr2:130895734
|
A | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-18252A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130895734 | ||||||
| chr2:130896156
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.40-17830A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130896156 | ||||||
| chr2:130896232
|
C | G | 1 | a0001c0001t0001g0135 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.40-17754C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130896232 | ||||||
| chr2:130896504
|
C | T | 1 | a0014c0023t0001g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.40-17482C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130896504 | ||||||
| chr2:130896817
|
G | A | 29 | a0001c0014t0001g0120a0001c0015t0001g0078a0001c0015t0001g0079others(26): Show | 29 | HG01175.hp2 HG01243.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.40-17169G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130896817 | ||||||
| chr2:130896883
|
G | A | 29 | a0001c0014t0001g0120a0001c0015t0001g0078a0001c0015t0001g0079others(26): Show | 29 | HG01175.hp2 HG01243.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.40-17103G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130896883 | ||||||
| chr2:130896948
|
A | C | 1 | a0003c0003t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.40-17038A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130896948 | ||||||
| chr2:130897182
|
G | A | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.40-16804G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130897182 | ||||||
| chr2:130897311
|
G | C | 83 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0046others(80): Show | 83 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.40-16675G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130897311 | ||||||
| chr2:130897311
|
G | T | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02647.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.40-16675G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130897311 | ||||||
| chr2:130897478
|
C | CA | 68 | a0001c0001t0001g0046a0001c0001t0001g0077a0001c0001t0001g0086others(65): Show | 68 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.40-16508_40-16507i others(3): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130897478 | ||||||
| chr2:130897527
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-16459G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130897527 | ||||||
| chr2:130897855
|
AC | A | 34 | a0001c0001t0001g0046a0001c0001t0001g0077a0001c0001t0001g0086others(31): Show | 34 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.40-16130delC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130897855 | ||||||
| chr2:130897977
|
C | T | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.40-16009C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130897977 | ||||||
| chr2:130898065
|
T | G | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-15921T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130898065 | ||||||
| chr2:130898193
|
C | G | 8 | a0002c0048t0001g0070a0009c0021t0001g0130a0009c0021t0001g0139others(5): Show | 8 | HG02258.hp2 HG02723.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-15793C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130898193 | ||||||
| chr2:130898196
|
G | A | 6 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.40-15790G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130898196 | ||||||
| chr2:130898279
|
G | A | 11 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0114others(8): Show | 11 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.40-15707G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130898279 | ||||||
| chr2:130898284
|
G | A | 11 | a0005c0006t0001g0052a0005c0006t0001g0100a0005c0006t0001g0102others(8): Show | 11 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.40-15702G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130898284 | ||||||
| chr2:130898377
|
G | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0114others(5): Show | 8 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-15609G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130898377 | ||||||
| chr2:130898640
|
C | A | 1 | a0001c0001t0001g0063 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.40-15346C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130898640 | ||||||
| chr2:130898732
|
G | A | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-15254G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130898732 | ||||||
| chr2:130898840
|
A | G | 76 | a0001c0001t0001g0046a0001c0001t0001g0077a0001c0001t0001g0086others(73): Show | 76 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.40-15146A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130898840 | ||||||
| chr2:130898893
|
G | T | 35 | a0001c0014t0001g0120a0001c0014t0002g0075a0001c0015t0001g0078others(32): Show | 35 | HG01243.hp2 HG02257.hp1 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.40-15093G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130898893 | ||||||
| chr2:130899012
|
A | G | 75 | a0001c0001t0001g0046a0001c0001t0001g0077a0001c0001t0001g0086others(72): Show | 75 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.40-14974A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130899012 | ||||||
| chr2:130899069
|
A | G | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-14917A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130899069 | ||||||
| chr2:130899135
|
C | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0135a0001c0002t0001g0020 | 3 | NA18747.hp1 NA18957.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.40-14851C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130899135 | ||||||
| chr2:130899277
|
C | T | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.40-14709C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130899277 | ||||||
| chr2:130899417
|
G | A | 1 | a0003c0003t0003g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.40-14569G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130899417 | ||||||
| chr2:130899593
|
G | C | 1 | a0006c0050t0001g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.40-14393G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130899593 | ||||||
| chr2:130899639
|
T | C | 63 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(60): Show | 63 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.40-14347T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130899639 | ||||||
| chr2:130899676
|
C | T | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.40-14310C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130899676 | ||||||
| chr2:130899784
|
G | A | 1 | a0004c0004t0001g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.40-14202G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130899784 | ||||||
| chr2:130899940
|
T | TCAATTCT others(344): Show |
1 | a0004c0004t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.40-14029_40-14028i others(353): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130899940 | |||||
| chr2:130899989
|
A | C | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-13997A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130899989 | ||||||
| chr2:130900088
|
C | G | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40-13898C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130900088 | ||||||
| chr2:130900152
|
C | T | 28 | a0001c0014t0001g0120a0001c0015t0001g0078a0001c0015t0001g0079others(25): Show | 28 | HG01243.hp2 HG02257.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.40-13834C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130900152 | ||||||
| chr2:130900322
|
C | T | 111 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(108): Show | 111 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.40-13664C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130900322 | ||||||
| chr2:130900463
|
A | G | 1 | a0007c0032t0001g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.40-13523A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130900463 | ||||||
| chr2:130900496
|
C | T | 35 | a0001c0014t0001g0120a0001c0014t0002g0075a0001c0015t0001g0078others(32): Show | 35 | HG01243.hp2 HG02257.hp1 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.40-13490C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130900496 | ||||||
| chr2:130900548
|
C | T | 112 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(109): Show | 112 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.40-13438C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130900548 | ||||||
| chr2:130900937
|
C | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-13049C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130900937 | ||||||
| chr2:130901523
|
CT | C | 43 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0114others(40): Show | 43 | HG01081.hp2 HG01243.hp2 HG01975.hp2 others(40): Show |
intron_variant | MODIFIER | c.40-12449delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130901523 | |||||
| chr2:130901582
|
G | A | 1 | a0003c0003t0001g0081 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.40-12404G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130901582 | ||||||
| chr2:130901642
|
T | C | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.40-12344T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130901642 | ||||||
| chr2:130901770
|
C | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-12216C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130901770 | ||||||
| chr2:130901772
|
C | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0002t0001g0041others(1): Show | 4 | HG01515.hp1 HG03017.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-12214C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130901772 | ||||||
| chr2:130901870
|
A | G | 2 | a0004c0004t0001g0005a0004c0004t0001g0008 | 2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.40-12116A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130901870 | ||||||
| chr2:130901904
|
A | G | 1 | a0011c0049t0001g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.40-12082A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130901904 | ||||||
| chr2:130902062
|
G | A | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.40-11924G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902062 | ||||||
| chr2:130902151
|
C | T | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.40-11835C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902151 | ||||||
| chr2:130902209
|
A | C | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-11777A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902209 | ||||||
| chr2:130902347
|
A | T | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-11639A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902347 | ||||||
| chr2:130902374
|
A | C | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-11612A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902374 | ||||||
| chr2:130902464
|
G | C | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40-11522G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902464 | ||||||
| chr2:130902465
|
G | A | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40-11521G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902465 | ||||||
| chr2:130902466
|
T | C | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40-11520T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902466 | ||||||
| chr2:130902467
|
G | A | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40-11519G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902467 | ||||||
| chr2:130902474
|
A | G | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40-11512A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902474 | ||||||
| chr2:130902484
|
CTCGGGAG others(239): Show |
C | 1 | a0001c0002t0001g0010 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.40-11501_40-11256d others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902484 | ||||||
| chr2:130902496
|
T | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0114others(5): Show | 8 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-11490T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902496 | ||||||
| chr2:130902526
|
G | A | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40-11460G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902526 | ||||||
| chr2:130902604
|
G | GGAAAGAA others(6): Show |
22 | a0001c0014t0001g0120a0002c0028t0001g0073a0002c0048t0001g0070others(19): Show | 22 | HG01175.hp2 HG02055.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.40-11370_40-11369i others(15): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130902604 | |||||
| chr2:130902704
|
T | TCGG | 11 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0114others(8): Show | 11 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.40-11280_40-11278d others(5): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130902704 | |||||
| chr2:130902725
|
T | C | 11 | a0005c0006t0001g0052a0005c0006t0001g0100a0005c0006t0001g0102others(8): Show | 11 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.40-11261T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902725 | ||||||
| chr2:130902901
|
G | A | 5 | a0006c0005t0001g0072a0006c0005t0001g0143a0006c0005t0003g0140others(2): Show | 5 | HG02257.hp1 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-11085G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902901 | ||||||
| chr2:130902915
|
G | GTCCTTAA | 95 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(92): Show | 95 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.40-11071_40-11070i others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902915 | ||||||
| chr2:130902958
|
G | A | 3 | a0007c0013t0001g0059a0013c0016t0003g0001a0013c0016t0003g0002 | 3 | HG02559.hp2 HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.40-11028G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130902958 | ||||||
| chr2:130903023
|
A | G | 14 | a0001c0014t0001g0120a0002c0048t0001g0070a0006c0005t0001g0072others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.40-10963A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130903023 | ||||||
| chr2:130903119
|
A | ATT | 55 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(52): Show | 55 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.40-10857_40-10856d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130903119 | |||||
| chr2:130903119
|
AT | A | 12 | a0003c0003t0001g0062a0005c0006t0001g0052a0005c0006t0001g0100others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.40-10856delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130903119 | |||||
| chr2:130903190
|
A | G | 38 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(35): Show | 38 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.40-10796A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130903190 | ||||||
| chr2:130903245
|
G | T | 21 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(18): Show | 21 | HG01175.hp2 HG01243.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.40-10741G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130903245 | ||||||
| chr2:130903247
|
C | CT | 113 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(110): Show | 113 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.40-10729dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130903247 | |||||
| chr2:130903265
|
C | CT | 8 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(5): Show | 8 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-10711dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130903265 | |||||
| chr2:130903301
|
C | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0114others(5): Show | 8 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-10685C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130903301 | ||||||
| chr2:130903328
|
G | A | 11 | a0005c0006t0001g0052a0005c0006t0001g0100a0005c0006t0001g0102others(8): Show | 11 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.40-10658G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130903328 | ||||||
| chr2:130903407
|
G | A | 11 | a0005c0006t0001g0052a0005c0006t0001g0100a0005c0006t0001g0102others(8): Show | 11 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.40-10579G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130903407 | ||||||
| chr2:130903658
|
C | T | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-10328C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130903658 | ||||||
| chr2:130903675
|
A | G | 1 | a0011c0049t0001g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.40-10311A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130903675 | ||||||
| chr2:130903700
|
C | G | 11 | a0005c0006t0001g0052a0005c0006t0001g0100a0005c0006t0001g0102others(8): Show | 11 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.40-10286C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130903700 | ||||||
| chr2:130903718
|
C | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-10268C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130903718 | ||||||
| chr2:130903760
|
C | T | 113 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(110): Show | 113 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.40-10226C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130903760 | ||||||
| chr2:130904073
|
T | C | 7 | a0003c0003t0001g0071a0003c0003t0002g0116a0003c0003t0002g0117others(4): Show | 7 | HG01175.hp2 HG02055.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.40-9913T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130904073 | ||||||
| chr2:130904097
|
T | C | 4 | a0009c0021t0001g0130a0009c0021t0001g0139a0009c0046t0009g0076others(1): Show | 4 | HG02723.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.40-9889T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130904097 | ||||||
| chr2:130904239
|
G | A | 5 | a0001c0045t0001g0085a0002c0011t0001g0132a0002c0011t0001g0133others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-9747G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130904239 | ||||||
| chr2:130904472
|
T | C | 8 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(5): Show | 8 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.40-9514T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130904472 | ||||||
| chr2:130904782
|
T | TAA | 51 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(48): Show | 51 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.40-9195_40-9194dup others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130904782 | |||||
| chr2:130904783
|
A | T | 11 | a0005c0006t0001g0052a0005c0006t0001g0100a0005c0006t0001g0102others(8): Show | 11 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.40-9203A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130904783 | ||||||
| chr2:130905023
|
G | A | 14 | a0001c0014t0001g0120a0002c0048t0001g0070a0006c0005t0001g0072others(11): Show | 14 | HG02257.hp1 HG02258.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.40-8963G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130905023 | ||||||
| chr2:130905109
|
AT | A | 94 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(91): Show | 94 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.40-8868delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130905109 | |||||
| chr2:130905408
|
A | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG02698.hp2 HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.40-8578A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130905408 | ||||||
| chr2:130905509
|
C | T | 113 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(110): Show | 113 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.40-8477C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130905509 | ||||||
| chr2:130905812
|
C | T | 8 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(5): Show | 8 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.40-8174C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130905812 | ||||||
| chr2:130906008
|
C | T | 8 | a0001c0014t0002g0075a0001c0018t0002g0105a0001c0018t0005g0106others(5): Show | 8 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.40-7978C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130906008 | ||||||
| chr2:130906106
|
T | C | 2 | a0004c0004t0001g0005a0004c0004t0001g0008 | 2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.40-7880T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130906106 | ||||||
| chr2:130906530
|
G | A | 42 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0114others(39): Show | 42 | HG01081.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.40-7456G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130906530 | ||||||
| chr2:130906694
|
C | T | 121 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(118): Show | 121 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.40-7292C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130906694 | ||||||
| chr2:130906735
|
C | T | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.40-7251C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130906735 | ||||||
| chr2:130906740
|
C | T | 120 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(117): Show | 120 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.40-7246C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130906740 | ||||||
| chr2:130906863
|
C | T | 20 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0114others(17): Show | 20 | HG01081.hp2 HG01243.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.40-7123C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130906863 | ||||||
| chr2:130906948
|
T | C | 15 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0114others(12): Show | 15 | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.40-7038T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130906948 | ||||||
| chr2:130906976
|
C | T | 3 | a0004c0004t0001g0128a0012c0019t0001g0127a0012c0019t0001g0129 | 3 | NA18948.hp2 NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.40-7010C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130906976 | ||||||
| chr2:130907103
|
G | A | 12 | a0001c0014t0002g0075a0005c0006t0001g0052a0005c0006t0001g0100others(9): Show | 12 | HG01243.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.40-6883G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907103 | ||||||
| chr2:130907208
|
C | CT | 19 | a0001c0007t0004g0093a0001c0014t0002g0075a0003c0003t0001g0062others(16): Show | 19 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.40-6756dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130907208 | |||||
| chr2:130907208
|
CT | C | 45 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 45 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.40-6756delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130907208 | |||||
| chr2:130907208
|
CTT | C | 19 | a0001c0001t0001g0035a0001c0001t0001g0114a0001c0001t0001g0115others(16): Show | 19 | HG01081.hp2 HG01243.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.40-6757_40-6756del others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130907208 | |||||
| chr2:130907250
|
G | T | 121 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(118): Show | 121 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.40-6736G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907250 | ||||||
| chr2:130907251
|
A | C | 121 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(118): Show | 121 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.40-6735A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907251 | ||||||
| chr2:130907253
|
A | C | 121 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(118): Show | 121 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.40-6733A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907253 | ||||||
| chr2:130907254
|
CTG | C | 121 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(118): Show | 121 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.40-6731_40-6730del others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907254 | ||||||
| chr2:130907257
|
G | A | 121 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(118): Show | 121 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.40-6729G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907257 | ||||||
| chr2:130907288
|
C | T | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40-6698C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907288 | ||||||
| chr2:130907316
|
G | C | 1 | a0004c0004t0001g0008 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.40-6670G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907316 | ||||||
| chr2:130907392
|
T | C | 99 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(96): Show | 99 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.40-6594T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907392 | ||||||
| chr2:130907452
|
C | T | 1 | a0006c0005t0003g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40-6534C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907452 | ||||||
| chr2:130907724
|
C | T | 26 | a0001c0001t0001g0087a0001c0014t0001g0036a0001c0044t0001g0011others(23): Show | 26 | HG00735.hp2 HG01081.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.40-6262C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907724 | ||||||
| chr2:130907725
|
A | G | 126 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(123): Show | 126 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.40-6261A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907725 | ||||||
| chr2:130907735
|
C | T | 1 | a0001c0034t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.40-6251C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907735 | ||||||
| chr2:130907972
|
T | A | 26 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(23): Show | 26 | HG00621.hp1 HG01175.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.40-6014T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130907972 | ||||||
| chr2:130908068
|
A | G | 6 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(3): Show | 6 | HG02559.hp1 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-5918A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130908068 | ||||||
| chr2:130908081
|
T | C | 1 | a0011c0022t0001g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.40-5905T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130908081 | ||||||
| chr2:130908601
|
G | A | 8 | a0002c0048t0001g0070a0009c0021t0001g0130a0009c0021t0001g0139others(5): Show | 8 | HG02258.hp2 HG02723.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-5385G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130908601 | ||||||
| chr2:130908607
|
T | C | 85 | a0001c0001t0001g0135a0001c0002t0001g0020a0001c0007t0004g0089others(82): Show | 85 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.40-5379T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130908607 | ||||||
| chr2:130908609
|
G | A | 10 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 10 | HG02080.hp2 HG02698.hp2 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-5377G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130908609 | ||||||
| chr2:130908697
|
T | A | 5 | a0001c0025t0005g0067a0010c0009t0001g0065a0010c0009t0001g0066others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-5289T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130908697 | ||||||
| chr2:130908725
|
G | A | 15 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(12): Show | 15 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.40-5261G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130908725 | ||||||
| chr2:130908849
|
A | C | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.40-5137A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130908849 | ||||||
| chr2:130908999
|
G | A | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40-4987G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130908999 | ||||||
| chr2:130909374
|
G | A | 1 | a0001c0045t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.40-4612G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130909374 | ||||||
| chr2:130909432
|
G | A | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.40-4554G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130909432 | ||||||
| chr2:130909437
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.40-4549G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130909437 | ||||||
| chr2:130909440
|
C | G | 4 | a0001c0001t0001g0135a0001c0002t0001g0020a0001c0044t0001g0011others(1): Show | 4 | HG00642.hp2 HG01257.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-4546C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130909440 | ||||||
| chr2:130909458
|
A | G | 7 | a0006c0005t0001g0072a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-4528A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130909458 | ||||||
| chr2:130909481
|
G | A | 1 | a0001c0034t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.40-4505G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130909481 | ||||||
| chr2:130909656
|
T | TA | 11 | a0001c0014t0001g0036a0001c0025t0005g0067a0005c0006t0002g0099others(8): Show | 11 | HG01243.hp1 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.40-4319dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130909656 | |||||
| chr2:130909656
|
T | TAA | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(2): Show | 5 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-4320_40-4319dup others(2): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130909656 | |||||
| chr2:130909656
|
TA | T | 25 | a0002c0010t0001g0003a0002c0010t0001g0047a0002c0010t0001g0051others(22): Show | 25 | HG00621.hp1 HG01884.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.40-4319delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130909656 | |||||
| chr2:130909729
|
C | T | 17 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(14): Show | 17 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.40-4257C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130909729 | ||||||
| chr2:130909766
|
A | G | 115 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(112): Show | 115 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.40-4220A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130909766 | ||||||
| chr2:130909819
|
C | CT | 3 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080 | 3 | HG02559.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40-4166dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130909819 | |||||
| chr2:130909908
|
A | G | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.40-4078A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130909908 | ||||||
| chr2:130910108
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.40-3878G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130910108 | ||||||
| chr2:130910175
|
G | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-3811G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130910175 | ||||||
| chr2:130910402
|
G | C | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.40-3584G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130910402 | ||||||
| chr2:130910437
|
G | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(43): Show | 46 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.40-3549G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130910437 | ||||||
| chr2:130910763
|
A | G | 46 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(43): Show | 46 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.40-3223A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130910763 | ||||||
| chr2:130910878
|
A | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-3108A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130910878 | ||||||
| chr2:130910881
|
T | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(67): Show | 70 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.40-3105T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130910881 | ||||||
| chr2:130911012
|
T | G | 114 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(111): Show | 114 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(111): Show |
intron_variant | MODIFIER | c.40-2974T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130911012 | ||||||
| chr2:130911571
|
G | A | 3 | a0007c0013t0001g0059a0013c0016t0003g0001a0013c0016t0003g0002 | 3 | HG02559.hp2 HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.40-2415G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130911571 | ||||||
| chr2:130911607
|
A | G | 60 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(57): Show | 60 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.40-2379A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130911607 | ||||||
| chr2:130911694
|
A | G | 4 | a0001c0045t0001g0085a0011c0022t0001g0084a0011c0022t0001g0096others(1): Show | 4 | HG02258.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.40-2292A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130911694 | ||||||
| chr2:130911785
|
C | T | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-2201C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130911785 | ||||||
| chr2:130911828
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.40-2158G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130911828 | ||||||
| chr2:130911990
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40-1996G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130911990 | ||||||
| chr2:130912076
|
G | A | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.40-1910G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130912076 | ||||||
| chr2:130912207
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.40-1779C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130912207 | ||||||
| chr2:130912410
|
C | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.40-1576C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130912410 | ||||||
| chr2:130912598
|
C | A | 68 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(65): Show | 68 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.40-1388C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130912598 | ||||||
| chr2:130912753
|
T | C | 1 | a0011c0022t0001g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.40-1233T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130912753 | ||||||
| chr2:130912865
|
C | G | 1 | a0021c0037t0001g0050 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.40-1121C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130912865 | ||||||
| chr2:130913057
|
C | T | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.40-929C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130913057 | ||||||
| chr2:130913065
|
G | C | 1 | a0001c0001t0002g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.40-921G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130913065 | ||||||
| chr2:130913083
|
A | C | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.40-903A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130913083 | ||||||
| chr2:130913279
|
A | T | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.40-707A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130913279 | ||||||
| chr2:130913517
|
G | T | 26 | a0001c0002t0001g0034a0001c0015t0001g0078a0001c0015t0001g0079others(23): Show | 26 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.40-469G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130913517 | ||||||
| chr2:130913535
|
T | A | 1 | a0001c0034t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.40-451T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130913535 | ||||||
| chr2:130913626
|
CAT | C | 7 | a0006c0005t0001g0072a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-357_40-356delAT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 130913626 | |||||
| chr2:130913714
|
C | T | 7 | a0006c0005t0001g0072a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-272C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130913714 | ||||||
| chr2:130913762
|
G | A | 1 | a0002c0010t0001g0047 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.40-224G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | 130913762 | ||||||
| chr2:130917517
|
C | T | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3552+19C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130917517 | ||||||
| chr2:130917639
|
C | A | 14 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(11): Show | 14 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.3552+141C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130917639 | ||||||
| chr2:130917655
|
A | C | 2 | a0002c0028t0001g0073a0023c0029t0001g0141 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3552+157A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130917655 | ||||||
| chr2:130917685
|
C | T | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3552+187C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130917685 | ||||||
| chr2:130917823
|
CTT | C | 15 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0077others(12): Show | 15 | HG02698.hp2 HG02965.hp1 HG03491.hp1 others(12): Show |
intron_variant | MODIFIER | c.3552+341_3552+342d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130917823 | |||||
| chr2:130917823
|
CTTT | C | 107 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(104): Show | 107 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.3552+340_3552+342d others(5): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130917823 | |||||
| chr2:130917823
|
CTTTT | C | 9 | a0005c0006t0001g0052a0005c0006t0001g0100a0005c0006t0001g0102others(6): Show | 9 | HG01243.hp2 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3552+339_3552+342d others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130917823 | |||||
| chr2:130917834
|
T | C | 1 | a0002c0010t0001g0051 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3552+336T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130917834 | ||||||
| chr2:130917931
|
T | C | 7 | a0006c0005t0001g0072a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3552+433T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130917931 | ||||||
| chr2:130917936
|
C | T | 7 | a0006c0005t0001g0072a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3552+438C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130917936 | ||||||
| chr2:130918047
|
C | T | 2 | a0009c0021t0001g0130a0009c0047t0001g0110 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3552+549C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130918047 | ||||||
| chr2:130918061
|
C | A | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3552+563C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130918061 | ||||||
| chr2:130918067
|
G | A | 14 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(11): Show | 14 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.3552+569G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130918067 | ||||||
| chr2:130918093
|
A | G | 14 | a0003c0003t0001g0030a0003c0003t0001g0062a0003c0003t0001g0071others(11): Show | 14 | HG01109.hp2 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.3552+595A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130918093 | ||||||
| chr2:130918356
|
A | G | 1 | a0001c0014t0002g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3552+858A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130918356 | ||||||
| chr2:130918371
|
C | T | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3552+873C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130918371 | ||||||
| chr2:130918462
|
CA | C | 21 | a0001c0018t0002g0105a0001c0018t0005g0106a0002c0048t0001g0070others(18): Show | 21 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(18): Show |
intron_variant | MODIFIER | c.3552+965delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130918462 | ||||||
| chr2:130918531
|
C | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3552+1033C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130918531 | ||||||
| chr2:130918546
|
T | C | 7 | a0006c0005t0001g0072a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3552+1048T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130918546 | ||||||
| chr2:130918570
|
A | G | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3552+1072A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130918570 | ||||||
| chr2:130918783
|
CTGTT | C | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3552+1289_3552+129 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130918783 | |||||
| chr2:130918948
|
T | C | 10 | a0005c0006t0001g0052a0005c0006t0001g0100a0005c0006t0001g0102others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3552+1450T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130918948 | ||||||
| chr2:130918990
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3552+1492T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130918990 | ||||||
| chr2:130919287
|
T | A | 19 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(16): Show | 19 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.3552+1789T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130919287 | ||||||
| chr2:130919650
|
C | T | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3552+2152C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130919650 | ||||||
| chr2:130919651
|
G | A | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3552+2153G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130919651 | ||||||
| chr2:130919678
|
C | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3552+2180C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130919678 | ||||||
| chr2:130919800
|
C | T | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3552+2302C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130919800 | ||||||
| chr2:130919841
|
A | G | 2 | a0001c0014t0001g0036a0023c0029t0001g0141 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3552+2343A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130919841 | ||||||
| chr2:130919849
|
C | T | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3552+2351C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130919849 | ||||||
| chr2:130919875
|
C | CA | 12 | a0001c0014t0001g0036a0001c0045t0001g0085a0005c0006t0001g0052others(9): Show | 12 | HG01243.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.3552+2390dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130919875 | |||||
| chr2:130919875
|
CA | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0046others(3): Show | 6 | HG02080.hp1 HG02080.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.3552+2390delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130919875 | |||||
| chr2:130919875
|
CAAAA | C | 18 | a0001c0027t0001g0107a0002c0010t0001g0003a0002c0010t0001g0047others(15): Show | 18 | HG00621.hp1 HG01884.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.3552+2387_3552+239 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130919875 | |||||
| chr2:130919960
|
C | T | 15 | a0003c0003t0001g0030a0003c0003t0001g0062a0003c0003t0001g0071others(12): Show | 15 | HG01109.hp2 HG01175.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.3552+2462C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130919960 | ||||||
| chr2:130920078
|
T | G | 61 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(58): Show | 61 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.3552+2580T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920078 | ||||||
| chr2:130920085
|
T | G | 7 | a0001c0018t0002g0105a0001c0018t0005g0106a0007c0013t0001g0059others(4): Show | 7 | HG02559.hp2 HG02572.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.3552+2587T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920085 | ||||||
| chr2:130920135
|
G | A | 1 | a0007c0013t0003g0060 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3552+2637G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920135 | ||||||
| chr2:130920135
|
G | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3552+2637G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920135 | ||||||
| chr2:130920209
|
A | G | 1 | a0005c0008t0001g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3552+2711A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920209 | ||||||
| chr2:130920353
|
G | A | 2 | a0001c0014t0001g0036a0023c0029t0001g0141 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3552+2855G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920353 | ||||||
| chr2:130920377
|
C | G | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3552+2879C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920377 | ||||||
| chr2:130920467
|
C | G | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3552+2969C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920467 | ||||||
| chr2:130920472
|
A | G | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3552+2974A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920472 | ||||||
| chr2:130920479
|
G | A | 2 | a0001c0014t0001g0036a0023c0029t0001g0141 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3552+2981G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920479 | ||||||
| chr2:130920493
|
G | A | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3552+2995G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920493 | ||||||
| chr2:130920538
|
CT | C | 2 | a0001c0039t0001g0039a0014c0023t0001g0057 | 2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3552+3041delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920538 | ||||||
| chr2:130920696
|
G | A | 1 | a0001c0034t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3552+3198G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920696 | ||||||
| chr2:130920795
|
A | G | 5 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(2): Show | 5 | HG01257.hp2 HG01258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3552+3297A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920795 | ||||||
| chr2:130920860
|
C | T | 11 | a0001c0045t0001g0085a0008c0012t0001g0026a0008c0012t0001g0027others(8): Show | 11 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.3552+3362C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130920860 | ||||||
| chr2:130921136
|
A | T | 2 | a0002c0048t0001g0070a0023c0029t0001g0141 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3552+3638A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130921136 | ||||||
| chr2:130921170
|
A | G | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3552+3672A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130921170 | ||||||
| chr2:130921306
|
G | T | 50 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(47): Show | 50 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.3552+3808G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130921306 | ||||||
| chr2:130921930
|
A | G | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3552+4432A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130921930 | ||||||
| chr2:130922056
|
G | A | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(46): Show | 49 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.3552+4558G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922056 | ||||||
| chr2:130922096
|
G | A | 28 | a0001c0014t0001g0036a0002c0010t0001g0003a0002c0010t0001g0047others(25): Show | 28 | HG00621.hp1 HG01884.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.3552+4598G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922096 | ||||||
| chr2:130922135
|
C | T | 8 | a0001c0045t0001g0085a0008c0012t0001g0026a0008c0012t0001g0027others(5): Show | 8 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.3552+4637C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922135 | ||||||
| chr2:130922174
|
A | C | 28 | a0001c0014t0001g0036a0002c0010t0001g0003a0002c0010t0001g0047others(25): Show | 28 | HG00621.hp1 HG01884.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.3552+4676A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922174 | ||||||
| chr2:130922246
|
A | G | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3552+4748A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922246 | ||||||
| chr2:130922251
|
A | G | 10 | a0005c0006t0001g0052a0005c0006t0001g0100a0005c0006t0001g0102others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3552+4753A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922251 | ||||||
| chr2:130922261
|
G | C | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3552+4763G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922261 | ||||||
| chr2:130922283
|
A | G | 1 | a0001c0002t0001g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3552+4785A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922283 | ||||||
| chr2:130922371
|
C | CA | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3552+4886dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130922371 | |||||
| chr2:130922373
|
A | G | 9 | a0001c0044t0001g0011a0001c0045t0001g0085a0008c0012t0001g0026others(6): Show | 9 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.3552+4875A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922373 | ||||||
| chr2:130922477
|
A | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3552+4979A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922477 | ||||||
| chr2:130922548
|
T | C | 59 | a0001c0014t0002g0075a0001c0015t0001g0078a0001c0015t0001g0079others(56): Show | 59 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.3552+5050T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922548 | ||||||
| chr2:130922568
|
C | T | 12 | a0002c0010t0001g0003a0002c0010t0001g0047a0002c0010t0001g0051others(9): Show | 12 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.3552+5070C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922568 | ||||||
| chr2:130922762
|
A | AT | 51 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(48): Show | 51 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3552+5275dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130922762 | |||||
| chr2:130922762
|
AT | A | 5 | a0001c0018t0002g0105a0001c0018t0005g0106a0010c0009t0001g0065others(2): Show | 5 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3552+5275delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130922762 | |||||
| chr2:130922777
|
T | G | 30 | a0001c0001t0001g0123a0001c0014t0001g0036a0001c0044t0001g0011others(27): Show | 30 | HG00621.hp1 HG01257.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.3552+5279T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922777 | ||||||
| chr2:130922838
|
T | C | 2 | a0010c0009t0001g0065a0010c0009t0001g0066 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.3552+5340T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130922838 | ||||||
| chr2:130922923
|
G | GAT | 39 | a0001c0014t0001g0036a0001c0044t0001g0011a0001c0045t0001g0085others(36): Show | 39 | HG00642.hp2 HG01081.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.3552+5442_3552+544 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130922923 | |||||
| chr2:130922923
|
G | GATAT | 2 | a0002c0010t0001g0003a0002c0010t0001g0136 | 2 | HG00621.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3552+5440_3552+544 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130922923 | |||||
| chr2:130922923
|
G | GATATAT | 42 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(39): Show | 42 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.3552+5438_3552+544 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130922923 | |||||
| chr2:130922923
|
G | GATATATA others(1): Show |
7 | a0001c0001t0001g0033a0001c0001t0001g0088a0001c0001t0001g0124others(4): Show | 7 | HG02080.hp1 HG02080.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3552+5436_3552+544 others(12): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130922923 | |||||
| chr2:130922923
|
G | GATATATA others(3): Show |
1 | a0014c0023t0001g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3552+5434_3552+544 others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130922923 | |||||
| chr2:130922923
|
G | GATATATA others(21): Show |
1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3552+5443_3552+544 others(32): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130922923 | |||||
| chr2:130923123
|
T | G | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3552+5625T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130923123 | ||||||
| chr2:130923220
|
G | A | 29 | a0001c0014t0001g0036a0002c0010t0001g0003a0002c0010t0001g0047others(26): Show | 29 | HG00621.hp1 HG01884.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3552+5722G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130923220 | ||||||
| chr2:130923254
|
A | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(46): Show | 49 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.3552+5756A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130923254 | ||||||
| chr2:130923398
|
T | G | 1 | a0001c0007t0004g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3552+5900T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130923398 | ||||||
| chr2:130923461
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3552+5963G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130923461 | ||||||
| chr2:130923545
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3552+6047G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130923545 | ||||||
| chr2:130923885
|
C | CT | 81 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(78): Show | 81 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.3552+6400dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130923885 | |||||
| chr2:130923885
|
CT | C | 14 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0002g0105others(11): Show | 14 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3552+6400delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130923885 | |||||
| chr2:130923942
|
A | G | 93 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(90): Show | 93 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.3552+6444A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130923942 | ||||||
| chr2:130923947
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3552+6449C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130923947 | ||||||
| chr2:130924033
|
A | G | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3552+6535A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924033 | ||||||
| chr2:130924039
|
C | T | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3552+6541C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924039 | ||||||
| chr2:130924069
|
T | G | 93 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(90): Show | 93 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.3552+6571T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924069 | ||||||
| chr2:130924218
|
G | A | 93 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(90): Show | 93 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.3552+6720G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924218 | ||||||
| chr2:130924281
|
CT | C | 92 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(89): Show | 92 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.3553-6658delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130924281 | |||||
| chr2:130924301
|
G | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3553-6651G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924301 | ||||||
| chr2:130924336
|
G | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3553-6616G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924336 | ||||||
| chr2:130924360
|
G | A | 4 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3553-6592G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924360 | ||||||
| chr2:130924366
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3553-6586G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924366 | ||||||
| chr2:130924383
|
C | G | 6 | a0001c0027t0001g0107a0007c0013t0001g0059a0007c0013t0003g0060others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3553-6569C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924383 | ||||||
| chr2:130924517
|
C | T | 14 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0002g0105others(11): Show | 14 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3553-6435C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924517 | ||||||
| chr2:130924639
|
C | T | 3 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068 | 3 | HG02717.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3553-6313C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924639 | ||||||
| chr2:130924712
|
G | A | 12 | a0003c0003t0001g0030a0003c0003t0001g0062a0003c0003t0001g0071others(9): Show | 12 | HG01109.hp2 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3553-6240G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924712 | ||||||
| chr2:130924861
|
C | T | 11 | a0001c0045t0001g0085a0008c0012t0001g0026a0008c0012t0001g0027others(8): Show | 11 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.3553-6091C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924861 | ||||||
| chr2:130924892
|
A | T | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3553-6060A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130924892 | ||||||
| chr2:130925035
|
A | AGT | 7 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.3553-5873_3553-587 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130925035 | |||||
| chr2:130925035
|
A | AGTGTGT | 4 | a0008c0012t0001g0026a0008c0012t0001g0027a0008c0012t0001g0045others(1): Show | 4 | HG00642.hp2 HG01081.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.3553-5877_3553-587 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130925035 | |||||
| chr2:130925035
|
AGT | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0126a0001c0002t0001g0083others(8): Show | 11 | HG01243.hp2 HG02257.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.3553-5873_3553-587 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130925035 | |||||
| chr2:130925035
|
AGTGT | A | 8 | a0001c0001t0001g0063a0001c0039t0001g0039a0005c0008t0001g0097others(5): Show | 8 | HG00621.hp2 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.3553-5875_3553-587 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130925035 | |||||
| chr2:130925035
|
AGTGTGT | A | 47 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(44): Show | 47 | HG00642.hp1 HG00735.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.3553-5877_3553-587 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130925035 | |||||
| chr2:130925035
|
AGTGTGTG others(1): Show |
A | 15 | a0001c0001t0001g0042a0001c0002t0001g0038a0001c0002t0001g0041others(12): Show | 15 | HG01515.hp2 HG02055.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.3553-5879_3553-587 others(12): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130925035 | |||||
| chr2:130925035
|
AGTGTGTG others(3): Show |
A | 10 | a0001c0014t0001g0036a0001c0018t0002g0105a0001c0018t0005g0106others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.3553-5881_3553-587 others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130925035 | |||||
| chr2:130925035
|
AGTGTGTG others(5): Show |
A | 13 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(10): Show | 13 | HG00621.hp1 HG01243.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.3553-5883_3553-587 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130925035 | |||||
| chr2:130925035
|
AGTGTGTG others(7): Show |
A | 21 | a0002c0011t0001g0132a0002c0011t0001g0133a0002c0011t0001g0134others(18): Show | 21 | HG01884.hp2 HG02280.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.3553-5885_3553-587 others(18): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130925035 | |||||
| chr2:130925035
|
AGTGTGTG others(9): Show |
A | 2 | a0002c0010t0001g0051a0009c0021t0001g0130 | 2 | HG02970.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3553-5887_3553-587 others(20): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130925035 | |||||
| chr2:130925046
|
G | A | 1 | a0011c0049t0001g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3553-5906G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130925046 | ||||||
| chr2:130925079
|
T | C | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3553-5873T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130925079 | ||||||
| chr2:130925085
|
T | TGA | 9 | a0001c0044t0001g0011a0001c0045t0001g0085a0008c0012t0001g0026others(6): Show | 9 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.3553-5848_3553-584 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130925085 | |||||
| chr2:130925085
|
TGA | T | 3 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068 | 3 | HG02717.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3553-5848_3553-584 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130925085 | |||||
| chr2:130925148
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3553-5804T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130925148 | ||||||
| chr2:130925266
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3553-5686G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130925266 | ||||||
| chr2:130925279
|
A | T | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3553-5673A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130925279 | ||||||
| chr2:130925326
|
A | C | 92 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(89): Show | 92 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.3553-5626A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130925326 | ||||||
| chr2:130925406
|
C | T | 2 | a0003c0003t0003g0112a0007c0017t0001g0109 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3553-5546C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130925406 | ||||||
| chr2:130925440
|
C | T | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3553-5512C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130925440 | ||||||
| chr2:130925498
|
T | C | 1 | a0001c0014t0002g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3553-5454T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130925498 | ||||||
| chr2:130925649
|
A | G | 42 | a0001c0001t0001g0017a0001c0014t0001g0036a0002c0010t0001g0003others(39): Show | 42 | HG00621.hp1 HG01109.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.3553-5303A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130925649 | ||||||
| chr2:130925753
|
T | C | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3553-5199T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130925753 | ||||||
| chr2:130926008
|
T | TTTTC | 4 | a0001c0001t0001g0086a0001c0002t0001g0020a0011c0022t0001g0084others(1): Show | 4 | HG00735.hp1 HG01258.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3553-4942_3553-493 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926008 | |||||
| chr2:130926008
|
T | TTTTCTTT others(1): Show |
13 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(10): Show | 13 | HG00642.hp1 HG01081.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.3553-4939_3553-493 others(12): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926008 | |||||
| chr2:130926008
|
T | TTTTCTTT others(5): Show |
13 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0035others(10): Show | 13 | HG01515.hp1 HG01515.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.3553-4939_3553-493 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926008 | |||||
| chr2:130926008
|
T | TTTTCTTT others(9): Show |
9 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0046others(6): Show | 9 | HG02698.hp2 HG03130.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.3553-4939_3553-493 others(20): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926008 | |||||
| chr2:130926008
|
T | TTTTCTTT others(13): Show |
5 | a0001c0001t0001g0063a0001c0001t0001g0124a0001c0002t0001g0034others(2): Show | 5 | HG00621.hp2 HG02080.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.3553-4939_3553-493 others(24): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926008 | |||||
| chr2:130926008
|
T | TTTTCTTT others(21): Show |
1 | a0001c0001t0001g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3553-4939_3553-493 others(32): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926008 | |||||
| chr2:130926014
|
C | CTCTTCCT others(5): Show |
1 | a0006c0005t0003g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3553-4934_3553-493 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926014 | |||||
| chr2:130926014
|
C | CTCTTTCT others(5): Show |
3 | a0001c0034t0001g0111a0006c0005t0001g0104a0006c0005t0005g0119 | 3 | HG02818.hp1 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3553-4930_3553-492 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926014 | |||||
| chr2:130926014
|
C | CTCTTTCT others(9): Show |
3 | a0001c0025t0005g0067a0001c0026t0001g0080a0006c0050t0001g0142 | 3 | HG01243.hp1 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3553-4930_3553-492 others(20): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926014 | |||||
| chr2:130926014
|
C | CTCTTTCT others(13): Show |
2 | a0001c0015t0001g0078a0001c0015t0001g0079 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3553-4930_3553-492 others(24): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926014 | |||||
| chr2:130926014
|
C | CTCTTTCT others(21): Show |
1 | a0003c0031t0006g0037 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3553-4930_3553-492 others(32): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926014 | |||||
| chr2:130926014
|
C | T | 92 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(89): Show | 92 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.3553-4938C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926014 | ||||||
| chr2:130926019
|
T | TCTTC | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3553-4930_3553-492 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926019 | |||||
| chr2:130926023
|
T | C | 1 | a0006c0005t0001g0094 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3553-4929T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926023 | ||||||
| chr2:130926034
|
T | TTCTTTCT others(3): Show |
1 | a0005c0006t0003g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3553-4916_3553-490 others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926034 | |||||
| chr2:130926042
|
T | C | 1 | a0005c0006t0002g0099 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3553-4910T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926042 | ||||||
| chr2:130926044
|
C | T | 1 | a0005c0006t0002g0099 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3553-4908C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926044 | ||||||
| chr2:130926044
|
CTTTCTCT others(5): Show |
C | 5 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3553-4906_3553-489 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926044 | |||||
| chr2:130926046
|
T | C | 1 | a0005c0006t0002g0099 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3553-4906T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926046 | ||||||
| chr2:130926048
|
C | CTCTT | 2 | a0001c0014t0002g0075a0002c0048t0001g0070 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3553-4878_3553-487 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTCTTTCT others(1): Show |
8 | a0005c0006t0001g0052a0005c0006t0001g0100a0005c0006t0001g0102others(5): Show | 8 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3553-4882_3553-487 others(12): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTCTTTCT others(5): Show |
2 | a0001c0007t0004g0093a0024c0033t0001g0021 | 2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.3553-4886_3553-487 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTCTTTCT others(13): Show |
1 | a0001c0001t0001g0017 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3553-4894_3553-487 others(24): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTT | 6 | a0001c0001t0001g0088a0005c0006t0003g0103a0006c0005t0001g0094others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3553-4903_3553-490 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTCT others(9): Show |
4 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3553-4903_3553-490 others(20): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTCT others(33): Show |
1 | a0003c0003t0001g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3553-4903_3553-490 others(44): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTT | 2 | a0001c0001t0001g0122a0007c0013t0002g0095 | 2 | HG01175.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.3553-4903_3553-490 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(9): Show |
1 | a0002c0010t0001g0051 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3553-4903_3553-490 others(20): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(17): Show |
5 | a0001c0014t0001g0036a0003c0003t0001g0062a0003c0003t0002g0116others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3553-4903_3553-490 others(28): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(21): Show |
4 | a0002c0010t0001g0136a0003c0003t0002g0117a0003c0003t0002g0118others(1): Show | 4 | HG02622.hp2 HG02818.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.3553-4903_3553-490 others(32): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(25): Show |
2 | a0003c0003t0001g0030a0007c0017t0001g0108 | 2 | HG01109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.3553-4903_3553-490 others(36): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(26): Show |
1 | a0003c0030t0004g0022 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3553-4903_3553-490 others(37): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(17): Show |
1 | a0004c0004t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3553-4903_3553-490 others(28): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(21): Show |
4 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0125others(1): Show | 4 | HG04199.hp2 HG04204.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.3553-4903_3553-490 others(32): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(25): Show |
4 | a0003c0003t0001g0081a0009c0047t0001g0110a0012c0019t0001g0127others(1): Show | 4 | HG03516.hp1 NA18971.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.3553-4903_3553-490 others(36): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(29): Show |
3 | a0002c0010t0001g0003a0002c0040t0001g0044a0007c0032t0001g0004 | 3 | HG00621.hp1 HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.3553-4903_3553-490 others(40): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(21): Show |
1 | a0004c0020t0001g0028 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3553-4903_3553-490 others(32): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(25): Show |
2 | a0004c0004t0007g0006a0004c0020t0001g0016 | 2 | HG04115.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.3553-4903_3553-490 others(36): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(29): Show |
5 | a0002c0011t0001g0133a0002c0011t0001g0134a0002c0011t0005g0054others(2): Show | 5 | HG02630.hp2 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3553-4903_3553-490 others(40): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(37): Show |
1 | a0002c0010t0001g0047 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3553-4903_3553-490 others(48): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(21): Show |
1 | a0009c0021t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3553-4903_3553-490 others(32): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(33): Show |
2 | a0002c0011t0001g0132a0018c0043t0001g0131 | 2 | HG01884.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3553-4903_3553-490 others(44): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(37): Show |
1 | a0002c0042t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3553-4903_3553-490 others(48): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | CTTTCTTT others(41): Show |
1 | a0009c0046t0009g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3553-4903_3553-490 others(52): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926048
|
C | T | 1 | a0005c0006t0002g0099 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3553-4904C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926048 | ||||||
| chr2:130926048
|
CTCTT | C | 9 | a0001c0044t0001g0011a0001c0045t0001g0085a0008c0012t0001g0026others(6): Show | 9 | HG00735.hp2 HG01081.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3553-4878_3553-487 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926048 | |||||
| chr2:130926050
|
C | T | 15 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0002g0105others(12): Show | 15 | HG00642.hp2 HG01243.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-4902C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926050 | ||||||
| chr2:130926052
|
T | C | 15 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0002g0105others(12): Show | 15 | HG00642.hp2 HG01243.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-4900T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926052 | ||||||
| chr2:130926052
|
T | TTC | 3 | a0001c0001t0001g0122a0010c0009t0001g0138a0023c0029t0001g0141 | 3 | HG02258.hp1 HG03130.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.3553-4898_3553-489 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926052 | |||||
| chr2:130926056
|
T | TTC | 3 | a0001c0001t0001g0088a0007c0013t0002g0095a0020c0038t0001g0032 | 3 | HG01175.hp2 HG03491.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.3553-4894_3553-489 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926056 | |||||
| chr2:130926066
|
CTTTCTTT others(5): Show |
C | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3553-4885_3553-487 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926066 | ||||||
| chr2:130926078
|
G | C | 97 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(94): Show | 97 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.3553-4874G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926078 | ||||||
| chr2:130926124
|
C | T | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3553-4828C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926124 | ||||||
| chr2:130926356
|
CTTTG | C | 13 | a0001c0044t0001g0011a0001c0045t0001g0085a0008c0012t0001g0026others(10): Show | 13 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.3553-4591_3553-458 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926356 | |||||
| chr2:130926578
|
T | C | 142 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(139): Show | 142 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.3553-4374T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926578 | ||||||
| chr2:130926601
|
A | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3553-4351A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926601 | ||||||
| chr2:130926736
|
GA | G | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3553-4213delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926736 | |||||
| chr2:130926757
|
C | A | 7 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3553-4195C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130926757 | ||||||
| chr2:130926810
|
A | AT | 6 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0002g0105others(3): Show | 6 | HG01081.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3553-4114dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATT | 12 | a0001c0025t0005g0067a0001c0026t0001g0080a0001c0044t0001g0011others(9): Show | 12 | HG00642.hp2 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3553-4115_3553-411 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATTTT | 20 | a0001c0001t0001g0017a0001c0027t0001g0107a0002c0010t0001g0003others(17): Show | 20 | HG00621.hp1 HG01109.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.3553-4117_3553-411 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATTTTT | 7 | a0002c0010t0001g0047a0002c0010t0001g0051a0002c0028t0001g0073others(4): Show | 7 | HG02615.hp2 HG03453.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.3553-4118_3553-411 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATTTTTCT others(3): Show |
1 | a0001c0001t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3553-4137_3553-413 others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATTTTTT | 10 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0002t0001g0038others(7): Show | 10 | HG01515.hp1 HG01515.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3553-4119_3553-411 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATTTTTTT | 13 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0046others(10): Show | 13 | HG02155.hp2 HG02818.hp2 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.3553-4120_3553-411 others(11): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATTTTTTT others(1): Show |
18 | a0001c0001t0001g0035a0001c0001t0001g0063a0001c0001t0001g0077others(15): Show | 18 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.3553-4121_3553-411 others(12): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATTTTTTT others(2): Show |
14 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(11): Show | 14 | HG02080.hp1 HG02080.hp2 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.3553-4122_3553-411 others(13): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0033a0001c0001t0001g0115a0001c0001t0008g0048others(1): Show | 4 | HG01884.hp1 HG01975.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3553-4123_3553-411 others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATTTTTTT others(5): Show |
2 | a0001c0014t0001g0036a0007c0013t0002g0095 | 2 | HG01175.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3553-4125_3553-411 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATTTTTTT others(6): Show |
1 | a0001c0039t0001g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3553-4126_3553-411 others(17): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATTTTTTT others(8): Show |
1 | a0011c0049t0001g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3553-4128_3553-411 others(19): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
A | ATTTTTTT others(12): Show |
1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3553-4132_3553-411 others(23): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
AT | A | 14 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(11): Show | 14 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.3553-4114delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
ATTTT | A | 7 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3553-4117_3553-411 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130926810
|
ATTTTTTT others(8): Show |
A | 4 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3553-4128_3553-411 others(19): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130926810 | |||||
| chr2:130927034
|
G | A | 14 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0002g0105others(11): Show | 14 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3553-3918G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130927034 | ||||||
| chr2:130927090
|
C | T | 42 | a0001c0001t0001g0017a0001c0014t0001g0036a0002c0010t0001g0003others(39): Show | 42 | HG00621.hp1 HG01109.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.3553-3862C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130927090 | ||||||
| chr2:130927436
|
G | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3553-3516G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130927436 | ||||||
| chr2:130927672
|
C | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3553-3280C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130927672 | ||||||
| chr2:130927694
|
G | GGTA | 42 | a0001c0001t0001g0017a0001c0014t0001g0036a0002c0010t0001g0003others(39): Show | 42 | HG00621.hp1 HG01109.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.3553-3257_3553-325 others(7): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130927694 | |||||
| chr2:130927704
|
C | T | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3553-3248C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130927704 | ||||||
| chr2:130927742
|
C | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3553-3210C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130927742 | ||||||
| chr2:130927764
|
T | C | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3553-3188T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130927764 | ||||||
| chr2:130927769
|
T | C | 1 | a0001c0034t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3553-3183T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130927769 | ||||||
| chr2:130927781
|
G | T | 92 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(89): Show | 92 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.3553-3171G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130927781 | ||||||
| chr2:130927940
|
T | C | 2 | a0002c0010t0001g0003a0002c0010t0001g0136 | 2 | HG00621.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3553-3012T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130927940 | ||||||
| chr2:130927968
|
C | T | 12 | a0001c0044t0001g0011a0001c0045t0001g0085a0008c0012t0001g0026others(9): Show | 12 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3553-2984C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130927968 | ||||||
| chr2:130927989
|
T | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3553-2963T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130927989 | ||||||
| chr2:130928117
|
T | C | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3553-2835T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928117 | ||||||
| chr2:130928132
|
A | C | 12 | a0001c0044t0001g0011a0001c0045t0001g0085a0008c0012t0001g0026others(9): Show | 12 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3553-2820A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928132 | ||||||
| chr2:130928169
|
T | G | 92 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(89): Show | 92 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.3553-2783T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928169 | ||||||
| chr2:130928220
|
A | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0137a0001c0002t0001g0113 | 3 | HG02155.hp1 HG04184.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.3553-2732A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928220 | ||||||
| chr2:130928244
|
G | A | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3553-2708G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928244 | ||||||
| chr2:130928302
|
T | C | 92 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(89): Show | 92 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.3553-2650T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928302 | ||||||
| chr2:130928347
|
G | A | 1 | a0009c0021t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3553-2605G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928347 | ||||||
| chr2:130928385
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3553-2567G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928385 | ||||||
| chr2:130928389
|
T | C | 1 | a0024c0033t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3553-2563T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928389 | ||||||
| chr2:130928396
|
T | C | 2 | a0001c0001t0008g0048a0001c0002t0001g0010 | 2 | HG00642.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.3553-2556T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928396 | ||||||
| chr2:130928499
|
T | C | 1 | a0010c0009t0001g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3553-2453T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928499 | ||||||
| chr2:130928634
|
T | C | 136 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(133): Show | 136 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(133): Show |
intron_variant | MODIFIER | c.3553-2318T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928634 | ||||||
| chr2:130928672
|
T | C | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3553-2280T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928672 | ||||||
| chr2:130928691
|
T | C | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3553-2261T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928691 | ||||||
| chr2:130928696
|
C | T | 2 | a0003c0003t0001g0071a0007c0032t0001g0004 | 2 | HG03195.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.3553-2256C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928696 | ||||||
| chr2:130928750
|
C | G | 6 | a0001c0027t0001g0107a0007c0013t0001g0059a0007c0013t0003g0060others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3553-2202C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130928750 | ||||||
| chr2:130929119
|
C | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3553-1833C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130929119 | ||||||
| chr2:130929191
|
T | G | 92 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(89): Show | 92 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.3553-1761T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130929191 | ||||||
| chr2:130929536
|
C | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3553-1416C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130929536 | ||||||
| chr2:130929569
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3553-1383G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130929569 | ||||||
| chr2:130929899
|
A | AT | 92 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(89): Show | 92 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.3553-1042dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 130929899 | |||||
| chr2:130929913
|
G | C | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(46): Show | 49 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.3553-1039G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130929913 | ||||||
| chr2:130929969
|
T | G | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3553-983T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130929969 | ||||||
| chr2:130929986
|
G | A | 1 | a0001c0014t0002g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3553-966G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130929986 | ||||||
| chr2:130930010
|
C | T | 1 | a0001c0044t0001g0011 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3553-942C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130930010 | ||||||
| chr2:130930018
|
C | T | 1 | a0001c0002t0001g0031 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3553-934C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130930018 | ||||||
| chr2:130930037
|
G | GC | 91 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(88): Show | 91 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.3553-915_3553-914i others(3): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130930037 | ||||||
| chr2:130930057
|
T | C | 1 | a0003c0003t0001g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3553-895T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130930057 | ||||||
| chr2:130930351
|
A | G | 1 | a0007c0032t0001g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3553-601A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130930351 | ||||||
| chr2:130930577
|
T | C | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3553-375T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130930577 | ||||||
| chr2:130930606
|
G | A | 39 | a0002c0010t0001g0003a0002c0010t0001g0047a0002c0010t0001g0051others(36): Show | 39 | HG00621.hp1 HG01109.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.3553-346G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130930606 | ||||||
| chr2:130930657
|
G | A | 1 | a0003c0003t0001g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3553-295G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130930657 | ||||||
| chr2:130930720
|
A | T | 28 | a0001c0001t0001g0017a0002c0010t0001g0003a0002c0010t0001g0047others(25): Show | 28 | HG00621.hp1 HG01884.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.3553-232A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130930720 | ||||||
| chr2:130930768
|
T | C | 5 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3553-184T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130930768 | ||||||
| chr2:130930809
|
G | T | 28 | a0001c0001t0001g0017a0002c0010t0001g0003a0002c0010t0001g0047others(25): Show | 28 | HG00621.hp1 HG01884.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.3553-143G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130930809 | ||||||
| chr2:130930884
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3553-68G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | chr2 | 130930884 | ||||||
| chr2:130931408
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3858+151A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130931408 | ||||||
| chr2:130931559
|
C | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3858+302C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130931559 | ||||||
| chr2:130931624
|
C | T | 51 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(48): Show | 51 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3858+367C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130931624 | ||||||
| chr2:130931828
|
T | G | 1 | a0018c0043t0001g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3858+571T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130931828 | ||||||
| chr2:130931934
|
G | A | 2 | a0002c0028t0001g0073a0007c0013t0002g0095 | 2 | HG01175.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3858+677G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130931934 | ||||||
| chr2:130931991
|
A | G | 1 | a0008c0012t0001g0026 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3858+734A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130931991 | ||||||
| chr2:130932143
|
G | A | 51 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(48): Show | 51 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3858+886G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130932143 | ||||||
| chr2:130932254
|
T | G | 1 | a0018c0043t0001g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3858+997T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130932254 | ||||||
| chr2:130932363
|
C | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3858+1106C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130932363 | ||||||
| chr2:130932500
|
C | T | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3858+1243C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130932500 | ||||||
| chr2:130932681
|
A | C | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3858+1424A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130932681 | ||||||
| chr2:130932929
|
C | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3858+1672C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130932929 | ||||||
| chr2:130933008
|
A | G | 51 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(48): Show | 51 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3858+1751A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130933008 | ||||||
| chr2:130933092
|
G | C | 1 | a0004c0004t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3858+1835G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130933092 | ||||||
| chr2:130933183
|
C | T | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3858+1926C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130933183 | ||||||
| chr2:130933214
|
CA | C | 18 | a0001c0001t0001g0017a0002c0010t0001g0003a0002c0010t0001g0047others(15): Show | 18 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.3858+1973delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130933214 | |||||
| chr2:130933214
|
CAA | C | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3858+1972_3858+197 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130933214 | |||||
| chr2:130933252
|
G | C | 1 | a0001c0001t0001g0012 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3858+1995G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130933252 | ||||||
| chr2:130933621
|
T | G | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3858+2364T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130933621 | ||||||
| chr2:130933636
|
T | G | 1 | a0005c0008t0001g0098 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3858+2379T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130933636 | ||||||
| chr2:130933788
|
G | A | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3858+2531G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130933788 | ||||||
| chr2:130933990
|
T | TC | 28 | a0001c0001t0001g0017a0002c0010t0001g0003a0002c0010t0001g0047others(25): Show | 28 | HG00621.hp1 HG01884.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.3858+2734dupC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130933990 | |||||
| chr2:130934097
|
GTTTCTA | G | 2 | a0001c0001t0001g0077a0001c0002t0001g0083 | 2 | NA18981.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.3858+2847_3858+285 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130934097 | |||||
| chr2:130934218
|
A | T | 51 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(48): Show | 51 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3858+2961A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130934218 | ||||||
| chr2:130934220
|
G | A | 3 | a0001c0014t0001g0036a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02922.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3858+2963G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130934220 | ||||||
| chr2:130934294
|
A | G | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3858+3037A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130934294 | ||||||
| chr2:130934317
|
T | C | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3858+3060T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130934317 | ||||||
| chr2:130934334
|
T | C | 2 | a0002c0028t0001g0073a0007c0013t0002g0095 | 2 | HG01175.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3858+3077T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130934334 | ||||||
| chr2:130934344
|
T | C | 24 | a0001c0027t0001g0107a0001c0044t0001g0011a0001c0045t0001g0085others(21): Show | 24 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.3858+3087T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130934344 | ||||||
| chr2:130934356
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3858+3099G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130934356 | ||||||
| chr2:130934385
|
C | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3858+3128C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130934385 | ||||||
| chr2:130934552
|
T | C | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3858+3295T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130934552 | ||||||
| chr2:130934839
|
C | T | 12 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(9): Show | 12 | HG01257.hp2 HG01258.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3858+3582C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130934839 | ||||||
| chr2:130934900
|
A | G | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(46): Show | 49 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.3858+3643A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130934900 | ||||||
| chr2:130934955
|
T | C | 2 | a0002c0028t0001g0073a0007c0013t0002g0095 | 2 | HG01175.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3858+3698T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130934955 | ||||||
| chr2:130935156
|
CTATTTAT others(5): Show |
C | 52 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(49): Show | 52 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.3858+3908_3858+391 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130935156 | |||||
| chr2:130935175
|
T | C | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3858+3918T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935175 | ||||||
| chr2:130935224
|
A | G | 52 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(49): Show | 52 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.3858+3967A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935224 | ||||||
| chr2:130935287
|
C | T | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3858+4030C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935287 | ||||||
| chr2:130935404
|
A | T | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3858+4147A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935404 | ||||||
| chr2:130935536
|
G | A | 52 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(49): Show | 52 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.3858+4279G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935536 | ||||||
| chr2:130935549
|
A | G | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3858+4292A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935549 | ||||||
| chr2:130935615
|
T | C | 3 | a0011c0022t0001g0084a0011c0022t0001g0096a0011c0049t0001g0056 | 3 | HG02258.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3858+4358T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935615 | ||||||
| chr2:130935688
|
T | C | 52 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(49): Show | 52 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.3858+4431T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935688 | ||||||
| chr2:130935804
|
T | C | 1 | a0005c0006t0003g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3858+4547T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935804 | ||||||
| chr2:130935809
|
G | A | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3858+4552G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935809 | ||||||
| chr2:130935818
|
G | C | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3858+4561G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935818 | ||||||
| chr2:130935841
|
T | C | 8 | a0001c0044t0001g0011a0001c0045t0001g0085a0008c0012t0001g0026others(5): Show | 8 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.3858+4584T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935841 | ||||||
| chr2:130935942
|
A | C | 3 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068 | 3 | HG02717.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3858+4685A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935942 | ||||||
| chr2:130935990
|
G | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3858+4733G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130935990 | ||||||
| chr2:130936028
|
G | A | 1 | a0006c0050t0001g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3858+4771G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130936028 | ||||||
| chr2:130936151
|
G | A | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3858+4894G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130936151 | ||||||
| chr2:130936255
|
G | A | 51 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(48): Show | 51 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3858+4998G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130936255 | ||||||
| chr2:130936258
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3858+5001T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130936258 | ||||||
| chr2:130936347
|
G | C | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3858+5090G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130936347 | ||||||
| chr2:130936632
|
G | T | 77 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(74): Show | 77 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.3858+5375G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130936632 | ||||||
| chr2:130936661
|
C | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3858+5404C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130936661 | ||||||
| chr2:130936684
|
T | C | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3858+5427T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130936684 | ||||||
| chr2:130936698
|
C | A | 4 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3858+5441C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130936698 | ||||||
| chr2:130936887
|
CT | C | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3858+5640delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130936887 | |||||
| chr2:130936905
|
CT | C | 9 | a0001c0002t0001g0024a0001c0014t0002g0075a0001c0027t0001g0107others(6): Show | 9 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3858+5667delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130936905 | |||||
| chr2:130936905
|
CTT | C | 70 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(67): Show | 70 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.3858+5666_3858+566 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130936905 | |||||
| chr2:130936905
|
CTTT | C | 46 | a0001c0001t0001g0017a0001c0044t0001g0011a0001c0045t0001g0085others(43): Show | 46 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.3858+5665_3858+566 others(7): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130936905 | |||||
| chr2:130936910
|
T | C | 1 | a0019c0036t0001g0049 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3858+5653T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130936910 | ||||||
| chr2:130937154
|
T | TC | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3858+5903dupC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130937154 | |||||
| chr2:130937599
|
C | T | 3 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068 | 3 | HG02717.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3858+6342C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130937599 | ||||||
| chr2:130937669
|
A | AT | 76 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(73): Show | 76 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.3858+6428dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130937669 | |||||
| chr2:130937669
|
AT | A | 20 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0002g0105others(17): Show | 20 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3858+6428delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130937669 | |||||
| chr2:130937698
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3858+6441C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130937698 | ||||||
| chr2:130937715
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3858+6458G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130937715 | ||||||
| chr2:130937816
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3858+6559C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130937816 | ||||||
| chr2:130937871
|
G | GT | 2 | a0002c0028t0001g0073a0007c0013t0002g0095 | 2 | HG01175.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3858+6616dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130937871 | |||||
| chr2:130937913
|
C | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3858+6656C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130937913 | ||||||
| chr2:130938069
|
C | G | 77 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(74): Show | 77 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.3858+6812C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130938069 | ||||||
| chr2:130938111
|
A | G | 1 | a0002c0010t0001g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3858+6854A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130938111 | ||||||
| chr2:130938372
|
A | G | 77 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(74): Show | 77 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.3858+7115A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130938372 | ||||||
| chr2:130938441
|
G | C | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3858+7184G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130938441 | ||||||
| chr2:130938456
|
A | G | 1 | a0010c0009t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3858+7199A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130938456 | ||||||
| chr2:130938818
|
C | T | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3858+7561C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130938818 | ||||||
| chr2:130938821
|
A | G | 3 | a0001c0014t0001g0036a0001c0018t0002g0105a0001c0018t0005g0106 | 3 | HG02922.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3858+7564A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130938821 | ||||||
| chr2:130939108
|
A | C | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3859-7401A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130939108 | ||||||
| chr2:130939432
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3859-7077G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130939432 | ||||||
| chr2:130939622
|
A | C | 3 | a0001c0001t0001g0042a0001c0002t0001g0038a0001c0002t0001g0041 | 3 | HG01515.hp2 HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3859-6887A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130939622 | ||||||
| chr2:130939753
|
T | C | 7 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3859-6756T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130939753 | ||||||
| chr2:130939922
|
G | A | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3859-6587G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130939922 | ||||||
| chr2:130939935
|
A | G | 1 | a0005c0006t0003g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3859-6574A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130939935 | ||||||
| chr2:130940069
|
A | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3859-6440A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940069 | ||||||
| chr2:130940213
|
G | A | 1 | a0021c0037t0001g0050 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3859-6296G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940213 | ||||||
| chr2:130940291
|
C | T | 2 | a0002c0048t0001g0070a0023c0029t0001g0141 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3859-6218C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940291 | ||||||
| chr2:130940334
|
G | C | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3859-6175G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940334 | ||||||
| chr2:130940440
|
T | C | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3859-6069T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940440 | ||||||
| chr2:130940533
|
A | G | 1 | a0003c0031t0006g0037 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3859-5976A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940533 | ||||||
| chr2:130940623
|
G | A | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3859-5886G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940623 | ||||||
| chr2:130940625
|
G | T | 24 | a0001c0027t0001g0107a0001c0044t0001g0011a0001c0045t0001g0085others(21): Show | 24 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.3859-5884G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940625 | ||||||
| chr2:130940703
|
C | T | 40 | a0001c0001t0001g0017a0002c0010t0001g0003a0002c0010t0001g0047others(37): Show | 40 | HG00621.hp1 HG01109.hp2 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.3859-5806C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940703 | ||||||
| chr2:130940739
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3859-5770G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940739 | ||||||
| chr2:130940764
|
A | G | 143 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(140): Show | 143 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(140): Show |
intron_variant | MODIFIER | c.3859-5745A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940764 | ||||||
| chr2:130940801
|
T | C | 87 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(84): Show | 87 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.3859-5708T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940801 | ||||||
| chr2:130940811
|
G | A | 1 | a0001c0014t0002g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3859-5698G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940811 | ||||||
| chr2:130940845
|
A | G | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3859-5664A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940845 | ||||||
| chr2:130940849
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3859-5660G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940849 | ||||||
| chr2:130940849
|
GA | G | 46 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(43): Show | 46 | HG00642.hp1 HG00735.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.3859-5649delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130940849 | |||||
| chr2:130940850
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3859-5659A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940850 | ||||||
| chr2:130940953
|
T | C | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3859-5556T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130940953 | ||||||
| chr2:130941007
|
G | C | 87 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(84): Show | 87 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.3859-5502G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130941007 | ||||||
| chr2:130941076
|
C | T | 28 | a0001c0001t0001g0017a0002c0010t0001g0003a0002c0010t0001g0047others(25): Show | 28 | HG00621.hp1 HG01884.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.3859-5433C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130941076 | ||||||
| chr2:130941135
|
G | A | 16 | a0001c0014t0001g0036a0001c0015t0001g0078a0001c0015t0001g0079others(13): Show | 16 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.3859-5374G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130941135 | ||||||
| chr2:130941210
|
A | AT | 59 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(56): Show | 59 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.3859-5285dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130941210 | |||||
| chr2:130941210
|
A | ATT | 82 | a0001c0001t0001g0017a0001c0015t0001g0078a0001c0015t0001g0079others(79): Show | 82 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.3859-5286_3859-528 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130941210 | |||||
| chr2:130941455
|
C | T | 5 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3859-5054C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130941455 | ||||||
| chr2:130941462
|
C | T | 1 | a0003c0003t0003g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3859-5047C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130941462 | ||||||
| chr2:130941597
|
T | C | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3859-4912T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130941597 | ||||||
| chr2:130941723
|
A | T | 1 | a0002c0010t0001g0047 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3859-4786A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130941723 | ||||||
| chr2:130941855
|
G | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3859-4654G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130941855 | ||||||
| chr2:130941870
|
A | C | 6 | a0001c0027t0001g0107a0007c0013t0001g0059a0007c0013t0003g0060others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3859-4639A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130941870 | ||||||
| chr2:130942040
|
G | C | 56 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(53): Show | 56 | HG00621.hp1 HG01109.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.3859-4469G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130942040 | ||||||
| chr2:130942106
|
G | C | 7 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3859-4403G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130942106 | ||||||
| chr2:130942149
|
T | A | 40 | a0001c0001t0001g0017a0002c0010t0001g0003a0002c0010t0001g0047others(37): Show | 40 | HG00621.hp1 HG01109.hp2 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.3859-4360T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130942149 | ||||||
| chr2:130942152
|
C | CT | 79 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0014t0001g0036others(76): Show | 79 | HG00621.hp1 HG01109.hp2 HG01175.hp2 others(76): Show |
intron_variant | MODIFIER | c.3859-4342dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130942152 | |||||
| chr2:130942152
|
CT | C | 7 | a0001c0044t0001g0011a0008c0012t0001g0026a0008c0012t0001g0027others(4): Show | 7 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.3859-4342delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 130942152 | |||||
| chr2:130942249
|
A | G | 1 | a0001c0002t0001g0010 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3859-4260A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130942249 | ||||||
| chr2:130942307
|
G | A | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(46): Show | 49 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.3859-4202G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130942307 | ||||||
| chr2:130942311
|
G | A | 1 | a0008c0012t0001g0026 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3859-4198G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130942311 | ||||||
| chr2:130942385
|
G | T | 2 | a0002c0010t0001g0003a0002c0010t0001g0136 | 2 | HG00621.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3859-4124G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130942385 | ||||||
| chr2:130942672
|
T | C | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3859-3837T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130942672 | ||||||
| chr2:130942725
|
G | A | 1 | a0007c0013t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3859-3784G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130942725 | ||||||
| chr2:130942797
|
A | G | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3859-3712A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130942797 | ||||||
| chr2:130942843
|
A | G | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3859-3666A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130942843 | ||||||
| chr2:130942904
|
A | G | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3859-3605A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130942904 | ||||||
| chr2:130943195
|
G | A | 7 | a0001c0044t0001g0011a0008c0012t0001g0026a0008c0012t0001g0027others(4): Show | 7 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.3859-3314G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130943195 | ||||||
| chr2:130943211
|
T | A | 40 | a0001c0001t0001g0017a0002c0010t0001g0003a0002c0010t0001g0047others(37): Show | 40 | HG00621.hp1 HG01109.hp2 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.3859-3298T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130943211 | ||||||
| chr2:130943620
|
A | G | 6 | a0001c0027t0001g0107a0007c0013t0001g0059a0007c0013t0003g0060others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3859-2889A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130943620 | ||||||
| chr2:130943649
|
G | A | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3859-2860G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130943649 | ||||||
| chr2:130943664
|
G | C | 1 | a0001c0014t0002g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3859-2845G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130943664 | ||||||
| chr2:130944066
|
A | T | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3859-2443A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130944066 | ||||||
| chr2:130944224
|
A | C | 80 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(77): Show | 80 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.3859-2285A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130944224 | ||||||
| chr2:130944225
|
G | A | 6 | a0001c0027t0001g0107a0007c0013t0001g0059a0007c0013t0003g0060others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3859-2284G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130944225 | ||||||
| chr2:130944315
|
T | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3859-2194T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130944315 | ||||||
| chr2:130944739
|
T | A | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3859-1770T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130944739 | ||||||
| chr2:130944983
|
C | G | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3859-1526C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130944983 | ||||||
| chr2:130945144
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3859-1365G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130945144 | ||||||
| chr2:130945313
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3859-1196G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130945313 | ||||||
| chr2:130945357
|
A | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3859-1152A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130945357 | ||||||
| chr2:130945955
|
T | C | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3859-554T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130945955 | ||||||
| chr2:130946103
|
A | G | 5 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(2): Show | 5 | HG01257.hp2 HG01258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3859-406A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130946103 | ||||||
| chr2:130946121
|
G | A | 45 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(42): Show | 45 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.3859-388G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130946121 | ||||||
| chr2:130946395
|
G | C | 56 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(53): Show | 56 | HG00621.hp1 HG01109.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.3859-114G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3/13 | chr2 | 130946395 | ||||||
| chr2:130946673
|
G | A | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3985+38G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130946673 | ||||||
| chr2:130946895
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3985+260G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130946895 | ||||||
| chr2:130946956
|
G | T | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3985+321G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130946956 | ||||||
| chr2:130947404
|
A | T | 1 | a0004c0020t0001g0016 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3985+769A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130947404 | ||||||
| chr2:130947410
|
A | G | 2 | a0002c0010t0001g0003a0002c0010t0001g0136 | 2 | HG00621.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3985+775A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130947410 | ||||||
| chr2:130947479
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3985+844G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130947479 | ||||||
| chr2:130947643
|
A | T | 2 | a0002c0011t0005g0054a0009c0021t0001g0130 | 2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3985+1008A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130947643 | ||||||
| chr2:130947653
|
A | G | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+1018A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130947653 | ||||||
| chr2:130947779
|
C | T | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3985+1144C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130947779 | ||||||
| chr2:130947800
|
G | C | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3985+1165G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130947800 | ||||||
| chr2:130948018
|
C | T | 1 | a0001c0044t0001g0011 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3985+1383C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130948018 | ||||||
| chr2:130948019
|
G | A | 6 | a0001c0027t0001g0107a0007c0013t0001g0059a0007c0013t0003g0060others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+1384G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130948019 | ||||||
| chr2:130948092
|
G | C | 1 | a0007c0032t0001g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3985+1457G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130948092 | ||||||
| chr2:130948104
|
G | A | 1 | a0001c0002t0001g0034 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3985+1469G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130948104 | ||||||
| chr2:130948393
|
C | T | 48 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 48 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.3985+1758C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130948393 | ||||||
| chr2:130948522
|
C | T | 1 | a0024c0033t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3985+1887C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130948522 | ||||||
| chr2:130948644
|
C | T | 32 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(29): Show | 32 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.3985+2009C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130948644 | ||||||
| chr2:130948659
|
C | A | 76 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(73): Show | 76 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.3985+2024C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130948659 | ||||||
| chr2:130948689
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+2054G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130948689 | ||||||
| chr2:130948777
|
T | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+2142T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130948777 | ||||||
| chr2:130948964
|
CTT | C | 72 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(69): Show | 72 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.3985+2331_3985+233 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130948964 | |||||
| chr2:130949085
|
T | C | 1 | a0022c0035t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3985+2450T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949085 | ||||||
| chr2:130949170
|
G | T | 77 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(74): Show | 77 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.3985+2535G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949170 | ||||||
| chr2:130949310
|
G | A | 77 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(74): Show | 77 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.3985+2675G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949310 | ||||||
| chr2:130949376
|
C | T | 2 | a0001c0001t0001g0046a0001c0002t0001g0074 | 2 | NA18962.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.3985+2741C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949376 | ||||||
| chr2:130949416
|
C | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3985+2781C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949416 | ||||||
| chr2:130949455
|
G | A | 1 | a0011c0049t0001g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3985+2820G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949455 | ||||||
| chr2:130949631
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3985+2996G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949631 | ||||||
| chr2:130949719
|
G | A | 10 | a0005c0006t0001g0052a0005c0006t0001g0100a0005c0006t0001g0102others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3985+3084G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949719 | ||||||
| chr2:130949759
|
C | T | 1 | a0014c0023t0001g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3985+3124C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949759 | ||||||
| chr2:130949868
|
C | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0088 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3985+3233C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949868 | ||||||
| chr2:130949892
|
G | A | 1 | a0001c0014t0002g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3985+3257G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949892 | ||||||
| chr2:130949900
|
C | G | 1 | a0001c0045t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3985+3265C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949900 | ||||||
| chr2:130949937
|
C | G | 1 | a0004c0020t0001g0016 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3985+3302C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130949937 | ||||||
| chr2:130950351
|
C | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3985+3716C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130950351 | ||||||
| chr2:130950358
|
C | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3985+3723C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130950358 | ||||||
| chr2:130950391
|
G | A | 2 | a0002c0048t0001g0070a0023c0029t0001g0141 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3985+3756G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130950391 | ||||||
| chr2:130950686
|
A | AC | 14 | a0002c0010t0001g0003a0002c0010t0001g0136a0002c0011t0001g0132others(11): Show | 14 | HG00621.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3985+4057dupC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130950686 | |||||
| chr2:130950689
|
C | G | 1 | a0007c0032t0001g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3985+4054C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130950689 | ||||||
| chr2:130950690
|
C | G | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+4055C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130950690 | ||||||
| chr2:130950693
|
A | C | 140 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(137): Show | 140 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.3985+4058A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130950693 | ||||||
| chr2:130950693
|
A | G | 1 | a0008c0053t0001g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3985+4058A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130950693 | ||||||
| chr2:130950694
|
C | G | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3985+4059C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130950694 | ||||||
| chr2:130951076
|
A | G | 89 | a0001c0001t0001g0017a0001c0014t0001g0036a0001c0015t0001g0078others(86): Show | 89 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.3985+4441A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130951076 | ||||||
| chr2:130951119
|
G | T | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3985+4484G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130951119 | ||||||
| chr2:130951131
|
T | C | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3985+4496T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130951131 | ||||||
| chr2:130951149
|
C | G | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+4514C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130951149 | ||||||
| chr2:130951168
|
T | C | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+4533T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130951168 | ||||||
| chr2:130951191
|
C | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(24): Show | 27 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.3985+4556C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130951191 | ||||||
| chr2:130951274
|
G | C | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+4639G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130951274 | ||||||
| chr2:130951722
|
C | T | 1 | a0010c0009t0001g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3985+5087C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130951722 | ||||||
| chr2:130951768
|
A | G | 1 | a0003c0003t0001g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3985+5133A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130951768 | ||||||
| chr2:130951773
|
A | T | 1 | a0001c0001t0002g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3985+5138A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130951773 | ||||||
| chr2:130951807
|
CT | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0088 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3985+5175delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130951807 | |||||
| chr2:130951958
|
C | T | 21 | a0001c0001t0001g0122a0001c0001t0001g0137a0001c0002t0001g0013others(18): Show | 21 | HG02155.hp1 HG02280.hp2 HG02723.hp1 others(18): Show |
intron_variant | MODIFIER | c.3985+5323C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130951958 | ||||||
| chr2:130952128
|
A | C | 1 | a0004c0020t0001g0016 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3985+5493A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130952128 | ||||||
| chr2:130952195
|
A | G | 6 | a0001c0027t0001g0107a0007c0013t0001g0059a0007c0013t0003g0060others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+5560A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130952195 | ||||||
| chr2:130952274
|
G | A | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3985+5639G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130952274 | ||||||
| chr2:130952279
|
G | A | 6 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+5644G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130952279 | ||||||
| chr2:130952443
|
C | G | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+5808C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130952443 | ||||||
| chr2:130952497
|
T | C | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3985+5862T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130952497 | ||||||
| chr2:130952993
|
T | C | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+6358T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130952993 | ||||||
| chr2:130953052
|
T | A | 42 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(39): Show | 42 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.3985+6417T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130953052 | ||||||
| chr2:130953088
|
C | T | 5 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+6453C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130953088 | ||||||
| chr2:130953126
|
T | C | 7 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3985+6491T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130953126 | ||||||
| chr2:130953154
|
G | C | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3985+6519G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130953154 | ||||||
| chr2:130953212
|
T | C | 1 | a0001c0014t0002g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3985+6577T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130953212 | ||||||
| chr2:130953382
|
C | T | 1 | a0005c0008t0001g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3985+6747C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130953382 | ||||||
| chr2:130953429
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0088 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3985+6794G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130953429 | ||||||
| chr2:130953622
|
C | G | 73 | a0001c0001t0001g0017a0001c0001t0001g0122a0001c0001t0001g0137others(70): Show | 73 | HG00621.hp1 HG01109.hp2 HG01243.hp1 others(70): Show |
intron_variant | MODIFIER | c.3985+6987C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130953622 | ||||||
| chr2:130953640
|
T | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3985+7005T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130953640 | ||||||
| chr2:130953848
|
A | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3985+7213A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130953848 | ||||||
| chr2:130954099
|
C | A | 4 | a0008c0012t0001g0026a0008c0012t0001g0027a0008c0012t0001g0045others(1): Show | 4 | HG00735.hp2 HG01081.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.3985+7464C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130954099 | ||||||
| chr2:130954148
|
C | T | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+7513C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130954148 | ||||||
| chr2:130954204
|
C | T | 7 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.3985+7569C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130954204 | ||||||
| chr2:130954550
|
A | T | 13 | a0003c0003t0001g0030a0003c0003t0001g0062a0003c0003t0001g0071others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.3985+7915A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130954550 | ||||||
| chr2:130954756
|
G | C | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+8121G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130954756 | ||||||
| chr2:130954879
|
C | T | 2 | a0004c0004t0001g0005a0004c0004t0001g0008 | 2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3985+8244C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130954879 | ||||||
| chr2:130954893
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3985+8258T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130954893 | ||||||
| chr2:130954963
|
A | AT | 41 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(38): Show | 41 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.3985+8337dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130954963 | |||||
| chr2:130954991
|
C | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3985+8356C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130954991 | ||||||
| chr2:130955135
|
G | A | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3985+8500G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130955135 | ||||||
| chr2:130955161
|
C | G | 1 | a0001c0014t0002g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3985+8526C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130955161 | ||||||
| chr2:130955759
|
C | G | 8 | a0001c0044t0001g0011a0001c0045t0001g0085a0008c0012t0001g0026others(5): Show | 8 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985+9124C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130955759 | ||||||
| chr2:130956204
|
A | C | 28 | a0001c0014t0001g0036a0001c0015t0001g0078a0001c0015t0001g0079others(25): Show | 28 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.3985+9569A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130956204 | ||||||
| chr2:130956466
|
C | G | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3985+9831C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130956466 | ||||||
| chr2:130956520
|
C | T | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3985+9885C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130956520 | ||||||
| chr2:130956524
|
T | G | 1 | a0001c0045t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3985+9889T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130956524 | ||||||
| chr2:130956534
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3985+9899G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130956534 | ||||||
| chr2:130956739
|
G | A | 14 | a0001c0027t0001g0107a0001c0044t0001g0011a0001c0045t0001g0085others(11): Show | 14 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.3985+10104G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130956739 | ||||||
| chr2:130956966
|
A | T | 14 | a0001c0027t0001g0107a0001c0044t0001g0011a0001c0045t0001g0085others(11): Show | 14 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.3985+10331A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130956966 | ||||||
| chr2:130957175
|
AT | A | 14 | a0001c0027t0001g0107a0001c0044t0001g0011a0001c0045t0001g0085others(11): Show | 14 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.3985+10541delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130957175 | ||||||
| chr2:130957177
|
A | G | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+10542A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130957177 | ||||||
| chr2:130957187
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+10552G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130957187 | ||||||
| chr2:130957206
|
C | A | 3 | a0001c0001t0001g0042a0001c0002t0001g0038a0001c0002t0001g0041 | 3 | HG01515.hp2 HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3985+10571C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130957206 | ||||||
| chr2:130957248
|
C | CT | 10 | a0001c0044t0001g0011a0001c0045t0001g0085a0002c0028t0001g0073others(7): Show | 10 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.3985+10625dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130957248 | |||||
| chr2:130957434
|
C | T | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3985+10799C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130957434 | ||||||
| chr2:130957592
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+10957G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130957592 | ||||||
| chr2:130957665
|
G | C | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3985+11030G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130957665 | ||||||
| chr2:130957795
|
G | T | 29 | a0001c0014t0001g0036a0001c0015t0001g0078a0001c0015t0001g0079others(26): Show | 29 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.3985+11160G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130957795 | ||||||
| chr2:130957840
|
GC | G | 14 | a0001c0027t0001g0107a0001c0044t0001g0011a0001c0045t0001g0085others(11): Show | 14 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.3985+11206delC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130957840 | ||||||
| chr2:130957934
|
T | C | 3 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068 | 3 | HG02717.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3985+11299T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130957934 | ||||||
| chr2:130957951
|
G | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3985+11316G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130957951 | ||||||
| chr2:130958015
|
C | CA | 15 | a0001c0014t0001g0036a0001c0015t0001g0078a0001c0015t0001g0079others(12): Show | 15 | HG01175.hp2 HG01243.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.3985+11392dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130958015 | |||||
| chr2:130958015
|
C | CAA | 11 | a0001c0044t0001g0011a0001c0045t0001g0085a0008c0012t0001g0026others(8): Show | 11 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.3985+11391_3985+11 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130958015 | |||||
| chr2:130958026
|
AAG | A | 5 | a0006c0005t0001g0094a0006c0005t0001g0143a0006c0005t0003g0140others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+11393_3985+11 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130958026 | |||||
| chr2:130958114
|
G | T | 1 | a0019c0036t0001g0049 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3985+11479G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130958114 | ||||||
| chr2:130958157
|
G | A | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3985+11522G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130958157 | ||||||
| chr2:130958259
|
A | G | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3985+11624A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130958259 | ||||||
| chr2:130958354
|
T | G | 1 | a0021c0037t0001g0050 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3985+11719T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130958354 | ||||||
| chr2:130958420
|
G | A | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3985+11785G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130958420 | ||||||
| chr2:130958422
|
T | G | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3985+11787T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130958422 | ||||||
| chr2:130958621
|
G | A | 34 | a0001c0014t0001g0036a0001c0015t0001g0078a0001c0015t0001g0079others(31): Show | 34 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.3985+11986G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130958621 | ||||||
| chr2:130958679
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+12044G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130958679 | ||||||
| chr2:130958796
|
G | A | 13 | a0001c0014t0001g0036a0001c0015t0001g0078a0001c0015t0001g0079others(10): Show | 13 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.3985+12161G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130958796 | ||||||
| chr2:130958946
|
C | CT | 19 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0123others(16): Show | 19 | HG00621.hp1 HG01884.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.3985+12324dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130958946 | |||||
| chr2:130959023
|
C | T | 1 | a0001c0002t0001g0041 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3985+12388C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959023 | ||||||
| chr2:130959066
|
C | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3985+12431C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959066 | ||||||
| chr2:130959090
|
C | T | 23 | a0003c0003t0001g0030a0003c0003t0001g0062a0003c0003t0001g0071others(20): Show | 23 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3985+12455C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959090 | ||||||
| chr2:130959091
|
C | G | 141 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(138): Show | 141 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(138): Show |
intron_variant | MODIFIER | c.3985+12456C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959091 | ||||||
| chr2:130959107
|
A | G | 1 | a0001c0002t0001g0023 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3985+12472A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959107 | ||||||
| chr2:130959254
|
T | C | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3985+12619T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959254 | ||||||
| chr2:130959255
|
T | A | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3985+12620T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959255 | ||||||
| chr2:130959257
|
A | T | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3985+12622A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959257 | ||||||
| chr2:130959262
|
C | T | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3985+12627C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959262 | ||||||
| chr2:130959263
|
C | G | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3985+12628C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959263 | ||||||
| chr2:130959264
|
TTCTTTTA others(61): Show |
T | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3985+12630_3985+12 others(74): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959264 | ||||||
| chr2:130959273
|
T | C | 33 | a0001c0014t0001g0036a0001c0015t0001g0078a0001c0015t0001g0079others(30): Show | 33 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.3985+12638T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959273 | ||||||
| chr2:130959333
|
A | G | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3985+12698A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959333 | ||||||
| chr2:130959633
|
T | C | 4 | a0001c0001t0001g0043a0001c0001t0001g0087a0001c0001t0001g0123others(1): Show | 4 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.3985+12998T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959633 | ||||||
| chr2:130959873
|
C | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3985+13238C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959873 | ||||||
| chr2:130959925
|
T | G | 1 | a0001c0002t0001g0038 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3985+13290T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130959925 | ||||||
| chr2:130960047
|
G | A | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+13412G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130960047 | ||||||
| chr2:130960095
|
G | A | 15 | a0001c0001t0001g0122a0001c0001t0001g0137a0001c0002t0001g0013others(12): Show | 15 | HG02155.hp1 HG02280.hp2 HG03704.hp1 others(12): Show |
intron_variant | MODIFIER | c.3985+13460G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130960095 | ||||||
| chr2:130960156
|
TA | T | 9 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(6): Show | 9 | HG00642.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3985+13530delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130960156 | |||||
| chr2:130960200
|
T | C | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3985+13565T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130960200 | ||||||
| chr2:130960210
|
C | T | 5 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+13575C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130960210 | ||||||
| chr2:130960223
|
T | TTATA | 7 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3985+13589_3985+13 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130960223 | |||||
| chr2:130960318
|
A | G | 41 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(38): Show | 41 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.3985+13683A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130960318 | ||||||
| chr2:130960352
|
G | C | 6 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+13717G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130960352 | ||||||
| chr2:130960393
|
A | C | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+13758A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130960393 | ||||||
| chr2:130960399
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3985+13764C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130960399 | ||||||
| chr2:130960706
|
C | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3985+14071C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130960706 | ||||||
| chr2:130960767
|
C | A | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3985+14132C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130960767 | ||||||
| chr2:130961217
|
A | C | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3985+14582A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130961217 | ||||||
| chr2:130961229
|
T | G | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3985+14594T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130961229 | ||||||
| chr2:130961602
|
C | T | 1 | a0003c0003t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3985+14967C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130961602 | ||||||
| chr2:130961672
|
G | A | 2 | a0001c0002t0001g0038a0002c0028t0001g0073 | 2 | HG01515.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3985+15037G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130961672 | ||||||
| chr2:130961689
|
G | A | 1 | a0019c0036t0001g0049 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3985+15054G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130961689 | ||||||
| chr2:130961909
|
C | A | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3985+15274C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130961909 | ||||||
| chr2:130961967
|
G | A | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3985+15332G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130961967 | ||||||
| chr2:130962110
|
G | A | 7 | a0002c0011t0001g0132a0002c0011t0001g0133a0002c0011t0001g0134others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3985+15475G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130962110 | ||||||
| chr2:130962166
|
G | T | 34 | a0001c0001t0001g0017a0001c0001t0001g0122a0001c0001t0001g0137others(31): Show | 34 | HG00621.hp1 HG01884.hp2 HG02155.hp1 others(31): Show |
intron_variant | MODIFIER | c.3985+15531G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130962166 | ||||||
| chr2:130962237
|
CA | C | 108 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(105): Show | 108 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.3985+15619delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130962237 | |||||
| chr2:130962276
|
G | A | 7 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3985+15641G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130962276 | ||||||
| chr2:130962559
|
C | T | 3 | a0004c0004t0001g0128a0012c0019t0001g0127a0012c0019t0001g0129 | 3 | NA18948.hp2 NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.3985+15924C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130962559 | ||||||
| chr2:130962739
|
A | G | 1 | a0003c0003t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3985+16104A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130962739 | ||||||
| chr2:130962830
|
A | C | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3985+16195A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130962830 | ||||||
| chr2:130963177
|
C | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3985+16542C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130963177 | ||||||
| chr2:130963181
|
C | T | 1 | a0010c0009t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3985+16546C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130963181 | ||||||
| chr2:130963215
|
G | T | 2 | a0002c0011t0005g0054a0009c0021t0001g0130 | 2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3985+16580G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130963215 | ||||||
| chr2:130963289
|
A | T | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3985+16654A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130963289 | ||||||
| chr2:130963345
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3985+16710C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130963345 | ||||||
| chr2:130963353
|
G | T | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+16718G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130963353 | ||||||
| chr2:130963445
|
G | A | 1 | a0001c0001t0008g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3985+16810G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130963445 | ||||||
| chr2:130963592
|
C | CG | 143 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(140): Show | 143 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(140): Show |
intron_variant | MODIFIER | c.3985+16959dupG | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130963592 | |||||
| chr2:130963651
|
C | T | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+17016C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130963651 | ||||||
| chr2:130963680
|
G | C | 4 | a0001c0001t0001g0017a0002c0010t0001g0003a0002c0010t0001g0051others(1): Show | 4 | HG00621.hp1 HG03654.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.3985+17045G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130963680 | ||||||
| chr2:130963819
|
T | G | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3985+17184T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130963819 | ||||||
| chr2:130963905
|
G | GGCCCGGA others(48): Show |
143 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(140): Show | 143 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(140): Show |
intron_variant | MODIFIER | c.3985+17275_3985+17 others(61): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130963905 | |||||
| chr2:130963945
|
G | C | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3985+17310G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130963945 | ||||||
| chr2:130963963
|
C | T | 23 | a0003c0003t0001g0030a0003c0003t0001g0062a0003c0003t0001g0071others(20): Show | 23 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3985+17328C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130963963 | ||||||
| chr2:130964195
|
C | G | 1 | a0002c0010t0001g0047 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3985+17560C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130964195 | ||||||
| chr2:130964337
|
T | C | 5 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+17702T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130964337 | ||||||
| chr2:130964383
|
TC | T | 34 | a0001c0001t0001g0017a0001c0001t0001g0122a0001c0001t0001g0137others(31): Show | 34 | HG00621.hp1 HG01884.hp2 HG02155.hp1 others(31): Show |
intron_variant | MODIFIER | c.3985+17750delC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130964383 | |||||
| chr2:130964437
|
T | G | 1 | a0001c0001t0001g0012 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3985+17802T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130964437 | ||||||
| chr2:130964670
|
G | A | 15 | a0001c0001t0001g0122a0001c0001t0001g0137a0001c0002t0001g0013others(12): Show | 15 | HG02155.hp1 HG02280.hp2 HG03704.hp1 others(12): Show |
intron_variant | MODIFIER | c.3985+18035G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130964670 | ||||||
| chr2:130964769
|
C | G | 28 | a0001c0014t0001g0036a0001c0015t0001g0078a0001c0015t0001g0079others(25): Show | 28 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.3985+18134C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130964769 | ||||||
| chr2:130965003
|
C | T | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3985+18368C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130965003 | ||||||
| chr2:130965212
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3985+18577G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130965212 | ||||||
| chr2:130965361
|
G | A | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0025t0005g0067others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+18726G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130965361 | ||||||
| chr2:130965370
|
A | G | 10 | a0003c0003t0001g0030a0003c0003t0001g0062a0003c0003t0001g0081others(7): Show | 10 | HG01109.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3985+18735A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130965370 | ||||||
| chr2:130965579
|
G | T | 101 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(98): Show | 101 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.3985+18944G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130965579 | ||||||
| chr2:130965662
|
C | T | 1 | a0008c0012t0001g0082 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3985+19027C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130965662 | ||||||
| chr2:130965693
|
C | T | 1 | a0002c0010t0001g0051 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3985+19058C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130965693 | ||||||
| chr2:130965830
|
C | T | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+19195C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130965830 | ||||||
| chr2:130965990
|
G | A | 1 | a0001c0002t0001g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3985+19355G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130965990 | ||||||
| chr2:130966037
|
C | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+19402C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130966037 | ||||||
| chr2:130966095
|
T | C | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+19460T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130966095 | ||||||
| chr2:130966311
|
C | T | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+19676C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130966311 | ||||||
| chr2:130966499
|
C | T | 15 | a0001c0001t0001g0122a0001c0001t0001g0137a0001c0002t0001g0013others(12): Show | 15 | HG02155.hp1 HG02280.hp2 HG03704.hp1 others(12): Show |
intron_variant | MODIFIER | c.3985+19864C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130966499 | ||||||
| chr2:130966586
|
A | G | 6 | a0001c0027t0001g0107a0007c0013t0001g0059a0007c0013t0003g0060others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+19951A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130966586 | ||||||
| chr2:130966659
|
C | T | 1 | a0008c0053t0001g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3985+20024C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130966659 | ||||||
| chr2:130966975
|
A | G | 5 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+20340A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130966975 | ||||||
| chr2:130967128
|
G | T | 7 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3985+20493G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130967128 | ||||||
| chr2:130967170
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+20535G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130967170 | ||||||
| chr2:130967330
|
C | T | 1 | a0004c0004t0001g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3985+20695C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130967330 | ||||||
| chr2:130967332
|
C | T | 97 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(94): Show | 97 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.3985+20697C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130967332 | ||||||
| chr2:130967488
|
T | C | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3985+20853T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130967488 | ||||||
| chr2:130967688
|
C | A | 10 | a0005c0006t0001g0052a0005c0006t0001g0100a0005c0006t0001g0102others(7): Show | 10 | HG01243.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3985+21053C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130967688 | ||||||
| chr2:130967715
|
G | C | 1 | a0010c0009t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3985+21080G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130967715 | ||||||
| chr2:130967754
|
G | A | 1 | a0001c0045t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3985+21119G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130967754 | ||||||
| chr2:130967949
|
T | A | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3985+21314T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130967949 | ||||||
| chr2:130967964
|
A | G | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3985+21329A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130967964 | ||||||
| chr2:130967982
|
G | A | 3 | a0001c0001t0001g0042a0001c0002t0001g0038a0001c0002t0001g0041 | 3 | HG01515.hp2 HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3985+21347G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130967982 | ||||||
| chr2:130967986
|
T | C | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+21351T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130967986 | ||||||
| chr2:130968198
|
A | G | 97 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(94): Show | 97 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.3985+21563A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968198 | ||||||
| chr2:130968212
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3985+21577A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968212 | ||||||
| chr2:130968274
|
C | G | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3985+21639C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968274 | ||||||
| chr2:130968338
|
A | G | 7 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3985+21703A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968338 | ||||||
| chr2:130968487
|
G | A | 97 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(94): Show | 97 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.3985+21852G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968487 | ||||||
| chr2:130968726
|
C | T | 5 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+22091C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968726 | ||||||
| chr2:130968729
|
C | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(10): Show | 13 | HG02080.hp1 HG02698.hp2 HG03491.hp1 others(10): Show |
intron_variant | MODIFIER | c.3985+22094C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968729 | ||||||
| chr2:130968744
|
C | T | 1 | a0022c0035t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3985+22109C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968744 | ||||||
| chr2:130968774
|
C | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3985+22139C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968774 | ||||||
| chr2:130968775
|
G | A | 6 | a0001c0044t0001g0011a0008c0012t0001g0026a0008c0012t0001g0027others(3): Show | 6 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+22140G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968775 | ||||||
| chr2:130968832
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3985+22197T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968832 | ||||||
| chr2:130968900
|
A | G | 5 | a0007c0013t0001g0059a0007c0013t0003g0060a0013c0016t0003g0001others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+22265A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968900 | ||||||
| chr2:130968901
|
G | A | 1 | a0001c0045t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3985+22266G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968901 | ||||||
| chr2:130968925
|
A | T | 9 | a0001c0044t0001g0011a0001c0045t0001g0085a0008c0012t0001g0026others(6): Show | 9 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.3985+22290A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968925 | ||||||
| chr2:130968951
|
T | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+22316T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968951 | ||||||
| chr2:130968974
|
C | T | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3985+22339C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968974 | ||||||
| chr2:130968998
|
G | C | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3985+22363G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130968998 | ||||||
| chr2:130969394
|
G | A | 3 | a0004c0004t0001g0125a0011c0022t0001g0084a0011c0022t0001g0096 | 3 | HG02258.hp2 HG02965.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3985+22759G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130969394 | ||||||
| chr2:130969469
|
G | A | 1 | a0001c0026t0001g0080 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3985+22834G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130969469 | ||||||
| chr2:130969548
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3985+22913G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130969548 | ||||||
| chr2:130969629
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+22994G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130969629 | ||||||
| chr2:130969631
|
T | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3985+22996T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130969631 | ||||||
| chr2:130969640
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+23005G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130969640 | ||||||
| chr2:130969784
|
A | C | 7 | a0007c0013t0002g0095a0010c0009t0001g0065a0010c0009t0001g0066others(4): Show | 7 | HG01175.hp2 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3985+23149A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130969784 | ||||||
| chr2:130969930
|
G | T | 6 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+23295G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130969930 | ||||||
| chr2:130969992
|
T | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(24): Show | 27 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.3985+23357T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130969992 | ||||||
| chr2:130970258
|
A | G | 7 | a0007c0013t0002g0095a0010c0009t0001g0065a0010c0009t0001g0066others(4): Show | 7 | HG01175.hp2 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3985+23623A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130970258 | ||||||
| chr2:130970439
|
A | G | 23 | a0003c0003t0001g0030a0003c0003t0001g0062a0003c0003t0001g0071others(20): Show | 23 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3985+23804A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130970439 | ||||||
| chr2:130970526
|
T | C | 7 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3985+23891T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130970526 | ||||||
| chr2:130970587
|
CA | C | 11 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.3985+23973delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130970587 | |||||
| chr2:130970587
|
CAA | C | 31 | a0001c0001t0001g0025a0001c0014t0001g0036a0001c0025t0005g0067others(28): Show | 31 | HG00642.hp2 HG01081.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.3985+23972_3985+23 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130970587 | |||||
| chr2:130970587
|
CAAA | C | 100 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(97): Show | 100 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.3985+23971_3985+23 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130970587 | |||||
| chr2:130970704
|
T | C | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+24069T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130970704 | ||||||
| chr2:130971020
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+24385G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971020 | ||||||
| chr2:130971135
|
T | C | 1 | a0022c0035t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3985+24500T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971135 | ||||||
| chr2:130971230
|
T | G | 7 | a0007c0013t0002g0095a0010c0009t0001g0065a0010c0009t0001g0066others(4): Show | 7 | HG01175.hp2 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3985+24595T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971230 | ||||||
| chr2:130971364
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3985+24729C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971364 | ||||||
| chr2:130971396
|
C | T | 1 | a0001c0018t0005g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3985+24761C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971396 | ||||||
| chr2:130971525
|
G | A | 1 | a0007c0017t0001g0109 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3985+24890G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971525 | ||||||
| chr2:130971655
|
C | CA | 89 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(86): Show | 89 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.3985+25041dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130971655 | |||||
| chr2:130971655
|
CA | C | 10 | a0001c0007t0004g0092a0001c0018t0002g0105a0001c0018t0005g0106others(7): Show | 10 | HG01243.hp1 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.3985+25041delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130971655 | |||||
| chr2:130971659
|
A | AG | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3985+25024_3985+25 others(7): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971659 | ||||||
| chr2:130971833
|
T | C | 142 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(139): Show | 142 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.3985+25198T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971833 | ||||||
| chr2:130971854
|
G | T | 7 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0005t0001g0104others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3985+25219G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971854 | ||||||
| chr2:130971876
|
T | C | 7 | a0007c0013t0002g0095a0010c0009t0001g0065a0010c0009t0001g0066others(4): Show | 7 | HG01175.hp2 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3985+25241T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971876 | ||||||
| chr2:130971926
|
C | A | 7 | a0007c0013t0002g0095a0010c0009t0001g0065a0010c0009t0001g0066others(4): Show | 7 | HG01175.hp2 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3985+25291C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971926 | ||||||
| chr2:130971943
|
A | G | 1 | a0011c0022t0001g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3985+25308A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971943 | ||||||
| chr2:130971982
|
G | A | 1 | a0003c0003t0002g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3985+25347G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130971982 | ||||||
| chr2:130972013
|
T | C | 9 | a0001c0014t0001g0036a0001c0025t0005g0067a0001c0034t0001g0111others(6): Show | 9 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.3985+25378T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130972013 | ||||||
| chr2:130972274
|
T | C | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3985+25639T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130972274 | ||||||
| chr2:130972309
|
C | A | 1 | a0005c0008t0001g0007 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3985+25674C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130972309 | ||||||
| chr2:130972393
|
A | G | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3985+25758A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130972393 | ||||||
| chr2:130972439
|
G | C | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3985+25804G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130972439 | ||||||
| chr2:130972517
|
G | A | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3985+25882G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130972517 | ||||||
| chr2:130972543
|
G | C | 23 | a0003c0003t0001g0030a0003c0003t0001g0062a0003c0003t0001g0071others(20): Show | 23 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3985+25908G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130972543 | ||||||
| chr2:130972717
|
GT | G | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3985+26084delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130972717 | |||||
| chr2:130972881
|
G | C | 131 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(128): Show | 131 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.3985+26246G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130972881 | ||||||
| chr2:130973019
|
T | C | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+26384T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130973019 | ||||||
| chr2:130973211
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+26576G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130973211 | ||||||
| chr2:130973306
|
C | T | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3985+26671C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130973306 | ||||||
| chr2:130973493
|
T | C | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+26858T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130973493 | ||||||
| chr2:130973749
|
C | G | 1 | a0001c0002t0001g0034 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3985+27114C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130973749 | ||||||
| chr2:130973831
|
A | T | 1 | a0001c0001t0001g0015 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3985+27196A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130973831 | ||||||
| chr2:130973891
|
T | C | 32 | a0001c0001t0001g0017a0001c0001t0001g0122a0001c0001t0001g0137others(29): Show | 32 | HG00621.hp1 HG01884.hp2 HG02155.hp1 others(29): Show |
intron_variant | MODIFIER | c.3985+27256T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130973891 | ||||||
| chr2:130974034
|
C | A | 1 | a0001c0001t0001g0017 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3985+27399C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974034 | ||||||
| chr2:130974048
|
T | G | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0026t0001g0080others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3985+27413T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974048 | ||||||
| chr2:130974139
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+27504G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974139 | ||||||
| chr2:130974201
|
G | T | 1 | a0008c0012t0001g0082 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3985+27566G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974201 | ||||||
| chr2:130974249
|
G | A | 3 | a0001c0025t0005g0067a0011c0022t0001g0084a0011c0022t0001g0096 | 3 | HG01243.hp1 HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3985+27614G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974249 | ||||||
| chr2:130974380
|
TTTA | T | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3985+27748_3985+27 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130974380 | |||||
| chr2:130974438
|
C | CTTTTTGT others(7): Show |
1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+27808_3985+27 others(20): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130974438 | |||||
| chr2:130974616
|
A | AT | 6 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+27998dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130974616 | |||||
| chr2:130974616
|
AT | A | 66 | a0001c0001t0001g0017a0001c0001t0001g0122a0001c0001t0001g0137others(63): Show | 66 | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.3985+27998delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130974616 | |||||
| chr2:130974616
|
ATT | A | 25 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(22): Show | 25 | HG00621.hp2 HG00735.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.3985+27997_3985+27 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130974616 | |||||
| chr2:130974616
|
ATTT | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(11): Show | 14 | HG02080.hp1 HG02698.hp2 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.3985+27996_3985+27 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130974616 | |||||
| chr2:130974632
|
T | G | 24 | a0002c0048t0001g0070a0003c0003t0001g0030a0003c0003t0001g0062others(21): Show | 24 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.3985+27997T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974632 | ||||||
| chr2:130974634
|
G | A | 24 | a0002c0048t0001g0070a0003c0003t0001g0030a0003c0003t0001g0062others(21): Show | 24 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.3985+27999G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974634 | ||||||
| chr2:130974635
|
TA | T | 24 | a0002c0048t0001g0070a0003c0003t0001g0030a0003c0003t0001g0062others(21): Show | 24 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.3985+28001delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974635 | ||||||
| chr2:130974652
|
G | A | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3985+28017G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974652 | ||||||
| chr2:130974701
|
A | G | 40 | a0001c0001t0001g0122a0001c0001t0001g0137a0001c0002t0001g0013others(37): Show | 40 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(37): Show |
intron_variant | MODIFIER | c.3985+28066A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974701 | ||||||
| chr2:130974886
|
A | G | 15 | a0001c0001t0001g0122a0001c0001t0001g0137a0001c0002t0001g0013others(12): Show | 15 | HG02155.hp1 HG02280.hp2 HG03704.hp1 others(12): Show |
intron_variant | MODIFIER | c.3985+28251A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974886 | ||||||
| chr2:130974948
|
A | G | 6 | a0001c0027t0001g0107a0007c0013t0001g0059a0007c0013t0003g0060others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+28313A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974948 | ||||||
| chr2:130974967
|
T | A | 127 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 127 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(124): Show |
intron_variant | MODIFIER | c.3985+28332T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130974967 | ||||||
| chr2:130975058
|
A | AC | 10 | a0001c0014t0001g0036a0001c0025t0005g0067a0002c0048t0001g0070others(7): Show | 10 | HG01243.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3985+28428dupC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130975058 | |||||
| chr2:130975131
|
T | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+28496T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130975131 | ||||||
| chr2:130975223
|
G | A | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3985+28588G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130975223 | ||||||
| chr2:130975286
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3985+28651C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130975286 | ||||||
| chr2:130975421
|
T | C | 10 | a0001c0027t0001g0107a0002c0011t0005g0054a0007c0013t0001g0059others(7): Show | 10 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.3985+28786T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130975421 | ||||||
| chr2:130975461
|
C | T | 1 | a0004c0004t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3985+28826C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130975461 | ||||||
| chr2:130975614
|
G | A | 5 | a0001c0014t0002g0075a0001c0015t0001g0078a0001c0015t0001g0079others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+28979G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130975614 | ||||||
| chr2:130975653
|
C | T | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+29018C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130975653 | ||||||
| chr2:130975741
|
C | T | 47 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(44): Show | 47 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.3985+29106C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130975741 | ||||||
| chr2:130975747
|
A | G | 12 | a0001c0001t0001g0017a0002c0010t0001g0003a0002c0010t0001g0051others(9): Show | 12 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.3985+29112A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130975747 | ||||||
| chr2:130975831
|
G | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(43): Show | 46 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3985+29196G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130975831 | ||||||
| chr2:130975858
|
C | T | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3985+29223C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130975858 | ||||||
| chr2:130975910
|
G | A | 10 | a0001c0044t0001g0011a0001c0045t0001g0085a0002c0028t0001g0073others(7): Show | 10 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.3985+29275G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130975910 | ||||||
| chr2:130976000
|
G | T | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3985+29365G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130976000 | ||||||
| chr2:130976011
|
G | T | 13 | a0001c0001t0001g0017a0001c0034t0001g0111a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3985+29376G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130976011 | ||||||
| chr2:130976038
|
G | A | 6 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(3): Show | 6 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+29403G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130976038 | ||||||
| chr2:130976082
|
C | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3985+29447C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130976082 | ||||||
| chr2:130976103
|
G | A | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3985+29468G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130976103 | ||||||
| chr2:130976195
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3985+29560C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130976195 | ||||||
| chr2:130976275
|
A | G | 42 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0025others(39): Show | 42 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.3985+29640A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130976275 | ||||||
| chr2:130976332
|
C | T | 5 | a0001c0027t0001g0107a0001c0045t0001g0085a0007c0013t0003g0060others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3985+29697C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130976332 | ||||||
| chr2:130976345
|
GTGTC | G | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3985+29714_3985+29 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130976345 | |||||
| chr2:130976349
|
C | CTG | 20 | a0001c0001t0001g0017a0001c0007t0004g0089a0001c0007t0004g0090others(17): Show | 20 | HG00621.hp1 HG01257.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.3985+29734_3985+29 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130976349 | |||||
| chr2:130976349
|
C | CTGTG | 54 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0025others(51): Show | 54 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.3985+29732_3985+29 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130976349 | |||||
| chr2:130976349
|
C | CTGTGTG | 24 | a0001c0001t0001g0137a0001c0002t0001g0083a0001c0002t0001g0113others(21): Show | 24 | HG01258.hp2 HG02155.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.3985+29730_3985+29 others(12): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130976349 | |||||
| chr2:130976349
|
C | CTGTGTGT others(1): Show |
3 | a0001c0034t0001g0111a0002c0011t0005g0054a0006c0005t0001g0104 | 3 | HG03041.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3985+29728_3985+29 others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130976349 | |||||
| chr2:130976349
|
CTG | C | 3 | a0004c0004t0001g0018a0004c0020t0001g0028a0007c0032t0001g0004 | 3 | HG03942.hp1 HG04184.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3985+29734_3985+29 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130976349 | |||||
| chr2:130976623
|
C | T | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3985+29988C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130976623 | ||||||
| chr2:130976730
|
G | A | 4 | a0001c0045t0001g0085a0007c0013t0003g0060a0013c0016t0003g0001others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3985+30095G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130976730 | ||||||
| chr2:130976795
|
C | A | 6 | a0001c0018t0002g0105a0001c0018t0005g0106a0002c0011t0005g0054others(3): Show | 6 | HG02723.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+30160C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130976795 | ||||||
| chr2:130976860
|
GTGTC | G | 8 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(5): Show | 8 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985+30228_3985+30 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130976860 | |||||
| chr2:130977223
|
G | A | 6 | a0001c0045t0001g0085a0007c0013t0003g0060a0011c0022t0001g0084others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+30588G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130977223 | ||||||
| chr2:130977341
|
G | T | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3985+30706G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130977341 | ||||||
| chr2:130977370
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+30735G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130977370 | ||||||
| chr2:130977374
|
C | T | 1 | a0002c0010t0001g0003 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3985+30739C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130977374 | ||||||
| chr2:130977449
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3985+30814G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130977449 | ||||||
| chr2:130977543
|
ATGTT | A | 4 | a0001c0045t0001g0085a0007c0013t0003g0060a0013c0016t0003g0001others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3985+30909_3985+30 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130977543 | ||||||
| chr2:130977654
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0035others(11): Show | 14 | HG02698.hp2 HG03491.hp1 HG03704.hp2 others(11): Show |
intron_variant | MODIFIER | c.3985+31019C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130977654 | ||||||
| chr2:130977655
|
G | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3985+31020G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130977655 | ||||||
| chr2:130977703
|
T | G | 2 | a0003c0003t0001g0081a0007c0017t0001g0109 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3985+31068T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130977703 | ||||||
| chr2:130977956
|
T | C | 1 | a0001c0001t0001g0017 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3985+31321T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130977956 | ||||||
| chr2:130978047
|
C | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3985+31412C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130978047 | ||||||
| chr2:130978066
|
C | T | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3985+31431C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130978066 | ||||||
| chr2:130978502
|
GC | G | 7 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.3985+31868delC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130978502 | ||||||
| chr2:130978575
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+31940G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130978575 | ||||||
| chr2:130978642
|
G | A | 1 | a0014c0023t0001g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3985+32007G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130978642 | ||||||
| chr2:130978688
|
A | C | 3 | a0007c0013t0002g0095a0011c0022t0001g0084a0011c0022t0001g0096 | 3 | HG01175.hp2 HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3985+32053A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130978688 | ||||||
| chr2:130978764
|
A | C | 6 | a0001c0018t0002g0105a0001c0018t0005g0106a0002c0011t0005g0054others(3): Show | 6 | HG02723.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3985+32129A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130978764 | ||||||
| chr2:130978999
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+32364G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130978999 | ||||||
| chr2:130979138
|
G | A | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3985+32503G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130979138 | ||||||
| chr2:130979502
|
G | A | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3985+32867G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130979502 | ||||||
| chr2:130979530
|
A | G | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3985+32895A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130979530 | ||||||
| chr2:130979597
|
T | A | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3985+32962T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130979597 | ||||||
| chr2:130979695
|
C | T | 1 | a0008c0053t0001g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3985+33060C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130979695 | ||||||
| chr2:130979734
|
T | TA | 17 | a0001c0001t0001g0025a0001c0001t0001g0122a0001c0002t0001g0013others(14): Show | 17 | HG01175.hp2 HG01243.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3985+33121dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130979734 | |||||
| chr2:130979734
|
T | TAA | 38 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0040others(35): Show | 38 | HG00735.hp1 HG00735.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.3985+33120_3985+33 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130979734 | |||||
| chr2:130979734
|
T | TAAA | 7 | a0001c0001t0001g0033a0001c0001t0001g0063a0001c0001t0001g0088others(4): Show | 7 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.3985+33119_3985+33 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130979734 | |||||
| chr2:130979734
|
TA | T | 24 | a0001c0001t0001g0017a0001c0027t0001g0107a0001c0034t0001g0111others(21): Show | 24 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.3985+33121delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130979734 | |||||
| chr2:130979763
|
AT | A | 20 | a0001c0018t0002g0105a0001c0018t0005g0106a0001c0034t0001g0111others(17): Show | 20 | HG01109.hp2 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.3985+33132delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130979763 | |||||
| chr2:130979819
|
C | G | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+33184C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130979819 | ||||||
| chr2:130979890
|
G | A | 13 | a0001c0001t0001g0017a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3985+33255G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130979890 | ||||||
| chr2:130979915
|
A | G | 7 | a0001c0018t0002g0105a0001c0018t0005g0106a0002c0011t0005g0054others(4): Show | 7 | HG02723.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.3985+33280A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130979915 | ||||||
| chr2:130979991
|
A | G | 1 | a0002c0011t0005g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3985+33356A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130979991 | ||||||
| chr2:130980166
|
G | A | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3985+33531G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130980166 | ||||||
| chr2:130980389
|
C | CA | 105 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(102): Show | 105 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.3985+33769dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130980389 | |||||
| chr2:130980389
|
C | CAA | 7 | a0001c0014t0002g0075a0001c0015t0001g0078a0001c0015t0001g0079others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3985+33768_3985+33 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130980389 | |||||
| chr2:130980535
|
A | C | 3 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068 | 3 | HG02717.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3985+33900A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130980535 | ||||||
| chr2:130980546
|
G | A | 106 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(103): Show | 106 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.3985+33911G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130980546 | ||||||
| chr2:130980624
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+33989G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130980624 | ||||||
| chr2:130981023
|
G | T | 4 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068others(1): Show | 4 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3985+34388G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130981023 | ||||||
| chr2:130981123
|
T | C | 20 | a0001c0018t0002g0105a0001c0018t0005g0106a0001c0034t0001g0111others(17): Show | 20 | HG01109.hp2 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.3985+34488T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130981123 | ||||||
| chr2:130981211
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3985+34576G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130981211 | ||||||
| chr2:130981237
|
A | G | 3 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068 | 3 | HG02717.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3985+34602A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130981237 | ||||||
| chr2:130981334
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0035others(10): Show | 13 | HG02698.hp2 HG03491.hp1 HG03704.hp2 others(10): Show |
intron_variant | MODIFIER | c.3985+34699C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130981334 | ||||||
| chr2:130981657
|
C | CA | 8 | a0001c0001t0001g0014a0001c0014t0002g0075a0001c0015t0001g0078others(5): Show | 8 | HG01243.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3985+35037dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130981657 | |||||
| chr2:130981707
|
C | T | 3 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068 | 3 | HG02717.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3985+35072C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130981707 | ||||||
| chr2:130981896
|
C | T | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3985+35261C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130981896 | ||||||
| chr2:130982041
|
G | A | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3985+35406G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130982041 | ||||||
| chr2:130982404
|
T | TA | 15 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(12): Show | 15 | HG02698.hp2 HG02717.hp1 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.3985+35770dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130982404 | |||||
| chr2:130982586
|
C | T | 4 | a0001c0045t0001g0085a0007c0013t0003g0060a0013c0016t0003g0001others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3985+35951C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130982586 | ||||||
| chr2:130982591
|
C | T | 1 | a0008c0053t0001g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3985+35956C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130982591 | ||||||
| chr2:130982612
|
CCTTTCTT others(5): Show |
C | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(46): Show | 49 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.3985+35985_3985+35 others(18): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130982612 | |||||
| chr2:130982809
|
G | C | 123 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(120): Show | 123 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.3985+36174G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130982809 | ||||||
| chr2:130983289
|
C | T | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3985+36654C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130983289 | ||||||
| chr2:130983378
|
A | G | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3985+36743A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130983378 | ||||||
| chr2:130983710
|
C | T | 1 | a0007c0017t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3985+37075C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130983710 | ||||||
| chr2:130983711
|
G | A | 18 | a0001c0034t0001g0111a0002c0011t0005g0054a0002c0048t0001g0070others(15): Show | 18 | HG01109.hp2 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.3985+37076G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130983711 | ||||||
| chr2:130983851
|
A | G | 123 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(120): Show | 123 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.3985+37216A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130983851 | ||||||
| chr2:130983870
|
T | C | 1 | a0006c0005t0001g0094 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3985+37235T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130983870 | ||||||
| chr2:130984118
|
C | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(46): Show | 49 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.3985+37483C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130984118 | ||||||
| chr2:130984175
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3985+37540G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130984175 | ||||||
| chr2:130984546
|
C | T | 5 | a0001c0014t0002g0075a0001c0015t0001g0078a0001c0015t0001g0079others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3985+37911C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130984546 | ||||||
| chr2:130984557
|
G | GC | 123 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(120): Show | 123 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.3985+37923dupC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130984557 | |||||
| chr2:130984603
|
C | T | 13 | a0001c0001t0001g0017a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3985+37968C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130984603 | ||||||
| chr2:130984615
|
G | GCA | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3985+37980_3985+37 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130984615 | ||||||
| chr2:130984688
|
T | TA | 58 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(55): Show | 58 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.3985+38070dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130984688 | |||||
| chr2:130984688
|
T | TAA | 27 | a0001c0007t0004g0090a0001c0007t0004g0091a0001c0007t0004g0092others(24): Show | 27 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.3985+38069_3985+38 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130984688 | |||||
| chr2:130984688
|
T | TAAA | 25 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(22): Show | 25 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(22): Show |
intron_variant | MODIFIER | c.3985+38068_3985+38 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130984688 | |||||
| chr2:130984754
|
C | A | 104 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(101): Show | 104 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.3985+38119C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130984754 | ||||||
| chr2:130984947
|
C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3985+38312C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130984947 | ||||||
| chr2:130985016
|
C | G | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(46): Show | 49 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.3985+38381C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985016 | ||||||
| chr2:130985017
|
A | C | 91 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(88): Show | 91 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.3985+38382A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985017 | ||||||
| chr2:130985155
|
G | A | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(46): Show | 49 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.3985+38520G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985155 | ||||||
| chr2:130985187
|
G | A | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3985+38552G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985187 | ||||||
| chr2:130985337
|
A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3985+38702A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985337 | ||||||
| chr2:130985439
|
C | A | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(46): Show | 49 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.3985+38804C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985439 | ||||||
| chr2:130985480
|
T | C | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3985+38845T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985480 | ||||||
| chr2:130985483
|
C | G | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3985+38848C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985483 | ||||||
| chr2:130985615
|
T | C | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3985+38980T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985615 | ||||||
| chr2:130985736
|
T | G | 1 | a0024c0033t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3985+39101T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985736 | ||||||
| chr2:130985759
|
T | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3985+39124T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985759 | ||||||
| chr2:130985804
|
GT | G | 13 | a0001c0001t0001g0017a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3985+39175delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130985804 | |||||
| chr2:130985837
|
C | T | 5 | a0001c0001t0001g0017a0002c0010t0001g0003a0002c0010t0001g0051others(2): Show | 5 | HG00621.hp1 HG02698.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.3985+39202C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985837 | ||||||
| chr2:130985918
|
G | A | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3985+39283G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985918 | ||||||
| chr2:130985948
|
TTG | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3985+39324_3985+39 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130985948 | |||||
| chr2:130985951
|
T | C | 113 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(110): Show | 113 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.3985+39316T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985951 | ||||||
| chr2:130985953
|
T | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3985+39318T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130985953 | ||||||
| chr2:130986032
|
TTG | T | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3985+39403_3985+39 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130986032 | |||||
| chr2:130986082
|
T | TTG | 3 | a0007c0013t0003g0060a0013c0016t0003g0001a0013c0016t0003g0002 | 3 | HG02559.hp2 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3985+39455_3985+39 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130986082 | |||||
| chr2:130986122
|
G | T | 92 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(89): Show | 92 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.3985+39487G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130986122 | ||||||
| chr2:130986148
|
T | C | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3985+39513T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130986148 | ||||||
| chr2:130986163
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3985+39528G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130986163 | ||||||
| chr2:130986203
|
T | C | 1 | a0007c0013t0003g0060 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3985+39568T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130986203 | ||||||
| chr2:130986318
|
T | C | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3985+39683T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130986318 | ||||||
| chr2:130986382
|
A | C | 4 | a0001c0045t0001g0085a0007c0013t0003g0060a0013c0016t0003g0001others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3985+39747A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130986382 | ||||||
| chr2:130986410
|
C | T | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3985+39775C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130986410 | ||||||
| chr2:130986561
|
G | A | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3985+39926G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130986561 | ||||||
| chr2:130986602
|
A | C | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3985+39967A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130986602 | ||||||
| chr2:130986935
|
G | A | 1 | a0007c0032t0001g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3985+40300G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130986935 | ||||||
| chr2:130987281
|
G | A | 93 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(90): Show | 93 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.3985+40646G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130987281 | ||||||
| chr2:130987319
|
C | G | 1 | a0001c0045t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3986-40626C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130987319 | ||||||
| chr2:130987322
|
G | A | 2 | a0011c0022t0001g0084a0011c0022t0001g0096 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3986-40623G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130987322 | ||||||
| chr2:130987428
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3986-40517G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130987428 | ||||||
| chr2:130987607
|
G | A | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3986-40338G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130987607 | ||||||
| chr2:130987704
|
C | T | 13 | a0001c0001t0001g0017a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3986-40241C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130987704 | ||||||
| chr2:130987712
|
T | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-40233T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130987712 | ||||||
| chr2:130987757
|
G | A | 68 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(65): Show | 68 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.3986-40188G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130987757 | ||||||
| chr2:130987770
|
T | C | 93 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(90): Show | 93 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.3986-40175T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130987770 | ||||||
| chr2:130988039
|
G | A | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3986-39906G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988039 | ||||||
| chr2:130988117
|
G | A | 2 | a0001c0001t0001g0009a0020c0038t0001g0032 | 2 | HG03491.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3986-39828G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988117 | ||||||
| chr2:130988182
|
C | T | 13 | a0001c0001t0001g0017a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3986-39763C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988182 | ||||||
| chr2:130988221
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3986-39724C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988221 | ||||||
| chr2:130988226
|
G | A | 1 | a0011c0022t0001g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3986-39719G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988226 | ||||||
| chr2:130988232
|
G | A | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3986-39713G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988232 | ||||||
| chr2:130988555
|
T | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-39390T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988555 | ||||||
| chr2:130988677
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3986-39268G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988677 | ||||||
| chr2:130988689
|
A | G | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3986-39256A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988689 | ||||||
| chr2:130988848
|
T | TTG | 2 | a0005c0006t0001g0052a0005c0008t0001g0101 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3986-39073_3986-39 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988848 | |||||
| chr2:130988868
|
GTGTGTAT others(5): Show |
G | 1 | a0001c0001t0001g0017 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3986-39075_3986-39 others(18): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988868 | |||||
| chr2:130988870
|
GTGTATAT others(1): Show |
G | 15 | a0001c0007t0004g0089a0001c0007t0004g0091a0001c0007t0004g0093others(12): Show | 15 | HG00621.hp1 HG01884.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.3986-39073_3986-39 others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988870 | |||||
| chr2:130988870
|
GTGTATAT others(3): Show |
G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3986-39073_3986-39 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988870 | |||||
| chr2:130988870
|
GTGTATAT others(5): Show |
G | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3986-39073_3986-39 others(18): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988870 | |||||
| chr2:130988872
|
G | A | 7 | a0001c0007t0004g0090a0001c0007t0004g0092a0001c0025t0005g0067others(4): Show | 7 | HG01175.hp2 HG01243.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.3986-39073G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988872 | ||||||
| chr2:130988872
|
GTA | G | 5 | a0001c0018t0002g0105a0001c0018t0005g0106a0010c0009t0001g0065others(2): Show | 5 | HG02717.hp1 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-39044_3986-39 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988872 | |||||
| chr2:130988872
|
GTATA | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0124a0001c0002t0001g0038others(3): Show | 6 | HG01515.hp1 HG01515.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.3986-39046_3986-39 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988872 | |||||
| chr2:130988872
|
GTATATA | G | 2 | a0001c0001t0001g0040a0001c0002t0001g0034 | 2 | HG02080.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.3986-39048_3986-39 others(12): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988872 | |||||
| chr2:130988872
|
GTATATAT others(1): Show |
G | 22 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0033others(19): Show | 22 | HG00621.hp2 HG00735.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3986-39050_3986-39 others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988872 | |||||
| chr2:130988872
|
GTATATAT others(3): Show |
G | 3 | a0001c0014t0002g0075a0001c0026t0001g0080a0024c0033t0001g0021 | 3 | HG02055.hp1 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.3986-39052_3986-39 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988872 | |||||
| chr2:130988872
|
GTATATAT others(5): Show |
G | 1 | a0003c0031t0006g0037 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3986-39054_3986-39 others(18): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988872 | |||||
| chr2:130988874
|
A | G | 42 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0114others(39): Show | 42 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.3986-39071A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988874 | ||||||
| chr2:130988876
|
A | G | 10 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0005t0001g0104others(7): Show | 10 | HG00735.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.3986-39069A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988876 | ||||||
| chr2:130988878
|
A | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0124a0001c0002t0001g0038others(3): Show | 6 | HG01515.hp1 HG01515.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.3986-39067A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988878 | ||||||
| chr2:130988880
|
A | G | 3 | a0001c0001t0001g0040a0001c0002t0001g0034a0022c0035t0001g0121 | 3 | HG02080.hp2 HG02155.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.3986-39065A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988880 | ||||||
| chr2:130988881
|
TATATATA others(19): Show |
T | 1 | a0019c0036t0001g0049 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3986-39062_3986-39 others(32): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988881 | |||||
| chr2:130988882
|
A | G | 21 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0033others(18): Show | 21 | HG00621.hp2 HG00735.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.3986-39063A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988882 | ||||||
| chr2:130988883
|
TATATATA others(19): Show |
T | 3 | a0001c0001t0001g0077a0001c0002t0001g0020a0004c0004t0001g0125 | 3 | NA18957.hp2 NA18990.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.3986-39060_3986-39 others(32): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988883 | |||||
| chr2:130988883
|
TATATATA others(25): Show |
T | 1 | a0001c0001t0001g0035 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3986-39060_3986-39 others(38): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988883 | |||||
| chr2:130988885
|
TATATATA others(17): Show |
T | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3986-39058_3986-39 others(30): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988885 | |||||
| chr2:130988885
|
TATATATA others(19): Show |
T | 5 | a0001c0001t0001g0015a0001c0001t0001g0087a0001c0001t0001g0123others(2): Show | 5 | HG02698.hp2 HG03831.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.3986-39058_3986-39 others(32): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988885 | |||||
| chr2:130988887
|
TATATATA others(11): Show |
T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3986-39056_3986-39 others(24): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988887 | |||||
| chr2:130988887
|
TATATATA others(19): Show |
T | 1 | a0001c0001t0001g0043 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3986-39056_3986-39 others(32): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988887 | |||||
| chr2:130988889
|
T | G | 1 | a0005c0006t0001g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3986-39056T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988889 | ||||||
| chr2:130988889
|
TATATATA others(7): Show |
T | 3 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118 | 3 | HG02622.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3986-39054_3986-39 others(20): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988889 | |||||
| chr2:130988889
|
TATATATA others(13): Show |
T | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3986-39054_3986-39 others(26): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988889 | |||||
| chr2:130988891
|
T | G | 1 | a0005c0006t0001g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3986-39054T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988891 | ||||||
| chr2:130988893
|
T | G | 2 | a0005c0006t0001g0052a0005c0008t0001g0101 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3986-39052T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988893 | ||||||
| chr2:130988893
|
TATATATA others(3): Show |
T | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0039t0001g0039others(1): Show | 4 | HG02486.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3986-39050_3986-39 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988893 | |||||
| chr2:130988893
|
TATATATA others(5): Show |
T | 5 | a0006c0005t0001g0104a0006c0005t0001g0143a0006c0005t0005g0119others(2): Show | 5 | HG00642.hp2 HG00735.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.3986-39050_3986-39 others(18): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988893 | |||||
| chr2:130988893
|
TATATATA others(7): Show |
T | 1 | a0008c0012t0001g0026 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3986-39050_3986-39 others(20): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988893 | |||||
| chr2:130988895
|
T | G | 5 | a0001c0018t0002g0105a0004c0004t0001g0018a0005c0006t0001g0052others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-39050T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988895 | ||||||
| chr2:130988895
|
T | TAGAG | 3 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0008t0001g0098 | 3 | HG02630.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3986-39049_3986-39 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988895 | |||||
| chr2:130988895
|
TATATATA others(1): Show |
T | 6 | a0001c0001t0001g0012a0001c0001t0002g0058a0001c0002t0001g0010others(3): Show | 6 | HG00642.hp1 HG01258.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.3986-39048_3986-39 others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988895 | |||||
| chr2:130988895
|
TATATATA others(5): Show |
T | 5 | a0001c0034t0001g0111a0006c0005t0001g0094a0006c0050t0001g0142others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-39048_3986-39 others(18): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988895 | |||||
| chr2:130988895
|
TATATATA others(7): Show |
T | 4 | a0001c0044t0001g0011a0003c0003t0001g0030a0005c0006t0003g0103others(1): Show | 4 | HG01081.hp1 HG01109.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.3986-39048_3986-39 others(20): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988895 | |||||
| chr2:130988897
|
T | G | 17 | a0001c0001t0001g0025a0001c0002t0001g0038a0001c0018t0002g0105others(14): Show | 17 | HG01515.hp1 HG01515.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.3986-39048T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988897 | ||||||
| chr2:130988897
|
T | TAGAGAG | 2 | a0003c0003t0001g0071a0004c0020t0001g0028 | 2 | HG03195.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3986-39047_3986-39 others(12): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988897 | |||||
| chr2:130988897
|
TATATAGA others(1): Show |
T | 2 | a0001c0001t0001g0046a0002c0010t0001g0047 | 2 | NA18962.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.3986-39046_3986-39 others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988897 | |||||
| chr2:130988897
|
TATATAGA others(3): Show |
T | 1 | a0008c0053t0001g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3986-39046_3986-39 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988897 | |||||
| chr2:130988897
|
TATATAGA others(5): Show |
T | 1 | a0011c0022t0001g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3986-39046_3986-39 others(18): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988897 | |||||
| chr2:130988899
|
T | G | 33 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0086others(30): Show | 33 | HG00735.hp1 HG01515.hp1 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.3986-39046T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988899 | ||||||
| chr2:130988899
|
T | TAGAGAGA others(5): Show |
1 | a0007c0017t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3986-39045_3986-39 others(18): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988899 | |||||
| chr2:130988899
|
T | TAGAGAGA others(9): Show |
1 | a0001c0002t0001g0083 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3986-39045_3986-39 others(22): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988899 | |||||
| chr2:130988899
|
TATAGAGA others(1): Show |
T | 2 | a0001c0007t0004g0090a0001c0007t0004g0092 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3986-39044_3986-39 others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988899 | |||||
| chr2:130988899
|
TATAGAGA others(5): Show |
T | 1 | a0006c0005t0003g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3986-39044_3986-39 others(18): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988899 | |||||
| chr2:130988901
|
T | G | 56 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0025others(53): Show | 56 | HG00621.hp2 HG00735.hp1 HG01515.hp1 others(53): Show |
intron_variant | MODIFIER | c.3986-39044T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988901 | ||||||
| chr2:130988901
|
T | TAGAG | 2 | a0005c0006t0002g0099a0005c0008t0001g0007 | 2 | HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.3986-39012_3986-39 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988901 | |||||
| chr2:130988901
|
T | TAGAGAGA others(5): Show |
1 | a0001c0002t0001g0113 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3986-39020_3986-39 others(18): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988901 | |||||
| chr2:130988903
|
G | T | 3 | a0001c0007t0004g0089a0001c0007t0004g0093a0009c0046t0009g0076 | 3 | HG02622.hp1 HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3986-39042G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988903 | ||||||
| chr2:130988907
|
G | T | 1 | a0001c0002t0001g0031 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3986-39038G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988907 | ||||||
| chr2:130988935
|
GA | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0124others(1): Show | 4 | HG01515.hp1 HG02080.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.3986-39007delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130988935 | |||||
| chr2:130988936
|
A | AGAGAGAG others(4): Show |
1 | a0001c0001t0001g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3986-39009_3986-39 others(17): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988936 | ||||||
| chr2:130988937
|
A | G | 12 | a0001c0001t0001g0017a0001c0027t0001g0107a0002c0010t0001g0003others(9): Show | 12 | HG00621.hp1 HG00642.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.3986-39008A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130988937 | ||||||
| chr2:130989048
|
A | G | 12 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(9): Show | 12 | HG02615.hp1 HG02698.hp2 HG03704.hp2 others(9): Show |
intron_variant | MODIFIER | c.3986-38897A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130989048 | ||||||
| chr2:130989240
|
C | T | 15 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(12): Show | 15 | HG01175.hp2 HG01257.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.3986-38705C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130989240 | ||||||
| chr2:130989356
|
A | C | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3986-38589A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130989356 | ||||||
| chr2:130989363
|
C | T | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3986-38582C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130989363 | ||||||
| chr2:130989769
|
C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-38176C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130989769 | ||||||
| chr2:130989858
|
C | A | 10 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(7): Show | 10 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.3986-38087C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130989858 | ||||||
| chr2:130990100
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3986-37845T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130990100 | ||||||
| chr2:130990380
|
T | G | 110 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(107): Show | 110 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.3986-37565T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130990380 | ||||||
| chr2:130990437
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0126 | 2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.3986-37508G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130990437 | ||||||
| chr2:130990483
|
G | T | 1 | a0003c0003t0001g0081 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3986-37462G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130990483 | ||||||
| chr2:130990644
|
G | GTC | 12 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(9): Show | 12 | HG02615.hp1 HG02698.hp2 HG03704.hp2 others(9): Show |
intron_variant | MODIFIER | c.3986-37300_3986-37 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130990644 | |||||
| chr2:130990707
|
A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-37238A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130990707 | ||||||
| chr2:130990876
|
T | A | 1 | a0001c0001t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3986-37069T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130990876 | ||||||
| chr2:130991068
|
T | C | 5 | a0002c0011t0005g0054a0002c0048t0001g0070a0009c0021t0001g0130others(2): Show | 5 | HG02723.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-36877T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991068 | ||||||
| chr2:130991089
|
G | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-36856G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991089 | ||||||
| chr2:130991099
|
A | C | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3986-36846A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991099 | ||||||
| chr2:130991101
|
T | C | 13 | a0001c0034t0001g0111a0003c0003t0001g0030a0003c0003t0002g0116others(10): Show | 13 | HG01109.hp2 HG02257.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.3986-36844T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991101 | ||||||
| chr2:130991277
|
G | T | 2 | a0003c0003t0001g0081a0007c0017t0001g0109 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3986-36668G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991277 | ||||||
| chr2:130991303
|
G | A | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3986-36642G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991303 | ||||||
| chr2:130991397
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3986-36548G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991397 | ||||||
| chr2:130991421
|
C | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(9): Show | 12 | HG02615.hp1 HG02698.hp2 HG03704.hp2 others(9): Show |
intron_variant | MODIFIER | c.3986-36524C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991421 | ||||||
| chr2:130991474
|
G | A | 13 | a0001c0001t0001g0017a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3986-36471G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991474 | ||||||
| chr2:130991512
|
G | A | 13 | a0001c0034t0001g0111a0003c0003t0001g0030a0003c0003t0002g0116others(10): Show | 13 | HG01109.hp2 HG02257.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.3986-36433G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991512 | ||||||
| chr2:130991522
|
C | A | 1 | a0001c0002t0001g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3986-36423C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991522 | ||||||
| chr2:130991523
|
G | A | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3986-36422G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991523 | ||||||
| chr2:130991529
|
G | C | 104 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(101): Show | 104 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.3986-36416G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991529 | ||||||
| chr2:130991557
|
C | T | 13 | a0001c0001t0001g0017a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3986-36388C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991557 | ||||||
| chr2:130991562
|
C | T | 9 | a0001c0001t0001g0137a0001c0002t0001g0013a0001c0002t0001g0083others(6): Show | 9 | HG02155.hp1 HG02280.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.3986-36383C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991562 | ||||||
| chr2:130991585
|
C | A | 18 | a0001c0034t0001g0111a0002c0011t0005g0054a0002c0048t0001g0070others(15): Show | 18 | HG01109.hp2 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.3986-36360C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991585 | ||||||
| chr2:130991877
|
G | A | 7 | a0001c0001t0002g0058a0001c0007t0004g0089a0001c0007t0004g0090others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3986-36068G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991877 | ||||||
| chr2:130991970
|
A | G | 12 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(9): Show | 12 | HG02615.hp1 HG02698.hp2 HG03704.hp2 others(9): Show |
intron_variant | MODIFIER | c.3986-35975A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130991970 | ||||||
| chr2:130992138
|
C | A | 1 | a0005c0006t0002g0099 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3986-35807C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130992138 | ||||||
| chr2:130992155
|
C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-35790C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130992155 | ||||||
| chr2:130992158
|
A | C | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3986-35787A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130992158 | ||||||
| chr2:130992176
|
A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-35769A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130992176 | ||||||
| chr2:130992273
|
A | G | 14 | a0001c0034t0001g0111a0003c0003t0001g0030a0003c0003t0002g0116others(11): Show | 14 | HG01109.hp2 HG01175.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3986-35672A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130992273 | ||||||
| chr2:130992387
|
A | ACGCT | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-35556_3986-35 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130992387 | |||||
| chr2:130992388
|
C | T | 4 | a0002c0011t0005g0054a0009c0021t0001g0130a0009c0021t0001g0139others(1): Show | 4 | HG02723.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3986-35557C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130992388 | ||||||
| chr2:130992614
|
A | G | 1 | a0007c0013t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3986-35331A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130992614 | ||||||
| chr2:130992692
|
C | T | 1 | a0001c0007t0004g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3986-35253C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130992692 | ||||||
| chr2:130992706
|
A | G | 5 | a0001c0018t0002g0105a0001c0018t0005g0106a0007c0013t0002g0095others(2): Show | 5 | HG01175.hp2 HG02258.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-35239A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130992706 | ||||||
| chr2:130992818
|
T | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3986-35127T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130992818 | ||||||
| chr2:130992848
|
C | T | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3986-35097C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130992848 | ||||||
| chr2:130992861
|
A | G | 1 | a0024c0033t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3986-35084A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130992861 | ||||||
| chr2:130993015
|
C | T | 1 | a0001c0002t0001g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3986-34930C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130993015 | ||||||
| chr2:130993057
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3986-34888C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130993057 | ||||||
| chr2:130993100
|
A | G | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3986-34845A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130993100 | ||||||
| chr2:130993160
|
A | G | 1 | a0001c0002t0001g0024 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3986-34785A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130993160 | ||||||
| chr2:130993291
|
C | T | 115 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(112): Show | 115 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.3986-34654C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130993291 | ||||||
| chr2:130993329
|
A | G | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3986-34616A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130993329 | ||||||
| chr2:130993336
|
T | C | 10 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(7): Show | 10 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.3986-34609T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130993336 | ||||||
| chr2:130993405
|
CAAT | C | 3 | a0007c0013t0003g0060a0013c0016t0003g0001a0013c0016t0003g0002 | 3 | HG02559.hp2 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3986-34536_3986-34 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130993405 | |||||
| chr2:130993446
|
ATTTTC | A | 12 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(9): Show | 12 | HG02615.hp1 HG02698.hp2 HG03704.hp2 others(9): Show |
intron_variant | MODIFIER | c.3986-34496_3986-34 others(11): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130993446 | |||||
| chr2:130993675
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3986-34270G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130993675 | ||||||
| chr2:130993717
|
C | T | 13 | a0001c0001t0001g0017a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3986-34228C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130993717 | ||||||
| chr2:130993935
|
G | A | 4 | a0002c0011t0005g0054a0009c0021t0001g0130a0009c0021t0001g0139others(1): Show | 4 | HG02723.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3986-34010G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130993935 | ||||||
| chr2:130994298
|
A | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0126 | 2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.3986-33647A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130994298 | ||||||
| chr2:130994371
|
A | G | 50 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(47): Show | 50 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.3986-33574A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130994371 | ||||||
| chr2:130994652
|
C | G | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3986-33293C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130994652 | ||||||
| chr2:130994864
|
A | C | 1 | a0001c0001t0001g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3986-33081A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130994864 | ||||||
| chr2:130994946
|
G | A | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3986-32999G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130994946 | ||||||
| chr2:130995090
|
A | G | 1 | a0007c0017t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3986-32855A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130995090 | ||||||
| chr2:130995393
|
A | G | 13 | a0001c0001t0001g0017a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3986-32552A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130995393 | ||||||
| chr2:130995434
|
A | G | 12 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(9): Show | 12 | HG02615.hp1 HG02698.hp2 HG03704.hp2 others(9): Show |
intron_variant | MODIFIER | c.3986-32511A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130995434 | ||||||
| chr2:130995460
|
C | T | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3986-32485C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130995460 | ||||||
| chr2:130995822
|
T | G | 6 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3986-32123T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130995822 | ||||||
| chr2:130995888
|
C | CT | 13 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0035others(10): Show | 13 | HG02615.hp1 HG02698.hp2 HG03704.hp2 others(10): Show |
intron_variant | MODIFIER | c.3986-32039dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130995888 | |||||
| chr2:130995888
|
CT | C | 11 | a0002c0011t0001g0132a0002c0011t0001g0133a0002c0011t0001g0134others(8): Show | 11 | HG01884.hp2 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-32039delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130995888 | |||||
| chr2:130995959
|
G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(8): Show | 11 | HG02698.hp2 HG03704.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-31986G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130995959 | ||||||
| chr2:130996034
|
C | T | 1 | a0002c0011t0001g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3986-31911C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130996034 | ||||||
| chr2:130996087
|
A | G | 1 | a0001c0001t0001g0015 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3986-31858A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130996087 | ||||||
| chr2:130996158
|
G | C | 1 | a0001c0001t0008g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3986-31787G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130996158 | ||||||
| chr2:130996201
|
A | G | 1 | a0001c0014t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3986-31744A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130996201 | ||||||
| chr2:130996291
|
C | G | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3986-31654C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130996291 | ||||||
| chr2:130996633
|
T | C | 7 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.3986-31312T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130996633 | ||||||
| chr2:130996647
|
G | C | 7 | a0001c0015t0001g0078a0001c0015t0001g0079a0003c0003t0001g0062others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3986-31298G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130996647 | ||||||
| chr2:130996667
|
G | A | 1 | a0001c0014t0002g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3986-31278G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130996667 | ||||||
| chr2:130996735
|
G | A | 94 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0077others(91): Show | 94 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.3986-31210G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130996735 | ||||||
| chr2:130996774
|
G | T | 26 | a0001c0001t0001g0033a0001c0001t0001g0088a0001c0001t0001g0137others(23): Show | 26 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.3986-31171G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130996774 | ||||||
| chr2:130996785
|
C | T | 23 | a0001c0001t0001g0137a0001c0002t0001g0013a0001c0002t0001g0083others(20): Show | 23 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.3986-31160C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130996785 | ||||||
| chr2:130997252
|
T | A | 1 | a0001c0026t0001g0080 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3986-30693T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130997252 | ||||||
| chr2:130997324
|
A | G | 3 | a0010c0009t0001g0065a0010c0009t0001g0066a0010c0009t0001g0068 | 3 | HG02717.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3986-30621A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130997324 | ||||||
| chr2:130997395
|
G | C | 11 | a0001c0002t0001g0013a0001c0002t0001g0083a0001c0002t0001g0113others(8): Show | 11 | HG00642.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-30550G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130997395 | ||||||
| chr2:130997453
|
T | C | 4 | a0005c0006t0001g0100a0005c0006t0001g0102a0005c0006t0002g0099others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3986-30492T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130997453 | ||||||
| chr2:130997494
|
A | G | 12 | a0001c0001t0001g0086a0001c0001t0001g0115a0001c0014t0001g0120others(9): Show | 12 | HG00735.hp1 HG01257.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.3986-30451A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130997494 | ||||||
| chr2:130997581
|
C | T | 68 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0035others(65): Show | 68 | HG00621.hp1 HG00642.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.3986-30364C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130997581 | ||||||
| chr2:130997585
|
G | A | 1 | a0001c0034t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3986-30360G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130997585 | ||||||
| chr2:130997615
|
A | G | 46 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0035others(43): Show | 46 | HG00621.hp2 HG00642.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.3986-30330A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130997615 | ||||||
| chr2:130997624
|
T | C | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3986-30321T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130997624 | ||||||
| chr2:130997818
|
A | G | 1 | a0003c0003t0001g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3986-30127A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130997818 | ||||||
| chr2:130997863
|
A | C | 75 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0035others(72): Show | 75 | HG00621.hp1 HG00642.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.3986-30082A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130997863 | ||||||
| chr2:130998089
|
A | G | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3986-29856A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130998089 | ||||||
| chr2:130998263
|
G | C | 6 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3986-29682G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130998263 | ||||||
| chr2:130998271
|
A | G | 3 | a0001c0014t0001g0036a0001c0025t0005g0067a0017c0051t0006g0069 | 3 | HG01243.hp1 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-29674A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130998271 | ||||||
| chr2:130998307
|
C | T | 2 | a0004c0004t0001g0005a0004c0004t0001g0008 | 2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3986-29638C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130998307 | ||||||
| chr2:130998594
|
A | G | 12 | a0001c0001t0001g0086a0001c0001t0001g0115a0001c0014t0001g0120others(9): Show | 12 | HG00735.hp1 HG01257.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.3986-29351A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130998594 | ||||||
| chr2:130998612
|
T | G | 1 | a0024c0033t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3986-29333T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130998612 | ||||||
| chr2:130998633
|
T | C | 2 | a0003c0003t0001g0030a0005c0006t0003g0103 | 2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3986-29312T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130998633 | ||||||
| chr2:130998809
|
C | T | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3986-29136C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130998809 | ||||||
| chr2:130998928
|
G | A | 88 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(85): Show | 88 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.3986-29017G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130998928 | ||||||
| chr2:130998958
|
C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0086a0001c0001t0001g0115others(10): Show | 13 | HG00735.hp1 HG01257.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.3986-28987C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130998958 | ||||||
| chr2:130999077
|
T | C | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3986-28868T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999077 | ||||||
| chr2:130999160
|
C | CT | 9 | a0001c0001t0001g0088a0001c0018t0002g0105a0001c0018t0005g0106others(6): Show | 9 | HG00621.hp1 HG02055.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3986-28769dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 130999160 | |||||
| chr2:130999221
|
C | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0043others(12): Show | 15 | HG02080.hp2 HG02258.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.3986-28724C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999221 | ||||||
| chr2:130999346
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3986-28599C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999346 | ||||||
| chr2:130999354
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0046 | 2 | HG03704.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.3986-28591T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999354 | ||||||
| chr2:130999358
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0046 | 2 | HG03704.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.3986-28587A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999358 | ||||||
| chr2:130999363
|
A | G | 15 | a0001c0001t0001g0035a0001c0001t0001g0123a0001c0001t0001g0124others(12): Show | 15 | HG00621.hp1 HG01884.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.3986-28582A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999363 | ||||||
| chr2:130999364
|
G | C | 1 | a0001c0001t0002g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3986-28581G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999364 | ||||||
| chr2:130999378
|
G | A | 1 | a0001c0002t0001g0024 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3986-28567G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999378 | ||||||
| chr2:130999391
|
T | C | 4 | a0001c0018t0002g0105a0001c0018t0005g0106a0011c0022t0001g0084others(1): Show | 4 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3986-28554T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999391 | ||||||
| chr2:130999403
|
G | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0086a0001c0001t0001g0115others(6): Show | 9 | HG00735.hp1 HG01257.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.3986-28542G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999403 | ||||||
| chr2:130999407
|
T | C | 9 | a0001c0001t0001g0015a0001c0001t0001g0086a0001c0001t0001g0115others(6): Show | 9 | HG00735.hp1 HG01257.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.3986-28538T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999407 | ||||||
| chr2:130999408
|
G | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0086a0001c0001t0001g0115others(6): Show | 9 | HG00735.hp1 HG01257.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.3986-28537G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999408 | ||||||
| chr2:130999436
|
A | G | 3 | a0002c0011t0005g0054a0002c0048t0001g0070a0009c0021t0001g0130 | 3 | HG02970.hp2 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3986-28509A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999436 | ||||||
| chr2:130999567
|
A | C | 3 | a0001c0014t0001g0036a0001c0025t0005g0067a0017c0051t0006g0069 | 3 | HG01243.hp1 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-28378A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999567 | ||||||
| chr2:130999637
|
C | CT | 3 | a0001c0014t0001g0036a0001c0025t0005g0067a0017c0051t0006g0069 | 3 | HG01243.hp1 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-28308_3986-28 others(7): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999637 | ||||||
| chr2:130999732
|
T | C | 21 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0043others(18): Show | 21 | HG01175.hp2 HG02080.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.3986-28213T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999732 | ||||||
| chr2:130999979
|
G | C | 2 | a0003c0003t0001g0030a0005c0006t0003g0103 | 2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3986-27966G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 130999979 | ||||||
| chr2:131000109
|
A | T | 3 | a0001c0014t0001g0036a0001c0025t0005g0067a0017c0051t0006g0069 | 3 | HG01243.hp1 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-27836A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131000109 | ||||||
| chr2:131000124
|
G | A | 44 | a0001c0001t0001g0123a0001c0002t0001g0031a0001c0002t0001g0083others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.3986-27821G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131000124 | ||||||
| chr2:131000474
|
C | A | 13 | a0001c0001t0001g0123a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.3986-27471C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131000474 | ||||||
| chr2:131000673
|
G | A | 44 | a0001c0001t0001g0123a0001c0002t0001g0031a0001c0002t0001g0083others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.3986-27272G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131000673 | ||||||
| chr2:131000843
|
A | C | 1 | a0020c0038t0001g0032 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3986-27102A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131000843 | ||||||
| chr2:131001043
|
A | G | 44 | a0001c0001t0001g0123a0001c0002t0001g0031a0001c0002t0001g0083others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.3986-26902A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001043 | ||||||
| chr2:131001075
|
C | T | 13 | a0001c0001t0001g0123a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.3986-26870C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001075 | ||||||
| chr2:131001159
|
C | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3986-26786C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001159 | ||||||
| chr2:131001160
|
G | A | 1 | a0006c0050t0001g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3986-26785G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001160 | ||||||
| chr2:131001164
|
G | A | 6 | a0001c0015t0001g0078a0001c0015t0001g0079a0002c0028t0001g0073others(3): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3986-26781G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001164 | ||||||
| chr2:131001234
|
C | T | 3 | a0001c0014t0002g0075a0001c0026t0001g0080a0009c0047t0001g0110 | 3 | HG02559.hp1 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3986-26711C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001234 | ||||||
| chr2:131001281
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3986-26664C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001281 | ||||||
| chr2:131001302
|
C | CA | 20 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0040others(17): Show | 20 | HG00621.hp2 HG00735.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.3986-26617dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131001302 | |||||
| chr2:131001302
|
C | CAA | 38 | a0001c0001t0001g0015a0001c0001t0001g0115a0001c0001t0001g0123others(35): Show | 38 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.3986-26618_3986-26 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131001302 | |||||
| chr2:131001302
|
C | CAAA | 18 | a0001c0001t0001g0086a0001c0002t0001g0031a0001c0002t0001g0083others(15): Show | 18 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.3986-26619_3986-26 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131001302 | |||||
| chr2:131001302
|
CAA | C | 8 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0002g0105others(5): Show | 8 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.3986-26618_3986-26 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131001302 | |||||
| chr2:131001352
|
C | T | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3986-26593C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001352 | ||||||
| chr2:131001400
|
T | C | 1 | a0001c0026t0001g0080 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3986-26545T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001400 | ||||||
| chr2:131001482
|
C | G | 12 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0063others(9): Show | 12 | HG00621.hp2 HG01109.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.3986-26463C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001482 | ||||||
| chr2:131001631
|
G | A | 3 | a0001c0014t0001g0036a0001c0025t0005g0067a0017c0051t0006g0069 | 3 | HG01243.hp1 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-26314G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001631 | ||||||
| chr2:131001645
|
A | G | 3 | a0001c0014t0001g0036a0001c0025t0005g0067a0017c0051t0006g0069 | 3 | HG01243.hp1 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-26300A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001645 | ||||||
| chr2:131001668
|
A | C | 22 | a0001c0002t0001g0031a0001c0002t0001g0083a0001c0002t0001g0113others(19): Show | 22 | HG00642.hp2 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.3986-26277A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001668 | ||||||
| chr2:131001705
|
A | AG | 6 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118others(3): Show | 6 | HG02622.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3986-26238dupG | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131001705 | |||||
| chr2:131001818
|
G | T | 42 | a0001c0001t0001g0123a0001c0002t0001g0031a0001c0002t0001g0083others(39): Show | 42 | HG00621.hp1 HG00642.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.3986-26127G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001818 | ||||||
| chr2:131001931
|
G | C | 22 | a0001c0002t0001g0031a0001c0002t0001g0083a0001c0002t0001g0113others(19): Show | 22 | HG00642.hp2 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.3986-26014G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131001931 | ||||||
| chr2:131002157
|
A | G | 1 | a0005c0008t0001g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3986-25788A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002157 | ||||||
| chr2:131002367
|
G | A | 22 | a0001c0002t0001g0031a0001c0002t0001g0083a0001c0002t0001g0113others(19): Show | 22 | HG00642.hp2 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.3986-25578G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002367 | ||||||
| chr2:131002437
|
G | A | 13 | a0001c0001t0001g0123a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.3986-25508G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002437 | ||||||
| chr2:131002523
|
A | C | 1 | a0004c0004t0001g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3986-25422A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002523 | ||||||
| chr2:131002574
|
T | G | 91 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0035others(88): Show | 91 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.3986-25371T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002574 | ||||||
| chr2:131002669
|
C | T | 13 | a0001c0001t0001g0123a0001c0027t0001g0107a0002c0010t0001g0003others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.3986-25276C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002669 | ||||||
| chr2:131002688
|
C | T | 1 | a0002c0041t0001g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3986-25257C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002688 | ||||||
| chr2:131002709
|
C | CA | 5 | a0005c0006t0001g0052a0005c0006t0001g0102a0005c0008t0001g0097others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-25204dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131002709 | |||||
| chr2:131002709
|
CA | C | 25 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0033others(22): Show | 25 | HG00642.hp1 HG01081.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.3986-25204delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131002709 | |||||
| chr2:131002709
|
CAA | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0088a0001c0002t0001g0013others(2): Show | 5 | HG01243.hp1 HG03453.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-25205_3986-25 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131002709 | |||||
| chr2:131002709
|
CAAA | C | 6 | a0001c0001t0001g0086a0001c0034t0001g0111a0002c0041t0001g0053others(3): Show | 6 | HG00735.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3986-25206_3986-25 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131002709 | |||||
| chr2:131002709
|
CAAAA | C | 14 | a0001c0001t0001g0015a0001c0001t0001g0115a0001c0014t0001g0120others(11): Show | 14 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.3986-25207_3986-25 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131002709 | |||||
| chr2:131002709
|
CAAAAA | C | 30 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0087others(27): Show | 30 | HG00621.hp1 HG01175.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.3986-25208_3986-25 others(11): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131002709 | |||||
| chr2:131002709
|
CAAAAAA | C | 34 | a0001c0001t0001g0035a0001c0001t0001g0123a0001c0002t0001g0031others(31): Show | 34 | HG00642.hp2 HG01081.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.3986-25209_3986-25 others(12): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131002709 | |||||
| chr2:131002738
|
A | G | 2 | a0003c0003t0001g0030a0005c0006t0003g0103 | 2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3986-25207A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002738 | ||||||
| chr2:131002741
|
A | C | 1 | a0002c0011t0001g0134 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3986-25204A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002741 | ||||||
| chr2:131002742
|
G | C | 1 | a0005c0006t0002g0099 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3986-25203G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002742 | ||||||
| chr2:131002755
|
T | C | 91 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0035others(88): Show | 91 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.3986-25190T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002755 | ||||||
| chr2:131002810
|
G | A | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3986-25135G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002810 | ||||||
| chr2:131002843
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3986-25102A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002843 | ||||||
| chr2:131002897
|
C | A | 5 | a0001c0034t0001g0111a0002c0041t0001g0053a0003c0003t0001g0081others(2): Show | 5 | HG02257.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3986-25048C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002897 | ||||||
| chr2:131002962
|
C | A | 1 | a0001c0002t0001g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3986-24983C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131002962 | ||||||
| chr2:131003236
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0088 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3986-24709A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131003236 | ||||||
| chr2:131003268
|
C | T | 1 | a0024c0033t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3986-24677C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131003268 | ||||||
| chr2:131003403
|
C | G | 76 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0043others(73): Show | 76 | HG00621.hp1 HG00642.hp2 HG01081.hp1 others(73): Show |
intron_variant | MODIFIER | c.3986-24542C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131003403 | ||||||
| chr2:131003405
|
C | T | 1 | a0006c0050t0001g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3986-24540C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131003405 | ||||||
| chr2:131003425
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3986-24520C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131003425 | ||||||
| chr2:131003731
|
G | A | 2 | a0001c0014t0001g0036a0001c0025t0005g0067 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-24214G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131003731 | ||||||
| chr2:131003818
|
T | A | 9 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(6): Show | 9 | HG01257.hp2 HG01258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.3986-24127T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131003818 | ||||||
| chr2:131003869
|
A | C | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3986-24076A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131003869 | ||||||
| chr2:131003883
|
G | C | 6 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118others(3): Show | 6 | HG02622.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3986-24062G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131003883 | ||||||
| chr2:131004054
|
A | G | 2 | a0001c0014t0001g0036a0001c0025t0005g0067 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-23891A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131004054 | ||||||
| chr2:131004077
|
T | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0126a0001c0002t0001g0013 | 3 | HG02698.hp2 HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.3986-23868T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131004077 | ||||||
| chr2:131004266
|
T | C | 2 | a0001c0014t0001g0036a0001c0025t0005g0067 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-23679T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131004266 | ||||||
| chr2:131004356
|
G | A | 1 | a0024c0033t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3986-23589G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131004356 | ||||||
| chr2:131004367
|
G | T | 2 | a0001c0034t0001g0111a0006c0050t0001g0142 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3986-23578G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131004367 | ||||||
| chr2:131004877
|
A | G | 76 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0043others(73): Show | 76 | HG00621.hp1 HG00642.hp2 HG01081.hp1 others(73): Show |
intron_variant | MODIFIER | c.3986-23068A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131004877 | ||||||
| chr2:131004923
|
G | A | 2 | a0001c0014t0001g0036a0001c0025t0005g0067 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-23022G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131004923 | ||||||
| chr2:131005005
|
G | A | 1 | a0001c0039t0001g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3986-22940G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131005005 | ||||||
| chr2:131005117
|
C | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3986-22828C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131005117 | ||||||
| chr2:131005209
|
A | T | 2 | a0001c0014t0001g0036a0001c0025t0005g0067 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-22736A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131005209 | ||||||
| chr2:131005332
|
A | G | 22 | a0001c0001t0001g0015a0001c0001t0001g0086a0001c0001t0001g0115others(19): Show | 22 | HG00621.hp1 HG00735.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.3986-22613A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131005332 | ||||||
| chr2:131005406
|
A | G | 2 | a0001c0014t0001g0036a0001c0025t0005g0067 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-22539A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131005406 | ||||||
| chr2:131005591
|
C | T | 2 | a0001c0014t0001g0036a0001c0025t0005g0067 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-22354C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131005591 | ||||||
| chr2:131006088
|
G | A | 2 | a0003c0003t0001g0030a0005c0006t0003g0103 | 2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3986-21857G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131006088 | ||||||
| chr2:131006225
|
G | A | 3 | a0001c0018t0002g0105a0001c0018t0005g0106a0024c0033t0001g0021 | 3 | HG02055.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3986-21720G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131006225 | ||||||
| chr2:131006380
|
G | T | 23 | a0001c0002t0001g0031a0001c0002t0001g0083a0001c0002t0001g0113others(20): Show | 23 | HG00642.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.3986-21565G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131006380 | ||||||
| chr2:131006439
|
A | G | 1 | a0001c0002t0001g0083 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3986-21506A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131006439 | ||||||
| chr2:131006516
|
A | G | 47 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0043others(44): Show | 47 | HG00642.hp2 HG01081.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.3986-21429A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131006516 | ||||||
| chr2:131006549
|
C | G | 1 | a0007c0017t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3986-21396C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131006549 | ||||||
| chr2:131006568
|
T | C | 2 | a0001c0018t0002g0105a0001c0018t0005g0106 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3986-21377T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131006568 | ||||||
| chr2:131006657
|
G | A | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3986-21288G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131006657 | ||||||
| chr2:131006670
|
TTTTGGGG others(10): Show |
T | 1 | a0001c0014t0002g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3986-21273_3986-21 others(23): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131006670 | |||||
| chr2:131006745
|
G | C | 7 | a0003c0003t0002g0116a0003c0003t0002g0117a0003c0003t0002g0118others(4): Show | 7 | HG02615.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3986-21200G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131006745 | ||||||
| chr2:131007030
|
G | A | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3986-20915G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131007030 | ||||||
| chr2:131007193
|
C | T | 6 | a0001c0015t0001g0078a0001c0015t0001g0079a0002c0028t0001g0073others(3): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3986-20752C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131007193 | ||||||
| chr2:131007428
|
C | T | 29 | a0001c0002t0001g0031a0001c0002t0001g0083a0001c0002t0001g0113others(26): Show | 29 | HG00642.hp2 HG01081.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.3986-20517C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131007428 | ||||||
| chr2:131007541
|
A | G | 1 | a0008c0012t0001g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3986-20404A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131007541 | ||||||
| chr2:131007790
|
C | A | 1 | a0001c0014t0001g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3986-20155C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131007790 | ||||||
| chr2:131007800
|
C | CT | 7 | a0001c0002t0001g0041a0003c0003t0001g0081a0005c0008t0001g0098others(4): Show | 7 | HG00735.hp2 HG01109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.3986-20117dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131007800 | |||||
| chr2:131007800
|
C | CTT | 12 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0043others(9): Show | 12 | HG02698.hp1 HG02698.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.3986-20118_3986-20 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131007800 | |||||
| chr2:131007800
|
CT | C | 37 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0115others(34): Show | 37 | HG00642.hp2 HG01081.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.3986-20117delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131007800 | |||||
| chr2:131007800
|
CTT | C | 17 | a0001c0002t0001g0031a0001c0007t0004g0090a0001c0014t0001g0036others(14): Show | 17 | HG01257.hp2 HG01884.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.3986-20118_3986-20 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131007800 | |||||
| chr2:131007800
|
CTTTTTTT others(3): Show |
C | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3986-20126_3986-20 others(16): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131007800 | |||||
| chr2:131007806
|
T | C | 3 | a0004c0004t0001g0128a0012c0019t0001g0127a0012c0019t0001g0129 | 3 | NA18948.hp2 NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.3986-20139T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131007806 | ||||||
| chr2:131007858
|
C | T | 2 | a0001c0014t0001g0036a0001c0025t0005g0067 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3986-20087C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131007858 | ||||||
| chr2:131007880
|
C | G | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3986-20065C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131007880 | ||||||
| chr2:131007999
|
G | T | 6 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3986-19946G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131007999 | ||||||
| chr2:131008199
|
A | C | 3 | a0001c0025t0005g0067a0001c0027t0001g0107a0009c0046t0009g0076 | 3 | HG01243.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3986-19746A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131008199 | ||||||
| chr2:131008351
|
AC | A | 2 | a0001c0025t0005g0067a0009c0046t0009g0076 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3986-19593delC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131008351 | ||||||
| chr2:131008434
|
T | TA | 2 | a0001c0025t0005g0067a0009c0046t0009g0076 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3986-19511_3986-19 others(7): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131008434 | ||||||
| chr2:131008502
|
G | C | 6 | a0001c0015t0001g0078a0001c0015t0001g0079a0002c0028t0001g0073others(3): Show | 6 | HG01109.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3986-19443G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131008502 | ||||||
| chr2:131008622
|
T | A | 1 | a0002c0010t0001g0051 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3986-19323T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131008622 | ||||||
| chr2:131008638
|
T | C | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3986-19307T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131008638 | ||||||
| chr2:131008642
|
T | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0137others(5): Show | 8 | HG02080.hp2 HG02723.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.3986-19303T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131008642 | ||||||
| chr2:131008645
|
T | A | 2 | a0001c0025t0005g0067a0009c0046t0009g0076 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3986-19300T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131008645 | ||||||
| chr2:131008809
|
A | G | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3986-19136A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131008809 | ||||||
| chr2:131008984
|
C | T | 1 | a0003c0003t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3986-18961C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131008984 | ||||||
| chr2:131009035
|
A | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0087others(13): Show | 16 | HG01258.hp2 HG02080.hp2 HG02698.hp1 others(13): Show |
intron_variant | MODIFIER | c.3986-18910A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131009035 | ||||||
| chr2:131009318
|
T | C | 14 | a0001c0001t0002g0058a0001c0014t0002g0075a0001c0015t0001g0078others(11): Show | 14 | HG01109.hp2 HG01175.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3986-18627T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131009318 | ||||||
| chr2:131009383
|
C | T | 4 | a0006c0005t0001g0072a0006c0005t0001g0143a0006c0005t0005g0119others(1): Show | 4 | HG02258.hp1 HG02818.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3986-18562C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131009383 | ||||||
| chr2:131009775
|
T | C | 4 | a0001c0045t0001g0085a0005c0006t0003g0103a0007c0013t0003g0060others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3986-18170T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131009775 | ||||||
| chr2:131009954
|
G | A | 6 | a0001c0025t0005g0067a0006c0005t0001g0072a0006c0005t0001g0143others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3986-17991G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131009954 | ||||||
| chr2:131009955
|
T | TTTTTGTT others(8): Show |
1 | a0005c0008t0001g0098 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3986-17980_3986-17 others(21): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131009955 | |||||
| chr2:131010408
|
A | T | 4 | a0001c0001t0002g0058a0003c0003t0002g0116a0003c0003t0002g0117others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3986-17537A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131010408 | ||||||
| chr2:131010507
|
G | A | 11 | a0001c0001t0001g0122a0001c0002t0001g0023a0001c0002t0001g0024others(8): Show | 11 | HG01515.hp2 HG01975.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-17438G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131010507 | ||||||
| chr2:131010509
|
TA | T | 7 | a0001c0034t0001g0111a0002c0011t0005g0054a0002c0048t0001g0070others(4): Show | 7 | HG00735.hp2 HG02257.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.3986-17435delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131010509 | ||||||
| chr2:131010623
|
A | G | 3 | a0001c0015t0001g0078a0001c0015t0001g0079a0003c0003t0001g0030 | 3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3986-17322A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131010623 | ||||||
| chr2:131010700
|
A | G | 1 | a0009c0047t0001g0110 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3986-17245A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131010700 | ||||||
| chr2:131010705
|
G | A | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3986-17240G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131010705 | ||||||
| chr2:131010866
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3986-17079C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131010866 | ||||||
| chr2:131010867
|
G | A | 7 | a0001c0034t0001g0111a0002c0011t0005g0054a0002c0048t0001g0070others(4): Show | 7 | HG00735.hp2 HG02257.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.3986-17078G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131010867 | ||||||
| chr2:131010877
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3986-17068C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131010877 | ||||||
| chr2:131010958
|
T | G | 78 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0017others(75): Show | 78 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.3986-16987T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131010958 | ||||||
| chr2:131011540
|
G | T | 1 | a0001c0018t0005g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3986-16405G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131011540 | ||||||
| chr2:131011573
|
T | A | 1 | a0008c0012t0001g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3986-16372T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131011573 | ||||||
| chr2:131011664
|
G | A | 56 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0017others(53): Show | 56 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.3986-16281G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131011664 | ||||||
| chr2:131011875
|
C | T | 1 | a0015c0054t0001g0061 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3986-16070C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131011875 | ||||||
| chr2:131011975
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3986-15970G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131011975 | ||||||
| chr2:131012018
|
C | T | 142 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(139): Show | 142 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.3986-15927C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131012018 | ||||||
| chr2:131012050
|
T | C | 7 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3986-15895T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131012050 | ||||||
| chr2:131012332
|
C | G | 1 | a0001c0044t0001g0011 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3986-15613C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131012332 | ||||||
| chr2:131012562
|
T | TTG | 88 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(85): Show | 88 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.3986-15369_3986-15 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131012562 | |||||
| chr2:131012562
|
T | TTGTG | 5 | a0001c0014t0001g0120a0005c0006t0002g0099a0006c0005t0001g0072others(2): Show | 5 | HG02257.hp2 HG02717.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.3986-15371_3986-15 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131012562 | |||||
| chr2:131012680
|
C | T | 10 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(7): Show | 10 | HG01175.hp2 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.3986-15265C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131012680 | ||||||
| chr2:131012900
|
A | G | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0007c0013t0002g0095 | 3 | HG01175.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3986-15045A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131012900 | ||||||
| chr2:131012978
|
A | G | 1 | a0019c0036t0001g0049 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3986-14967A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131012978 | ||||||
| chr2:131013150
|
C | G | 5 | a0001c0014t0001g0036a0001c0027t0001g0107a0006c0005t0001g0094others(2): Show | 5 | HG01258.hp2 HG02486.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-14795C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131013150 | ||||||
| chr2:131013185
|
A | T | 1 | a0006c0005t0001g0094 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3986-14760A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131013185 | ||||||
| chr2:131013337
|
G | A | 2 | a0010c0009t0001g0065a0010c0009t0001g0066 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.3986-14608G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131013337 | ||||||
| chr2:131013490
|
G | A | 1 | a0002c0010t0001g0047 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3986-14455G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131013490 | ||||||
| chr2:131013625
|
G | A | 1 | a0022c0035t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3986-14320G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131013625 | ||||||
| chr2:131013832
|
A | C | 130 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0015others(127): Show | 130 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(127): Show |
intron_variant | MODIFIER | c.3986-14113A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131013832 | ||||||
| chr2:131014189
|
A | G | 78 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(75): Show | 78 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.3986-13756A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131014189 | ||||||
| chr2:131014275
|
C | T | 1 | a0018c0043t0001g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3986-13670C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131014275 | ||||||
| chr2:131014276
|
T | C | 5 | a0003c0003t0001g0081a0005c0006t0003g0103a0007c0013t0003g0060others(2): Show | 5 | HG02723.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-13669T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131014276 | ||||||
| chr2:131014292
|
C | T | 5 | a0003c0003t0001g0081a0005c0006t0003g0103a0007c0013t0003g0060others(2): Show | 5 | HG02723.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-13653C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131014292 | ||||||
| chr2:131014350
|
A | G | 117 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(114): Show | 117 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.3986-13595A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131014350 | ||||||
| chr2:131014424
|
C | T | 77 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(74): Show | 77 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.3986-13521C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131014424 | ||||||
| chr2:131014505
|
G | A | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0007c0013t0002g0095 | 3 | HG01175.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3986-13440G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131014505 | ||||||
| chr2:131014698
|
C | T | 3 | a0004c0004t0001g0128a0012c0019t0001g0127a0012c0019t0001g0129 | 3 | NA18948.hp2 NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.3986-13247C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131014698 | ||||||
| chr2:131014874
|
T | A | 7 | a0002c0011t0001g0132a0002c0011t0001g0133a0002c0011t0001g0134others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3986-13071T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131014874 | ||||||
| chr2:131014941
|
G | A | 2 | a0002c0011t0005g0054a0003c0031t0006g0037 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3986-13004G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131014941 | ||||||
| chr2:131015214
|
C | T | 2 | a0001c0014t0001g0120a0005c0006t0002g0099 | 2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3986-12731C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131015214 | ||||||
| chr2:131015292
|
A | T | 5 | a0001c0014t0001g0036a0001c0027t0001g0107a0006c0005t0001g0094others(2): Show | 5 | HG01258.hp2 HG02486.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-12653A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131015292 | ||||||
| chr2:131015369
|
A | G | 1 | a0013c0016t0003g0002 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3986-12576A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131015369 | ||||||
| chr2:131015521
|
C | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0035others(9): Show | 12 | HG02698.hp1 HG02895.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.3986-12424C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131015521 | ||||||
| chr2:131015535
|
C | T | 7 | a0002c0011t0001g0132a0002c0011t0001g0133a0002c0011t0001g0134others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3986-12410C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131015535 | ||||||
| chr2:131015583
|
A | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0035others(9): Show | 12 | HG02698.hp1 HG02895.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.3986-12362A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131015583 | ||||||
| chr2:131015586
|
C | A | 2 | a0002c0011t0005g0054a0003c0031t0006g0037 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3986-12359C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131015586 | ||||||
| chr2:131015662
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3986-12283G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131015662 | ||||||
| chr2:131015852
|
G | C | 1 | a0009c0046t0009g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3986-12093G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131015852 | ||||||
| chr2:131015956
|
T | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0035others(9): Show | 12 | HG02698.hp1 HG02895.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.3986-11989T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131015956 | ||||||
| chr2:131015965
|
T | G | 1 | a0020c0038t0001g0032 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3986-11980T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131015965 | ||||||
| chr2:131016191
|
A | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0035others(9): Show | 12 | HG02698.hp1 HG02895.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.3986-11754A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131016191 | ||||||
| chr2:131016344
|
A | G | 1 | a0007c0013t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3986-11601A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131016344 | ||||||
| chr2:131016613
|
T | C | 15 | a0001c0001t0001g0046a0001c0001t0001g0063a0001c0001t0001g0114others(12): Show | 15 | HG00621.hp1 HG00621.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.3986-11332T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131016613 | ||||||
| chr2:131016739
|
C | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0035others(9): Show | 12 | HG02698.hp1 HG02895.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.3986-11206C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131016739 | ||||||
| chr2:131016773
|
C | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0035others(9): Show | 12 | HG02698.hp1 HG02895.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.3986-11172C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131016773 | ||||||
| chr2:131016805
|
T | A | 86 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(83): Show | 86 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.3986-11140T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131016805 | ||||||
| chr2:131016858
|
A | G | 142 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(139): Show | 142 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.3986-11087A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131016858 | ||||||
| chr2:131017371
|
C | T | 142 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(139): Show | 142 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.3986-10574C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131017371 | ||||||
| chr2:131017639
|
AC | A | 7 | a0001c0025t0005g0067a0001c0045t0001g0085a0005c0008t0001g0007others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3986-10302delC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131017639 | |||||
| chr2:131017730
|
G | A | 1 | a0021c0037t0001g0050 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3986-10215G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131017730 | ||||||
| chr2:131017950
|
T | G | 87 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(84): Show | 87 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.3986-9995T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131017950 | ||||||
| chr2:131018028
|
T | G | 1 | a0002c0028t0001g0073 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3986-9917T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131018028 | ||||||
| chr2:131018278
|
A | C | 132 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0015others(129): Show | 132 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.3986-9667A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131018278 | ||||||
| chr2:131018296
|
C | T | 3 | a0001c0001t0001g0042a0001c0002t0001g0041a0004c0004t0001g0008 | 3 | HG03017.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3986-9649C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131018296 | ||||||
| chr2:131018338
|
C | T | 2 | a0002c0011t0005g0054a0003c0031t0006g0037 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3986-9607C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131018338 | ||||||
| chr2:131018429
|
A | G | 11 | a0001c0001t0002g0058a0002c0011t0001g0132a0002c0011t0001g0133others(8): Show | 11 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.3986-9516A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131018429 | ||||||
| chr2:131018654
|
A | T | 11 | a0001c0001t0002g0058a0002c0011t0001g0132a0002c0011t0001g0133others(8): Show | 11 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.3986-9291A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131018654 | ||||||
| chr2:131018738
|
T | C | 14 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(11): Show | 14 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3986-9207T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131018738 | ||||||
| chr2:131018900
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3986-9045G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131018900 | ||||||
| chr2:131019156
|
T | G | 1 | a0007c0013t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3986-8789T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019156 | ||||||
| chr2:131019296
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3986-8649C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019296 | ||||||
| chr2:131019354
|
G | A | 23 | a0001c0001t0002g0058a0001c0014t0002g0075a0001c0015t0001g0078others(20): Show | 23 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.3986-8591G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019354 | ||||||
| chr2:131019644
|
G | GT | 84 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(81): Show | 84 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.3986-8294dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131019644 | |||||
| chr2:131019656
|
T | C | 109 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(106): Show | 109 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.3986-8289T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019656 | ||||||
| chr2:131019697
|
G | C | 2 | a0001c0002t0001g0020a0001c0002t0001g0034 | 2 | HG02080.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.3986-8248G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019697 | ||||||
| chr2:131019702
|
C | T | 1 | a0007c0013t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3986-8243C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019702 | ||||||
| chr2:131019718
|
C | T | 86 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(83): Show | 86 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.3986-8227C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019718 | ||||||
| chr2:131019720
|
G | T | 2 | a0010c0009t0001g0065a0010c0009t0001g0066 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.3986-8225G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019720 | ||||||
| chr2:131019782
|
T | C | 2 | a0001c0014t0001g0120a0005c0006t0002g0099 | 2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3986-8163T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019782 | ||||||
| chr2:131019825
|
G | A | 5 | a0001c0014t0001g0036a0001c0027t0001g0107a0006c0005t0001g0094others(2): Show | 5 | HG01258.hp2 HG02486.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-8120G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019825 | ||||||
| chr2:131019835
|
T | C | 2 | a0007c0017t0001g0108a0011c0022t0001g0096 | 2 | HG02895.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3986-8110T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019835 | ||||||
| chr2:131019869
|
C | T | 142 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(139): Show | 142 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.3986-8076C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019869 | ||||||
| chr2:131019929
|
T | C | 142 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(139): Show | 142 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.3986-8016T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131019929 | ||||||
| chr2:131020113
|
G | A | 135 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0015others(132): Show | 135 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.3986-7832G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131020113 | ||||||
| chr2:131020202
|
A | G | 85 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(82): Show | 85 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.3986-7743A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131020202 | ||||||
| chr2:131020296
|
T | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0124a0001c0002t0001g0020others(8): Show | 11 | HG01515.hp2 HG01975.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-7649T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131020296 | ||||||
| chr2:131020304
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0124a0001c0002t0001g0020others(8): Show | 11 | HG01515.hp2 HG01975.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.3986-7641A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131020304 | ||||||
| chr2:131020405
|
G | C | 6 | a0001c0014t0001g0036a0001c0027t0001g0107a0003c0003t0001g0030others(3): Show | 6 | HG01109.hp2 HG01258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.3986-7540G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131020405 | ||||||
| chr2:131020424
|
G | A | 5 | a0003c0003t0001g0081a0005c0006t0003g0103a0007c0013t0003g0060others(2): Show | 5 | HG02723.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-7521G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131020424 | ||||||
| chr2:131020431
|
T | C | 123 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(120): Show | 123 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.3986-7514T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131020431 | ||||||
| chr2:131020436
|
G | A | 87 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(84): Show | 87 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.3986-7509G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131020436 | ||||||
| chr2:131020479
|
G | A | 2 | a0001c0001t0001g0115a0002c0010t0001g0003 | 2 | HG00621.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.3986-7466G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131020479 | ||||||
| chr2:131020549
|
T | C | 87 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(84): Show | 87 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.3986-7396T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131020549 | ||||||
| chr2:131020628
|
T | C | 1 | a0025c0024t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3986-7317T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131020628 | ||||||
| chr2:131021265
|
T | C | 109 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(106): Show | 109 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.3986-6680T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131021265 | ||||||
| chr2:131021279
|
G | C | 7 | a0002c0011t0001g0132a0002c0011t0001g0133a0002c0011t0001g0134others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3986-6666G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131021279 | ||||||
| chr2:131021366
|
A | G | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0007c0013t0002g0095 | 3 | HG01175.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3986-6579A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131021366 | ||||||
| chr2:131021387
|
C | G | 1 | a0007c0013t0002g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3986-6558C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131021387 | ||||||
| chr2:131021777
|
G | A | 1 | a0007c0013t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3986-6168G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131021777 | ||||||
| chr2:131021850
|
A | C | 1 | a0001c0002t0001g0113 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3986-6095A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131021850 | ||||||
| chr2:131021870
|
G | A | 13 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(10): Show | 13 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.3986-6075G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131021870 | ||||||
| chr2:131022243
|
A | G | 5 | a0003c0003t0001g0081a0005c0006t0003g0103a0007c0013t0003g0060others(2): Show | 5 | HG02723.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-5702A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131022243 | ||||||
| chr2:131022652
|
T | C | 1 | a0009c0021t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3986-5293T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131022652 | ||||||
| chr2:131022657
|
CA | C | 33 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0017others(30): Show | 33 | HG01257.hp2 HG01258.hp1 HG02257.hp1 others(30): Show |
intron_variant | MODIFIER | c.3986-5274delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131022657 | |||||
| chr2:131022657
|
CAA | C | 22 | a0001c0001t0002g0058a0001c0014t0001g0120a0001c0015t0001g0078others(19): Show | 22 | HG01175.hp2 HG01884.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.3986-5275_3986-527 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131022657 | |||||
| chr2:131022657
|
CAAA | C | 85 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(82): Show | 85 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.3986-5276_3986-527 others(7): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131022657 | |||||
| chr2:131022716
|
CT | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0035others(9): Show | 12 | HG02698.hp1 HG02895.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.3986-5225delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131022716 | |||||
| chr2:131022854
|
T | C | 83 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(80): Show | 83 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.3986-5091T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131022854 | ||||||
| chr2:131022923
|
AT | A | 19 | a0001c0001t0002g0058a0001c0014t0002g0075a0001c0015t0001g0078others(16): Show | 19 | HG01175.hp2 HG01884.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.3986-5021delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131022923 | ||||||
| chr2:131022931
|
A | G | 23 | a0001c0001t0002g0058a0001c0014t0001g0120a0001c0014t0002g0075others(20): Show | 23 | HG01175.hp2 HG01884.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.3986-5014A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131022931 | ||||||
| chr2:131023024
|
T | G | 5 | a0003c0003t0001g0081a0005c0006t0003g0103a0007c0013t0003g0060others(2): Show | 5 | HG02723.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-4921T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131023024 | ||||||
| chr2:131023072
|
CTCAAA | C | 2 | a0002c0010t0001g0047a0004c0020t0001g0016 | 2 | NA18970.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3986-4872_3986-486 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131023072 | ||||||
| chr2:131023073
|
T | A | 83 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(80): Show | 83 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.3986-4872T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131023073 | ||||||
| chr2:131023074
|
C | CA | 17 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0035others(14): Show | 17 | HG01243.hp1 HG02572.hp1 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.3986-4850dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131023074 | |||||
| chr2:131023074
|
C | CAAAA | 7 | a0002c0011t0001g0132a0002c0011t0001g0133a0002c0011t0001g0134others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3986-4853_3986-485 others(8): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131023074 | |||||
| chr2:131023074
|
C | CAAAAAA | 8 | a0001c0001t0001g0115a0001c0015t0001g0078a0001c0015t0001g0079others(5): Show | 8 | HG01975.hp2 HG02717.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3986-4855_3986-485 others(10): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131023074 | |||||
| chr2:131023074
|
C | CAAAAAAA | 45 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0040others(42): Show | 45 | HG00621.hp1 HG00621.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.3986-4856_3986-485 others(11): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131023074 | |||||
| chr2:131023074
|
C | CAAAAAAA others(1): Show |
17 | a0001c0001t0001g0033a0001c0001t0001g0086a0001c0001t0001g0137others(14): Show | 17 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.3986-4857_3986-485 others(12): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131023074 | |||||
| chr2:131023074
|
CA | C | 14 | a0001c0002t0001g0113a0001c0007t0004g0089a0001c0007t0004g0090others(11): Show | 14 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3986-4850delA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131023074 | |||||
| chr2:131023075
|
A | G | 3 | a0010c0009t0001g0068a0017c0051t0006g0069a0023c0029t0001g0141 | 3 | HG02615.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3986-4870A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131023075 | ||||||
| chr2:131023079
|
A | C | 2 | a0002c0010t0001g0047a0004c0020t0001g0016 | 2 | NA18970.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3986-4866A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131023079 | ||||||
| chr2:131023131
|
T | G | 8 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3986-4814T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131023131 | ||||||
| chr2:131023250
|
G | A | 83 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(80): Show | 83 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.3986-4695G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131023250 | ||||||
| chr2:131023276
|
C | T | 134 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0015others(131): Show | 134 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(131): Show |
intron_variant | MODIFIER | c.3986-4669C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131023276 | ||||||
| chr2:131023589
|
A | G | 14 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(11): Show | 14 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3986-4356A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131023589 | ||||||
| chr2:131023895
|
G | GCATGGAA others(13): Show |
1 | a0008c0012t0001g0082 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3986-4040_3986-402 others(24): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131023895 | |||||
| chr2:131024177
|
A | G | 108 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(105): Show | 108 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.3986-3768A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024177 | ||||||
| chr2:131024204
|
T | G | 7 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.3986-3741T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024204 | ||||||
| chr2:131024206
|
T | TGTCAC | 14 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(11): Show | 14 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3986-3739_3986-373 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024206 | ||||||
| chr2:131024214
|
T | C | 1 | a0006c0005t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3986-3731T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024214 | ||||||
| chr2:131024251
|
C | G | 134 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0015others(131): Show | 134 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(131): Show |
intron_variant | MODIFIER | c.3986-3694C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024251 | ||||||
| chr2:131024314
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3986-3631C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024314 | ||||||
| chr2:131024322
|
T | C | 108 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(105): Show | 108 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.3986-3623T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024322 | ||||||
| chr2:131024326
|
A | C | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0002c0028t0001g0073others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3986-3619A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024326 | ||||||
| chr2:131024413
|
C | CT | 87 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(84): Show | 87 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.3986-3531dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 131024413 | |||||
| chr2:131024436
|
C | T | 1 | a0007c0013t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3986-3509C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024436 | ||||||
| chr2:131024496
|
T | G | 1 | a0009c0046t0009g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3986-3449T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024496 | ||||||
| chr2:131024554
|
C | T | 21 | a0001c0001t0002g0058a0001c0014t0002g0075a0001c0015t0001g0078others(18): Show | 21 | HG01175.hp2 HG01884.hp2 HG02622.hp2 others(18): Show |
intron_variant | MODIFIER | c.3986-3391C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024554 | ||||||
| chr2:131024564
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3986-3381C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024564 | ||||||
| chr2:131024593
|
A | G | 134 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0015others(131): Show | 134 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(131): Show |
intron_variant | MODIFIER | c.3986-3352A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024593 | ||||||
| chr2:131024681
|
A | G | 85 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(82): Show | 85 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.3986-3264A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024681 | ||||||
| chr2:131024700
|
C | T | 108 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(105): Show | 108 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.3986-3245C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024700 | ||||||
| chr2:131024751
|
T | C | 7 | a0002c0011t0001g0132a0002c0011t0001g0133a0002c0011t0001g0134others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3986-3194T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131024751 | ||||||
| chr2:131025161
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3986-2784C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131025161 | ||||||
| chr2:131025183
|
G | A | 6 | a0001c0014t0001g0036a0001c0027t0001g0107a0003c0003t0001g0030others(3): Show | 6 | HG01109.hp2 HG01258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.3986-2762G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131025183 | ||||||
| chr2:131025254
|
T | C | 109 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(106): Show | 109 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.3986-2691T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131025254 | ||||||
| chr2:131025506
|
C | T | 87 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(84): Show | 87 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.3986-2439C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131025506 | ||||||
| chr2:131025599
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3986-2346T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131025599 | ||||||
| chr2:131025601
|
T | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0077a0001c0001t0001g0135 | 3 | NA18612.hp1 NA18747.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.3986-2344T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131025601 | ||||||
| chr2:131025813
|
G | A | 87 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(84): Show | 87 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.3986-2132G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131025813 | ||||||
| chr2:131025814
|
A | G | 1 | a0004c0004t0001g0008 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3986-2131A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131025814 | ||||||
| chr2:131026399
|
G | A | 19 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(16): Show | 19 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.3986-1546G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131026399 | ||||||
| chr2:131026473
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0035others(10): Show | 13 | HG02698.hp1 HG02895.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.3986-1472C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131026473 | ||||||
| chr2:131026530
|
A | C | 21 | a0001c0001t0002g0058a0001c0014t0002g0075a0001c0015t0001g0078others(18): Show | 21 | HG01175.hp2 HG01884.hp2 HG02622.hp2 others(18): Show |
intron_variant | MODIFIER | c.3986-1415A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131026530 | ||||||
| chr2:131026605
|
C | T | 87 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(84): Show | 87 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.3986-1340C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131026605 | ||||||
| chr2:131026753
|
C | A | 17 | a0001c0014t0002g0075a0001c0015t0001g0078a0001c0015t0001g0079others(14): Show | 17 | HG01175.hp2 HG01884.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.3986-1192C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131026753 | ||||||
| chr2:131026782
|
C | T | 8 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3986-1163C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131026782 | ||||||
| chr2:131026850
|
G | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3986-1095G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131026850 | ||||||
| chr2:131027089
|
G | A | 2 | a0004c0004t0001g0144a0014c0023t0001g0057 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3986-856G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131027089 | ||||||
| chr2:131027165
|
C | T | 5 | a0003c0003t0001g0081a0005c0006t0003g0103a0007c0013t0003g0060others(2): Show | 5 | HG02723.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-780C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131027165 | ||||||
| chr2:131027178
|
A | G | 1 | a0002c0010t0001g0003 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3986-767A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131027178 | ||||||
| chr2:131027198
|
G | A | 87 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(84): Show | 87 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.3986-747G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131027198 | ||||||
| chr2:131027279
|
A | G | 1 | a0009c0021t0001g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3986-666A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131027279 | ||||||
| chr2:131027408
|
G | A | 5 | a0003c0003t0001g0081a0005c0006t0003g0103a0007c0013t0003g0060others(2): Show | 5 | HG02723.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3986-537G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131027408 | ||||||
| chr2:131027790
|
G | T | 1 | a0012c0019t0001g0127 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3986-155G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | chr2 | 131027790 | ||||||
| chr2:131028148
|
C | T | 5 | a0003c0003t0001g0081a0005c0006t0003g0103a0007c0013t0003g0060others(2): Show | 5 | HG02723.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4125+64C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131028148 | ||||||
| chr2:131028214
|
A | G | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0005g0106others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.4125+130A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131028214 | ||||||
| chr2:131028217
|
G | A | 16 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0035others(13): Show | 16 | HG02698.hp1 HG02895.hp1 HG02896.hp1 others(13): Show |
intron_variant | MODIFIER | c.4125+133G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131028217 | ||||||
| chr2:131028537
|
T | A | 87 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(84): Show | 87 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.4125+453T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131028537 | ||||||
| chr2:131028549
|
G | A | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0005g0106others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.4125+465G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131028549 | ||||||
| chr2:131028587
|
G | A | 87 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(84): Show | 87 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.4125+503G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131028587 | ||||||
| chr2:131028658
|
A | G | 134 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0015others(131): Show | 134 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(131): Show |
intron_variant | MODIFIER | c.4125+574A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131028658 | ||||||
| chr2:131028742
|
T | G | 21 | a0001c0001t0002g0058a0001c0014t0002g0075a0001c0015t0001g0078others(18): Show | 21 | HG01175.hp2 HG01884.hp2 HG02622.hp2 others(18): Show |
intron_variant | MODIFIER | c.4125+658T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131028742 | ||||||
| chr2:131028744
|
T | G | 21 | a0001c0001t0002g0058a0001c0014t0002g0075a0001c0015t0001g0078others(18): Show | 21 | HG01175.hp2 HG01884.hp2 HG02622.hp2 others(18): Show |
intron_variant | MODIFIER | c.4125+660T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131028744 | ||||||
| chr2:131028752
|
C | T | 2 | a0002c0011t0005g0054a0003c0031t0006g0037 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4125+668C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131028752 | ||||||
| chr2:131028815
|
T | C | 132 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0015others(129): Show | 132 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.4125+731T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131028815 | ||||||
| chr2:131028945
|
G | T | 85 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(82): Show | 85 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.4125+861G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131028945 | ||||||
| chr2:131029037
|
CTAGA | C | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0007c0013t0002g0095 | 3 | HG01175.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.4125+954_4125+957d others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029037 | ||||||
| chr2:131029042
|
G | A | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0007c0013t0002g0095 | 3 | HG01175.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.4125+958G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029042 | ||||||
| chr2:131029043
|
G | T | 3 | a0001c0014t0002g0075a0001c0018t0002g0105a0007c0013t0002g0095 | 3 | HG01175.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.4125+959G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029043 | ||||||
| chr2:131029082
|
C | T | 4 | a0001c0001t0001g0115a0002c0010t0001g0003a0003c0003t0001g0081others(1): Show | 4 | HG00621.hp1 HG01975.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4125+998C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029082 | ||||||
| chr2:131029096
|
C | CA | 2 | a0001c0001t0001g0126a0001c0001t0008g0048 | 2 | HG01884.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.4125+1013dupA | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 131029096 | |||||
| chr2:131029096
|
C | T | 7 | a0002c0011t0001g0132a0002c0011t0001g0133a0002c0011t0001g0134others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.4125+1012C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029096 | ||||||
| chr2:131029172
|
C | A | 5 | a0003c0003t0001g0081a0005c0006t0003g0103a0007c0013t0003g0060others(2): Show | 5 | HG02723.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4125+1088C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029172 | ||||||
| chr2:131029314
|
G | A | 11 | a0001c0001t0002g0058a0002c0011t0001g0132a0002c0011t0001g0133others(8): Show | 11 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.4125+1230G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029314 | ||||||
| chr2:131029427
|
T | G | 8 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.4125+1343T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029427 | ||||||
| chr2:131029497
|
G | A | 1 | a0003c0003t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4125+1413G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029497 | ||||||
| chr2:131029551
|
C | CTTT | 11 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0005g0106others(8): Show | 11 | HG01884.hp2 HG02630.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.4125+1481_4125+148 others(7): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 131029551 | |||||
| chr2:131029551
|
C | CTTTTT | 5 | a0001c0001t0002g0058a0001c0014t0002g0075a0003c0003t0002g0116others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4125+1479_4125+148 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 131029551 | |||||
| chr2:131029551
|
CTTT | C | 83 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(80): Show | 83 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.4125+1481_4125+148 others(7): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 131029551 | |||||
| chr2:131029672
|
G | A | 1 | a0007c0013t0001g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4125+1588G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029672 | ||||||
| chr2:131029768
|
A | G | 106 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(103): Show | 106 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.4125+1684A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029768 | ||||||
| chr2:131029774
|
A | G | 85 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(82): Show | 85 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.4125+1690A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029774 | ||||||
| chr2:131029814
|
A | T | 1 | a0001c0001t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4125+1730A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029814 | ||||||
| chr2:131029834
|
G | A | 1 | a0001c0007t0004g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4125+1750G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029834 | ||||||
| chr2:131029867
|
C | T | 11 | a0001c0001t0002g0058a0002c0011t0001g0132a0002c0011t0001g0133others(8): Show | 11 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.4125+1783C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029867 | ||||||
| chr2:131029904
|
G | A | 16 | a0001c0001t0002g0058a0001c0015t0001g0078a0001c0015t0001g0079others(13): Show | 16 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.4125+1820G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029904 | ||||||
| chr2:131029940
|
G | A | 1 | a0004c0020t0001g0028 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4125+1856G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029940 | ||||||
| chr2:131029968
|
G | A | 85 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(82): Show | 85 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.4125+1884G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131029968 | ||||||
| chr2:131030056
|
A | G | 85 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(82): Show | 85 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.4125+1972A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131030056 | ||||||
| chr2:131030242
|
G | GT | 85 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(82): Show | 85 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.4125+2165dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 131030242 | |||||
| chr2:131030385
|
G | C | 1 | a0001c0034t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4125+2301G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131030385 | ||||||
| chr2:131030445
|
G | A | 85 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(82): Show | 85 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.4125+2361G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131030445 | ||||||
| chr2:131030496
|
G | A | 3 | a0006c0005t0003g0140a0013c0016t0003g0001a0013c0016t0003g0002 | 3 | HG02559.hp2 HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4125+2412G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131030496 | ||||||
| chr2:131030847
|
C | T | 4 | a0001c0015t0001g0078a0001c0015t0001g0079a0002c0028t0001g0073others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4125+2763C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131030847 | ||||||
| chr2:131030853
|
A | G | 85 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(82): Show | 85 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.4125+2769A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131030853 | ||||||
| chr2:131031167
|
G | A | 1 | a0001c0002t0001g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4125+3083G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131031167 | ||||||
| chr2:131031242
|
C | T | 6 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4125+3158C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131031242 | ||||||
| chr2:131031251
|
G | T | 6 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4125+3167G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131031251 | ||||||
| chr2:131031260
|
C | G | 5 | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0005g0106others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.4125+3176C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131031260 | ||||||
| chr2:131031396
|
C | T | 16 | a0001c0014t0001g0036a0001c0025t0005g0067a0001c0027t0001g0107others(13): Show | 16 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.4125+3312C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131031396 | ||||||
| chr2:131031705
|
C | T | 1 | a0001c0027t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4125+3621C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131031705 | ||||||
| chr2:131031811
|
T | C | 16 | a0001c0014t0001g0036a0001c0025t0005g0067a0001c0027t0001g0107others(13): Show | 16 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.4125+3727T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131031811 | ||||||
| chr2:131031918
|
C | T | 7 | a0002c0011t0001g0132a0002c0011t0001g0133a0002c0011t0001g0134others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.4125+3834C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131031918 | ||||||
| chr2:131031981
|
C | T | 16 | a0001c0014t0001g0036a0001c0025t0005g0067a0001c0027t0001g0107others(13): Show | 16 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.4125+3897C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131031981 | ||||||
| chr2:131032014
|
G | A | 1 | a0001c0002t0001g0010 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4125+3930G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032014 | ||||||
| chr2:131032057
|
C | T | 5 | a0003c0003t0001g0081a0005c0006t0003g0103a0007c0013t0003g0060others(2): Show | 5 | HG02723.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4125+3973C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032057 | ||||||
| chr2:131032173
|
G | A | 2 | a0002c0011t0005g0054a0003c0031t0006g0037 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4125+4089G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032173 | ||||||
| chr2:131032215
|
G | T | 16 | a0001c0014t0001g0036a0001c0025t0005g0067a0001c0027t0001g0107others(13): Show | 16 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.4125+4131G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032215 | ||||||
| chr2:131032231
|
C | G | 16 | a0001c0014t0001g0036a0001c0025t0005g0067a0001c0027t0001g0107others(13): Show | 16 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.4125+4147C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032231 | ||||||
| chr2:131032290
|
C | T | 16 | a0001c0014t0001g0036a0001c0025t0005g0067a0001c0027t0001g0107others(13): Show | 16 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.4125+4206C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032290 | ||||||
| chr2:131032460
|
G | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0035others(9): Show | 12 | HG02698.hp1 HG02895.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.4125+4376G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032460 | ||||||
| chr2:131032547
|
G | A | 16 | a0001c0014t0001g0036a0001c0025t0005g0067a0001c0027t0001g0107others(13): Show | 16 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.4125+4463G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032547 | ||||||
| chr2:131032596
|
G | A | 6 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4125+4512G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032596 | ||||||
| chr2:131032822
|
C | CTTTCTTT others(10): Show |
14 | a0001c0014t0001g0036a0001c0025t0005g0067a0001c0027t0001g0107others(11): Show | 14 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.4125+4746_4125+474 others(21): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 131032822 | |||||
| chr2:131032822
|
C | CTTTCTTT others(15): Show |
1 | a0003c0003t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4125+4746_4125+474 others(26): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 131032822 | |||||
| chr2:131032822
|
CTTTCT | C | 2 | a0002c0011t0005g0054a0003c0031t0006g0037 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4125+4757_4125+476 others(9): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 131032822 | |||||
| chr2:131032848
|
C | CT | 9 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0002t0001g0013others(6): Show | 9 | HG02698.hp1 HG02965.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.4125+4786dupT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 131032848 | |||||
| chr2:131032848
|
C | CTT | 5 | a0001c0001t0001g0009a0001c0014t0002g0075a0001c0018t0002g0105others(2): Show | 5 | HG02647.hp2 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4125+4785_4125+478 others(6): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 131032848 | |||||
| chr2:131032848
|
CT | C | 30 | a0001c0001t0002g0058a0001c0002t0001g0031a0001c0015t0001g0078others(27): Show | 30 | HG01243.hp2 HG01884.hp2 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.4125+4786delT | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 131032848 | |||||
| chr2:131032854
|
T | C | 57 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(54): Show | 57 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.4125+4770T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032854 | ||||||
| chr2:131032854
|
T | TC | 11 | a0001c0001t0001g0035a0001c0025t0005g0067a0002c0048t0001g0070others(8): Show | 11 | HG00735.hp2 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.4125+4770_4125+477 others(5): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032854 | ||||||
| chr2:131032855
|
T | C | 34 | a0001c0001t0002g0058a0001c0002t0001g0031a0001c0014t0001g0036others(31): Show | 34 | HG01109.hp2 HG01243.hp2 HG01258.hp2 others(31): Show |
intron_variant | MODIFIER | c.4125+4771T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032855 | ||||||
| chr2:131032914
|
A | G | 120 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(117): Show | 120 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.4125+4830A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032914 | ||||||
| chr2:131032916
|
A | C | 1 | a0001c0014t0001g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4125+4832A>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032916 | ||||||
| chr2:131032980
|
G | A | 2 | a0002c0011t0005g0054a0003c0031t0006g0037 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4125+4896G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131032980 | ||||||
| chr2:131033001
|
T | C | 121 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(118): Show | 121 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.4125+4917T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131033001 | ||||||
| chr2:131033073
|
G | A | 85 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(82): Show | 85 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.4125+4989G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131033073 | ||||||
| chr2:131033111
|
G | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0025others(70): Show | 73 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.4125+5027G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131033111 | ||||||
| chr2:131033226
|
G | A | 49 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0033others(46): Show | 49 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.4125+5142G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131033226 | ||||||
| chr2:131033716
|
C | G | 18 | a0001c0014t0001g0036a0001c0014t0002g0075a0001c0018t0002g0105others(15): Show | 18 | HG00735.hp2 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.4126-5137C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131033716 | ||||||
| chr2:131033719
|
A | G | 2 | a0001c0007t0004g0090a0001c0007t0004g0092 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.4126-5134A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131033719 | ||||||
| chr2:131033839
|
C | T | 6 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4126-5014C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131033839 | ||||||
| chr2:131033872
|
C | T | 7 | a0002c0011t0001g0132a0002c0011t0001g0133a0002c0011t0001g0134others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.4126-4981C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131033872 | ||||||
| chr2:131034152
|
A | T | 16 | a0001c0001t0002g0058a0001c0014t0001g0120a0001c0018t0005g0106others(13): Show | 16 | HG01175.hp2 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.4126-4701A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131034152 | ||||||
| chr2:131034165
|
G | A | 1 | a0003c0003t0001g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4126-4688G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131034165 | ||||||
| chr2:131034279
|
C | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4126-4574C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131034279 | ||||||
| chr2:131034525
|
G | A | 45 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(42): Show | 45 | HG00642.hp1 HG01109.hp2 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.4126-4328G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131034525 | ||||||
| chr2:131034571
|
A | G | 118 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(115): Show | 118 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.4126-4282A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131034571 | ||||||
| chr2:131034805
|
T | G | 7 | a0001c0014t0001g0036a0001c0014t0001g0120a0001c0027t0001g0107others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.4126-4048T>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131034805 | ||||||
| chr2:131034835
|
G | T | 1 | a0001c0025t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4126-4018G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131034835 | ||||||
| chr2:131035085
|
G | A | 4 | a0005c0008t0001g0007a0005c0008t0001g0098a0009c0021t0001g0130others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4126-3768G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131035085 | ||||||
| chr2:131035105
|
C | A | 2 | a0005c0008t0001g0007a0009c0021t0001g0130 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.4126-3748C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131035105 | ||||||
| chr2:131035337
|
C | G | 1 | a0001c0001t0001g0040 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4126-3516C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131035337 | ||||||
| chr2:131035393
|
T | C | 1 | a0003c0003t0001g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4126-3460T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131035393 | ||||||
| chr2:131035462
|
C | T | 7 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.4126-3391C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131035462 | ||||||
| chr2:131035673
|
A | G | 6 | a0001c0014t0001g0036a0001c0025t0005g0067a0001c0027t0001g0107others(3): Show | 6 | HG00735.hp2 HG01243.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.4126-3180A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131035673 | ||||||
| chr2:131035734
|
C | T | 1 | a0025c0024t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4126-3119C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131035734 | ||||||
| chr2:131035831
|
C | T | 1 | a0001c0039t0001g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4126-3022C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131035831 | ||||||
| chr2:131035952
|
C | G | 1 | a0001c0044t0001g0011 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4126-2901C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131035952 | ||||||
| chr2:131035996
|
T | C | 1 | a0006c0005t0001g0143 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4126-2857T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131035996 | ||||||
| chr2:131036025
|
A | G | 3 | a0012c0019t0001g0127a0012c0019t0001g0129a0019c0036t0001g0049 | 3 | NA18948.hp1 NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.4126-2828A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131036025 | ||||||
| chr2:131036158
|
A | G | 1 | a0001c0001t0008g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4126-2695A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131036158 | ||||||
| chr2:131036320
|
C | T | 49 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(46): Show | 49 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.4126-2533C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131036320 | ||||||
| chr2:131036334
|
T | A | 7 | a0001c0001t0002g0058a0001c0014t0002g0075a0001c0018t0002g0105others(4): Show | 7 | HG01175.hp2 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.4126-2519T>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131036334 | ||||||
| chr2:131036632
|
A | G | 51 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(48): Show | 51 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.4126-2221A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131036632 | ||||||
| chr2:131036636
|
G | A | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4126-2217G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131036636 | ||||||
| chr2:131036691
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4126-2162G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131036691 | ||||||
| chr2:131036857
|
A | G | 51 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(48): Show | 51 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.4126-1996A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131036857 | ||||||
| chr2:131037040
|
G | C | 3 | a0012c0019t0001g0127a0012c0019t0001g0129a0019c0036t0001g0049 | 3 | NA18948.hp1 NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.4126-1813G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131037040 | ||||||
| chr2:131037122
|
A | G | 52 | a0001c0001t0001g0009a0001c0001t0002g0058a0001c0002t0001g0010others(49): Show | 52 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.4126-1731A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131037122 | ||||||
| chr2:131037178
|
C | T | 1 | a0004c0004t0007g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4126-1675C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131037178 | ||||||
| chr2:131037235
|
A | T | 52 | a0001c0001t0001g0009a0001c0001t0002g0058a0001c0002t0001g0010others(49): Show | 52 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.4126-1618A>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131037235 | ||||||
| chr2:131037243
|
G | A | 1 | a0023c0029t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4126-1610G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131037243 | ||||||
| chr2:131037697
|
G | C | 1 | a0009c0046t0009g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4126-1156G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131037697 | ||||||
| chr2:131037772
|
G | A | 31 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0020others(28): Show | 31 | HG00642.hp1 HG01243.hp2 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.4126-1081G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131037772 | ||||||
| chr2:131037860
|
GC | G | 34 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0020others(31): Show | 34 | HG00642.hp1 HG01243.hp2 HG01515.hp2 others(31): Show |
intron_variant | MODIFIER | c.4126-992delC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131037860 | ||||||
| chr2:131038051
|
G | A | 32 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0020others(29): Show | 32 | HG00642.hp1 HG01243.hp2 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.4126-802G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131038051 | ||||||
| chr2:131038317
|
C | A | 3 | a0001c0015t0001g0078a0001c0015t0001g0079a0002c0028t0001g0073 | 3 | HG02896.hp1 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4126-536C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131038317 | ||||||
| chr2:131038431
|
C | CCCAGCCT others(22): Show |
7 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.4126-422_4126-421i others(31): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131038431 | ||||||
| chr2:131038497
|
G | T | 1 | a0001c0001t0001g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4126-356G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131038497 | ||||||
| chr2:131038683
|
T | C | 57 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(54): Show | 57 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.4126-170T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131038683 | ||||||
| chr2:131038759
|
C | G | 1 | a0010c0009t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4126-94C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131038759 | ||||||
| chr2:131038836
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4126-17C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | chr2 | 131038836 | ||||||
| chr2:131039199
|
T | C | 6 | a0003c0003t0003g0112a0005c0006t0003g0103a0006c0005t0003g0140others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.4305+167T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 6/13 | chr2 | 131039199 | ||||||
| chr2:131039735
|
C | G | 55 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(52): Show | 55 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.4306-281C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 6/13 | chr2 | 131039735 | ||||||
| chr2:131039794
|
A | G | 54 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(51): Show | 54 | HG00642.hp1 HG01175.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.4306-222A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 6/13 | chr2 | 131039794 | ||||||
| chr2:131039871
|
G | C | 33 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0020others(30): Show | 33 | HG00642.hp1 HG01243.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.4306-145G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 6/13 | chr2 | 131039871 | ||||||
| chr2:131039911
|
A | G | 57 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(54): Show | 57 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.4306-105A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 6/13 | chr2 | 131039911 | ||||||
| chr2:131039916
|
C | A | 7 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.4306-100C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 6/13 | chr2 | 131039916 | ||||||
| chr2:131039936
|
G | T | 1 | a0002c0048t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4306-80G>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 6/13 | chr2 | 131039936 | ||||||
| chr2:131040874
|
G | A | 20 | a0001c0001t0002g0058a0001c0007t0004g0089a0001c0007t0004g0090others(17): Show | 20 | HG01175.hp2 HG01257.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.4663-356G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 8/13 | chr2 | 131040874 | ||||||
| chr2:131040936
|
A | AC | 57 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(54): Show | 57 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.4663-289dupC | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 131040936 | |||||
| chr2:131040944
|
C | A | 33 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0020others(30): Show | 33 | HG00642.hp1 HG01243.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.4663-286C>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 8/13 | chr2 | 131040944 | ||||||
| chr2:131041164
|
C | G | 55 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(52): Show | 55 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.4663-66C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 8/13 | chr2 | 131041164 | ||||||
| chr2:131041212
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4663-18T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 8/13 | chr2 | 131041212 | ||||||
| chr2:131041496
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4895+34G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 9/13 | chr2 | 131041496 | ||||||
| chr2:131041952
|
C | T | 7 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.5025+8C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 10/13 | chr2 | 131041952 | ||||||
| chr2:131041990
|
C | T | 55 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(52): Show | 55 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.5025+46C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 10/13 | chr2 | 131041990 | ||||||
| chr2:131042129
|
C | T | 3 | a0001c0015t0001g0078a0001c0015t0001g0079a0002c0028t0001g0073 | 3 | HG02896.hp1 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.5025+185C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 10/13 | chr2 | 131042129 | ||||||
| chr2:131042213
|
A | G | 1 | a0001c0045t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5025+269A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 10/13 | chr2 | 131042213 | ||||||
| chr2:131042779
|
C | G | 1 | a0017c0051t0006g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5026-673C>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 10/13 | chr2 | 131042779 | ||||||
| chr2:131042789
|
G | A | 6 | a0003c0003t0003g0112a0005c0006t0003g0103a0006c0005t0003g0140others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5026-663G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 10/13 | chr2 | 131042789 | ||||||
| chr2:131043020
|
T | C | 56 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(53): Show | 56 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.5026-432T>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 10/13 | chr2 | 131043020 | ||||||
| chr2:131043115
|
C | CTAAAA | 25 | a0001c0001t0002g0058a0001c0007t0004g0089a0001c0007t0004g0090others(22): Show | 25 | HG01175.hp2 HG01243.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.5026-335_5026-334i others(7): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 131043115 | |||||
| chr2:131043116
|
T | TAAAAC | 31 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0020others(28): Show | 31 | HG00642.hp1 HG01243.hp2 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.5026-335_5026-334i others(7): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 131043116 | |||||
| chr2:131043194
|
A | G | 3 | a0001c0025t0005g0067a0002c0011t0005g0054a0006c0005t0005g0119 | 3 | HG01243.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5026-258A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 10/13 | chr2 | 131043194 | ||||||
| chr2:131043370
|
G | C | 56 | a0001c0001t0002g0058a0001c0002t0001g0010a0001c0002t0001g0013others(53): Show | 56 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.5026-82G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 10/13 | chr2 | 131043370 | ||||||
| chr2:131043713
|
GGGCTGGG others(21): Show |
G | 32 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0020others(29): Show | 32 | HG00642.hp1 HG01243.hp2 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.5157+132_5157+159d others(30): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 131043713 | |||||
| chr2:131043742
|
G | A | 3 | a0003c0003t0001g0081a0007c0017t0001g0109a0010c0009t0001g0138 | 3 | HG02258.hp1 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5157+159G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 11/13 | chr2 | 131043742 | ||||||
| chr2:131043792
|
G | A | 1 | a0003c0031t0006g0037 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5157+209G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 11/13 | chr2 | 131043792 | ||||||
| chr2:131043843
|
A | G | 1 | a0001c0002t0001g0038 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.5157+260A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 11/13 | chr2 | 131043843 | ||||||
| chr2:131043893
|
C | T | 5 | a0001c0001t0002g0058a0003c0003t0002g0116a0003c0003t0002g0117others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5157+310C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 11/13 | chr2 | 131043893 | ||||||
| chr2:131044175
|
G | C | 10 | a0001c0026t0001g0080a0001c0045t0001g0085a0002c0041t0001g0053others(7): Show | 10 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.5158-124G>C | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 11/13 | chr2 | 131044175 | ||||||
| chr2:131044590
|
G | A | 2 | a0001c0018t0005g0106a0009c0047t0001g0110 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5401+48G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 12/13 | chr2 | 131044590 | ||||||
| chr2:131044683
|
CCA | C | 21 | a0001c0001t0002g0058a0001c0007t0004g0089a0001c0007t0004g0090others(18): Show | 21 | HG01175.hp2 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.5401+142_5401+143d others(4): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 12/13 | chr2 | 131044683 | ||||||
| chr2:131044758
|
C | T | 1 | a0001c0018t0005g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5401+216C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 12/13 | chr2 | 131044758 | ||||||
| chr2:131044759
|
G | A | 32 | a0001c0002t0001g0010a0001c0002t0001g0013a0001c0002t0001g0020others(29): Show | 32 | HG00642.hp1 HG01243.hp2 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.5401+217G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 12/13 | chr2 | 131044759 | ||||||
| chr2:131044904
|
G | A | 1 | a0003c0003t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5401+362G>A | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 12/13 | chr2 | 131044904 | ||||||
| chr2:131045034
|
A | G | 11 | a0001c0001t0002g0058a0001c0014t0002g0075a0001c0015t0001g0078others(8): Show | 11 | HG01175.hp2 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.5402-335A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 12/13 | chr2 | 131045034 | ||||||
| chr2:131045089
|
A | G | 6 | a0003c0003t0003g0112a0005c0006t0003g0103a0006c0005t0003g0140others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5402-280A>G | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 12/13 | chr2 | 131045089 | ||||||
| chr2:131045136
|
C | T | 7 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.5402-233C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 12/13 | chr2 | 131045136 | ||||||
| chr2:131045189
|
C | T | 17 | a0001c0001t0002g0058a0001c0014t0002g0075a0001c0015t0001g0078others(14): Show | 17 | HG01175.hp2 HG02257.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.5402-180C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 12/13 | chr2 | 131045189 | ||||||
| chr2:131045619
|
C | T | 8 | a0001c0007t0004g0089a0001c0007t0004g0090a0001c0007t0004g0091others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.5479+173C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 13/13 | chr2 | 131045619 | ||||||
| chr2:131045788
|
C | T | 6 | a0003c0003t0003g0112a0005c0006t0003g0103a0006c0005t0003g0140others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5480-250C>T | ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 13/13 | chr2 | 131045788 |