Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9826 |
|---|---|
| ensemblid | ENSG00000132694.19 |
| hgncid | 14580 |
| symbol | ARHGEF11 |
| name | Rho guanine nucleotide exchange factor 11 |
| refseq_nuc | NM_198236.3 |
| refseq_prot | NP_937879.1 |
| ensembl_nuc | ENST00000368194.8 |
| ensembl_prot | ENSP00000357177.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 156934840 |
| end | 157045742 |
| strand | - |
| ver | v1.2 |
| region | chr1:156934840-157045742 |
| region5000 | chr1:156929840-157050742 |
| regionname0 | ARHGEF11_chr1_156934840_157045742 |
| regionname5000 | ARHGEF11_chr1_156929840_157050742 |
| 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 | 1562 | 150 | 23 | 39 | 62 | 6 | 20 | 49 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002 | 0/0 | 1562 | 144 | 48 | 18 | 62 | 3 | 13 | 48 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0003 | 1/1 | 1562 | 59 | 12 | 10 | 22 | 5 | 8 | 17 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0004 | 0/0 | 1562 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0005 | 0/0 | 1562 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0006 | 0/0 | 1562 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0007 | 0/0 | 1562 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0008 | 0/0 | 1562 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0009 | 0/0 | 1562 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0010 | 0/0 | 1562 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| 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 | 4689 | 146 | 23 | 36 | 61 | 6 | 20 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0002 | 0/0 | 4689 | 86 | 13 | 12 | 51 | 3 | 7 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0003 | 1/1 | 4689 | 59 | 12 | 10 | 22 | 5 | 8 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0004 | 0/0 | 4689 | 57 | 35 | 6 | 11 | 0 | 5 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0005 | 0/0 | 4689 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0006 | 0/0 | 4689 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0007 | 0/0 | 4689 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0008 | 0/0 | 4689 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0009 | 0/0 | 4689 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0010 | 0/0 | 4689 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0011 | 0/0 | 4689 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0012 | 0/0 | 4689 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0013 | 0/0 | 4689 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| c0014 | 0/0 | 4689 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2573 | 76 | 3 | 18 | 44 | 3 | 8 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0002 | 0/0 | 2573 | 68 | 11 | 12 | 34 | 3 | 8 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0003 | 0/0 | 2573 | 53 | 8 | 9 | 26 | 3 | 7 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0004 | 0/0 | 2573 | 38 | 5 | 17 | 7 | 3 | 6 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0005 | 0/0 | 2573 | 28 | 14 | 2 | 9 | 0 | 3 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0006 | 1/1 | 2573 | 17 | 8 | 2 | 2 | 2 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0007 | 0/0 | 2573 | 9 | 0 | 1 | 1 | 0 | 7 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0008 | 0/0 | 2574 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0009 | 0/0 | 2573 | 6 | 0 | 4 | 0 | 0 | 2 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0010 | 0/0 | 2573 | 6 | 0 | 0 | 6 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0011 | 0/0 | 2573 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0012 | 0/0 | 2574 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0013 | 0/0 | 2574 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0014 | 0/0 | 2574 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0015 | 0/0 | 2574 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0016 | 0/0 | 2573 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0017 | 0/0 | 2573 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0018 | 0/0 | 2573 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0019 | 0/0 | 2572 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0020 | 0/0 | 2573 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0021 | 0/0 | 2575 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0022 | 0/0 | 2573 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0023 | 0/0 | 2573 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0024 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0025 | 0/0 | 2573 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0026 | 0/0 | 2575 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0027 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0028 | 0/0 | 2573 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0029 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0030 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0031 | 0/0 | 2573 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0032 | 0/0 | 2573 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0033 | 0/0 | 2573 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0034 | 0/0 | 2573 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0035 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| t0036 | 0/0 | 2573 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0017 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0106 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| 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 | 4689 | 146 | 23 | 36 | 61 | 6 | 20 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0005 | 0/0 | 4689 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0011 | 0/0 | 4689 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0002 | 0/0 | 4689 | 86 | 13 | 12 | 51 | 3 | 7 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004 | 0/0 | 4689 | 57 | 35 | 6 | 11 | 0 | 5 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0008 | 0/0 | 4689 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0003c0003 | 1/1 | 4689 | 59 | 12 | 10 | 22 | 5 | 8 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0004c0007 | 0/0 | 4689 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0005c0006 | 0/0 | 4689 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0006c0009 | 0/0 | 4689 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0007c0012 | 0/0 | 4689 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0008c0013 | 0/0 | 4689 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0009c0010 | 0/0 | 4689 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0010c0014 | 0/0 | 4689 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7261 | 73 | 3 | 16 | 43 | 3 | 8 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0003 | 0/0 | 7261 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0004 | 0/0 | 7261 | 37 | 5 | 16 | 7 | 3 | 6 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0006 | 0/0 | 7261 | 7 | 5 | 0 | 2 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0007 | 0/0 | 7261 | 8 | 0 | 1 | 1 | 0 | 6 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0010 | 0/0 | 7261 | 6 | 0 | 0 | 6 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0015 | 0/0 | 7262 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0020 | 0/0 | 7261 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0028 | 0/0 | 7261 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0030 | 0/0 | 7261 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0032 | 0/0 | 7261 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0034 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0035 | 0/0 | 7262 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0001t0036 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0005t0001 | 0/0 | 7261 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0001c0011t0004 | 0/0 | 7261 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0002t0002 | 0/0 | 7261 | 67 | 11 | 12 | 34 | 3 | 7 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0002t0011 | 0/0 | 7261 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0002t0012 | 0/0 | 7262 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0002t0016 | 0/0 | 7261 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0002t0017 | 0/0 | 7261 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0002t0023 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0002t0024 | 0/0 | 7261 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0002t0029 | 0/0 | 7262 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004t0005 | 0/0 | 7261 | 26 | 12 | 2 | 9 | 0 | 3 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004t0008 | 0/0 | 7262 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004t0009 | 0/0 | 7261 | 6 | 0 | 4 | 0 | 0 | 2 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004t0013 | 0/0 | 7262 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004t0014 | 0/0 | 7262 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004t0018 | 0/0 | 7261 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004t0021 | 0/0 | 7263 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004t0022 | 0/0 | 7261 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004t0025 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004t0026 | 0/0 | 7263 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004t0027 | 0/0 | 7261 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0004t0033 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0002c0008t0002 | 0/0 | 7261 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0003c0003t0003 | 0/0 | 7261 | 45 | 6 | 7 | 22 | 3 | 7 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0003c0003t0006 | 1/1 | 7261 | 10 | 3 | 2 | 0 | 2 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0003c0003t0019 | 0/0 | 7260 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0003c0003t0031 | 0/0 | 7261 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0004c0007t0003 | 0/0 | 7261 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0005c0006t0005 | 0/0 | 7261 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0006c0009t0003 | 0/0 | 7261 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0007c0012t0003 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0008c0013t0007 | 0/0 | 7261 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0009c0010t0003 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| a0010c0014t0014 | 0/0 | 7262 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | copy fasta | chr1 | 156929840 | 157050742 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0010g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0010g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0010g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0010g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0010g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0010g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0015g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0015g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0015g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0015g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0020g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0020g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0028g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0030g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0032g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0034g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0035g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0036g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0005t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0005t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0005t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0011t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0011g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0011g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0011g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0011g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0012g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0012g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0012g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0012g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0016g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0016g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0016g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0016g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0017g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0017g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0017g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0023g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0024g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0029g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0009g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0009g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0009g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0009g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0009g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0013g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0014g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0014g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0014g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0018g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0018g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0018g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0021g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0021g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0022g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0022g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0025g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0026g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0027g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0033g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0008t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0017 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0106 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0019g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0019g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0019g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0031g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0004c0007t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0004c0007t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0005c0006t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0005c0006t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0006c0009t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0007c0012t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0008c0013t0007g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0009c0010t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0010c0014t0014g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0006 | g0016 | EUR | GBR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0332 | EUR | GBR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0087 | EUR | FIN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00280 | hp2 | a0003 | c0003 | t0003 | g0230 | EUR | FIN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00323 | hp1 | a0003 | c0003 | t0003 | g0231 | EUR | FIN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0150 | EUR | FIN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00408 | hp2 | a0002 | c0004 | t0005 | g0128 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00438 | hp2 | a0003 | c0003 | t0003 | g0220 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00597 | hp1 | a0003 | c0003 | t0003 | g0233 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00609 | hp2 | a0002 | c0002 | t0012 | g0193 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00621 | hp2 | a0002 | c0004 | t0033 | g0285 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0167 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00639 | hp2 | a0003 | c0003 | t0003 | g0243 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00642 | hp1 | a0002 | c0004 | t0009 | g0116 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0039 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00741 | hp1 | a0002 | c0004 | t0005 | g0008 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0049 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0101 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0163 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01071 | hp1 | a0003 | c0003 | t0003 | g0216 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0100 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0089 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0180 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01167 | hp2 | a0003 | c0003 | t0003 | g0271 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01169 | hp2 | a0003 | c0003 | t0003 | g0270 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0050 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01192 | hp2 | a0003 | c0003 | t0031 | g0215 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0145 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0168 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01257 | hp1 | a0003 | c0003 | t0006 | g0011 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01257 | hp2 | a0002 | c0004 | t0009 | g0002 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01258 | hp1 | a0002 | c0004 | t0009 | g0002 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0162 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01346 | hp2 | a0002 | c0004 | t0009 | g0114 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0053 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01433 | hp2 | a0002 | c0004 | t0005 | g0018 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01496 | hp2 | a0003 | c0003 | t0006 | g0012 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0157 | EUR | IBS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01515 | hp2 | a0003 | c0003 | t0006 | g0013 | EUR | IBS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0158 | EUR | IBS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01517 | hp2 | a0003 | c0003 | t0003 | g0214 | EUR | IBS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01884 | hp1 | a0003 | c0003 | t0003 | g0212 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01891 | hp1 | a0002 | c0004 | t0005 | g0109 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0030 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01928 | hp1 | a0001 | c0001 | t0028 | g0184 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01928 | hp2 | a0001 | c0005 | t0001 | g0284 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01934 | hp2 | a0003 | c0003 | t0003 | g0269 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01943 | hp1 | a0001 | c0005 | t0001 | g0289 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0090 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01975 | hp2 | a0003 | c0003 | t0003 | g0227 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01978 | hp1 | a0003 | c0003 | t0003 | g0267 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0166 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02004 | hp1 | a0001 | c0001 | t0032 | g0258 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0139 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02015 | hp1 | a0002 | c0004 | t0005 | g0052 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02055 | hp1 | a0005 | c0006 | t0005 | g0022 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02055 | hp2 | a0003 | c0003 | t0003 | g0266 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02071 | hp2 | a0001 | c0001 | t0007 | g0146 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0134 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02083 | hp1 | a0001 | c0001 | t0036 | g0357 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0088 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02132 | hp1 | a0003 | c0003 | t0003 | g0253 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02135 | hp1 | a0003 | c0003 | t0003 | g0252 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02145 | hp1 | a0002 | c0004 | t0027 | g0173 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02145 | hp2 | a0002 | c0004 | t0013 | g0190 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0179 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02257 | hp1 | a0002 | c0004 | t0018 | g0250 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02257 | hp2 | a0005 | c0006 | t0005 | g0023 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02258 | hp2 | a0002 | c0004 | t0008 | g0196 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0164 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02280 | hp1 | a0002 | c0004 | t0008 | g0198 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02280 | hp2 | a0002 | c0004 | t0005 | g0015 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02300 | hp1 | a0001 | c0011 | t0004 | g0165 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02300 | hp2 | a0006 | c0009 | t0003 | g0219 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0028 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02451 | hp2 | a0003 | c0003 | t0003 | g0251 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02523 | hp1 | a0003 | c0003 | t0003 | g0224 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02572 | hp1 | a0002 | c0004 | t0021 | g0175 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02572 | hp2 | a0003 | c0003 | t0019 | g0359 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0148 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0079 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02615 | hp2 | a0001 | c0001 | t0030 | g0209 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02622 | hp1 | a0002 | c0002 | t0024 | g0004 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02622 | hp2 | a0003 | c0003 | t0019 | g0358 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02630 | hp1 | a0002 | c0004 | t0008 | g0199 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02630 | hp2 | a0002 | c0004 | t0005 | g0007 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02647 | hp2 | a0002 | c0004 | t0008 | g0200 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02683 | hp1 | a0003 | c0003 | t0003 | g0226 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02683 | hp2 | a0002 | c0004 | t0005 | g0021 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0055 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02723 | hp1 | a0003 | c0003 | t0003 | g0247 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0125 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02735 | hp1 | a0003 | c0003 | t0003 | g0225 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02735 | hp2 | a0002 | c0008 | t0002 | g0063 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02738 | hp1 | a0002 | c0004 | t0005 | g0126 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0143 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0122 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02809 | hp2 | a0001 | c0001 | t0020 | g0170 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0038 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0169 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02895 | hp1 | a0002 | c0004 | t0005 | g0024 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0112 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02896 | hp1 | a0001 | c0001 | t0015 | g0202 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02896 | hp2 | a0002 | c0004 | t0022 | g0132 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02897 | hp1 | a0001 | c0001 | t0015 | g0201 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02897 | hp2 | a0002 | c0004 | t0005 | g0025 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0123 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02922 | hp2 | a0002 | c0004 | t0014 | g0206 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0036 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02965 | hp2 | a0003 | c0003 | t0003 | g0248 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02976 | hp1 | a0002 | c0004 | t0005 | g0009 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02976 | hp2 | a0002 | c0004 | t0013 | g0185 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03041 | hp1 | a0003 | c0003 | t0006 | g0027 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03098 | hp1 | a0010 | c0014 | t0014 | g0205 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03130 | hp2 | a0002 | c0004 | t0005 | g0014 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03139 | hp1 | a0002 | c0004 | t0005 | g0006 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03139 | hp2 | a0002 | c0004 | t0021 | g0174 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03195 | hp1 | a0002 | c0004 | t0013 | g0186 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0094 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03209 | hp2 | a0002 | c0004 | t0005 | g0105 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03225 | hp1 | a0003 | c0003 | t0006 | g0026 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03225 | hp2 | a0002 | c0004 | t0008 | g0197 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03239 | hp1 | a0003 | c0003 | t0003 | g0228 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03453 | hp2 | a0002 | c0004 | t0008 | g0194 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0204 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0033 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03490 | hp1 | a0003 | c0003 | t0003 | g0229 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0153 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0154 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03540 | hp1 | a0002 | c0004 | t0013 | g0189 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03540 | hp2 | a0001 | c0001 | t0015 | g0208 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03654 | hp1 | a0003 | c0003 | t0003 | g0245 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0044 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03669 | hp2 | a0008 | c0013 | t0007 | g0144 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0103 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03704 | hp2 | a0002 | c0004 | t0009 | g0118 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0095 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0056 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0147 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03942 | hp1 | a0003 | c0003 | t0003 | g0241 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0176 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04115 | hp1 | a0001 | c0001 | t0007 | g0142 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0082 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04184 | hp1 | a0002 | c0004 | t0009 | g0115 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0149 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0151 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04199 | hp2 | a0003 | c0003 | t0006 | g0069 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04204 | hp2 | a0002 | c0004 | t0005 | g0119 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0040 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0140 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0124 | AFR | YRI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18522 | hp2 | a0002 | c0004 | t0005 | g0107 | AFR | YRI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | CHB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18906 | hp1 | a0002 | c0004 | t0014 | g0207 | AFR | YRI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | YRI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18943 | hp1 | a0002 | c0004 | t0005 | g0111 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18943 | hp2 | a0002 | c0002 | t0012 | g0191 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18944 | hp2 | a0002 | c0002 | t0016 | g0256 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18948 | hp1 | a0002 | c0002 | t0012 | g0187 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18948 | hp2 | a0003 | c0003 | t0003 | g0268 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0110 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18952 | hp2 | a0002 | c0002 | t0017 | g0045 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18960 | hp1 | a0003 | c0003 | t0003 | g0260 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18960 | hp2 | a0002 | c0002 | t0011 | g0075 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18963 | hp2 | a0003 | c0003 | t0003 | g0222 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18964 | hp2 | a0002 | c0004 | t0005 | g0113 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18966 | hp1 | a0001 | c0001 | t0010 | g0353 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18966 | hp2 | a0002 | c0002 | t0023 | g0003 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18967 | hp2 | a0007 | c0012 | t0003 | g0242 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18968 | hp1 | a0002 | c0002 | t0017 | g0093 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18968 | hp2 | a0003 | c0003 | t0003 | g0262 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18979 | hp1 | a0003 | c0003 | t0003 | g0221 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18981 | hp2 | a0003 | c0003 | t0003 | g0264 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18987 | hp1 | a0002 | c0004 | t0005 | g0120 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18987 | hp2 | a0001 | c0001 | t0034 | g0349 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18988 | hp2 | a0002 | c0002 | t0016 | g0235 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18994 | hp2 | a0001 | c0001 | t0010 | g0350 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18995 | hp2 | a0004 | c0007 | t0003 | g0254 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18997 | hp1 | a0004 | c0007 | t0003 | g0255 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18997 | hp2 | a0001 | c0001 | t0010 | g0355 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18998 | hp1 | a0003 | c0003 | t0003 | g0217 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18998 | hp2 | a0002 | c0002 | t0011 | g0074 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19000 | hp2 | a0001 | c0001 | t0010 | g0354 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19002 | hp1 | a0002 | c0002 | t0011 | g0078 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19002 | hp2 | a0002 | c0004 | t0025 | g0121 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19004 | hp1 | a0003 | c0003 | t0003 | g0218 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19004 | hp2 | a0002 | c0002 | t0017 | g0091 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19005 | hp2 | a0003 | c0003 | t0003 | g0239 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19010 | hp1 | a0003 | c0003 | t0003 | g0259 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19010 | hp2 | a0002 | c0002 | t0012 | g0192 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19011 | hp1 | a0003 | c0003 | t0003 | g0237 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19011 | hp2 | a0001 | c0001 | t0010 | g0352 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19030 | hp1 | a0002 | c0004 | t0022 | g0131 | AFR | LWK | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19030 | hp2 | a0003 | c0003 | t0019 | g0360 | AFR | LWK | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19043 | hp1 | a0002 | c0004 | t0008 | g0195 | AFR | LWK | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | LWK | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19055 | hp2 | a0001 | c0005 | t0001 | g0281 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19056 | hp1 | a0002 | c0002 | t0011 | g0077 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19056 | hp2 | a0003 | c0003 | t0003 | g0238 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19060 | hp2 | a0002 | c0002 | t0016 | g0257 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19063 | hp1 | a0003 | c0003 | t0003 | g0263 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19064 | hp1 | a0003 | c0003 | t0003 | g0240 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19068 | hp1 | a0002 | c0002 | t0011 | g0076 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19068 | hp2 | a0002 | c0004 | t0005 | g0117 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19070 | hp2 | a0002 | c0002 | t0016 | g0236 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19074 | hp2 | a0003 | c0003 | t0003 | g0223 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19078 | hp1 | a0003 | c0003 | t0003 | g0265 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19080 | hp2 | a0001 | c0001 | t0010 | g0351 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19083 | hp2 | a0002 | c0004 | t0005 | g0129 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19084 | hp1 | a0002 | c0004 | t0005 | g0054 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19085 | hp1 | a0009 | c0010 | t0003 | g0234 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19087 | hp1 | a0002 | c0004 | t0005 | g0127 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19090 | hp1 | a0003 | c0003 | t0003 | g0261 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19240 | hp1 | a0001 | c0001 | t0035 | g0356 | AFR | YRI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19240 | hp2 | a0002 | c0004 | t0005 | g0019 | AFR | YRI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20129 | hp1 | a0003 | c0003 | t0006 | g0010 | AFR | ASW | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20129 | hp2 | a0002 | c0004 | t0026 | g0108 | AFR | ASW | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0104 | EUR | TSI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0299 | EUR | TSI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0048 | EUR | TSI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | TSI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20905 | hp1 | a0003 | c0003 | t0003 | g0244 | SAS | GIH | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0141 | SAS | GIH | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0102 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02109 | hp1 | a0003 | c0003 | t0003 | g0232 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02109 | hp2 | a0002 | c0004 | t0005 | g0020 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02486 | hp1 | a0002 | c0004 | t0018 | g0249 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02486 | hp2 | a0002 | c0002 | t0029 | g0188 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03471 | hp1 | a0002 | c0004 | t0014 | g0203 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG06807 | hp1 | a0002 | c0004 | t0018 | g0246 | AFR | USA | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | USA | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0006 | g0017 | REF | REF | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0006 | g0106 | REF | REF | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156937289
|
T | C | 5 | a0001a0002a0005others(2): Show | 298 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(295): Show |
missense_variant | MODERATE | c.4400A>G | p.His1467Arg | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/41 | 5812/7261 | 4400/4689 | 1467/1562 | chr1 | 156937289 | ||
| chr1:156937323
|
T | C | 2 | a0001a0008 | 151 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(148): Show |
missense_variant | MODERATE | c.4366A>G | p.Ser1456Gly | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/41 | 5778/7261 | 4366/4689 | 1456/1562 | chr1 | 156937323 | ||
| chr1:156937340
|
G | A | 1 | a0007 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.4349C>T | p.Pro1450Leu | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/41 | 5761/7261 | 4349/4689 | 1450/1562 | chr1 | 156937340 | ||
| chr1:156939704
|
G | A | 1 | a0008 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.3940C>T | p.Arg1314Trp | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/41 | 5352/7261 | 3940/4689 | 1314/1562 | chr1 | 156939704 | ||
| chr1:156939892
|
A | C | 1 | a0009 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.3752T>G | p.Leu1251Arg | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/41 | 5164/7261 | 3752/4689 | 1251/1562 | chr1 | 156939892 | ||
| chr1:156941907
|
G | A | 1 | a0005 | 2 | HG02055.hp1 HG02257.hp2 |
missense_variant | MODERATE | c.3409C>T | p.Pro1137Ser | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/41 | 4821/7261 | 3409/4689 | 1137/1562 | chr1 | 156941907 | ||
| chr1:156941926
|
C | T | 1 | a0006 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.3390G>A | p.Met1130Ile | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/41 | 4802/7261 | 3390/4689 | 1130/1562 | chr1 | 156941926 | ||
| chr1:156948185
|
G | A | 1 | a0004 | 2 | NA18995.hp2 NA18997.hp1 |
missense_variant | MODERATE | c.2149C>T | p.Arg717Cys | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 24/41 | 3561/7261 | 2149/4689 | 717/1562 | chr1 | 156948185 | ||
| chr1:156969356
|
G | A | 1 | a0010 | 1 | HG03098.hp1 | missense_variant&splice_region_variant | MODERATE | c.751C>T | p.Arg251Trp | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/41 | 2163/7261 | 751/4689 | 251/1562 | chr1 | 156969356 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156936940
|
C | T | 1 | a0001c0011 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.4506G>A | p.Thr1502Thr | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/41 | 5918/7261 | 4506/4689 | 1502/1562 | chr1 | 156936940 | ||
| chr1:156939903
|
G | A | 2 | a0002c0002a0002c0008 | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
synonymous_variant | LOW | c.3741C>T | p.Asn1247Asn | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/41 | 5153/7261 | 3741/4689 | 1247/1562 | chr1 | 156939903 | ||
| chr1:156968104
|
C | T | 1 | a0002c0008 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.846G>A | p.Ser282Ser | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/41 | 2258/7261 | 846/4689 | 282/1562 | chr1 | 156968104 | ||
| chr1:156984427
|
T | C | 1 | a0001c0005 | 3 | HG01928.hp2 HG01943.hp1 NA19055.hp2 |
synonymous_variant | LOW | c.135A>G | p.Gln45Gln | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/41 | 1547/7261 | 135/4689 | 45/1562 | chr1 | 156984427 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156934852
|
A | G | 10 | a0002c0002t0002a0002c0002t0011a0002c0002t0012others(7): Show | 89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1148T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 1148 | chr1 | 156934852 | |||||
| chr1:156934967
|
T | TTA | 2 | a0002c0004t0021a0002c0004t0026 | 3 | HG02572.hp1 HG03139.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1031_*1032dupTA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 1032 | chr1 | 156934967 | |||||
| chr1:156934982
|
T | G | 1 | a0002c0002t0011 | 5 | NA18960.hp2 NA18998.hp2 NA19002.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1018A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 1018 | chr1 | 156934982 | |||||
| chr1:156935026
|
G | A | 10 | a0002c0002t0002a0002c0002t0011a0002c0002t0012others(7): Show | 89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*974C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 974 | chr1 | 156935026 | |||||
| chr1:156935045
|
G | T | 3 | a0001c0001t0007a0001c0001t0032a0008c0013t0007 | 10 | HG01243.hp1 HG02004.hp1 HG02071.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*955C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 955 | chr1 | 156935045 | |||||
| chr1:156935103
|
C | T | 2 | a0002c0002t0029a0002c0004t0021 | 3 | HG02486.hp2 HG02572.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*897G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 897 | chr1 | 156935103 | |||||
| chr1:156935172
|
C | T | 1 | a0003c0003t0031 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*828G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 828 | chr1 | 156935172 | |||||
| chr1:156935525
|
C | T | 1 | a0002c0004t0009 | 6 | HG00642.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*475G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 475 | chr1 | 156935525 | |||||
| chr1:156935594
|
G | T | 1 | a0002c0004t0025 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*406C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 406 | chr1 | 156935594 | |||||
| chr1:156935743
|
G | A | 1 | a0002c0002t0017 | 3 | NA18952.hp2 NA18968.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*257C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 257 | chr1 | 156935743 | |||||
| chr1:156935792
|
A | G | 21 | a0002c0002t0002a0002c0002t0011a0002c0002t0012others(18): Show | 136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*208T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 208 | chr1 | 156935792 | |||||
| chr1:156935860
|
C | G | 1 | a0002c0004t0021 | 2 | HG02572.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*140G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 140 | chr1 | 156935860 | |||||
| chr1:156935890
|
C | G | 1 | a0001c0001t0020 | 2 | HG02809.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*110G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 110 | chr1 | 156935890 | |||||
| chr1:157044443
|
T | C | 1 | a0001c0001t0034 | 1 | NA18987.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-113A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | chr1 | 157044443 | ||||||
| chr1:157044500
|
C | T | 1 | a0002c0002t0024 | 1 | HG02622.hp1 | 5_prime_UTR_variant | MODIFIER | c.-170G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 170 | chr1 | 157044500 | |||||
| chr1:157044799
|
G | T | 2 | a0001c0001t0035a0002c0004t0008 | 8 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-469C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 469 | chr1 | 157044799 | |||||
| chr1:157044910
|
G | A | 25 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(22): Show | 134 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-580C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | chr1 | 157044910 | ||||||
| chr1:157044975
|
C | A | 1 | a0001c0001t0028 | 1 | HG01928.hp1 | 5_prime_UTR_variant | MODIFIER | c.-645G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 645 | chr1 | 157044975 | |||||
| chr1:157045078
|
C | CA | 8 | a0001c0001t0015a0001c0001t0035a0002c0002t0012others(5): Show | 25 | HG00609.hp2 HG02145.hp2 HG02258.hp2 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-749dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 749 | chr1 | 157045078 | |||||
| chr1:157045085
|
A | T | 7 | a0001c0001t0001a0001c0001t0010a0001c0001t0030others(4): Show | 86 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
5_prime_UTR_variant | MODIFIER | c.-755T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 755 | chr1 | 157045085 | |||||
| chr1:157045172
|
T | A | 11 | a0001c0001t0003a0001c0001t0030a0001c0001t0032others(8): Show | 63 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(60): Show |
5_prime_UTR_variant | MODIFIER | c.-842A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 842 | chr1 | 157045172 | |||||
| chr1:157045233
|
G | C | 1 | a0001c0001t0010 | 6 | NA18966.hp1 NA18994.hp2 NA18997.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-903C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 903 | chr1 | 157045233 | |||||
| chr1:157045234
|
C | A | 6 | a0001c0001t0001a0001c0001t0010a0001c0001t0034others(3): Show | 85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
5_prime_UTR_variant | MODIFIER | c.-904G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 904 | chr1 | 157045234 | |||||
| chr1:157045424
|
T | C | 1 | a0001c0001t0035 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1094A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 1094 | chr1 | 157045424 | |||||
| chr1:157045571
|
G | A | 1 | a0001c0001t0036 | 1 | HG02083.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1241C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | chr1 | 157045571 | ||||||
| chr1:157045641
|
G | T | 1 | a0002c0002t0023 | 1 | NA18966.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1311C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 1311 | chr1 | 157045641 | |||||
| chr1:157045642
|
AC | A | 1 | a0003c0003t0019 | 3 | HG02572.hp2 HG02622.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-1313delG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 1313 | chr1 | 157045642 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156936301
|
C | T | 1 | a0003c0003t0003g0231 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4631-243G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936301 | ||||||
| chr1:156936320
|
G | A | 3 | a0002c0004t0018g0246a0005c0006t0005g0022a0005c0006t0005g0023 | 3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4631-262C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936320 | ||||||
| chr1:156936354
|
C | T | 1 | a0003c0003t0003g0241 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4631-296G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936354 | ||||||
| chr1:156936355
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4631-297C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936355 | ||||||
| chr1:156936378
|
T | C | 9 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(6): Show | 9 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.4631-320A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936378 | ||||||
| chr1:156936480
|
GA | G | 6 | a0003c0003t0003g0251a0003c0003t0003g0263a0003c0003t0003g0266others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.4630+335delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936480 | ||||||
| chr1:156936493
|
A | AATATAT | 6 | a0001c0001t0001g0275a0001c0001t0001g0294a0001c0001t0001g0295others(3): Show | 6 | HG02015.hp2 HG02258.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.4630+322_4630+323i others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | ||||||
| chr1:156936493
|
A | AATATATA others(3): Show |
3 | a0001c0001t0001g0327a0001c0001t0001g0329a0001c0001t0007g0142 | 3 | HG01123.hp2 HG01256.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.4630+322_4630+323i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | ||||||
| chr1:156936493
|
A | AATATATA others(5): Show |
2 | a0001c0001t0001g0301a0002c0002t0002g0032 | 2 | NA18747.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.4630+322_4630+323i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | ||||||
| chr1:156936493
|
A | AATATATA others(13): Show |
2 | a0001c0001t0001g0276a0001c0005t0001g0281 | 2 | HG00558.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.4630+322_4630+323i others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | ||||||
| chr1:156936493
|
A | AATATATA others(23): Show |
1 | a0001c0001t0001g0287 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4630+322_4630+323i others(32): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | ||||||
| chr1:156936493
|
A | ATATATAT others(12): Show |
1 | a0002c0002t0002g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4630+322_4630+323i others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | ||||||
| chr1:156936493
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0288 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4630+322_4630+323i others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | ||||||
| chr1:156936493
|
A | T | 3 | a0002c0004t0005g0105a0002c0004t0005g0107a0002c0004t0026g0108 | 3 | HG03209.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4630+323T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | ||||||
| chr1:156936495
|
A | AATAT | 7 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0290others(4): Show | 7 | HG01167.hp1 HG02074.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | AATATAT | 26 | a0001c0001t0001g0279a0001c0001t0001g0282a0001c0001t0001g0292others(23): Show | 27 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | AATATATA others(1): Show |
14 | a0001c0001t0001g0313a0001c0001t0001g0319a0001c0001t0001g0337others(11): Show | 14 | HG01106.hp1 HG01123.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | AATATATA others(3): Show |
10 | a0001c0001t0001g0321a0001c0001t0001g0326a0001c0001t0001g0328others(7): Show | 10 | HG01433.hp1 HG01934.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | AATATATA others(5): Show |
3 | a0001c0001t0007g0143a0001c0001t0007g0146a0001c0001t0010g0350 | 3 | HG02071.hp2 HG02738.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.4630+320_4630+321i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | AATATATA others(7): Show |
2 | a0001c0001t0001g0331a0001c0001t0007g0147 | 2 | HG03927.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.4630+320_4630+321i others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | AATATATA others(9): Show |
1 | a0001c0001t0006g0088 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4630+320_4630+321i others(18): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | AATATATA others(11): Show |
1 | a0001c0005t0001g0284 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4630+320_4630+321i others(20): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | AATATATA others(15): Show |
1 | a0002c0002t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4630+320_4630+321i others(24): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | AATATATA others(21): Show |
1 | a0001c0001t0001g0316 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4630+320_4630+321i others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | AATATATA others(23): Show |
1 | a0002c0004t0008g0199 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4630+320_4630+321i others(32): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | AATATATA others(25): Show |
1 | a0002c0004t0008g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4630+320_4630+321i others(34): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | ATATAT | 12 | a0001c0001t0001g0274a0001c0001t0001g0306a0001c0001t0001g0310others(9): Show | 12 | HG00323.hp2 HG01099.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | ATATATAT | 13 | a0001c0001t0001g0278a0001c0001t0001g0311a0001c0001t0004g0135others(10): Show | 13 | HG01070.hp2 HG01346.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(9): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | ATATATAT others(2): Show |
8 | a0001c0001t0001g0280a0001c0001t0001g0307a0001c0001t0004g0178others(5): Show | 8 | HG01192.hp1 HG01255.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | ATATATAT others(4): Show |
4 | a0001c0001t0004g0158a0002c0002t0002g0047a0002c0002t0002g0071others(1): Show | 4 | HG01517.hp1 NA18955.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0004g0157a0008c0013t0007g0144 | 2 | HG01515.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.4630+320_4630+321i others(15): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0297 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4630+320_4630+321i others(31): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
A | T | 26 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0283others(23): Show | 26 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.4630+321T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936495
|
AAAATATA others(3): Show |
A | 1 | a0002c0004t0008g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4630+311_4630+320d others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | ||||||
| chr1:156936497
|
A | AAAAAAAA others(23): Show |
1 | a0002c0004t0005g0105 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(32): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAAAAAA others(27): Show |
1 | a0002c0004t0026g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(36): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAAAAAA others(29): Show |
1 | a0002c0004t0005g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(38): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAAAAAA others(17): Show |
1 | a0002c0004t0005g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(26): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAAAAAA others(4): Show |
2 | a0002c0004t0005g0111a0002c0004t0009g0002 | 3 | HG01257.hp2 HG01258.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.4630+318_4630+319i others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAAAAAA others(3): Show |
3 | a0002c0004t0005g0128a0002c0004t0005g0129a0002c0004t0025g0121 | 3 | HG00408.hp2 NA19002.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.4630+318_4630+319i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAAAAAA others(5): Show |
1 | a0002c0004t0009g0114 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAAAAAT others(4): Show |
1 | a0002c0004t0009g0118 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAAAATA others(3): Show |
1 | a0002c0004t0033g0285 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAAAATA others(5): Show |
1 | a0002c0002t0002g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAAATAT others(22): Show |
1 | a0002c0004t0008g0195 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(31): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAAATAT others(24): Show |
1 | a0002c0004t0013g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(33): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAATAT | 8 | a0001c0001t0001g0315a0002c0002t0002g0028a0002c0002t0002g0039others(5): Show | 8 | HG00642.hp2 HG02451.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.4630+318_4630+319i others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAATATA others(3): Show |
3 | a0002c0002t0002g0055a0002c0002t0002g0060a0002c0002t0029g0188 | 3 | HG02486.hp2 HG02698.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.4630+318_4630+319i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAATATA others(5): Show |
1 | a0002c0002t0002g0056 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAAATATA others(25): Show |
2 | a0002c0004t0013g0186a0002c0004t0013g0190 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4630+318_4630+319i others(34): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AAATATAT others(4): Show |
3 | a0001c0001t0004g0152a0001c0001t0010g0352a0002c0002t0002g0042 | 3 | HG01169.hp1 HG02071.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.4630+318_4630+319i others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AATATAT | 28 | a0001c0001t0001g0286a0001c0001t0001g0304a0001c0001t0001g0312others(25): Show | 28 | HG00609.hp2 HG01074.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.4630+313_4630+318d others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AATATATA others(3): Show |
3 | a0001c0001t0001g0325a0001c0001t0006g0110a0002c0002t0002g0081 | 3 | NA18947.hp1 NA18951.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.4630+309_4630+318d others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AATATATA others(5): Show |
2 | a0001c0001t0007g0140a0002c0002t0002g0064 | 2 | HG04228.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.4630+307_4630+318d others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AATATATA others(7): Show |
1 | a0002c0002t0002g0043 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4630+305_4630+318d others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AATATATA others(13): Show |
1 | a0001c0001t0004g0139 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4630+299_4630+318d others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AATATATA others(21): Show |
1 | a0002c0004t0008g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4630+291_4630+318d others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | AATATATA others(23): Show |
1 | a0002c0004t0008g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(32): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | ATATAT | 6 | a0001c0001t0004g0168a0002c0002t0002g0033a0002c0002t0002g0038others(3): Show | 6 | HG01243.hp2 HG02818.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.4630+318_4630+319i others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | ATATATAT | 11 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0004g0151others(8): Show | 11 | HG01099.hp2 HG01175.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.4630+318_4630+319i others(9): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | ATATATAT others(2): Show |
4 | a0001c0001t0001g0314a0001c0001t0004g0155a0002c0002t0002g0036others(1): Show | 4 | HG01496.hp1 HG02965.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.4630+318_4630+319i others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | ATATATAT others(4): Show |
2 | a0002c0002t0002g0073a0002c0002t0016g0257 | 2 | NA19009.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.4630+318_4630+319i others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0004g0156 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | ATATATAT others(12): Show |
1 | a0001c0005t0001g0289 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | ATATATAT others(14): Show |
1 | a0002c0004t0013g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0277 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(25): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0036g0357 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(29): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936497
|
A | T | 152 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(149): Show | 153 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.4630+319T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | ||||||
| chr1:156936498
|
AT | A | 5 | a0002c0004t0022g0132a0003c0003t0006g0011a0003c0003t0031g0215others(2): Show | 5 | HG01192.hp2 HG01257.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.4630+317delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936498 | ||||||
| chr1:156936499
|
T | A | 19 | a0001c0001t0020g0169a0001c0001t0020g0170a0002c0004t0005g0006others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.4630+317A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936499 | ||||||
| chr1:156936501
|
T | A | 5 | a0002c0004t0005g0007a0002c0004t0022g0132a0004c0007t0003g0254others(2): Show | 5 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.4630+315A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936501 | ||||||
| chr1:156936527
|
A | T | 1 | a0001c0001t0006g0088 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4630+289T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936527 | ||||||
| chr1:156936532
|
A | T | 1 | a0002c0002t0002g0060 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.4630+284T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936532 | ||||||
| chr1:156936565
|
C | T | 4 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0030g0209others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4630+251G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936565 | ||||||
| chr1:156936647
|
G | A | 1 | a0003c0003t0003g0245 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4630+169C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936647 | ||||||
| chr1:156936658
|
A | G | 88 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(85): Show | 88 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.4630+158T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936658 | ||||||
| chr1:156936781
|
A | G | 19 | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0109others(16): Show | 20 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.4630+35T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936781 | ||||||
| chr1:156937016
|
C | T | 1 | a0002c0004t0005g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4441-11G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937016 | ||||||
| chr1:156937089
|
G | A | 86 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.4441-84C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937089 | ||||||
| chr1:156937118
|
C | T | 134 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(131): Show | 136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.4441-113G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937118 | ||||||
| chr1:156937234
|
C | G | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4440+15G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937234 | ||||||
| chr1:156937235
|
C | G | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4440+14G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937235 | ||||||
| chr1:156937236
|
C | A | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4440+13G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937236 | ||||||
| chr1:156937237
|
T | A | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4440+12A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937237 | ||||||
| chr1:156937238
|
G | A | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4440+11C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937238 | ||||||
| chr1:156937239
|
C | T | 100 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(97): Show | 101 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.4440+10G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937239 | ||||||
| chr1:156937627
|
C | T | 2 | a0001c0001t0004g0171a0001c0001t0004g0172 | 2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4193-131G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937627 | ||||||
| chr1:156937656
|
C | T | 3 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0030g0209 | 3 | HG01884.hp2 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4193-160G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937656 | ||||||
| chr1:156937674
|
G | A | 1 | a0001c0001t0006g0125 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4193-178C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937674 | ||||||
| chr1:156937717
|
G | A | 1 | a0001c0001t0007g0140 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4193-221C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937717 | ||||||
| chr1:156937758
|
C | A | 88 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(85): Show | 89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.4193-262G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937758 | ||||||
| chr1:156937774
|
G | A | 1 | a0002c0002t0002g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4193-278C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937774 | ||||||
| chr1:156937843
|
G | A | 13 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(10): Show | 13 | HG00741.hp1 HG02280.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.4193-347C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937843 | ||||||
| chr1:156938374
|
C | T | 18 | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0111others(15): Show | 19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.4192+44G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156938374 | ||||||
| chr1:156938534
|
C | T | 1 | a0001c0001t0004g0138 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.4097-21G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156938534 | ||||||
| chr1:156938797
|
G | A | 18 | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0111others(15): Show | 19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.4097-284C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156938797 | ||||||
| chr1:156938835
|
C | A | 3 | a0002c0004t0018g0246a0005c0006t0005g0022a0005c0006t0005g0023 | 3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4097-322G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156938835 | ||||||
| chr1:156938943
|
C | T | 1 | a0002c0002t0002g0083 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4097-430G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156938943 | ||||||
| chr1:156939122
|
T | A | 4 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0204others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4096+426A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156939122 | ||||||
| chr1:156939194
|
T | C | 113 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(110): Show | 114 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.4096+354A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156939194 | ||||||
| chr1:156939453
|
CAGGGGGA others(4): Show |
C | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4096+84_4096+94del others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156939453 | ||||||
| chr1:156939511
|
T | A | 88 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(85): Show | 89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.4096+37A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156939511 | ||||||
| chr1:156940104
|
C | T | 1 | a0001c0001t0001g0331 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3733+103G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 36/40 | chr1 | 156940104 | ||||||
| chr1:156940157
|
G | A | 1 | a0001c0001t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3733+50C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 36/40 | chr1 | 156940157 | ||||||
| chr1:156940470
|
G | A | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3515-45C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940470 | ||||||
| chr1:156940473
|
C | T | 1 | a0002c0002t0002g0029 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3515-48G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940473 | ||||||
| chr1:156940695
|
C | T | 1 | a0002c0002t0002g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3515-270G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940695 | ||||||
| chr1:156940696
|
A | G | 118 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(115): Show | 120 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.3515-271T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940696 | ||||||
| chr1:156940702
|
T | C | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3515-277A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940702 | ||||||
| chr1:156940704
|
C | A | 9 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(6): Show | 9 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.3515-279G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940704 | ||||||
| chr1:156940757
|
C | T | 86 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.3515-332G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940757 | ||||||
| chr1:156940806
|
C | T | 18 | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0111others(15): Show | 19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.3515-381G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940806 | ||||||
| chr1:156940921
|
C | T | 1 | a0003c0003t0003g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3514+451G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940921 | ||||||
| chr1:156941004
|
C | T | 3 | a0002c0004t0018g0246a0005c0006t0005g0022a0005c0006t0005g0023 | 3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3514+368G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941004 | ||||||
| chr1:156941051
|
A | G | 3 | a0002c0004t0018g0246a0005c0006t0005g0022a0005c0006t0005g0023 | 3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3514+321T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941051 | ||||||
| chr1:156941085
|
G | A | 2 | a0002c0004t0005g0052a0002c0004t0005g0054 | 2 | HG02015.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3514+287C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941085 | ||||||
| chr1:156941100
|
GCTCGTCT others(1): Show |
G | 88 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(85): Show | 89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.3514+264_3514+271d others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941100 | ||||||
| chr1:156941116
|
A | G | 144 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(141): Show | 146 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.3514+256T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941116 | ||||||
| chr1:156941158
|
T | C | 1 | a0003c0003t0006g0069 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3514+214A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941158 | ||||||
| chr1:156941229
|
C | G | 2 | a0003c0003t0003g0270a0003c0003t0003g0271 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3514+143G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941229 | ||||||
| chr1:156941336
|
T | A | 5 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0001g0337others(2): Show | 5 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.3514+36A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941336 | ||||||
| chr1:156941496
|
G | A | 11 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0030g0209others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.3453-63C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/40 | chr1 | 156941496 | ||||||
| chr1:156941516
|
TC | T | 13 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(10): Show | 13 | HG00741.hp1 HG02280.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3453-84delG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/40 | chr1 | 156941516 | ||||||
| chr1:156941579
|
G | A | 1 | a0010c0014t0014g0205 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3453-146C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/40 | chr1 | 156941579 | ||||||
| chr1:156941587
|
A | G | 102 | a0001c0001t0001g0317a0001c0001t0004g0150a0002c0002t0002g0001others(99): Show | 103 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.3453-154T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/40 | chr1 | 156941587 | ||||||
| chr1:156941670
|
G | A | 1 | a0003c0003t0003g0229 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3452+194C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/40 | chr1 | 156941670 | ||||||
| chr1:156942277
|
A | T | 2 | a0003c0003t0006g0026a0003c0003t0006g0027 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3327-288T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 33/40 | chr1 | 156942277 | ||||||
| chr1:156942904
|
C | T | 1 | a0002c0004t0005g0019 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3236-124G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156942904 | ||||||
| chr1:156942991
|
C | T | 2 | a0001c0001t0004g0171a0001c0001t0004g0172 | 2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3236-211G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156942991 | ||||||
| chr1:156943065
|
C | CTTTTTT | 17 | a0002c0004t0005g0054a0002c0004t0005g0111a0002c0004t0005g0113others(14): Show | 18 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.3236-291_3236-286d others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943065 | ||||||
| chr1:156943065
|
C | CTTTTTTT | 32 | a0002c0002t0002g0028a0002c0002t0002g0040a0002c0002t0002g0073others(29): Show | 32 | HG01070.hp1 HG01433.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.3236-292_3236-286d others(9): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943065 | ||||||
| chr1:156943065
|
C | CTTTTTTT others(1): Show |
91 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0029others(88): Show | 92 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.3236-293_3236-286d others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943065 | ||||||
| chr1:156943079
|
G | T | 1 | a0001c0001t0004g0159 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3236-299C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943079 | ||||||
| chr1:156943183
|
C | T | 3 | a0002c0002t0002g0094a0002c0004t0021g0174a0002c0004t0021g0175 | 3 | HG02572.hp1 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3236-403G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943183 | ||||||
| chr1:156943357
|
G | C | 1 | a0001c0001t0004g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3236-577C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943357 | ||||||
| chr1:156943657
|
C | T | 102 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.3235+278G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943657 | ||||||
| chr1:156943659
|
C | A | 1 | a0001c0001t0001g0300 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3235+276G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943659 | ||||||
| chr1:156943786
|
C | T | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3235+149G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943786 | ||||||
| chr1:156944278
|
C | A | 118 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(115): Show | 120 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.3067+80G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 31/40 | chr1 | 156944278 | ||||||
| chr1:156944310
|
G | A | 2 | a0002c0004t0005g0052a0002c0004t0005g0054 | 2 | HG02015.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3067+48C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 31/40 | chr1 | 156944310 | ||||||
| chr1:156944448
|
C | A | 1 | a0002c0004t0005g0105 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2992-15G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944448 | ||||||
| chr1:156944448
|
CCATT | C | 169 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(166): Show | 169 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.2992-19_2992-16del others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944448 | ||||||
| chr1:156944448
|
CCATTCAT others(1): Show |
C | 123 | a0001c0001t0001g0312a0001c0001t0001g0315a0002c0002t0002g0001others(120): Show | 125 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2992-23_2992-16del others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944448 | ||||||
| chr1:156944644
|
C | T | 1 | a0002c0004t0014g0206 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2992-211G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944644 | ||||||
| chr1:156944671
|
T | C | 1 | a0001c0001t0036g0357 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2992-238A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944671 | ||||||
| chr1:156944676
|
C | A | 2 | a0003c0003t0003g0270a0003c0003t0003g0271 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2992-243G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944676 | ||||||
| chr1:156944676
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2992-243G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944676 | ||||||
| chr1:156944832
|
C | T | 1 | a0001c0001t0007g0146 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2991+187G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944832 | ||||||
| chr1:156944915
|
C | G | 3 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0006g0125 | 3 | HG02723.hp2 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2991+104G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944915 | ||||||
| chr1:156944927
|
C | T | 1 | a0010c0014t0014g0205 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2991+92G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944927 | ||||||
| chr1:156944931
|
T | G | 1 | a0002c0002t0002g0097 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2991+88A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944931 | ||||||
| chr1:156945220
|
T | C | 4 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0204others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2813-23A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945220 | ||||||
| chr1:156945246
|
C | T | 145 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(142): Show | 147 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.2813-49G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945246 | ||||||
| chr1:156945417
|
C | A | 6 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 6 | HG00735.hp1 HG00735.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.2813-220G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945417 | ||||||
| chr1:156945454
|
A | T | 9 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(6): Show | 9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2813-257T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945454 | ||||||
| chr1:156945457
|
T | G | 9 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(6): Show | 9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2813-260A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945457 | ||||||
| chr1:156945530
|
T | C | 1 | a0002c0002t0002g0039 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2813-333A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945530 | ||||||
| chr1:156945746
|
C | A | 14 | a0002c0002t0002g0040a0002c0002t0002g0055a0002c0002t0002g0056others(11): Show | 14 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2812+299G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945746 | ||||||
| chr1:156945787
|
G | A | 3 | a0003c0003t0003g0237a0003c0003t0003g0238a0003c0003t0003g0239 | 3 | NA19005.hp2 NA19011.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2812+258C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945787 | ||||||
| chr1:156946848
|
G | GCCTATCC others(3): Show |
145 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(142): Show | 147 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.2569-62_2569-61ins others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 27/40 | chr1 | 156946848 | ||||||
| chr1:156947133
|
T | C | 1 | a0001c0001t0007g0148 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2489-118A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 26/40 | chr1 | 156947133 | ||||||
| chr1:156947248
|
G | T | 1 | a0001c0001t0004g0138 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2488+56C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 26/40 | chr1 | 156947248 | ||||||
| chr1:156947738
|
C | T | 3 | a0002c0004t0018g0246a0005c0006t0005g0022a0005c0006t0005g0023 | 3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2341+31G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 25/40 | chr1 | 156947738 | ||||||
| chr1:156948556
|
T | C | 23 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(20): Show | 23 | HG00741.hp1 HG01433.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1926-58A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156948556 | ||||||
| chr1:156948652
|
A | G | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0036g0357 | 3 | HG00558.hp2 HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1926-154T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156948652 | ||||||
| chr1:156948800
|
T | C | 1 | a0006c0009t0003g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1926-302A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156948800 | ||||||
| chr1:156949124
|
A | G | 1 | a0002c0002t0002g0080 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1926-626T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949124 | ||||||
| chr1:156949188
|
C | T | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1926-690G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949188 | ||||||
| chr1:156949276
|
G | A | 3 | a0002c0004t0018g0249a0002c0004t0018g0250a0002c0004t0027g0173 | 3 | HG02145.hp1 HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1926-778C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949276 | ||||||
| chr1:156949298
|
C | T | 4 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0204others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1926-800G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949298 | ||||||
| chr1:156949332
|
T | C | 134 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(131): Show | 136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1926-834A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949332 | ||||||
| chr1:156949388
|
A | G | 97 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(94): Show | 98 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1926-890T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949388 | ||||||
| chr1:156949607
|
T | C | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1926-1109A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949607 | ||||||
| chr1:156949659
|
C | A | 9 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(6): Show | 9 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1926-1161G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949659 | ||||||
| chr1:156949823
|
A | G | 9 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(6): Show | 9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1926-1325T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949823 | ||||||
| chr1:156949990
|
A | G | 145 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(142): Show | 147 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1926-1492T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949990 | ||||||
| chr1:156950119
|
C | A | 1 | a0001c0001t0004g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1925+1454G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156950119 | ||||||
| chr1:156950433
|
C | T | 2 | a0002c0004t0008g0197a0002c0004t0008g0198 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1925+1140G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156950433 | ||||||
| chr1:156950677
|
AAACAAAC others(1): Show |
A | 4 | a0002c0004t0005g0015a0002c0004t0005g0105a0002c0004t0005g0107others(1): Show | 4 | HG02280.hp2 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1925+888_1925+895d others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156950677 | ||||||
| chr1:156950685
|
G | A | 10 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(7): Show | 10 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1925+888C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156950685 | ||||||
| chr1:156951166
|
A | G | 18 | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0111others(15): Show | 19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1925+407T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156951166 | ||||||
| chr1:156951370
|
G | A | 9 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(6): Show | 9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1925+203C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156951370 | ||||||
| chr1:156951418
|
T | C | 1 | a0002c0004t0005g0021 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1925+155A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156951418 | ||||||
| chr1:156951428
|
A | G | 46 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(43): Show | 46 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.1925+145T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156951428 | ||||||
| chr1:156951484
|
G | A | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1925+89C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156951484 | ||||||
| chr1:156951808
|
G | C | 1 | a0001c0001t0001g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1799-109C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156951808 | ||||||
| chr1:156951884
|
G | A | 1 | a0003c0003t0006g0010 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1799-185C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156951884 | ||||||
| chr1:156952604
|
C | T | 18 | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0111others(15): Show | 19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1799-905G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156952604 | ||||||
| chr1:156952784
|
G | T | 134 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(131): Show | 136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1799-1085C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156952784 | ||||||
| chr1:156953112
|
CAG | C | 18 | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0111others(15): Show | 19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1799-1415_1799-141 others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953112 | ||||||
| chr1:156953117
|
G | C | 8 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(5): Show | 8 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1799-1418C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953117 | ||||||
| chr1:156953295
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1799-1596G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953295 | ||||||
| chr1:156953424
|
C | T | 1 | a0001c0001t0004g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1798+1468G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953424 | ||||||
| chr1:156953432
|
T | C | 1 | a0008c0013t0007g0144 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1798+1460A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953432 | ||||||
| chr1:156953445
|
A | G | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1798+1447T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953445 | ||||||
| chr1:156953514
|
AC | A | 3 | a0003c0003t0019g0358a0003c0003t0019g0359a0003c0003t0019g0360 | 3 | HG02572.hp2 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1798+1377delG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953514 | ||||||
| chr1:156953523
|
C | A | 3 | a0003c0003t0019g0358a0003c0003t0019g0359a0003c0003t0019g0360 | 3 | HG02572.hp2 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1798+1369G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953523 | ||||||
| chr1:156953684
|
C | A | 1 | a0001c0001t0004g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1798+1208G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953684 | ||||||
| chr1:156953686
|
C | A | 92 | a0001c0001t0001g0273a0001c0001t0001g0275a0001c0001t0001g0277others(89): Show | 92 | HG00438.hp1 HG00609.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.1798+1206G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953686 | ||||||
| chr1:156953688
|
C | A | 126 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(123): Show | 126 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.1798+1204G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953688 | ||||||
| chr1:156953690
|
C | A | 349 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(346): Show | 351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.1798+1202G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953690 | ||||||
| chr1:156953841
|
A | G | 13 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(10): Show | 13 | HG00741.hp1 HG02280.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1798+1051T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953841 | ||||||
| chr1:156953934
|
G | A | 18 | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0111others(15): Show | 19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1798+958C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953934 | ||||||
| chr1:156954027
|
C | T | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1798+865G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954027 | ||||||
| chr1:156954102
|
G | A | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1798+790C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954102 | ||||||
| chr1:156954164
|
G | A | 1 | a0002c0004t0005g0105 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1798+728C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954164 | ||||||
| chr1:156954287
|
C | T | 1 | a0002c0004t0025g0121 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1798+605G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954287 | ||||||
| chr1:156954336
|
C | T | 2 | a0003c0003t0003g0216a0003c0003t0031g0215 | 2 | HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1798+556G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954336 | ||||||
| chr1:156954380
|
C | CA | 18 | a0003c0003t0003g0216a0003c0003t0003g0225a0003c0003t0003g0229others(15): Show | 18 | HG00597.hp1 HG00639.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1798+511dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
C | CAA | 7 | a0003c0003t0003g0212a0003c0003t0003g0237a0003c0003t0003g0240others(4): Show | 7 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1798+510_1798+511d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
C | CAAAAAAA others(6): Show |
1 | a0003c0003t0003g0223 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1798+499_1798+511d others(15): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CA | C | 13 | a0003c0003t0003g0217a0003c0003t0003g0226a0003c0003t0003g0248others(10): Show | 13 | HG00099.hp1 HG01515.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1798+511delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CAAAAAAA others(1): Show |
C | 10 | a0001c0001t0001g0277a0001c0001t0001g0309a0001c0001t0004g0136others(7): Show | 10 | HG02135.hp2 HG03669.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.1798+504_1798+511d others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CAAAAAAA others(2): Show |
C | 81 | a0001c0001t0001g0275a0001c0001t0001g0278a0001c0001t0001g0279others(78): Show | 81 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1798+503_1798+511d others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CAAAAAAA others(3): Show |
C | 144 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0286others(141): Show | 145 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.1798+502_1798+511d others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CAAAAAAA others(4): Show |
C | 9 | a0001c0001t0001g0276a0001c0001t0004g0159a0001c0001t0015g0202others(6): Show | 9 | HG00558.hp2 HG01255.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1798+501_1798+511d others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0015g0201a0002c0004t0005g0019a0002c0004t0022g0131others(1): Show | 4 | HG02896.hp2 HG02897.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1798+500_1798+511d others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CAAAAAAA others(7): Show |
C | 6 | a0002c0004t0005g0015a0002c0004t0005g0105a0002c0004t0005g0107others(3): Show | 6 | HG02280.hp2 HG03041.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1798+498_1798+511d others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CAAAAAAA others(8): Show |
C | 26 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(23): Show | 27 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1798+497_1798+511d others(17): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CAAAAAAA others(9): Show |
C | 2 | a0002c0004t0005g0113a0002c0004t0005g0129 | 2 | NA18964.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1798+496_1798+511d others(18): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CAAAAAAA others(10): Show |
C | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1798+495_1798+511d others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CAAAAAAA others(12): Show |
C | 1 | a0003c0003t0003g0214 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1798+493_1798+511d others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CAAAAAAA others(17): Show |
C | 1 | a0003c0003t0003g0267 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1798+488_1798+511d others(26): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954380
|
CAAAAAAA others(19): Show |
C | 13 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(10): Show | 13 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1798+486_1798+511d others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | ||||||
| chr1:156954456
|
G | C | 3 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0208 | 3 | HG02896.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1798+436C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954456 | ||||||
| chr1:156954467
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1798+425G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954467 | ||||||
| chr1:156954532
|
AG | A | 6 | a0002c0002t0002g0030a0002c0002t0002g0033a0002c0002t0002g0034others(3): Show | 6 | HG01891.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1798+359delC | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954532 | ||||||
| chr1:156954616
|
C | A | 3 | a0002c0004t0018g0246a0005c0006t0005g0022a0005c0006t0005g0023 | 3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1798+276G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954616 | ||||||
| chr1:156954680
|
G | C | 1 | a0002c0004t0005g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1798+212C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954680 | ||||||
| chr1:156955091
|
G | A | 1 | a0002c0004t0005g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1769-170C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955091 | ||||||
| chr1:156955215
|
T | C | 1 | a0002c0004t0005g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1769-294A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955215 | ||||||
| chr1:156955297
|
CT | C | 117 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(114): Show | 119 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1769-377delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955297 | ||||||
| chr1:156955327
|
G | A | 9 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(6): Show | 9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1768+376C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955327 | ||||||
| chr1:156955621
|
C | A | 4 | a0003c0003t0003g0222a0003c0003t0003g0223a0003c0003t0003g0224others(1): Show | 4 | HG02523.hp1 NA18963.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1768+82G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955621 | ||||||
| chr1:156955643
|
T | C | 97 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(94): Show | 98 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1768+60A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955643 | ||||||
| chr1:156955684
|
T | C | 1 | a0003c0003t0003g0227 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1768+19A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955684 | ||||||
| chr1:156955849
|
C | T | 3 | a0002c0004t0018g0246a0005c0006t0005g0022a0005c0006t0005g0023 | 3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1672-50G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 19/40 | chr1 | 156955849 | ||||||
| chr1:156955850
|
G | A | 1 | a0003c0003t0006g0017 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1672-51C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 19/40 | chr1 | 156955850 | ||||||
| chr1:156955877
|
C | A | 1 | a0002c0002t0002g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1672-78G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 19/40 | chr1 | 156955877 | ||||||
| chr1:156956307
|
GGTTTCAC others(3): Show |
G | 18 | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0111others(15): Show | 19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1671+103_1671+112d others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 19/40 | chr1 | 156956307 | ||||||
| chr1:156956317
|
T | C | 1 | a0003c0003t0003g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1671+103A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 19/40 | chr1 | 156956317 | ||||||
| chr1:156956641
|
C | T | 4 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0030g0209others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1527-77G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 18/40 | chr1 | 156956641 | ||||||
| chr1:156956849
|
T | C | 1 | a0001c0001t0004g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1527-285A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 18/40 | chr1 | 156956849 | ||||||
| chr1:156956901
|
G | T | 1 | a0003c0003t0003g0221 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1527-337C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 18/40 | chr1 | 156956901 | ||||||
| chr1:156957532
|
G | A | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1526+260C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 18/40 | chr1 | 156957532 | ||||||
| chr1:156957772
|
C | T | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG02129.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1526+20G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 18/40 | chr1 | 156957772 | ||||||
| chr1:156957959
|
T | C | 119 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0208others(116): Show | 121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1503-144A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 17/40 | chr1 | 156957959 | ||||||
| chr1:156958234
|
C | T | 3 | a0002c0004t0018g0246a0005c0006t0005g0022a0005c0006t0005g0023 | 3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1503-419G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 17/40 | chr1 | 156958234 | ||||||
| chr1:156958348
|
A | G | 3 | a0002c0004t0018g0246a0005c0006t0005g0022a0005c0006t0005g0023 | 3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1502+394T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 17/40 | chr1 | 156958348 | ||||||
| chr1:156958423
|
A | G | 2 | a0002c0004t0005g0014a0002c0004t0005g0018 | 2 | HG01433.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1502+319T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 17/40 | chr1 | 156958423 | ||||||
| chr1:156958530
|
T | C | 1 | a0002c0002t0011g0074 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1502+212A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 17/40 | chr1 | 156958530 | ||||||
| chr1:156958700
|
C | T | 9 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(6): Show | 9 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1502+42G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 17/40 | chr1 | 156958700 | ||||||
| chr1:156958984
|
A | T | 100 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(97): Show | 101 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1379+62T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 16/40 | chr1 | 156958984 | ||||||
| chr1:156958992
|
C | A | 2 | a0003c0003t0003g0222a0003c0003t0003g0262 | 2 | NA18963.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1379+54G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 16/40 | chr1 | 156958992 | ||||||
| chr1:156959231
|
C | T | 13 | a0001c0001t0001g0344a0001c0001t0004g0130a0001c0001t0004g0133others(10): Show | 13 | HG01243.hp1 HG02004.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1283-89G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959231 | ||||||
| chr1:156959471
|
T | C | 2 | a0002c0004t0008g0197a0002c0004t0008g0198 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1283-329A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959471 | ||||||
| chr1:156959530
|
A | G | 1 | a0001c0001t0006g0125 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1283-388T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959530 | ||||||
| chr1:156959788
|
C | G | 1 | a0002c0004t0025g0121 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1282+630G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959788 | ||||||
| chr1:156959802
|
T | C | 100 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(97): Show | 101 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1282+616A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959802 | ||||||
| chr1:156959843
|
G | A | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1282+575C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959843 | ||||||
| chr1:156959924
|
A | AC | 10 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(7): Show | 10 | HG00741.hp1 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1282+493dupG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959924 | ||||||
| chr1:156959927
|
CCCCCT | C | 85 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1282+486_1282+490d others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959927 | ||||||
| chr1:156959932
|
T | C | 44 | a0002c0004t0005g0009a0002c0004t0005g0014a0002c0004t0005g0015others(41): Show | 45 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1282+486A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959932 | ||||||
| chr1:156959932
|
TC | T | 68 | a0001c0001t0001g0278a0001c0001t0001g0344a0001c0001t0003g0210others(65): Show | 68 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1282+485delG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959932 | ||||||
| chr1:156959933
|
C | T | 42 | a0002c0004t0005g0009a0002c0004t0005g0014a0002c0004t0005g0015others(39): Show | 43 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1282+485G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959933 | ||||||
| chr1:156959936
|
C | G | 4 | a0003c0003t0003g0260a0003c0003t0003g0261a0003c0003t0003g0265others(1): Show | 4 | NA18948.hp2 NA18960.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282+482G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959936 | ||||||
| chr1:156959939
|
C | A | 1 | a0001c0001t0004g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1282+479G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959939 | ||||||
| chr1:156959940
|
C | A | 6 | a0002c0002t0002g0032a0002c0002t0002g0047a0002c0002t0002g0071others(3): Show | 6 | HG00597.hp2 NA18955.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282+478G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959940 | ||||||
| chr1:156959941
|
C | A | 89 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1282+477G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959941 | ||||||
| chr1:156959941
|
C | CA | 3 | a0001c0001t0001g0277a0001c0001t0001g0315a0001c0001t0001g0325 | 3 | NA18963.hp1 NA18979.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1282+476_1282+477i others(3): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959941 | ||||||
| chr1:156959942
|
C | A | 182 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0277others(179): Show | 184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1282+476G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959942 | ||||||
| chr1:156959942
|
C | CA | 28 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0001g0276others(25): Show | 28 | HG00438.hp1 HG00558.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1282+475_1282+476i others(3): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959942 | ||||||
| chr1:156959943
|
C | A | 280 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(277): Show | 282 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.1282+475G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959943 | ||||||
| chr1:156959943
|
C | CA | 6 | a0001c0001t0001g0290a0001c0001t0015g0201a0001c0001t0015g0208others(3): Show | 6 | HG00741.hp1 HG02602.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1282+474dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959943 | ||||||
| chr1:156960073
|
A | G | 146 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(143): Show | 148 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1282+345T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156960073 | ||||||
| chr1:156960109
|
C | T | 13 | a0001c0001t0004g0149a0002c0004t0005g0006a0002c0004t0005g0007others(10): Show | 13 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.1282+309G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156960109 | ||||||
| chr1:156960188
|
G | A | 6 | a0002c0002t0002g0030a0002c0002t0002g0033a0002c0002t0002g0034others(3): Show | 6 | HG01891.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282+230C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156960188 | ||||||
| chr1:156960261
|
C | T | 100 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(97): Show | 101 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1282+157G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156960261 | ||||||
| chr1:156960351
|
A | G | 1 | a0002c0002t0002g0042 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1282+67T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156960351 | ||||||
| chr1:156960361
|
G | A | 3 | a0002c0004t0008g0194a0002c0004t0008g0195a0002c0004t0008g0196 | 3 | HG02258.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1282+57C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156960361 | ||||||
| chr1:156960495
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1240-35C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960495 | ||||||
| chr1:156960503
|
A | G | 1 | a0003c0003t0003g0224 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1240-43T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960503 | ||||||
| chr1:156960531
|
C | T | 9 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(6): Show | 9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240-71G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960531 | ||||||
| chr1:156960611
|
C | A | 18 | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0111others(15): Show | 19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1240-151G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960611 | ||||||
| chr1:156960668
|
T | C | 1 | a0006c0009t0003g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1240-208A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960668 | ||||||
| chr1:156960687
|
C | T | 1 | a0002c0002t0002g0097 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1240-227G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960687 | ||||||
| chr1:156960744
|
A | C | 3 | a0002c0004t0005g0105a0002c0004t0005g0107a0002c0004t0026g0108 | 3 | HG03209.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1240-284T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960744 | ||||||
| chr1:156960849
|
A | C | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1240-389T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960849 | ||||||
| chr1:156961437
|
T | G | 2 | a0002c0004t0005g0009a0002c0004t0005g0015 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1239+240A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156961437 | ||||||
| chr1:156961586
|
T | C | 2 | a0002c0002t0002g0046a0002c0002t0002g0092 | 2 | NA18952.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1239+91A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156961586 | ||||||
| chr1:156962235
|
A | G | 1 | a0001c0001t0004g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1141-460T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962235 | ||||||
| chr1:156962290
|
C | T | 4 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0204others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-515G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962290 | ||||||
| chr1:156962312
|
C | A | 4 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0204others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-537G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962312 | ||||||
| chr1:156962460
|
C | T | 1 | a0003c0003t0003g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1141-685G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962460 | ||||||
| chr1:156962772
|
G | A | 13 | a0001c0001t0001g0275a0001c0001t0001g0280a0001c0001t0001g0286others(10): Show | 13 | HG01255.hp1 HG02040.hp1 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.1140+431C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962772 | ||||||
| chr1:156962842
|
G | A | 1 | a0001c0001t0006g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1140+361C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962842 | ||||||
| chr1:156962862
|
G | A | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1140+341C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962862 | ||||||
| chr1:156962878
|
C | CA | 91 | a0001c0001t0001g0277a0001c0001t0001g0279a0001c0001t0001g0286others(88): Show | 91 | HG00280.hp2 HG00621.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.1140+324dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962878 | ||||||
| chr1:156962878
|
C | CAA | 20 | a0001c0001t0001g0309a0001c0001t0001g0312a0001c0001t0001g0315others(17): Show | 20 | HG00438.hp1 HG00741.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.1140+323_1140+324d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962878 | ||||||
| chr1:156962878
|
CA | C | 32 | a0001c0001t0015g0208a0002c0002t0002g0005a0002c0002t0002g0029others(29): Show | 32 | HG00621.hp1 HG01123.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.1140+324delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962878 | ||||||
| chr1:156962878
|
CAA | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0028a0002c0002t0002g0030others(54): Show | 58 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1140+323_1140+324d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962878 | ||||||
| chr1:156962878
|
CAAAAAAA others(6): Show |
C | 2 | a0003c0003t0003g0252a0003c0003t0003g0253 | 2 | HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1140+312_1140+324d others(15): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962878 | ||||||
| chr1:156962908
|
A | T | 1 | a0001c0001t0001g0278 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1140+295T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962908 | ||||||
| chr1:156963000
|
T | A | 1 | a0003c0003t0003g0217 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1140+203A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156963000 | ||||||
| chr1:156963355
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1039-51G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 12/40 | chr1 | 156963355 | ||||||
| chr1:156963509
|
G | C | 9 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(6): Show | 9 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1038+11C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 12/40 | chr1 | 156963509 | ||||||
| chr1:156963775
|
G | A | 2 | a0002c0004t0005g0052a0002c0004t0005g0054 | 2 | HG02015.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.964-181C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156963775 | ||||||
| chr1:156963821
|
G | T | 151 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(148): Show | 151 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.964-227C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156963821 | ||||||
| chr1:156964075
|
C | T | 1 | a0001c0001t0003g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.964-481G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156964075 | ||||||
| chr1:156964170
|
A | G | 98 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(95): Show | 99 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.964-576T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156964170 | ||||||
| chr1:156964356
|
A | G | 2 | a0003c0003t0006g0026a0003c0003t0006g0027 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.964-762T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156964356 | ||||||
| chr1:156964637
|
G | A | 1 | a0002c0002t0002g0058 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.964-1043C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156964637 | ||||||
| chr1:156964767
|
T | C | 9 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(6): Show | 9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.964-1173A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156964767 | ||||||
| chr1:156965101
|
T | C | 151 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(148): Show | 151 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.964-1507A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965101 | ||||||
| chr1:156965256
|
A | G | 8 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(5): Show | 8 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-1662T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965256 | ||||||
| chr1:156965310
|
C | T | 3 | a0002c0002t0002g0040a0002c0002t0002g0055a0002c0002t0002g0056 | 3 | HG02698.hp2 HG03927.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.964-1716G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965310 | ||||||
| chr1:156965340
|
G | C | 1 | a0002c0002t0002g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.964-1746C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965340 | ||||||
| chr1:156965437
|
C | A | 1 | a0002c0002t0002g0060 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.964-1843G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965437 | ||||||
| chr1:156965576
|
T | C | 1 | a0002c0002t0002g0060 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.964-1982A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965576 | ||||||
| chr1:156965650
|
G | A | 18 | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0111others(15): Show | 19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.964-2056C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965650 | ||||||
| chr1:156965697
|
G | C | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.964-2103C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965697 | ||||||
| chr1:156965717
|
G | C | 1 | a0001c0001t0015g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.964-2123C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965717 | ||||||
| chr1:156966201
|
T | C | 1 | a0001c0001t0007g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.963+1786A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156966201 | ||||||
| chr1:156966252
|
A | C | 3 | a0001c0005t0001g0281a0001c0005t0001g0284a0001c0005t0001g0289 | 3 | HG01928.hp2 HG01943.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.963+1735T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156966252 | ||||||
| chr1:156966490
|
T | C | 118 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(115): Show | 120 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.963+1497A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156966490 | ||||||
| chr1:156966624
|
A | C | 1 | a0001c0001t0007g0148 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.963+1363T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156966624 | ||||||
| chr1:156966868
|
T | C | 18 | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0111others(15): Show | 19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.963+1119A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156966868 | ||||||
| chr1:156966904
|
G | A | 1 | a0001c0001t0001g0316 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.963+1083C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156966904 | ||||||
| chr1:156967139
|
A | G | 11 | a0002c0004t0008g0194a0002c0004t0008g0195a0002c0004t0008g0196others(8): Show | 11 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.963+848T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967139 | ||||||
| chr1:156967184
|
A | G | 1 | a0001c0001t0004g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.963+803T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967184 | ||||||
| chr1:156967322
|
G | A | 1 | a0001c0001t0004g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.963+665C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967322 | ||||||
| chr1:156967399
|
T | C | 2 | a0002c0004t0014g0206a0002c0004t0014g0207 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.963+588A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967399 | ||||||
| chr1:156967500
|
C | T | 3 | a0002c0004t0005g0105a0002c0004t0005g0107a0002c0004t0026g0108 | 3 | HG03209.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.963+487G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967500 | ||||||
| chr1:156967653
|
C | T | 2 | a0002c0004t0005g0009a0002c0004t0005g0015 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.963+334G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967653 | ||||||
| chr1:156967781
|
T | C | 1 | a0001c0001t0001g0298 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.963+206A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967781 | ||||||
| chr1:156968243
|
C | T | 1 | a0003c0003t0003g0230 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.826-119G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156968243 | ||||||
| chr1:156968548
|
AT | A | 97 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(94): Show | 98 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.826-425delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156968548 | ||||||
| chr1:156968775
|
C | T | 3 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008 | 3 | HG00741.hp1 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.825+507G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156968775 | ||||||
| chr1:156968918
|
C | T | 7 | a0001c0001t0001g0307a0002c0004t0005g0014a0002c0004t0005g0020others(4): Show | 7 | HG01255.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.825+364G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156968918 | ||||||
| chr1:156968969
|
T | C | 1 | a0001c0001t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.825+313A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156968969 | ||||||
| chr1:156969039
|
C | T | 2 | a0002c0004t0005g0009a0002c0004t0005g0015 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.825+243G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156969039 | ||||||
| chr1:156969085
|
G | T | 1 | a0002c0002t0002g0049 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.825+197C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156969085 | ||||||
| chr1:156969275
|
G | A | 82 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0028others(79): Show | 83 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(80): Show |
splice_region_variant&intron_variant | LOW | c.825+7C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156969275 | ||||||
| chr1:156969379
|
A | G | 23 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(20): Show | 24 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.749-21T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 9/40 | chr1 | 156969379 | ||||||
| chr1:156969383
|
C | T | 281 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(278): Show | 283 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.749-25G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 9/40 | chr1 | 156969383 | ||||||
| chr1:156969516
|
C | T | 1 | a0002c0004t0033g0285 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.749-158G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 9/40 | chr1 | 156969516 | ||||||
| chr1:156969929
|
G | C | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.748+69C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 9/40 | chr1 | 156969929 | ||||||
| chr1:156969991
|
G | T | 2 | a0003c0003t0003g0270a0003c0003t0003g0271 | 2 | HG01167.hp2 HG01169.hp2 |
splice_region_variant&intron_variant | LOW | c.748+7C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 9/40 | chr1 | 156969991 | ||||||
| chr1:156970385
|
G | A | 1 | a0002c0004t0005g0128 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.703-342C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156970385 | ||||||
| chr1:156970454
|
T | C | 6 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(3): Show | 6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-411A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156970454 | ||||||
| chr1:156970533
|
A | G | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.703-490T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156970533 | ||||||
| chr1:156970602
|
A | G | 1 | a0001c0001t0004g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.703-559T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156970602 | ||||||
| chr1:156970785
|
A | G | 8 | a0002c0004t0018g0246a0002c0004t0018g0249a0002c0004t0018g0250others(5): Show | 8 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.703-742T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156970785 | ||||||
| chr1:156971304
|
G | C | 1 | a0001c0001t0001g0282 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.702+393C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156971304 | ||||||
| chr1:156971620
|
T | G | 86 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.702+77A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156971620 | ||||||
| chr1:156971920
|
C | T | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.583-104G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156971920 | ||||||
| chr1:156972232
|
G | A | 1 | a0001c0001t0007g0142 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.583-416C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156972232 | ||||||
| chr1:156972244
|
C | T | 5 | a0002c0004t0005g0009a0002c0004t0005g0015a0003c0003t0019g0358others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.583-428G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156972244 | ||||||
| chr1:156972344
|
T | C | 1 | a0002c0008t0002g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.583-528A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156972344 | ||||||
| chr1:156972363
|
C | T | 1 | a0003c0003t0003g0225 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.583-547G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156972363 | ||||||
| chr1:156972436
|
C | T | 90 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(87): Show | 90 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.583-620G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156972436 | ||||||
| chr1:156972835
|
A | AC | 116 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0110others(113): Show | 118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.583-1020dupG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156972835 | ||||||
| chr1:156973181
|
G | A | 1 | a0002c0002t0002g0039 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.583-1365C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973181 | ||||||
| chr1:156973330
|
C | T | 1 | a0001c0001t0015g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.583-1514G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973330 | ||||||
| chr1:156973395
|
T | C | 2 | a0003c0003t0003g0216a0003c0003t0031g0215 | 2 | HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.583-1579A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973395 | ||||||
| chr1:156973509
|
C | T | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-1693G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973509 | ||||||
| chr1:156973512
|
A | T | 9 | a0001c0001t0007g0140a0001c0001t0007g0141a0001c0001t0007g0142others(6): Show | 9 | HG01243.hp1 HG02004.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.583-1696T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973512 | ||||||
| chr1:156973620
|
C | T | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.583-1804G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973620 | ||||||
| chr1:156973778
|
T | C | 1 | a0002c0004t0033g0285 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.583-1962A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973778 | ||||||
| chr1:156973884
|
C | A | 1 | a0001c0001t0001g0346 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.583-2068G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973884 | ||||||
| chr1:156973890
|
G | A | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.583-2074C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973890 | ||||||
| chr1:156973933
|
T | C | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.583-2117A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973933 | ||||||
| chr1:156974027
|
A | G | 5 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(2): Show | 5 | HG01433.hp2 HG02109.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.583-2211T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974027 | ||||||
| chr1:156974090
|
G | A | 1 | a0002c0002t0012g0192 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.583-2274C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974090 | ||||||
| chr1:156974385
|
G | A | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.583-2569C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974385 | ||||||
| chr1:156974407
|
T | C | 116 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0110others(113): Show | 118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.582+2576A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974407 | ||||||
| chr1:156974578
|
C | T | 2 | a0001c0001t0001g0283a0001c0001t0001g0307 | 2 | HG01255.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.582+2405G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974578 | ||||||
| chr1:156974590
|
G | C | 1 | a0001c0001t0004g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.582+2393C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974590 | ||||||
| chr1:156974650
|
G | A | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.582+2333C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974650 | ||||||
| chr1:156974668
|
T | C | 10 | a0001c0001t0001g0278a0001c0001t0004g0160a0001c0001t0004g0161others(7): Show | 10 | HG01070.hp2 HG01346.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.582+2315A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974668 | ||||||
| chr1:156974760
|
G | A | 4 | a0002c0004t0005g0009a0003c0003t0019g0358a0003c0003t0019g0359others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+2223C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974760 | ||||||
| chr1:156974885
|
G | C | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.582+2098C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974885 | ||||||
| chr1:156974991
|
T | G | 85 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(82): Show | 85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.582+1992A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974991 | ||||||
| chr1:156975211
|
C | T | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.582+1772G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975211 | ||||||
| chr1:156975290
|
T | C | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.582+1693A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975290 | ||||||
| chr1:156975302
|
T | A | 5 | a0001c0001t0001g0279a0001c0001t0001g0318a0001c0001t0001g0319others(2): Show | 5 | NA18949.hp2 NA18973.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.582+1681A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975302 | ||||||
| chr1:156975570
|
A | T | 1 | a0002c0002t0002g0067 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.582+1413T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975570 | ||||||
| chr1:156975578
|
G | T | 15 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(12): Show | 15 | HG00408.hp2 HG02723.hp2 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.582+1405C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975578 | ||||||
| chr1:156975642
|
T | C | 5 | a0002c0004t0005g0009a0002c0004t0005g0015a0003c0003t0019g0358others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.582+1341A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975642 | ||||||
| chr1:156975701
|
C | T | 12 | a0001c0001t0035g0356a0002c0004t0008g0194a0002c0004t0008g0195others(9): Show | 12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.582+1282G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975701 | ||||||
| chr1:156975892
|
C | T | 1 | a0002c0002t0002g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.582+1091G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975892 | ||||||
| chr1:156975916
|
C | G | 217 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(214): Show | 219 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.582+1067G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975916 | ||||||
| chr1:156976134
|
C | T | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.582+849G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976134 | ||||||
| chr1:156976197
|
T | G | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.582+786A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976197 | ||||||
| chr1:156976258
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.582+725T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976258 | ||||||
| chr1:156976307
|
T | C | 293 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(290): Show | 295 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.582+676A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976307 | ||||||
| chr1:156976754
|
T | A | 1 | a0001c0001t0004g0161 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.582+229A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976754 | ||||||
| chr1:156976797
|
G | A | 1 | a0002c0002t0024g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.582+186C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976797 | ||||||
| chr1:156976848
|
C | A | 10 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(7): Show | 10 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.582+135G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976848 | ||||||
| chr1:156977106
|
T | G | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.511-52A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156977106 | ||||||
| chr1:156977203
|
T | C | 2 | a0005c0006t0005g0022a0005c0006t0005g0023 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.511-149A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156977203 | ||||||
| chr1:156977499
|
A | G | 218 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(215): Show | 220 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.511-445T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156977499 | ||||||
| chr1:156977566
|
C | A | 86 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.511-512G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156977566 | ||||||
| chr1:156977717
|
A | G | 2 | a0002c0002t0002g0046a0002c0002t0002g0092 | 2 | NA18952.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.510+487T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156977717 | ||||||
| chr1:156977756
|
T | C | 1 | a0001c0001t0004g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.510+448A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156977756 | ||||||
| chr1:156978110
|
C | T | 2 | a0002c0004t0005g0014a0002c0004t0005g0018 | 2 | HG01433.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.510+94G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156978110 | ||||||
| chr1:156978136
|
T | C | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.510+68A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156978136 | ||||||
| chr1:156978161
|
A | T | 89 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.510+43T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156978161 | ||||||
| chr1:156978164
|
G | C | 5 | a0002c0004t0005g0009a0002c0004t0005g0015a0003c0003t0019g0358others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+40C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156978164 | ||||||
| chr1:156978448
|
G | A | 10 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(7): Show | 10 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-66C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156978448 | ||||||
| chr1:156978450
|
A | G | 5 | a0002c0004t0005g0105a0002c0004t0005g0107a0002c0004t0026g0108others(2): Show | 5 | HG03041.hp1 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-68T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156978450 | ||||||
| chr1:156978465
|
C | T | 1 | a0010c0014t0014g0205 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.332-83G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156978465 | ||||||
| chr1:156978700
|
T | C | 20 | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0123others(17): Show | 21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.332-318A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156978700 | ||||||
| chr1:156978716
|
A | G | 1 | a0002c0004t0009g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.332-334T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156978716 | ||||||
| chr1:156978838
|
C | T | 1 | a0001c0001t0003g0210 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.331+391G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156978838 | ||||||
| chr1:156979088
|
C | A | 115 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0112others(112): Show | 117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.331+141G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156979088 | ||||||
| chr1:156979164
|
CCCT | C | 85 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(82): Show | 85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.331+62_331+64delAG others(1): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156979164 | ||||||
| chr1:156979361
|
C | CT | 97 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(94): Show | 98 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.274-76dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979361 | ||||||
| chr1:156979361
|
C | CTT | 74 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0004g0133others(71): Show | 74 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.274-77_274-76dupAA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979361 | ||||||
| chr1:156979361
|
C | CTTT | 8 | a0001c0001t0001g0278a0001c0001t0004g0151a0001c0001t0004g0179others(5): Show | 8 | HG01175.hp2 HG02148.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-78_274-76dupAA others(1): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979361 | ||||||
| chr1:156979361
|
CT | C | 86 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0001g0277others(83): Show | 86 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.274-76delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979361 | ||||||
| chr1:156979361
|
CTTTT | C | 14 | a0002c0004t0005g0111a0002c0004t0005g0113a0002c0004t0005g0117others(11): Show | 15 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.274-79_274-76delAA others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979361 | ||||||
| chr1:156979406
|
C | T | 10 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(7): Show | 10 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-120G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979406 | ||||||
| chr1:156979555
|
G | A | 4 | a0002c0004t0013g0185a0002c0004t0013g0186a0002c0004t0013g0189others(1): Show | 4 | HG02145.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-269C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979555 | ||||||
| chr1:156979606
|
C | T | 1 | a0001c0001t0004g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.274-320G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979606 | ||||||
| chr1:156979610
|
C | T | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-324G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979610 | ||||||
| chr1:156979655
|
C | T | 100 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(97): Show | 100 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.274-369G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979655 | ||||||
| chr1:156979921
|
T | C | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.273+516A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979921 | ||||||
| chr1:156979946
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.273+491G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979946 | ||||||
| chr1:156980603
|
A | G | 1 | a0002c0002t0011g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.224-117T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980603 | ||||||
| chr1:156980603
|
A | T | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-117T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980603 | ||||||
| chr1:156980791
|
G | A | 38 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(35): Show | 38 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.224-305C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980791 | ||||||
| chr1:156980833
|
C | CG | 35 | a0001c0001t0004g0134a0001c0001t0004g0138a0001c0001t0004g0153others(32): Show | 35 | HG01071.hp1 HG01192.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.224-348dupC | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980833 | ||||||
| chr1:156980833
|
C | CGG | 20 | a0001c0001t0004g0180a0001c0001t0004g0181a0001c0001t0007g0141others(17): Show | 20 | HG01099.hp2 HG01175.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.224-349_224-348dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980833 | ||||||
| chr1:156980833
|
C | CGGGGGGG others(4): Show |
2 | a0001c0001t0004g0130a0002c0004t0022g0131 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.224-358_224-348dup others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980833 | ||||||
| chr1:156980833
|
CG | C | 20 | a0001c0001t0001g0295a0001c0001t0001g0298a0001c0001t0001g0325others(17): Show | 20 | HG00639.hp1 HG01255.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-348delC | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980833 | ||||||
| chr1:156980833
|
CGG | C | 87 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(84): Show | 87 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.224-349_224-348del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980833 | ||||||
| chr1:156980833
|
CGGGG | C | 20 | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0123others(17): Show | 21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.224-351_224-348del others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980833 | ||||||
| chr1:156980847
|
GA | G | 11 | a0002c0002t0002g0028a0002c0002t0002g0029a0002c0002t0002g0031others(8): Show | 11 | HG00642.hp2 HG02071.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.224-362delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980847 | ||||||
| chr1:156980847
|
GAA | G | 70 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(67): Show | 71 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.224-363_224-362del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980847 | ||||||
| chr1:156980848
|
A | G | 9 | a0001c0001t0004g0130a0002c0002t0002g0043a0002c0002t0002g0058others(6): Show | 9 | HG00621.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.224-362T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980848 | ||||||
| chr1:156980849
|
A | G | 18 | a0001c0001t0004g0130a0002c0002t0002g0028a0002c0002t0002g0029others(15): Show | 18 | HG00621.hp1 HG00642.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.224-363T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980849 | ||||||
| chr1:156980864
|
T | G | 5 | a0002c0002t0002g0100a0002c0002t0002g0101a0002c0002t0002g0102others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-378A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980864 | ||||||
| chr1:156980991
|
C | A | 218 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(215): Show | 220 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.224-505G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980991 | ||||||
| chr1:156981003
|
A | G | 85 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.224-517T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981003 | ||||||
| chr1:156981121
|
T | G | 20 | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0123others(17): Show | 21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.224-635A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981121 | ||||||
| chr1:156981200
|
TA | T | 21 | a0001c0001t0001g0296a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.224-715delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981200 | ||||||
| chr1:156981212
|
A | T | 1 | a0002c0004t0014g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.224-726T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981212 | ||||||
| chr1:156981212
|
AT | A | 92 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(89): Show | 93 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.224-727delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981212 | ||||||
| chr1:156981213
|
T | A | 3 | a0002c0002t0002g0056a0002c0002t0002g0059a0002c0002t0002g0097 | 3 | HG02129.hp2 HG03927.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.224-727A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981213 | ||||||
| chr1:156981214
|
T | A | 94 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(91): Show | 95 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.224-728A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981214 | ||||||
| chr1:156981270
|
T | C | 5 | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0123others(2): Show | 5 | HG02723.hp2 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.224-784A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981270 | ||||||
| chr1:156981366
|
C | A | 2 | a0001c0001t0004g0180a0001c0001t0004g0181 | 2 | HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.224-880G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981366 | ||||||
| chr1:156981535
|
G | A | 20 | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0123others(17): Show | 21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.224-1049C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981535 | ||||||
| chr1:156981579
|
T | C | 116 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0110others(113): Show | 118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.224-1093A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981579 | ||||||
| chr1:156981583
|
C | CCTCCCAT others(8): Show |
1 | a0002c0002t0002g0097 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.224-1112_224-1098d others(17): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981583 | ||||||
| chr1:156981944
|
A | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.224-1458T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981944 | ||||||
| chr1:156982050
|
TA | T | 3 | a0002c0004t0005g0105a0002c0004t0005g0107a0002c0004t0026g0108 | 3 | HG03209.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.224-1565delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982050 | ||||||
| chr1:156982172
|
G | A | 6 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(3): Show | 6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.224-1686C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982172 | ||||||
| chr1:156982262
|
C | A | 115 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0112others(112): Show | 117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.224-1776G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982262 | ||||||
| chr1:156982334
|
C | T | 10 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(7): Show | 10 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-1848G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982334 | ||||||
| chr1:156982350
|
A | G | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.224-1864T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982350 | ||||||
| chr1:156982455
|
T | A | 20 | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0123others(17): Show | 21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.223+1884A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982455 | ||||||
| chr1:156982625
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.223+1714G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982625 | ||||||
| chr1:156983267
|
G | A | 1 | a0007c0012t0003g0242 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.223+1072C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156983267 | ||||||
| chr1:156983282
|
G | A | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.223+1057C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156983282 | ||||||
| chr1:156983700
|
G | C | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.223+639C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156983700 | ||||||
| chr1:156983777
|
A | G | 1 | a0002c0002t0002g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.223+562T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156983777 | ||||||
| chr1:156983928
|
A | G | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.223+411T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156983928 | ||||||
| chr1:156984051
|
G | A | 1 | a0002c0002t0002g0097 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.223+288C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156984051 | ||||||
| chr1:156984088
|
C | T | 1 | a0001c0001t0001g0300 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.223+251G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156984088 | ||||||
| chr1:156984475
|
C | T | 229 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(226): Show | 231 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.125-38G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984475 | ||||||
| chr1:156984571
|
C | A | 1 | a0002c0002t0002g0039 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.125-134G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984571 | ||||||
| chr1:156984576
|
C | T | 1 | a0002c0002t0002g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.125-139G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984576 | ||||||
| chr1:156984592
|
T | C | 218 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(215): Show | 220 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.125-155A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984592 | ||||||
| chr1:156984611
|
T | C | 1 | a0002c0004t0005g0021 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.125-174A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984611 | ||||||
| chr1:156984641
|
T | C | 86 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.125-204A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984641 | ||||||
| chr1:156984689
|
T | C | 15 | a0002c0004t0005g0111a0002c0004t0005g0113a0002c0004t0005g0117others(12): Show | 16 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.125-252A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984689 | ||||||
| chr1:156984764
|
C | T | 1 | a0002c0004t0033g0285 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.125-327G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984764 | ||||||
| chr1:156984799
|
C | G | 1 | a0001c0001t0001g0342 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.125-362G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984799 | ||||||
| chr1:156985289
|
T | C | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.124+793A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985289 | ||||||
| chr1:156985487
|
G | A | 20 | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0123others(17): Show | 21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.124+595C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985487 | ||||||
| chr1:156985492
|
C | T | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.124+590G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985492 | ||||||
| chr1:156985515
|
C | G | 7 | a0001c0001t0007g0140a0001c0001t0007g0141a0001c0001t0007g0142others(4): Show | 7 | HG01243.hp1 HG02071.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+567G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985515 | ||||||
| chr1:156985545
|
T | A | 1 | a0001c0001t0004g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.124+537A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985545 | ||||||
| chr1:156985730
|
C | CT | 172 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0276others(169): Show | 173 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.124+351dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985730 | ||||||
| chr1:156985748
|
T | A | 3 | a0003c0003t0003g0260a0003c0003t0003g0265a0003c0003t0003g0268 | 3 | NA18948.hp2 NA18960.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.124+334A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985748 | ||||||
| chr1:156985749
|
A | T | 1 | a0001c0001t0001g0338 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124+333T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985749 | ||||||
| chr1:156986001
|
T | C | 5 | a0002c0002t0011g0074a0002c0002t0011g0075a0002c0002t0011g0076others(2): Show | 5 | NA18960.hp2 NA18998.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+81A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156986001 | ||||||
| chr1:156986077
|
G | T | 1 | a0001c0001t0001g0344 | 1 | HG03041.hp2 | splice_region_variant&intron_variant | LOW | c.124+5C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156986077 | ||||||
| chr1:156986197
|
T | C | 1 | a0001c0001t0007g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33-24A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986197 | ||||||
| chr1:156986265
|
T | C | 87 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(84): Show | 87 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.33-92A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986265 | ||||||
| chr1:156986326
|
T | C | 1 | a0001c0001t0004g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.33-153A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986326 | ||||||
| chr1:156986469
|
G | A | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-296C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986469 | ||||||
| chr1:156986554
|
G | C | 4 | a0001c0001t0004g0171a0001c0001t0004g0172a0001c0001t0020g0169others(1): Show | 4 | HG02809.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-381C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986554 | ||||||
| chr1:156986566
|
G | A | 115 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0112others(112): Show | 117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.33-393C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986566 | ||||||
| chr1:156986736
|
C | T | 1 | a0002c0004t0005g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.33-563G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986736 | ||||||
| chr1:156986839
|
T | C | 12 | a0001c0001t0035g0356a0002c0004t0008g0194a0002c0004t0008g0195others(9): Show | 12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-666A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986839 | ||||||
| chr1:156986889
|
T | C | 4 | a0002c0004t0005g0009a0003c0003t0019g0358a0003c0003t0019g0359others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-716A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986889 | ||||||
| chr1:156986946
|
C | A | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-773G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986946 | ||||||
| chr1:156987240
|
T | C | 35 | a0001c0001t0001g0278a0001c0001t0004g0134a0001c0001t0004g0135others(32): Show | 35 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.33-1067A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156987240 | ||||||
| chr1:156987450
|
A | T | 86 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.33-1277T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156987450 | ||||||
| chr1:156987559
|
G | T | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-1386C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156987559 | ||||||
| chr1:156987613
|
T | G | 1 | a0001c0001t0020g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.33-1440A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156987613 | ||||||
| chr1:156988272
|
C | T | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-2099G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156988272 | ||||||
| chr1:156988306
|
C | T | 3 | a0002c0002t0002g0044a0002c0002t0002g0095a0002c0008t0002g0063 | 3 | HG02735.hp2 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.33-2133G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156988306 | ||||||
| chr1:156988555
|
T | C | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-2382A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156988555 | ||||||
| chr1:156988680
|
G | A | 15 | a0001c0001t0004g0151a0001c0001t0004g0152a0001c0001t0004g0153others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.33-2507C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156988680 | ||||||
| chr1:156988718
|
T | G | 1 | a0002c0002t0002g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.33-2545A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156988718 | ||||||
| chr1:156988833
|
G | A | 20 | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0123others(17): Show | 21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-2660C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156988833 | ||||||
| chr1:156989015
|
G | C | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-2842C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989015 | ||||||
| chr1:156989129
|
G | C | 100 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(97): Show | 100 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.33-2956C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989129 | ||||||
| chr1:156989132
|
G | A | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-2959C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989132 | ||||||
| chr1:156989141
|
C | T | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-2968G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989141 | ||||||
| chr1:156989330
|
T | G | 1 | a0002c0004t0014g0207 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.33-3157A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989330 | ||||||
| chr1:156989656
|
T | C | 2 | a0002c0004t0005g0120a0002c0004t0025g0121 | 2 | NA18987.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.33-3483A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989656 | ||||||
| chr1:156989727
|
C | T | 8 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0204others(5): Show | 8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-3554G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989727 | ||||||
| chr1:156989735
|
A | G | 1 | a0001c0001t0004g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.33-3562T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989735 | ||||||
| chr1:156989804
|
G | A | 2 | a0002c0004t0005g0107a0002c0004t0026g0108 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.33-3631C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989804 | ||||||
| chr1:156989888
|
T | C | 2 | a0002c0002t0011g0076a0002c0002t0011g0077 | 2 | NA19056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.33-3715A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989888 | ||||||
| chr1:156990121
|
G | A | 1 | a0002c0004t0005g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.33-3948C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990121 | ||||||
| chr1:156990123
|
C | A | 2 | a0002c0002t0002g0080a0002c0002t0002g0081 | 2 | HG02040.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.33-3950G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990123 | ||||||
| chr1:156990277
|
T | A | 1 | a0002c0002t0012g0191 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.33-4104A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990277 | ||||||
| chr1:156990340
|
T | C | 1 | a0002c0002t0016g0257 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.33-4167A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990340 | ||||||
| chr1:156990472
|
A | G | 1 | a0003c0003t0003g0241 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.33-4299T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990472 | ||||||
| chr1:156990476
|
C | T | 1 | a0002c0002t0002g0057 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.33-4303G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990476 | ||||||
| chr1:156990497
|
C | T | 90 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(87): Show | 90 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-4324G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990497 | ||||||
| chr1:156990613
|
T | C | 2 | a0002c0002t0002g0033a0002c0002t0002g0038 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.33-4440A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990613 | ||||||
| chr1:156990631
|
G | A | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG02129.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.33-4458C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990631 | ||||||
| chr1:156990699
|
T | TA | 115 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0110others(112): Show | 117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.33-4527dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990699 | ||||||
| chr1:156990942
|
T | C | 3 | a0002c0002t0017g0045a0002c0002t0017g0091a0002c0002t0017g0093 | 3 | NA18952.hp2 NA18968.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.33-4769A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990942 | ||||||
| chr1:156991091
|
T | C | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-4918A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991091 | ||||||
| chr1:156991111
|
G | A | 3 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0030g0209 | 3 | HG01884.hp2 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.33-4938C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991111 | ||||||
| chr1:156991350
|
C | T | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-5177G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991350 | ||||||
| chr1:156991362
|
C | T | 4 | a0001c0001t0004g0171a0001c0001t0004g0172a0001c0001t0020g0169others(1): Show | 4 | HG02809.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-5189G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991362 | ||||||
| chr1:156991438
|
G | C | 12 | a0001c0001t0035g0356a0002c0004t0008g0194a0002c0004t0008g0195others(9): Show | 12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-5265C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991438 | ||||||
| chr1:156991476
|
C | T | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-5303G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991476 | ||||||
| chr1:156991707
|
CTTATTT | C | 11 | a0001c0001t0035g0356a0002c0004t0008g0194a0002c0004t0008g0195others(8): Show | 11 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-5540_33-5535del others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991707 | ||||||
| chr1:156991710
|
A | AT | 79 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0275others(76): Show | 79 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.33-5538dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | ||||||
| chr1:156991710
|
A | ATT | 21 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0001g0279others(18): Show | 21 | HG00438.hp1 HG00558.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-5539_33-5538dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | ||||||
| chr1:156991710
|
A | ATTTTTTT | 10 | a0001c0001t0006g0110a0002c0004t0005g0113a0002c0004t0005g0119others(7): Show | 10 | HG00408.hp2 HG01346.hp2 HG03704.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-5544_33-5538dup others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | ||||||
| chr1:156991710
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0006g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.33-5547_33-5538dup others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | ||||||
| chr1:156991710
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0006g0122a0001c0001t0006g0125 | 2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.33-5548_33-5538dup others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | ||||||
| chr1:156991710
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0006g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.33-5549_33-5538dup others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | ||||||
| chr1:156991710
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0006g0124 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.33-5550_33-5538dup others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | ||||||
| chr1:156991710
|
A | T | 1 | a0002c0004t0009g0002 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.33-5537T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | ||||||
| chr1:156991710
|
ATTTTTTT others(3): Show |
A | 3 | a0002c0002t0017g0045a0002c0002t0017g0091a0002c0002t0017g0093 | 3 | NA18952.hp2 NA18968.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.33-5547_33-5538del others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | ||||||
| chr1:156991710
|
ATTTTTTT others(4): Show |
A | 92 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(89): Show | 93 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-5548_33-5538del others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | ||||||
| chr1:156991715
|
T | A | 3 | a0002c0004t0005g0009a0003c0003t0019g0358a0003c0003t0019g0359 | 3 | HG02572.hp2 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.33-5542A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991715 | ||||||
| chr1:156991719
|
T | A | 1 | a0003c0003t0019g0360 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.33-5546A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991719 | ||||||
| chr1:156991720
|
T | A | 3 | a0002c0004t0005g0009a0003c0003t0019g0358a0003c0003t0019g0359 | 3 | HG02572.hp2 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.33-5547A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991720 | ||||||
| chr1:156991740
|
G | A | 1 | a0001c0001t0004g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.33-5567C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991740 | ||||||
| chr1:156991777
|
C | T | 6 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(3): Show | 6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-5604G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991777 | ||||||
| chr1:156991938
|
G | A | 1 | a0002c0002t0002g0097 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.33-5765C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991938 | ||||||
| chr1:156992023
|
T | C | 1 | a0002c0004t0008g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.33-5850A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992023 | ||||||
| chr1:156992148
|
G | T | 1 | a0001c0001t0001g0317 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.33-5975C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992148 | ||||||
| chr1:156992379
|
T | TCCTG | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-6210_33-6207dup others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992379 | ||||||
| chr1:156992389
|
T | C | 116 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0110others(113): Show | 118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.33-6216A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992389 | ||||||
| chr1:156992399
|
G | T | 86 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.33-6226C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992399 | ||||||
| chr1:156992414
|
T | G | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-6241A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992414 | ||||||
| chr1:156992509
|
G | A | 5 | a0002c0004t0005g0105a0002c0004t0005g0107a0002c0004t0026g0108others(2): Show | 5 | HG03041.hp1 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-6336C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992509 | ||||||
| chr1:156992603
|
ATG | A | 128 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0110others(125): Show | 130 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.33-6432_33-6431del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992603 | ||||||
| chr1:156992615
|
GTA | G | 90 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(87): Show | 90 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-6444_33-6443del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992615 | ||||||
| chr1:156992927
|
C | T | 116 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0110others(113): Show | 118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.33-6754G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992927 | ||||||
| chr1:156992943
|
C | T | 2 | a0001c0001t0004g0171a0001c0001t0004g0172 | 2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.33-6770G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992943 | ||||||
| chr1:156993304
|
A | G | 5 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(2): Show | 5 | HG01433.hp2 HG02109.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-7131T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993304 | ||||||
| chr1:156993470
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.33-7297G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993470 | ||||||
| chr1:156993564
|
A | G | 1 | a0001c0001t0001g0299 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.33-7391T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993564 | ||||||
| chr1:156993619
|
G | C | 4 | a0001c0001t0004g0171a0001c0001t0004g0172a0001c0001t0020g0169others(1): Show | 4 | HG02809.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-7446C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993619 | ||||||
| chr1:156993685
|
T | C | 1 | a0002c0002t0002g0064 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.33-7512A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993685 | ||||||
| chr1:156993722
|
G | C | 1 | a0001c0001t0004g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.33-7549C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993722 | ||||||
| chr1:156993868
|
T | C | 5 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(2): Show | 5 | HG01433.hp2 HG02109.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-7695A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993868 | ||||||
| chr1:156993932
|
T | C | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-7759A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993932 | ||||||
| chr1:156994082
|
T | C | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-7909A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994082 | ||||||
| chr1:156994183
|
G | A | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-8010C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994183 | ||||||
| chr1:156994207
|
A | T | 3 | a0002c0002t0002g0029a0002c0002t0002g0036a0002c0002t0002g0037 | 3 | HG02647.hp1 HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.33-8034T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994207 | ||||||
| chr1:156994260
|
C | T | 102 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(99): Show | 102 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.33-8087G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994260 | ||||||
| chr1:156994386
|
T | TTG | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-8215_33-8214dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994386 | ||||||
| chr1:156994392
|
G | GT | 136 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0004g0133others(133): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.33-8220dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994392 | ||||||
| chr1:156994392
|
G | GTGT | 85 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.33-8220_33-8219ins others(3): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994392 | ||||||
| chr1:156994392
|
G | GTT | 22 | a0001c0001t0001g0299a0001c0001t0001g0307a0001c0001t0004g0182others(19): Show | 22 | HG00597.hp1 HG01255.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-8221_33-8220dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994392 | ||||||
| chr1:156994392
|
G | GTTT | 79 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(76): Show | 79 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.33-8222_33-8220dup others(3): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994392 | ||||||
| chr1:156994675
|
C | A | 116 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0110others(113): Show | 118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.33-8502G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994675 | ||||||
| chr1:156994784
|
C | G | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-8611G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994784 | ||||||
| chr1:156994836
|
AGGTAATA others(15): Show |
A | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-8685_33-8664del others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994836 | ||||||
| chr1:156994859
|
G | A | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-8686C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994859 | ||||||
| chr1:156994990
|
C | T | 1 | a0002c0002t0002g0041 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.33-8817G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994990 | ||||||
| chr1:156995010
|
CTT | C | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-8839_33-8838del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156995010 | ||||||
| chr1:156995310
|
G | T | 359 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(356): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.33-9137C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156995310 | ||||||
| chr1:156995559
|
C | CT | 23 | a0001c0001t0001g0317a0001c0001t0006g0112a0001c0001t0006g0122others(20): Show | 24 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.33-9387dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156995559 | ||||||
| chr1:156995596
|
C | T | 1 | a0002c0004t0005g0019 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.33-9423G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156995596 | ||||||
| chr1:156995704
|
G | GT | 91 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(88): Show | 91 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.33-9532dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156995704 | ||||||
| chr1:156995722
|
T | TA | 3 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0340 | 3 | NA18995.hp1 NA19062.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.33-9550dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156995722 | ||||||
| chr1:156996153
|
C | A | 1 | a0002c0002t0002g0042 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.33-9980G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996153 | ||||||
| chr1:156996156
|
A | G | 115 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0112others(112): Show | 117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.33-9983T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996156 | ||||||
| chr1:156996634
|
G | A | 6 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(3): Show | 6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-10461C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996634 | ||||||
| chr1:156996645
|
C | T | 86 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.33-10472G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996645 | ||||||
| chr1:156996653
|
G | A | 6 | a0002c0002t0002g0030a0002c0002t0002g0033a0002c0002t0002g0034others(3): Show | 6 | HG01891.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-10480C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996653 | ||||||
| chr1:156996689
|
C | T | 2 | a0003c0003t0006g0026a0003c0003t0006g0027 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.33-10516G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996689 | ||||||
| chr1:156996705
|
G | A | 4 | a0002c0004t0005g0009a0003c0003t0019g0358a0003c0003t0019g0359others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-10532C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996705 | ||||||
| chr1:156996766
|
C | T | 5 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0001g0334others(2): Show | 5 | HG00099.hp2 HG01074.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-10593G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996766 | ||||||
| chr1:156996772
|
C | CA | 58 | a0001c0001t0001g0277a0001c0001t0001g0279a0001c0001t0001g0292others(55): Show | 58 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.33-10600dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | ||||||
| chr1:156996772
|
C | CAA | 9 | a0001c0001t0001g0275a0001c0001t0001g0280a0001c0001t0001g0286others(6): Show | 9 | HG02040.hp1 HG02132.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-10601_33-10600d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | ||||||
| chr1:156996772
|
C | CAAA | 67 | a0001c0001t0001g0301a0001c0001t0001g0302a0001c0001t0004g0130others(64): Show | 68 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-10602_33-10600d others(5): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | ||||||
| chr1:156996772
|
C | CAAAA | 23 | a0001c0001t0001g0347a0002c0002t0002g0034a0002c0002t0002g0035others(20): Show | 23 | HG00642.hp2 HG01175.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.33-10603_33-10600d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | ||||||
| chr1:156996772
|
C | CAAAAA | 9 | a0001c0001t0001g0348a0002c0002t0002g0049a0002c0002t0002g0067others(6): Show | 9 | HG00741.hp2 HG01433.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-10604_33-10600d others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | ||||||
| chr1:156996772
|
CA | C | 6 | a0001c0001t0004g0172a0002c0004t0005g0006a0002c0004t0005g0007others(3): Show | 6 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-10600delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | ||||||
| chr1:156996772
|
CAAAAA | C | 19 | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0123others(16): Show | 20 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.33-10604_33-10600d others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | ||||||
| chr1:156996794
|
AG | A | 3 | a0001c0001t0001g0287a0001c0001t0001g0297a0001c0001t0001g0345 | 3 | HG02273.hp1 HG02523.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.33-10622delC | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996794 | ||||||
| chr1:156996795
|
G | A | 82 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(79): Show | 82 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.33-10622C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996795 | ||||||
| chr1:156996797
|
C | A | 85 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(82): Show | 85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.33-10624G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996797 | ||||||
| chr1:156996808
|
A | G | 115 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0112others(112): Show | 117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.33-10635T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996808 | ||||||
| chr1:156996859
|
A | ATT | 21 | a0001c0001t0001g0272a0001c0001t0001g0305a0001c0001t0001g0325others(18): Show | 22 | HG00408.hp2 HG01167.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-10688_33-10687d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996859 | ||||||
| chr1:156996859
|
A | ATTT | 86 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(83): Show | 86 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.33-10689_33-10687d others(5): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996859 | ||||||
| chr1:156996859
|
A | ATTTT | 12 | a0001c0001t0001g0279a0001c0001t0001g0310a0001c0001t0001g0312others(9): Show | 12 | HG00621.hp2 HG01361.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-10690_33-10687d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996859 | ||||||
| chr1:156996859
|
AT | A | 87 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(84): Show | 88 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.33-10687delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996859 | ||||||
| chr1:156996948
|
A | G | 1 | a0003c0003t0003g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.33-10775T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996948 | ||||||
| chr1:156996973
|
C | T | 8 | a0002c0002t0016g0235a0002c0002t0016g0236a0002c0002t0016g0256others(5): Show | 8 | HG02523.hp1 NA18944.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-10800G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996973 | ||||||
| chr1:156996984
|
C | A | 2 | a0005c0006t0005g0022a0005c0006t0005g0023 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.33-10811G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996984 | ||||||
| chr1:156997038
|
A | T | 19 | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0123others(16): Show | 20 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.33-10865T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997038 | ||||||
| chr1:156997039
|
T | A | 11 | a0001c0001t0001g0275a0001c0001t0001g0280a0001c0001t0001g0286others(8): Show | 11 | HG02040.hp1 HG03704.hp1 HG04204.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-10866A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997039 | ||||||
| chr1:156997313
|
T | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-11140A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997313 | ||||||
| chr1:156997544
|
C | A | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-11371G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997544 | ||||||
| chr1:156997550
|
G | A | 1 | a0001c0001t0020g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-11377C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997550 | ||||||
| chr1:156997609
|
C | T | 1 | a0002c0002t0002g0051 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.33-11436G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997609 | ||||||
| chr1:156997685
|
A | T | 4 | a0001c0001t0007g0140a0001c0001t0007g0143a0001c0001t0007g0146others(1): Show | 4 | HG02071.hp2 HG02738.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-11512T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997685 | ||||||
| chr1:156997747
|
G | GA | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-11575dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997747 | ||||||
| chr1:156997852
|
AT | A | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-11680delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997852 | ||||||
| chr1:156997892
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.33-11719G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997892 | ||||||
| chr1:156998031
|
C | CAG | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-11860_33-11859d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998031 | ||||||
| chr1:156998123
|
G | A | 3 | a0001c0001t0004g0135a0001c0001t0004g0137a0001c0001t0004g0182 | 3 | NA18977.hp1 NA19000.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.33-11950C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998123 | ||||||
| chr1:156998151
|
G | A | 100 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(97): Show | 100 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.33-11978C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998151 | ||||||
| chr1:156998330
|
T | C | 4 | a0002c0004t0013g0185a0002c0004t0013g0186a0002c0004t0013g0189others(1): Show | 4 | HG02145.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-12157A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998330 | ||||||
| chr1:156998488
|
C | T | 8 | a0002c0002t0016g0235a0002c0002t0016g0236a0002c0002t0016g0256others(5): Show | 8 | HG02523.hp1 NA18944.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-12315G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998488 | ||||||
| chr1:156998506
|
T | A | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-12333A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998506 | ||||||
| chr1:156998776
|
C | T | 89 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.33-12603G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998776 | ||||||
| chr1:156998908
|
G | A | 3 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008 | 3 | HG00741.hp1 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.33-12735C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998908 | ||||||
| chr1:156998953
|
A | T | 89 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.33-12780T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998953 | ||||||
| chr1:156999055
|
G | A | 1 | a0002c0002t0002g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.33-12882C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999055 | ||||||
| chr1:156999058
|
C | A | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-12885G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999058 | ||||||
| chr1:156999101
|
A | C | 2 | a0005c0006t0005g0022a0005c0006t0005g0023 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.33-12928T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999101 | ||||||
| chr1:156999266
|
T | A | 61 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(58): Show | 61 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.33-13093A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999266 | ||||||
| chr1:156999274
|
A | G | 3 | a0002c0004t0005g0105a0002c0004t0005g0107a0002c0004t0026g0108 | 3 | HG03209.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.33-13101T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999274 | ||||||
| chr1:156999281
|
G | A | 1 | a0002c0004t0005g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33-13108C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999281 | ||||||
| chr1:156999302
|
A | G | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-13129T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999302 | ||||||
| chr1:156999710
|
G | A | 2 | a0001c0001t0001g0297a0001c0001t0001g0341 | 2 | NA18947.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.33-13537C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999710 | ||||||
| chr1:156999718
|
T | C | 6 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(3): Show | 6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-13545A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999718 | ||||||
| chr1:156999811
|
A | G | 116 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0110others(113): Show | 118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.33-13638T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999811 | ||||||
| chr1:156999815
|
C | A | 1 | a0001c0001t0003g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.33-13642G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999815 | ||||||
| chr1:156999967
|
C | T | 5 | a0002c0004t0009g0002a0002c0004t0009g0114a0002c0004t0009g0115others(2): Show | 6 | HG00642.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-13794G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999967 | ||||||
| chr1:157000076
|
A | G | 218 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(215): Show | 220 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.33-13903T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000076 | ||||||
| chr1:157000104
|
G | T | 345 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(342): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.33-13931C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000104 | ||||||
| chr1:157000108
|
G | A | 6 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0303others(3): Show | 6 | HG01361.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-13935C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000108 | ||||||
| chr1:157000154
|
C | G | 218 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(215): Show | 220 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.33-13981G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000154 | ||||||
| chr1:157000252
|
C | T | 100 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(97): Show | 100 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.33-14079G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000252 | ||||||
| chr1:157000253
|
G | A | 1 | a0003c0003t0003g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.33-14080C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000253 | ||||||
| chr1:157000335
|
T | C | 99 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(96): Show | 99 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.33-14162A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000335 | ||||||
| chr1:157000343
|
A | G | 1 | a0001c0001t0006g0124 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.33-14170T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000343 | ||||||
| chr1:157000545
|
A | G | 2 | a0002c0004t0005g0019a0002c0004t0005g0021 | 2 | HG02683.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.33-14372T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000545 | ||||||
| chr1:157000648
|
G | A | 3 | a0002c0002t0002g0048a0002c0002t0002g0049a0002c0002t0002g0050 | 3 | HG00741.hp2 HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.33-14475C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000648 | ||||||
| chr1:157000803
|
C | T | 2 | a0005c0006t0005g0022a0005c0006t0005g0023 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.33-14630G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000803 | ||||||
| chr1:157000961
|
G | A | 12 | a0001c0001t0035g0356a0002c0004t0008g0194a0002c0004t0008g0195others(9): Show | 12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-14788C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000961 | ||||||
| chr1:157001183
|
G | A | 12 | a0001c0001t0035g0356a0002c0004t0008g0194a0002c0004t0008g0195others(9): Show | 12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-15010C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001183 | ||||||
| chr1:157001368
|
T | C | 6 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(3): Show | 6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-15195A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001368 | ||||||
| chr1:157001485
|
C | T | 1 | a0002c0004t0005g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33-15312G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001485 | ||||||
| chr1:157001551
|
T | A | 1 | a0002c0002t0016g0257 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.33-15378A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001551 | ||||||
| chr1:157001815
|
G | T | 95 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-15642C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001815 | ||||||
| chr1:157001875
|
G | A | 10 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(7): Show | 10 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.33-15702C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001875 | ||||||
| chr1:157001995
|
C | T | 1 | a0002c0004t0005g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33-15822G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001995 | ||||||
| chr1:157002189
|
T | C | 293 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(290): Show | 295 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.33-16016A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002189 | ||||||
| chr1:157002269
|
G | C | 1 | a0002c0004t0009g0002 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.33-16096C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002269 | ||||||
| chr1:157002295
|
A | G | 2 | a0001c0001t0001g0316a0001c0001t0034g0349 | 2 | HG00438.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.33-16122T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002295 | ||||||
| chr1:157002354
|
C | G | 4 | a0001c0001t0001g0288a0001c0005t0001g0281a0001c0005t0001g0284others(1): Show | 4 | HG00609.hp1 HG01928.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-16181G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002354 | ||||||
| chr1:157002588
|
T | C | 10 | a0001c0001t0004g0139a0001c0001t0007g0140a0001c0001t0007g0141others(7): Show | 10 | HG01243.hp1 HG02004.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-16415A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002588 | ||||||
| chr1:157002613
|
T | G | 2 | a0002c0002t0002g0065a0002c0002t0002g0066 | 2 | NA18970.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.33-16440A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002613 | ||||||
| chr1:157002626
|
C | G | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-16453G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002626 | ||||||
| chr1:157002675
|
T | C | 293 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(290): Show | 295 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.33-16502A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002675 | ||||||
| chr1:157002686
|
A | G | 293 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(290): Show | 295 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.33-16513T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002686 | ||||||
| chr1:157002693
|
C | T | 61 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(58): Show | 61 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.33-16520G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002693 | ||||||
| chr1:157002745
|
T | C | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-16572A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002745 | ||||||
| chr1:157002766
|
T | C | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-16593A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002766 | ||||||
| chr1:157002942
|
A | G | 3 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG02698.hp1 HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.33-16769T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002942 | ||||||
| chr1:157003068
|
T | G | 1 | a0002c0002t0002g0039 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.33-16895A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157003068 | ||||||
| chr1:157003104
|
A | G | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-16931T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157003104 | ||||||
| chr1:157003372
|
C | G | 1 | a0002c0004t0005g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.33-17199G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157003372 | ||||||
| chr1:157003485
|
T | C | 1 | a0003c0003t0003g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.33-17312A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157003485 | ||||||
| chr1:157003704
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.33-17531G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157003704 | ||||||
| chr1:157003974
|
G | A | 1 | a0002c0004t0005g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33-17801C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157003974 | ||||||
| chr1:157004153
|
C | T | 2 | a0005c0006t0005g0022a0005c0006t0005g0023 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.33-17980G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004153 | ||||||
| chr1:157004234
|
G | A | 3 | a0002c0002t0002g0065a0002c0002t0002g0066a0002c0002t0023g0003 | 3 | NA18966.hp2 NA18970.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.33-18061C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004234 | ||||||
| chr1:157004530
|
C | T | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-18357G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004530 | ||||||
| chr1:157004613
|
C | T | 4 | a0002c0004t0005g0006a0002c0004t0005g0008a0002c0004t0005g0024others(1): Show | 4 | HG00741.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-18440G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004613 | ||||||
| chr1:157004625
|
C | G | 84 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(81): Show | 84 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.33-18452G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004625 | ||||||
| chr1:157004824
|
C | A | 2 | a0003c0003t0006g0026a0003c0003t0006g0027 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.33-18651G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004824 | ||||||
| chr1:157004829
|
C | A | 1 | a0002c0002t0012g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.33-18656G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004829 | ||||||
| chr1:157004831
|
A | G | 90 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(87): Show | 90 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-18658T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004831 | ||||||
| chr1:157004940
|
G | T | 2 | a0002c0002t0002g0036a0002c0002t0002g0037 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.33-18767C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004940 | ||||||
| chr1:157005204
|
C | G | 2 | a0003c0003t0006g0026a0003c0003t0006g0027 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.33-19031G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157005204 | ||||||
| chr1:157005209
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.33-19036G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157005209 | ||||||
| chr1:157005230
|
T | A | 66 | a0001c0001t0032g0258a0002c0002t0016g0235a0002c0002t0016g0236others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.33-19057A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157005230 | ||||||
| chr1:157005838
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.33-19665G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157005838 | ||||||
| chr1:157005918
|
C | G | 3 | a0003c0003t0019g0358a0003c0003t0019g0359a0003c0003t0019g0360 | 3 | HG02572.hp2 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.33-19745G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157005918 | ||||||
| chr1:157006015
|
C | T | 258 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.33-19842G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006015 | ||||||
| chr1:157006157
|
T | A | 1 | a0002c0002t0002g0060 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.33-19984A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006157 | ||||||
| chr1:157006277
|
A | G | 238 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.33-20104T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006277 | ||||||
| chr1:157006433
|
C | T | 258 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.33-20260G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006433 | ||||||
| chr1:157006440
|
G | A | 12 | a0001c0001t0035g0356a0002c0004t0008g0194a0002c0004t0008g0195others(9): Show | 12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-20267C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006440 | ||||||
| chr1:157006472
|
C | T | 10 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(7): Show | 10 | NA18966.hp1 NA18979.hp2 NA18994.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-20299G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006472 | ||||||
| chr1:157006483
|
C | CT | 12 | a0001c0001t0035g0356a0002c0004t0008g0194a0002c0004t0008g0195others(9): Show | 12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-20311_33-20310i others(3): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006483 | ||||||
| chr1:157006484
|
C | CG | 345 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(342): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.33-20312_33-20311i others(3): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006484 | ||||||
| chr1:157006484
|
C | G | 12 | a0001c0001t0035g0356a0002c0004t0008g0194a0002c0004t0008g0195others(9): Show | 12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-20311G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006484 | ||||||
| chr1:157006601
|
A | C | 66 | a0001c0001t0032g0258a0002c0002t0016g0235a0002c0002t0016g0236others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.33-20428T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006601 | ||||||
| chr1:157006695
|
A | G | 1 | a0002c0004t0005g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33-20522T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006695 | ||||||
| chr1:157006772
|
C | T | 1 | a0002c0002t0002g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.33-20599G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006772 | ||||||
| chr1:157006820
|
G | A | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-20647C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006820 | ||||||
| chr1:157007026
|
G | A | 1 | a0003c0003t0003g0262 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.33-20853C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007026 | ||||||
| chr1:157007384
|
C | T | 353 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(350): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.33-21211G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007384 | ||||||
| chr1:157007389
|
T | C | 354 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(351): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.33-21216A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007389 | ||||||
| chr1:157007469
|
C | A | 1 | a0002c0002t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.33-21296G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007469 | ||||||
| chr1:157007662
|
C | T | 1 | a0006c0009t0003g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.33-21489G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007662 | ||||||
| chr1:157007756
|
C | T | 6 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(3): Show | 6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-21583G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007756 | ||||||
| chr1:157007899
|
GT | G | 87 | a0001c0001t0001g0341a0001c0001t0004g0130a0001c0001t0006g0088others(84): Show | 88 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.33-21727delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007899 | ||||||
| chr1:157007906
|
T | G | 4 | a0002c0004t0014g0203a0002c0004t0014g0206a0002c0004t0014g0207others(1): Show | 4 | HG02922.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-21733A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007906 | ||||||
| chr1:157007910
|
T | G | 3 | a0003c0003t0003g0260a0003c0003t0003g0261a0003c0003t0003g0268 | 3 | NA18948.hp2 NA18960.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.33-21737A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007910 | ||||||
| chr1:157007911
|
T | G | 2 | a0002c0002t0012g0187a0003c0003t0003g0265 | 2 | NA18948.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.33-21738A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007911 | ||||||
| chr1:157007911
|
TTG | T | 168 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(165): Show | 168 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.33-21740_33-21739d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007911 | ||||||
| chr1:157007912
|
T | G | 8 | a0002c0002t0002g0067a0002c0002t0002g0068a0002c0002t0002g0083others(5): Show | 8 | HG00558.hp1 HG02132.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-21739A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007912 | ||||||
| chr1:157007912
|
TG | T | 5 | a0002c0002t0002g0040a0002c0002t0002g0055a0002c0002t0002g0056others(2): Show | 5 | HG02698.hp2 HG03927.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-21740delC | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007912 | ||||||
| chr1:157007913
|
G | T | 10 | a0002c0002t0002g0067a0002c0002t0002g0068a0002c0002t0002g0083others(7): Show | 10 | HG00558.hp1 HG02132.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-21740C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007913 | ||||||
| chr1:157007913
|
GT | G | 80 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(77): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.33-21741delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007913 | ||||||
| chr1:157007914
|
T | G | 173 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(170): Show | 173 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.33-21741A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007914 | ||||||
| chr1:157007919
|
T | G | 1 | a0003c0003t0003g0263 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.33-21746A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007919 | ||||||
| chr1:157007920
|
T | G | 62 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(59): Show | 62 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.33-21747A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007920 | ||||||
| chr1:157007963
|
CA | C | 356 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(353): Show | 358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.33-21791delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007963 | ||||||
| chr1:157007989
|
T | C | 1 | a0002c0004t0005g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.33-21816A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007989 | ||||||
| chr1:157008098
|
C | T | 4 | a0001c0001t0001g0288a0001c0005t0001g0281a0001c0005t0001g0284others(1): Show | 4 | HG00609.hp1 HG01928.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-21925G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008098 | ||||||
| chr1:157008113
|
A | G | 238 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.33-21940T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008113 | ||||||
| chr1:157008216
|
C | T | 5 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(2): Show | 5 | HG01433.hp2 HG02109.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-22043G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008216 | ||||||
| chr1:157008226
|
T | A | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-22053A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008226 | ||||||
| chr1:157008233
|
T | G | 5 | a0002c0004t0005g0009a0002c0004t0005g0015a0003c0003t0019g0358others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-22060A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008233 | ||||||
| chr1:157008406
|
G | GCA | 13 | a0001c0001t0004g0130a0002c0002t0002g0038a0002c0002t0002g0094others(10): Show | 13 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-22235_33-22234d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008406 | ||||||
| chr1:157008406
|
G | GCACA | 68 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(65): Show | 69 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.33-22237_33-22234d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008406 | ||||||
| chr1:157008406
|
G | GCACACA | 9 | a0002c0002t0002g0031a0002c0002t0002g0061a0002c0002t0002g0083others(6): Show | 9 | HG00558.hp1 HG02630.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-22239_33-22234d others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008406 | ||||||
| chr1:157008406
|
G | GCACACAC others(7): Show |
1 | a0002c0002t0029g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.33-22247_33-22234d others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008406 | ||||||
| chr1:157008406
|
GCA | G | 98 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(95): Show | 98 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.33-22235_33-22234d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008406 | ||||||
| chr1:157008406
|
GCACA | G | 161 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(158): Show | 162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.33-22237_33-22234d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008406 | ||||||
| chr1:157008523
|
C | T | 2 | a0003c0003t0003g0217a0003c0003t0003g0218 | 2 | NA18998.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.33-22350G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008523 | ||||||
| chr1:157008727
|
A | C | 1 | a0002c0002t0002g0042 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.33-22554T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008727 | ||||||
| chr1:157009073
|
C | T | 1 | a0003c0003t0003g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.33-22900G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157009073 | ||||||
| chr1:157009554
|
A | G | 1 | a0002c0004t0005g0119 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.33-23381T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157009554 | ||||||
| chr1:157009903
|
C | T | 2 | a0003c0003t0003g0261a0003c0003t0003g0268 | 2 | NA18948.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.33-23730G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157009903 | ||||||
| chr1:157010009
|
G | C | 9 | a0003c0003t0003g0233a0003c0003t0003g0237a0003c0003t0003g0238others(6): Show | 9 | HG00597.hp1 NA18967.hp2 NA18981.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-23836C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010009 | ||||||
| chr1:157010029
|
C | G | 1 | a0001c0001t0001g0318 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.33-23856G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010029 | ||||||
| chr1:157010058
|
G | A | 2 | a0001c0001t0001g0304a0001c0001t0001g0345 | 2 | HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.33-23885C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010058 | ||||||
| chr1:157010080
|
C | A | 4 | a0001c0001t0004g0135a0001c0001t0004g0136a0001c0001t0004g0137others(1): Show | 4 | NA18977.hp1 NA19000.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-23907G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010080 | ||||||
| chr1:157010094
|
G | T | 1 | a0002c0002t0002g0064 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.33-23921C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010094 | ||||||
| chr1:157010197
|
C | A | 1 | a0010c0014t0014g0205 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.33-24024G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010197 | ||||||
| chr1:157010237
|
T | C | 1 | a0003c0003t0003g0260 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.33-24064A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010237 | ||||||
| chr1:157010369
|
C | CA | 238 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.33-24197dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010369 | ||||||
| chr1:157010488
|
C | A | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-24315G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010488 | ||||||
| chr1:157010595
|
G | C | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-24422C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010595 | ||||||
| chr1:157010597
|
T | TG | 354 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(351): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.33-24425dupC | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010597 | ||||||
| chr1:157010901
|
A | G | 1 | a0002c0004t0005g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33-24728T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010901 | ||||||
| chr1:157011045
|
C | T | 259 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(256): Show | 261 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.33-24872G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011045 | ||||||
| chr1:157011193
|
T | G | 1 | a0001c0001t0020g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-25020A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011193 | ||||||
| chr1:157011240
|
T | C | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-25067A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011240 | ||||||
| chr1:157011359
|
C | T | 354 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(351): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.33-25186G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011359 | ||||||
| chr1:157011456
|
C | A | 356 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(353): Show | 358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.33-25283G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011456 | ||||||
| chr1:157011493
|
T | C | 3 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0208 | 3 | HG02896.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.33-25320A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011493 | ||||||
| chr1:157011556
|
G | A | 116 | a0001c0001t0004g0130a0001c0001t0006g0088a0001c0001t0006g0110others(113): Show | 118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.33-25383C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011556 | ||||||
| chr1:157011856
|
T | C | 1 | a0002c0004t0005g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.33-25683A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011856 | ||||||
| chr1:157011857
|
G | A | 2 | a0002c0002t0002g0044a0002c0002t0002g0095 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.33-25684C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011857 | ||||||
| chr1:157012036
|
T | C | 5 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(2): Show | 5 | HG01433.hp2 HG02109.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-25863A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157012036 | ||||||
| chr1:157012127
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.33-25954G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157012127 | ||||||
| chr1:157012400
|
G | C | 1 | a0002c0004t0005g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.33-26227C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157012400 | ||||||
| chr1:157012838
|
T | C | 6 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(3): Show | 6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-26665A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157012838 | ||||||
| chr1:157013104
|
G | A | 254 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.33-26931C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013104 | ||||||
| chr1:157013144
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.33-26971G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013144 | ||||||
| chr1:157013145
|
C | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-26972G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013145 | ||||||
| chr1:157013170
|
T | C | 8 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0204others(5): Show | 8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-26997A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013170 | ||||||
| chr1:157013259
|
T | TCA | 3 | a0001c0001t0001g0279a0001c0001t0001g0336a0002c0004t0027g0173 | 3 | HG02145.hp1 HG03831.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.33-27088_33-27087d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACA | 51 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(48): Show | 51 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACA | 19 | a0001c0001t0001g0273a0001c0001t0001g0291a0001c0001t0001g0292others(16): Show | 19 | HG01074.hp1 HG01361.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(1): Show |
8 | a0001c0001t0001g0305a0001c0001t0001g0311a0001c0001t0001g0312others(5): Show | 8 | HG01106.hp1 HG02074.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(3): Show |
3 | a0001c0001t0001g0272a0001c0001t0001g0274a0003c0003t0003g0266 | 3 | HG01099.hp1 HG01167.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.33-27087_33-27086i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(5): Show |
6 | a0001c0001t0004g0153a0001c0001t0004g0154a0002c0004t0014g0203others(3): Show | 6 | HG02723.hp1 HG03098.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(7): Show |
5 | a0002c0004t0008g0199a0002c0004t0008g0200a0002c0004t0014g0206others(2): Show | 5 | HG02451.hp2 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(9): Show |
11 | a0001c0001t0004g0137a0001c0001t0004g0139a0001c0001t0007g0148others(8): Show | 11 | HG02004.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(18): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(11): Show |
16 | a0001c0001t0001g0342a0001c0001t0004g0135a0001c0001t0007g0140others(13): Show | 16 | HG01257.hp1 HG02004.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(20): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(13): Show |
13 | a0001c0001t0004g0136a0001c0001t0004g0182a0001c0001t0007g0141others(10): Show | 13 | HG01192.hp2 HG01517.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(15): Show |
7 | a0001c0001t0007g0142a0003c0003t0003g0228a0003c0003t0003g0253others(4): Show | 7 | HG00099.hp1 HG02132.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(24): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(17): Show |
23 | a0001c0001t0007g0143a0001c0001t0020g0170a0002c0004t0008g0197others(20): Show | 23 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(26): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(19): Show |
6 | a0002c0002t0016g0235a0002c0002t0016g0257a0002c0004t0013g0189others(3): Show | 6 | HG03139.hp2 HG03540.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(21): Show |
9 | a0001c0001t0004g0171a0002c0004t0008g0198a0002c0004t0013g0185others(6): Show | 9 | HG00639.hp2 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(23): Show |
5 | a0001c0001t0004g0172a0002c0002t0016g0236a0003c0003t0003g0237others(2): Show | 5 | NA18906.hp2 NA19011.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(32): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(25): Show |
2 | a0003c0003t0003g0239a0003c0003t0003g0259 | 2 | NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.33-27087_33-27086i others(34): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(31): Show |
2 | a0002c0002t0016g0256a0003c0003t0003g0240 | 2 | NA18944.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.33-27087_33-27086i others(40): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCACACAC others(33): Show |
1 | a0003c0003t0003g0264 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.33-27087_33-27086i others(42): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCTCACAC others(3): Show |
2 | a0001c0001t0003g0210a0001c0001t0004g0150 | 2 | HG00323.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.33-27087_33-27086i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCTCACAC others(5): Show |
2 | a0001c0001t0001g0278a0001c0001t0004g0160 | 2 | NA19055.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.33-27087_33-27086i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCTCACAC others(7): Show |
6 | a0001c0001t0004g0149a0001c0001t0004g0151a0001c0001t0004g0152others(3): Show | 6 | HG01169.hp1 HG01192.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCTCACAC others(9): Show |
4 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0168others(1): Show | 4 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(18): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCTCACAC others(11): Show |
10 | a0001c0001t0003g0211a0001c0001t0004g0134a0001c0001t0004g0157others(7): Show | 10 | HG01070.hp2 HG01099.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(20): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCTCACAC others(13): Show |
4 | a0001c0001t0004g0138a0001c0001t0004g0179a0001c0001t0028g0184others(1): Show | 4 | HG01928.hp1 HG02148.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCTCACAC others(15): Show |
2 | a0001c0001t0004g0159a0001c0001t0004g0166 | 2 | HG01255.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.33-27087_33-27086i others(24): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013259
|
T | TCTCACAC others(17): Show |
1 | a0001c0001t0030g0209 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.33-27087_33-27086i others(26): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | ||||||
| chr1:157013261
|
A | T | 1 | a0001c0001t0004g0167 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.33-27088T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013261 | ||||||
| chr1:157013263
|
T | A | 253 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(250): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.33-27090A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013263 | ||||||
| chr1:157013263
|
T | TCACA | 51 | a0001c0001t0006g0088a0002c0002t0002g0005a0002c0002t0002g0030others(48): Show | 51 | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.33-27094_33-27091d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013263 | ||||||
| chr1:157013263
|
T | TCACACA | 10 | a0002c0002t0002g0001a0002c0002t0002g0029a0002c0002t0002g0037others(7): Show | 11 | HG00280.hp1 HG00741.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.33-27096_33-27091d others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013263 | ||||||
| chr1:157013263
|
T | TCACACAC others(1): Show |
5 | a0002c0002t0002g0042a0002c0002t0023g0003a0002c0004t0005g0019others(2): Show | 5 | HG02071.hp1 HG03041.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-27098_33-27091d others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013263 | ||||||
| chr1:157013263
|
T | TCACACAC others(3): Show |
4 | a0002c0002t0002g0028a0002c0004t0005g0014a0002c0004t0005g0021others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-27100_33-27091d others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013263 | ||||||
| chr1:157013263
|
TCACACA | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-27096_33-27091d others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013263 | ||||||
| chr1:157013299
|
A | ACACACAC others(21): Show |
1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.33-27127_33-27126i others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | ||||||
| chr1:157013299
|
A | ACACACAC others(13): Show |
5 | a0002c0004t0005g0113a0002c0004t0005g0117a0002c0004t0005g0119others(2): Show | 5 | HG00642.hp1 HG04204.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-27127_33-27126i others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | ||||||
| chr1:157013299
|
A | ACACACAC others(11): Show |
2 | a0002c0004t0005g0127a0002c0004t0005g0128 | 2 | HG00408.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.33-27127_33-27126i others(20): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | ||||||
| chr1:157013299
|
A | ACACACAC others(9): Show |
5 | a0002c0002t0012g0192a0002c0004t0005g0111a0002c0004t0005g0120others(2): Show | 5 | HG02738.hp1 NA18943.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-27127_33-27126i others(18): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | ||||||
| chr1:157013299
|
A | ACACACAC others(7): Show |
1 | a0002c0004t0009g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.33-27127_33-27126i others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | ||||||
| chr1:157013299
|
A | ACACACAC others(5): Show |
1 | a0002c0004t0009g0118 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.33-27127_33-27126i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | ||||||
| chr1:157013299
|
A | ACACACAC others(3): Show |
4 | a0002c0002t0012g0191a0002c0002t0012g0193a0002c0004t0009g0002others(1): Show | 5 | HG00609.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-27127_33-27126i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | ||||||
| chr1:157013299
|
A | ACACACAC others(1): Show |
4 | a0001c0001t0006g0123a0001c0001t0006g0124a0002c0002t0012g0187others(1): Show | 4 | HG02735.hp2 HG02922.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-27127_33-27126i others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | ||||||
| chr1:157013299
|
A | ACACACC | 3 | a0002c0002t0002g0044a0002c0002t0002g0062a0002c0002t0002g0095 | 3 | HG00408.hp1 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.33-27127_33-27126i others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | ||||||
| chr1:157013299
|
A | ACACC | 21 | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0125others(18): Show | 21 | HG00741.hp2 HG01175.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-27127_33-27126i others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | ||||||
| chr1:157013299
|
A | C | 1 | a0002c0002t0002g0053 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.33-27126T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | ||||||
| chr1:157013300
|
C | CACACACA others(6): Show |
1 | a0001c0001t0007g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33-27128_33-27127i others(15): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013300 | ||||||
| chr1:157013300
|
C | CACACACA others(10): Show |
1 | a0001c0001t0004g0167 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.33-27128_33-27127i others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013300 | ||||||
| chr1:157013300
|
C | CACACACA others(16): Show |
1 | a0001c0001t0007g0146 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.33-27128_33-27127i others(25): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013300 | ||||||
| chr1:157013300
|
C | CACACACA others(18): Show |
1 | a0001c0001t0007g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.33-27128_33-27127i others(27): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013300 | ||||||
| chr1:157013387
|
C | T | 8 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(5): Show | 8 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-27214G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013387 | ||||||
| chr1:157013536
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.33-27363A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013536 | ||||||
| chr1:157013545
|
T | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-27372A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013545 | ||||||
| chr1:157013701
|
G | GA | 88 | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(85): Show | 89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.33-27529dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013701 | ||||||
| chr1:157013859
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.33-27686A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013859 | ||||||
| chr1:157013913
|
C | T | 96 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(93): Show | 96 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.33-27740G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013913 | ||||||
| chr1:157014004
|
A | C | 101 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(98): Show | 101 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.33-27831T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014004 | ||||||
| chr1:157014090
|
C | T | 1 | a0001c0001t0004g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.33-27917G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014090 | ||||||
| chr1:157014247
|
T | G | 229 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(226): Show | 230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.33-28074A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014247 | ||||||
| chr1:157014309
|
A | G | 86 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.33-28136T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014309 | ||||||
| chr1:157014330
|
T | C | 356 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(353): Show | 358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.33-28157A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014330 | ||||||
| chr1:157014658
|
C | T | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | NA18955.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.33-28485G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014658 | ||||||
| chr1:157014741
|
C | T | 3 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0208 | 3 | HG02896.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.33-28568G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014741 | ||||||
| chr1:157014934
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-28761G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014934 | ||||||
| chr1:157015058
|
G | A | 86 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.33-28885C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015058 | ||||||
| chr1:157015125
|
T | C | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-28952A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015125 | ||||||
| chr1:157015150
|
A | T | 61 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(58): Show | 61 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.33-28977T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015150 | ||||||
| chr1:157015219
|
T | C | 1 | a0002c0004t0005g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.33-29046A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015219 | ||||||
| chr1:157015535
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.32+28764G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015535 | ||||||
| chr1:157015638
|
G | C | 85 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.32+28661C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015638 | ||||||
| chr1:157015739
|
C | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0307 | 2 | HG01255.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.32+28560G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015739 | ||||||
| chr1:157016103
|
T | C | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+28196A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016103 | ||||||
| chr1:157016235
|
T | C | 26 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(23): Show | 27 | HG00408.hp2 HG00642.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.32+28064A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016235 | ||||||
| chr1:157016344
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+27955G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016344 | ||||||
| chr1:157016354
|
GGATTATA others(2): Show |
G | 12 | a0001c0001t0035g0356a0002c0004t0008g0194a0002c0004t0008g0195others(9): Show | 12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+27936_32+27944d others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016354 | ||||||
| chr1:157016711
|
T | C | 1 | a0002c0004t0005g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+27588A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016711 | ||||||
| chr1:157016798
|
A | ATTAT | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+27497_32+27500d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016798 | ||||||
| chr1:157016798
|
ATTAT | A | 316 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(313): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.32+27497_32+27500d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016798 | ||||||
| chr1:157016798
|
ATTATTTA others(5): Show |
A | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+27489_32+27500d others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016798 | ||||||
| chr1:157016906
|
G | C | 1 | a0002c0002t0002g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.32+27393C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016906 | ||||||
| chr1:157017080
|
G | A | 352 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(349): Show | 354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.32+27219C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017080 | ||||||
| chr1:157017089
|
A | G | 3 | a0002c0002t0002g0092a0002c0002t0017g0091a0002c0002t0017g0093 | 3 | NA18952.hp1 NA18968.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.32+27210T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017089 | ||||||
| chr1:157017121
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+27178G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017121 | ||||||
| chr1:157017306
|
C | A | 1 | a0001c0001t0001g0323 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.32+26993G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017306 | ||||||
| chr1:157017492
|
G | A | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+26807C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017492 | ||||||
| chr1:157017570
|
G | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+26729C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017570 | ||||||
| chr1:157017577
|
C | T | 1 | a0001c0001t0004g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.32+26722G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017577 | ||||||
| chr1:157017662
|
G | A | 4 | a0002c0004t0013g0185a0002c0004t0013g0186a0002c0004t0013g0189others(1): Show | 4 | HG02145.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+26637C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017662 | ||||||
| chr1:157017701
|
C | T | 1 | a0002c0004t0005g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+26598G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017701 | ||||||
| chr1:157017702
|
G | A | 11 | a0001c0001t0004g0139a0001c0001t0007g0140a0001c0001t0007g0141others(8): Show | 11 | HG01243.hp1 HG02004.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+26597C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017702 | ||||||
| chr1:157017706
|
C | CA | 107 | a0001c0001t0001g0278a0001c0001t0001g0308a0001c0001t0001g0309others(104): Show | 108 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.32+26592dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017706 | ||||||
| chr1:157017706
|
CA | C | 9 | a0001c0001t0004g0161a0001c0001t0004g0180a0001c0001t0006g0112others(6): Show | 9 | HG00741.hp1 HG01099.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+26592delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017706 | ||||||
| chr1:157017706
|
CAAAAAAA others(3): Show |
C | 3 | a0002c0002t0002g0051a0002c0002t0002g0098a0002c0002t0002g0099 | 3 | NA18973.hp1 NA18977.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.32+26583_32+26592d others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017706 | ||||||
| chr1:157017725
|
A | G | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0287others(4): Show | 7 | HG00558.hp2 HG00609.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+26574T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017725 | ||||||
| chr1:157017745
|
G | C | 4 | a0001c0001t0004g0135a0001c0001t0004g0136a0001c0001t0004g0137others(1): Show | 4 | NA18977.hp1 NA19000.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+26554C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017745 | ||||||
| chr1:157017905
|
C | T | 85 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(82): Show | 85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+26394G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017905 | ||||||
| chr1:157018204
|
A | T | 8 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0204others(5): Show | 8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+26095T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018204 | ||||||
| chr1:157018257
|
T | C | 2 | a0001c0001t0001g0278a0001c0001t0004g0160 | 2 | NA19055.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.32+26042A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018257 | ||||||
| chr1:157018370
|
G | A | 1 | a0001c0001t0004g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.32+25929C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018370 | ||||||
| chr1:157018371
|
C | T | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+25928G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018371 | ||||||
| chr1:157018469
|
C | T | 85 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(82): Show | 85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+25830G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018469 | ||||||
| chr1:157018506
|
G | A | 87 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(84): Show | 87 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.32+25793C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018506 | ||||||
| chr1:157018513
|
C | T | 6 | a0003c0003t0003g0217a0003c0003t0003g0218a0003c0003t0003g0260others(3): Show | 6 | NA18948.hp2 NA18960.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+25786G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018513 | ||||||
| chr1:157018540
|
G | A | 86 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.32+25759C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018540 | ||||||
| chr1:157018561
|
C | T | 2 | a0003c0003t0006g0026a0003c0003t0006g0027 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.32+25738G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018561 | ||||||
| chr1:157018712
|
C | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+25587G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018712 | ||||||
| chr1:157018780
|
T | C | 1 | a0001c0001t0001g0331 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.32+25519A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018780 | ||||||
| chr1:157018829
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+25470G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018829 | ||||||
| chr1:157018830
|
G | A | 1 | a0001c0001t0006g0124 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.32+25469C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018830 | ||||||
| chr1:157018931
|
C | T | 354 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(351): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.32+25368G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018931 | ||||||
| chr1:157018981
|
C | T | 8 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0204others(5): Show | 8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+25318G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018981 | ||||||
| chr1:157019000
|
T | C | 224 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(221): Show | 225 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.32+25299A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157019000 | ||||||
| chr1:157019006
|
G | C | 3 | a0003c0003t0003g0244a0003c0003t0003g0270a0003c0003t0003g0271 | 3 | HG01167.hp2 HG01169.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.32+25293C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157019006 | ||||||
| chr1:157019502
|
C | A | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+24797G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157019502 | ||||||
| chr1:157019505
|
T | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+24794A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157019505 | ||||||
| chr1:157019995
|
C | T | 1 | a0001c0001t0007g0140 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.32+24304G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157019995 | ||||||
| chr1:157020019
|
C | T | 42 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(39): Show | 42 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.32+24280G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020019 | ||||||
| chr1:157020080
|
C | T | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+24219G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020080 | ||||||
| chr1:157020111
|
G | A | 3 | a0001c0001t0004g0167a0001c0001t0004g0168a0001c0001t0004g0177 | 3 | HG00639.hp1 HG00735.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.32+24188C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020111 | ||||||
| chr1:157020125
|
G | GA | 135 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(132): Show | 135 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.32+24173dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020125 | ||||||
| chr1:157020154
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.32+24145G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020154 | ||||||
| chr1:157020383
|
T | G | 1 | a0003c0003t0003g0251 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.32+23916A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020383 | ||||||
| chr1:157020444
|
A | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+23855T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020444 | ||||||
| chr1:157020499
|
G | A | 1 | a0002c0002t0002g0083 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.32+23800C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020499 | ||||||
| chr1:157020570
|
A | G | 1 | a0003c0003t0003g0260 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.32+23729T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020570 | ||||||
| chr1:157020652
|
A | G | 1 | a0003c0003t0003g0223 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.32+23647T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020652 | ||||||
| chr1:157020844
|
C | G | 1 | a0003c0003t0006g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.32+23455G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020844 | ||||||
| chr1:157020845
|
G | A | 1 | a0001c0001t0004g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.32+23454C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020845 | ||||||
| chr1:157020865
|
T | C | 1 | a0010c0014t0014g0205 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.32+23434A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020865 | ||||||
| chr1:157020894
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.32+23405A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020894 | ||||||
| chr1:157021018
|
T | C | 1 | a0003c0003t0003g0245 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.32+23281A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021018 | ||||||
| chr1:157021047
|
G | A | 1 | a0002c0002t0002g0084 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.32+23252C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021047 | ||||||
| chr1:157021168
|
G | A | 8 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0204others(5): Show | 8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+23131C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021168 | ||||||
| chr1:157021517
|
A | C | 86 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.32+22782T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021517 | ||||||
| chr1:157021661
|
CA | C | 85 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(82): Show | 85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+22637delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021661 | ||||||
| chr1:157021736
|
A | G | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+22563T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021736 | ||||||
| chr1:157021779
|
C | T | 135 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(132): Show | 135 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.32+22520G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021779 | ||||||
| chr1:157021896
|
T | C | 12 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(9): Show | 12 | HG00099.hp1 HG01257.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.32+22403A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021896 | ||||||
| chr1:157022317
|
AAGTC | A | 7 | a0002c0004t0018g0246a0002c0004t0018g0249a0002c0004t0018g0250others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+21978_32+21981d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022317 | ||||||
| chr1:157022329
|
T | G | 1 | a0001c0001t0020g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+21970A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022329 | ||||||
| chr1:157022428
|
A | G | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.32+21871T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022428 | ||||||
| chr1:157022495
|
A | C | 1 | a0002c0004t0005g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+21804T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022495 | ||||||
| chr1:157022840
|
T | C | 2 | a0005c0006t0005g0022a0005c0006t0005g0023 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.32+21459A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022840 | ||||||
| chr1:157022947
|
C | T | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.32+21352G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022947 | ||||||
| chr1:157022961
|
C | T | 213 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(210): Show | 215 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.32+21338G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022961 | ||||||
| chr1:157022973
|
C | T | 1 | a0002c0002t0002g0029 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.32+21326G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022973 | ||||||
| chr1:157022991
|
T | C | 85 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(82): Show | 85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+21308A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022991 | ||||||
| chr1:157023207
|
A | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+21092T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023207 | ||||||
| chr1:157023495
|
GTGGCTCA others(4): Show |
G | 1 | a0001c0001t0035g0356 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.32+20793_32+20803d others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023495 | ||||||
| chr1:157023626
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.32+20673G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023626 | ||||||
| chr1:157023697
|
G | A | 1 | a0002c0002t0002g0085 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.32+20602C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023697 | ||||||
| chr1:157023747
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+20552G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023747 | ||||||
| chr1:157023765
|
C | CA | 146 | a0001c0001t0001g0278a0001c0001t0001g0312a0001c0001t0001g0331others(143): Show | 146 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.32+20533dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023765 | ||||||
| chr1:157023787
|
TAAC | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+20509_32+20511d others(5): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023787 | ||||||
| chr1:157023789
|
A | C | 2 | a0003c0003t0003g0223a0003c0003t0003g0224 | 2 | HG02523.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.32+20510T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023789 | ||||||
| chr1:157023891
|
A | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+20408T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023891 | ||||||
| chr1:157023912
|
T | A | 5 | a0002c0004t0005g0006a0002c0004t0005g0007a0002c0004t0005g0008others(2): Show | 5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+20387A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023912 | ||||||
| chr1:157024068
|
C | T | 1 | a0001c0001t0004g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.32+20231G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024068 | ||||||
| chr1:157024101
|
T | TA | 352 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(349): Show | 354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.32+20197dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024101 | ||||||
| chr1:157024365
|
G | T | 1 | a0001c0001t0001g0273 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.32+19934C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024365 | ||||||
| chr1:157024463
|
C | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+19836G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024463 | ||||||
| chr1:157024519
|
T | C | 1 | a0002c0002t0002g0050 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.32+19780A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024519 | ||||||
| chr1:157024687
|
T | C | 3 | a0003c0003t0019g0358a0003c0003t0019g0359a0003c0003t0019g0360 | 3 | HG02572.hp2 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.32+19612A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024687 | ||||||
| chr1:157024732
|
GCA | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+19565_32+19566d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024732 | ||||||
| chr1:157024827
|
T | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+19472A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024827 | ||||||
| chr1:157024849
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+19450G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024849 | ||||||
| chr1:157025004
|
T | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+19295A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025004 | ||||||
| chr1:157025082
|
A | G | 8 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0204others(5): Show | 8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+19217T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025082 | ||||||
| chr1:157025156
|
A | G | 3 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0020 | 3 | HG01433.hp2 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.32+19143T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025156 | ||||||
| chr1:157025335
|
C | T | 1 | a0002c0004t0005g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+18964G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025335 | ||||||
| chr1:157025360
|
A | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(2): Show | 5 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+18939T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025360 | ||||||
| chr1:157025620
|
G | A | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+18679C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025620 | ||||||
| chr1:157025866
|
T | C | 3 | a0002c0002t0002g0048a0002c0002t0002g0049a0002c0002t0002g0050 | 3 | HG00741.hp2 HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.32+18433A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025866 | ||||||
| chr1:157025991
|
T | C | 2 | a0003c0003t0006g0026a0003c0003t0006g0027 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.32+18308A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025991 | ||||||
| chr1:157026398
|
G | A | 2 | a0002c0004t0005g0120a0002c0004t0025g0121 | 2 | NA18987.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.32+17901C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026398 | ||||||
| chr1:157026452
|
T | C | 4 | a0003c0003t0003g0252a0003c0003t0003g0253a0004c0007t0003g0254others(1): Show | 4 | HG02132.hp1 HG02135.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+17847A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026452 | ||||||
| chr1:157026463
|
C | T | 8 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0287others(5): Show | 8 | HG00558.hp2 HG00609.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+17836G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026463 | ||||||
| chr1:157026586
|
G | A | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | NA18955.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.32+17713C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026586 | ||||||
| chr1:157026656
|
C | G | 1 | a0001c0001t0001g0287 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.32+17643G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026656 | ||||||
| chr1:157026811
|
T | C | 1 | a0001c0001t0004g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.32+17488A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026811 | ||||||
| chr1:157026855
|
A | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+17444T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026855 | ||||||
| chr1:157027092
|
T | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+17207A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157027092 | ||||||
| chr1:157027359
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.32+16940C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157027359 | ||||||
| chr1:157027389
|
A | C | 1 | a0002c0004t0005g0019 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.32+16910T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157027389 | ||||||
| chr1:157027683
|
G | A | 1 | a0002c0004t0005g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+16616C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157027683 | ||||||
| chr1:157027706
|
C | T | 5 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0001g0334others(2): Show | 5 | HG00099.hp2 HG01074.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+16593G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157027706 | ||||||
| chr1:157027852
|
C | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+16447G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157027852 | ||||||
| chr1:157028158
|
A | G | 1 | a0001c0001t0001g0286 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.32+16141T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028158 | ||||||
| chr1:157028252
|
T | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+16047A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028252 | ||||||
| chr1:157028304
|
T | C | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0036g0357 | 3 | HG00558.hp2 HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.32+15995A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028304 | ||||||
| chr1:157028435
|
G | C | 1 | a0002c0002t0002g0086 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.32+15864C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028435 | ||||||
| chr1:157028555
|
A | G | 3 | a0002c0002t0002g0048a0002c0002t0002g0049a0002c0002t0002g0050 | 3 | HG00741.hp2 HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.32+15744T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028555 | ||||||
| chr1:157028734
|
CAAAGA | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+15560_32+15564d others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028734 | ||||||
| chr1:157028932
|
T | C | 1 | a0001c0001t0001g0277 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.32+15367A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028932 | ||||||
| chr1:157029128
|
T | C | 1 | a0002c0002t0016g0256 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.32+15171A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029128 | ||||||
| chr1:157029167
|
C | CA | 15 | a0001c0001t0001g0278a0001c0001t0001g0316a0001c0001t0004g0137others(12): Show | 15 | HG00280.hp1 HG00438.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.32+15131dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029167 | ||||||
| chr1:157029261
|
T | TTTG | 84 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(81): Show | 84 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.32+15035_32+15037d others(5): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029261 | ||||||
| chr1:157029261
|
T | TTTGTTG | 170 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(167): Show | 171 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.32+15032_32+15037d others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029261 | ||||||
| chr1:157029261
|
T | TTTGTTGT others(2): Show |
89 | a0001c0001t0006g0088a0001c0001t0015g0204a0001c0001t0032g0258others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.32+15029_32+15037d others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029261 | ||||||
| chr1:157029261
|
T | TTTGTTGT others(5): Show |
3 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0024g0004 | 3 | HG02622.hp1 HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.32+15026_32+15037d others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029261 | ||||||
| chr1:157029331
|
G | A | 6 | a0002c0002t0002g0042a0002c0004t0005g0009a0002c0004t0005g0015others(3): Show | 6 | HG02071.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+14968C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029331 | ||||||
| chr1:157029519
|
GC | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+14779delG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029519 | ||||||
| chr1:157029842
|
A | C | 1 | a0002c0004t0014g0206 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.32+14457T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029842 | ||||||
| chr1:157029845
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+14454G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029845 | ||||||
| chr1:157029981
|
G | T | 1 | a0002c0004t0005g0113 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.32+14318C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029981 | ||||||
| chr1:157030325
|
T | C | 1 | a0001c0001t0006g0088 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.32+13974A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157030325 | ||||||
| chr1:157030562
|
T | G | 88 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(85): Show | 89 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.32+13737A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157030562 | ||||||
| chr1:157030659
|
C | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+13640G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157030659 | ||||||
| chr1:157030830
|
C | A | 2 | a0001c0001t0004g0137a0001c0001t0004g0182 | 2 | NA18977.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.32+13469G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157030830 | ||||||
| chr1:157030924
|
G | A | 136 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(133): Show | 136 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.32+13375C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157030924 | ||||||
| chr1:157030925
|
C | T | 2 | a0003c0003t0003g0222a0003c0003t0003g0262 | 2 | NA18963.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.32+13374G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157030925 | ||||||
| chr1:157031025
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.32+13274G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031025 | ||||||
| chr1:157031090
|
A | T | 1 | a0002c0004t0033g0285 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.32+13209T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031090 | ||||||
| chr1:157031163
|
G | A | 2 | a0002c0004t0008g0199a0002c0004t0008g0200 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.32+13136C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031163 | ||||||
| chr1:157031183
|
A | G | 2 | a0002c0002t0002g0046a0002c0002t0017g0045 | 2 | NA18952.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.32+13116T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031183 | ||||||
| chr1:157031235
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+13064G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031235 | ||||||
| chr1:157031483
|
A | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+12816T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031483 | ||||||
| chr1:157031484
|
T | C | 1 | a0001c0001t0006g0125 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.32+12815A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031484 | ||||||
| chr1:157031529
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.32+12770G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031529 | ||||||
| chr1:157031537
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01099.hp1 HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.32+12762G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031537 | ||||||
| chr1:157031805
|
G | C | 12 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(9): Show | 12 | HG00099.hp1 HG01257.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.32+12494C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031805 | ||||||
| chr1:157031813
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.32+12486T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031813 | ||||||
| chr1:157031816
|
C | T | 1 | a0001c0001t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.32+12483G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031816 | ||||||
| chr1:157031869
|
C | A | 84 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(81): Show | 84 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.32+12430G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031869 | ||||||
| chr1:157031873
|
G | A | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+12426C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031873 | ||||||
| chr1:157031927
|
T | C | 1 | a0002c0002t0002g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.32+12372A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031927 | ||||||
| chr1:157032141
|
A | G | 1 | a0001c0001t0001g0339 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.32+12158T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032141 | ||||||
| chr1:157032147
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+12152G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032147 | ||||||
| chr1:157032345
|
TAA | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+11952_32+11953d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032345 | ||||||
| chr1:157032431
|
G | C | 1 | a0002c0002t0024g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.32+11868C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032431 | ||||||
| chr1:157032651
|
T | C | 135 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(132): Show | 135 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.32+11648A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032651 | ||||||
| chr1:157032707
|
A | G | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+11592T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032707 | ||||||
| chr1:157032849
|
A | G | 1 | a0001c0005t0001g0284 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.32+11450T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032849 | ||||||
| chr1:157032972
|
T | C | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+11327A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032972 | ||||||
| chr1:157032996
|
G | T | 2 | a0002c0002t0002g0102a0002c0002t0002g0103 | 2 | HG01123.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.32+11303C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032996 | ||||||
| chr1:157033074
|
T | C | 1 | a0002c0002t0012g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.32+11225A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033074 | ||||||
| chr1:157033391
|
T | C | 1 | a0003c0003t0003g0268 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.32+10908A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033391 | ||||||
| chr1:157033480
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+10819G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033480 | ||||||
| chr1:157033572
|
T | C | 9 | a0001c0001t0001g0279a0001c0001t0001g0282a0001c0001t0001g0317others(6): Show | 9 | HG02129.hp1 NA18949.hp2 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+10727A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033572 | ||||||
| chr1:157033632
|
G | C | 1 | a0001c0001t0001g0344 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+10667C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033632 | ||||||
| chr1:157033735
|
C | A | 356 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(353): Show | 358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.32+10564G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033735 | ||||||
| chr1:157033944
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.32+10355T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033944 | ||||||
| chr1:157034072
|
T | C | 8 | a0002c0004t0005g0019a0002c0004t0005g0021a0003c0003t0006g0010others(5): Show | 8 | HG00099.hp1 HG01257.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+10227A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157034072 | ||||||
| chr1:157034107
|
C | A | 6 | a0003c0003t0003g0217a0003c0003t0003g0218a0003c0003t0003g0260others(3): Show | 6 | NA18948.hp2 NA18960.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+10192G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157034107 | ||||||
| chr1:157034330
|
C | T | 5 | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0123others(2): Show | 5 | HG02723.hp2 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+9969G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157034330 | ||||||
| chr1:157034477
|
T | C | 1 | a0002c0004t0005g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.32+9822A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157034477 | ||||||
| chr1:157034629
|
A | G | 8 | a0001c0001t0035g0356a0002c0004t0008g0194a0002c0004t0008g0195others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+9670T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157034629 | ||||||
| chr1:157034738
|
A | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+9561T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157034738 | ||||||
| chr1:157035035
|
C | T | 8 | a0001c0001t0015g0201a0001c0001t0015g0202a0001c0001t0015g0204others(5): Show | 8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+9264G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035035 | ||||||
| chr1:157035076
|
G | C | 84 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(81): Show | 84 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.32+9223C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035076 | ||||||
| chr1:157035362
|
C | A | 63 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0213others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.32+8937G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035362 | ||||||
| chr1:157035401
|
C | CT | 7 | a0001c0001t0001g0282a0001c0005t0001g0281a0002c0004t0005g0111others(4): Show | 7 | HG00438.hp2 HG03098.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+8897dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035401 | ||||||
| chr1:157035401
|
CT | C | 22 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(19): Show | 22 | HG01070.hp2 HG01123.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.32+8897delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035401 | ||||||
| chr1:157035437
|
C | T | 1 | a0002c0004t0005g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+8862G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035437 | ||||||
| chr1:157035474
|
C | T | 1 | a0003c0003t0003g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.32+8825G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035474 | ||||||
| chr1:157035530
|
C | A | 1 | a0001c0001t0001g0334 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.32+8769G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035530 | ||||||
| chr1:157035550
|
A | C | 354 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(351): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.32+8749T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035550 | ||||||
| chr1:157035566
|
C | T | 90 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(87): Show | 91 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.32+8733G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035566 | ||||||
| chr1:157035759
|
A | AAT | 84 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(81): Show | 84 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.32+8538_32+8539dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035759 | ||||||
| chr1:157035773
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8526G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035773 | ||||||
| chr1:157035773
|
CAGGAATA others(9): Show |
C | 12 | a0002c0004t0005g0014a0002c0004t0005g0018a0002c0004t0005g0019others(9): Show | 12 | HG00099.hp1 HG01257.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.32+8510_32+8525del others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035773 | ||||||
| chr1:157035775
|
G | T | 2 | a0001c0001t0004g0130a0002c0004t0022g0132 | 2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.32+8524C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035775 | ||||||
| chr1:157035776
|
G | A | 2 | a0001c0001t0004g0130a0002c0004t0022g0132 | 2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.32+8523C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035776 | ||||||
| chr1:157035777
|
A | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8522T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035777 | ||||||
| chr1:157035791
|
G | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8508C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035791 | ||||||
| chr1:157035792
|
G | A | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8507C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035792 | ||||||
| chr1:157035793
|
A | T | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8506T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035793 | ||||||
| chr1:157035803
|
C | T | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8496G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035803 | ||||||
| chr1:157035805
|
G | T | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8494C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035805 | ||||||
| chr1:157035817
|
T | C | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8482A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035817 | ||||||
| chr1:157035818
|
AGGAATAT others(6): Show |
A | 170 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0001g0334others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.32+8468_32+8480del others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035818 | ||||||
| chr1:157035820
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.32+8479C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035820 | ||||||
| chr1:157035831
|
T | A | 2 | a0001c0001t0004g0130a0002c0004t0005g0009 | 2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.32+8468A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035831 | ||||||
| chr1:157035831
|
T | TA | 185 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(182): Show | 186 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.32+8467_32+8468ins others(1): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035831 | ||||||
| chr1:157035833
|
G | A | 4 | a0002c0002t0012g0187a0002c0002t0012g0191a0002c0002t0012g0192others(1): Show | 4 | HG00609.hp2 NA18943.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+8466C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035833 | ||||||
| chr1:157035843
|
ATGTATAT others(3): Show |
A | 11 | a0001c0001t0004g0130a0001c0001t0007g0140a0001c0001t0007g0141others(8): Show | 11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8446_32+8455del others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035843 | ||||||
| chr1:157035846
|
T | A | 1 | a0001c0001t0004g0139 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+8453A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035846 | ||||||
| chr1:157035853
|
T | A | 2 | a0001c0001t0004g0139a0002c0004t0005g0009 | 2 | HG02004.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.32+8446A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035853 | ||||||
| chr1:157035854
|
T | C | 2 | a0002c0004t0022g0131a0002c0004t0022g0132 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8445A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035854 | ||||||
| chr1:157035856
|
G | T | 1 | a0001c0001t0004g0139 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+8443C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035856 | ||||||
| chr1:157035858
|
A | T | 1 | a0001c0001t0004g0139 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+8441T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035858 | ||||||
| chr1:157035860
|
TATATATA others(3): Show |
T | 9 | a0001c0001t0004g0130a0001c0001t0007g0140a0001c0001t0007g0141others(6): Show | 9 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+8429_32+8438del others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035860 | ||||||
| chr1:157035862
|
T | C | 2 | a0001c0001t0004g0133a0001c0001t0007g0148 | 2 | HG02602.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.32+8437A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035862 | ||||||
| chr1:157035865
|
A | T | 1 | a0001c0001t0004g0139 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+8434T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035865 | ||||||
| chr1:157035868
|
G | T | 1 | a0002c0004t0005g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+8431C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035868 | ||||||
| chr1:157035870
|
A | T | 1 | a0002c0004t0005g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+8429T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035870 | ||||||
| chr1:157035871
|
ATATATAT others(33): Show |
A | 2 | a0002c0002t0002g0044a0002c0002t0002g0095 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.32+8388_32+8427del others(40): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035871 | ||||||
| chr1:157035871
|
ATATATAT others(61): Show |
A | 1 | a0006c0009t0003g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.32+8360_32+8427del others(68): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035871 | ||||||
| chr1:157035874
|
T | C | 1 | a0001c0001t0004g0139 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+8425A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035874 | ||||||
| chr1:157035877
|
A | T | 1 | a0002c0004t0005g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+8422T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035877 | ||||||
| chr1:157035883
|
ATATATAT others(21): Show |
A | 264 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.32+8388_32+8415del others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035883 | ||||||
| chr1:157035883
|
ATATATAT others(49): Show |
A | 65 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0213others(62): Show | 65 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.32+8360_32+8415del others(56): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035883 | ||||||
| chr1:157035886
|
T | C | 11 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0006g0124others(8): Show | 11 | HG00621.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+8413A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035886 | ||||||
| chr1:157035892
|
G | T | 11 | a0001c0001t0004g0130a0001c0001t0007g0140a0001c0001t0007g0141others(8): Show | 11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8407C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035892 | ||||||
| chr1:157035893
|
GAA | G | 11 | a0001c0001t0004g0130a0001c0001t0007g0140a0001c0001t0007g0141others(8): Show | 11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8404_32+8405del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035893 | ||||||
| chr1:157035894
|
AATATATA others(23): Show |
A | 1 | a0010c0014t0014g0205 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.32+8375_32+8404del others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035894 | ||||||
| chr1:157035895
|
ATATATAT others(37): Show |
A | 1 | a0001c0001t0004g0139 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+8360_32+8403del others(44): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035895 | ||||||
| chr1:157035903
|
A | T | 11 | a0001c0001t0004g0130a0001c0001t0007g0140a0001c0001t0007g0141others(8): Show | 11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8396T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035903 | ||||||
| chr1:157035906
|
T | G | 12 | a0001c0001t0004g0130a0001c0001t0007g0140a0001c0001t0007g0141others(9): Show | 12 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+8393A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035906 | ||||||
| chr1:157035909
|
ATC | A | 12 | a0001c0001t0004g0130a0001c0001t0007g0140a0001c0001t0007g0141others(9): Show | 12 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+8388_32+8389del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035909 | ||||||
| chr1:157035914
|
T | C | 275 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(272): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.32+8385A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035914 | ||||||
| chr1:157035922
|
AAT | A | 11 | a0001c0001t0004g0130a0001c0001t0007g0140a0001c0001t0007g0141others(8): Show | 11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8375_32+8376del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035922 | ||||||
| chr1:157035934
|
T | G | 11 | a0001c0001t0004g0130a0001c0001t0007g0140a0001c0001t0007g0141others(8): Show | 11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8365A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035934 | ||||||
| chr1:157035937
|
ATC | A | 11 | a0001c0001t0004g0130a0001c0001t0007g0140a0001c0001t0007g0141others(8): Show | 11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8360_32+8361del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035937 | ||||||
| chr1:157035942
|
T | C | 78 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0213others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.32+8357A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035942 | ||||||
| chr1:157035950
|
AATATATA others(23): Show |
A | 1 | a0002c0004t0005g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+8319_32+8348del others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035950 | ||||||
| chr1:157035952
|
TATATATA others(47): Show |
T | 2 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.32+8293_32+8346del others(54): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035952 | ||||||
| chr1:157035978
|
AAT | A | 4 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0006g0124others(1): Show | 4 | HG02723.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+8319_32+8320del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035978 | ||||||
| chr1:157036006
|
AATATATA others(23): Show |
A | 4 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0006g0124others(1): Show | 4 | HG02723.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+8263_32+8292del others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036006 | ||||||
| chr1:157036032
|
AAT | A | 90 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(87): Show | 91 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.32+8265_32+8266del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036032 | ||||||
| chr1:157036078
|
AAT | A | 5 | a0001c0001t0004g0171a0001c0001t0004g0172a0001c0001t0020g0169others(2): Show | 5 | HG02145.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+8219_32+8220del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036078 | ||||||
| chr1:157036099
|
A | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8200T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036099 | ||||||
| chr1:157036107
|
A | C | 1 | a0001c0001t0001g0280 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.32+8192T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036107 | ||||||
| chr1:157036126
|
AAAAT | A | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8169_32+8172del others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036126 | ||||||
| chr1:157036140
|
AATATATG others(5): Show |
A | 2 | a0002c0004t0008g0199a0002c0004t0008g0200 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.32+8147_32+8158del others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036140 | ||||||
| chr1:157036148
|
AATAC | A | 3 | a0002c0002t0002g0092a0002c0002t0017g0091a0002c0002t0017g0093 | 3 | NA18952.hp1 NA18968.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.32+8147_32+8150del others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036148 | ||||||
| chr1:157036164
|
T | TATATATG others(17): Show |
2 | a0001c0001t0004g0167a0001c0001t0004g0168 | 2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.32+8111_32+8134dup others(24): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036164 | ||||||
| chr1:157036186
|
TACATATA others(3): Show |
T | 9 | a0001c0001t0004g0139a0001c0001t0007g0140a0001c0001t0007g0141others(6): Show | 9 | HG01243.hp1 HG02004.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+8103_32+8112del others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036186 | ||||||
| chr1:157036196
|
A | AAT | 100 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.32+8101_32+8102dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036196 | ||||||
| chr1:157036196
|
AATATATA others(3): Show |
A | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8093_32+8102del others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036196 | ||||||
| chr1:157036204
|
TAC | T | 37 | a0001c0001t0004g0171a0001c0001t0004g0172a0001c0001t0006g0110others(34): Show | 38 | HG00408.hp2 HG00642.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.32+8093_32+8094del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036204 | ||||||
| chr1:157036206
|
C | T | 314 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(311): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.32+8093G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036206 | ||||||
| chr1:157036308
|
CT | C | 7 | a0002c0004t0005g0009a0002c0004t0005g0015a0003c0003t0019g0358others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+7990delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036308 | ||||||
| chr1:157036385
|
G | A | 5 | a0001c0001t0004g0171a0001c0001t0004g0172a0001c0001t0020g0169others(2): Show | 5 | HG02145.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+7914C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036385 | ||||||
| chr1:157036943
|
T | C | 2 | a0002c0004t0014g0206a0002c0004t0014g0207 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32+7356A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036943 | ||||||
| chr1:157036997
|
A | G | 135 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(132): Show | 135 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.32+7302T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036997 | ||||||
| chr1:157037082
|
C | T | 1 | a0002c0004t0005g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+7217G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037082 | ||||||
| chr1:157037116
|
A | G | 354 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(351): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.32+7183T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037116 | ||||||
| chr1:157037184
|
T | C | 132 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(129): Show | 132 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.32+7115A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037184 | ||||||
| chr1:157037256
|
G | A | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+7043C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037256 | ||||||
| chr1:157037352
|
C | T | 51 | a0001c0001t0001g0278a0001c0001t0004g0133a0001c0001t0004g0134others(48): Show | 51 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.32+6947G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037352 | ||||||
| chr1:157037416
|
T | C | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.32+6883A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037416 | ||||||
| chr1:157037710
|
C | T | 135 | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(132): Show | 135 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.32+6589G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037710 | ||||||
| chr1:157037736
|
C | A | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+6563G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037736 | ||||||
| chr1:157037873
|
A | C | 1 | a0001c0001t0004g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.32+6426T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037873 | ||||||
| chr1:157037967
|
G | A | 2 | a0003c0003t0003g0263a0003c0003t0003g0264 | 2 | NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.32+6332C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037967 | ||||||
| chr1:157037988
|
C | T | 26 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(23): Show | 27 | HG00408.hp2 HG00642.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.32+6311G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037988 | ||||||
| chr1:157038009
|
G | A | 1 | a0001c0001t0001g0341 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.32+6290C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038009 | ||||||
| chr1:157038029
|
C | CA | 157 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0276others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.32+6269dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038029 | ||||||
| chr1:157038029
|
C | CAA | 22 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(19): Show | 22 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+6268_32+6269dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038029 | ||||||
| chr1:157038029
|
CA | C | 23 | a0001c0001t0004g0130a0001c0001t0004g0133a0001c0001t0006g0110others(20): Show | 23 | HG00741.hp1 HG01891.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.32+6269delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038029 | ||||||
| chr1:157038146
|
G | A | 1 | a0003c0003t0003g0269 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.32+6153C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038146 | ||||||
| chr1:157038153
|
G | A | 1 | a0001c0001t0015g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+6146C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038153 | ||||||
| chr1:157038194
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.32+6105C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038194 | ||||||
| chr1:157038222
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.32+6077A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038222 | ||||||
| chr1:157038240
|
C | T | 2 | a0001c0001t0003g0213a0003c0003t0003g0214 | 2 | HG00735.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.32+6059G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038240 | ||||||
| chr1:157038252
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+6047G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038252 | ||||||
| chr1:157038278
|
G | GGAGA | 356 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(353): Show | 358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.32+6020_32+6021ins others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038278 | ||||||
| chr1:157038447
|
C | T | 357 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(354): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.32+5852G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038447 | ||||||
| chr1:157038718
|
A | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+5581T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038718 | ||||||
| chr1:157039063
|
C | A | 2 | a0005c0006t0005g0022a0005c0006t0005g0023 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.32+5236G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157039063 | ||||||
| chr1:157039384
|
C | T | 6 | a0001c0001t0004g0134a0001c0001t0004g0135a0001c0001t0004g0136others(3): Show | 6 | HG02074.hp1 NA18977.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+4915G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157039384 | ||||||
| chr1:157039508
|
T | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+4791A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157039508 | ||||||
| chr1:157039508
|
T | TTTTTTCT others(39): Show |
1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4745_32+4790dup others(46): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157039508 | ||||||
| chr1:157039654
|
A | C | 1 | a0003c0003t0003g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.32+4645T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157039654 | ||||||
| chr1:157039880
|
T | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+4419A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157039880 | ||||||
| chr1:157040236
|
C | T | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0036g0357 | 3 | HG00558.hp2 HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.32+4063G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040236 | ||||||
| chr1:157040245
|
T | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+4054A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040245 | ||||||
| chr1:157040268
|
T | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4031A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040268 | ||||||
| chr1:157040270
|
T | C | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4029A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040270 | ||||||
| chr1:157040274
|
T | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4025A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040274 | ||||||
| chr1:157040278
|
G | T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4021C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040278 | ||||||
| chr1:157040282
|
G | T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4017C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040282 | ||||||
| chr1:157040290
|
T | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4009A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040290 | ||||||
| chr1:157040300
|
G | T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3999C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040300 | ||||||
| chr1:157040310
|
CAGCTAAA others(7): Show |
C | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3975_32+3988del others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040310 | ||||||
| chr1:157040325
|
G | T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3974C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040325 | ||||||
| chr1:157040332
|
T | C | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3967A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040332 | ||||||
| chr1:157040334
|
G | T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3965C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040334 | ||||||
| chr1:157040348
|
A | T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3951T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040348 | ||||||
| chr1:157040358
|
G | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3941C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040358 | ||||||
| chr1:157040359
|
A | T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3940T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040359 | ||||||
| chr1:157040406
|
A | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+3893T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040406 | ||||||
| chr1:157040479
|
T | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3820A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040479 | ||||||
| chr1:157040487
|
C | G | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3812G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040487 | ||||||
| chr1:157040503
|
TTAAGGTG others(14): Show |
T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3775_32+3795del others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040503 | ||||||
| chr1:157040530
|
T | C | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3769A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040530 | ||||||
| chr1:157040531
|
C | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3768G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040531 | ||||||
| chr1:157040533
|
C | T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3766G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040533 | ||||||
| chr1:157040618
|
T | C | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3681A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040618 | ||||||
| chr1:157040619
|
C | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3680G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040619 | ||||||
| chr1:157040624
|
C | T | 1 | a0001c0001t0004g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.32+3675G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040624 | ||||||
| chr1:157040697
|
T | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3602A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040697 | ||||||
| chr1:157040710
|
G | T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3589C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040710 | ||||||
| chr1:157040711
|
T | G | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3588A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040711 | ||||||
| chr1:157040712
|
T | C | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3587A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040712 | ||||||
| chr1:157040713
|
T | C | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3586A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040713 | ||||||
| chr1:157040714
|
T | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3585A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040714 | ||||||
| chr1:157040716
|
T | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3583A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040716 | ||||||
| chr1:157040717
|
T | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3582A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040717 | ||||||
| chr1:157040718
|
T | G | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3581A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040718 | ||||||
| chr1:157040719
|
T | C | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3580A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040719 | ||||||
| chr1:157040720
|
G | T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3579C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040720 | ||||||
| chr1:157040721
|
G | C | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3578C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040721 | ||||||
| chr1:157040722
|
G | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3577C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040722 | ||||||
| chr1:157040727
|
T | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3572A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040727 | ||||||
| chr1:157040728
|
T | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3571A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040728 | ||||||
| chr1:157040732
|
T | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3567A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040732 | ||||||
| chr1:157040751
|
G | C | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3548C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040751 | ||||||
| chr1:157040752
|
C | T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3547G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040752 | ||||||
| chr1:157040759
|
A | C | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3540T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040759 | ||||||
| chr1:157040772
|
T | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3527A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040772 | ||||||
| chr1:157040787
|
A | T | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3512T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040787 | ||||||
| chr1:157040902
|
C | A | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3397G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040902 | ||||||
| chr1:157040903
|
A | C | 1 | a0001c0001t0006g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3396T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040903 | ||||||
| chr1:157041353
|
T | C | 2 | a0002c0004t0005g0024a0002c0004t0005g0025 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.32+2946A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041353 | ||||||
| chr1:157041502
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.32+2797G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041502 | ||||||
| chr1:157041533
|
A | G | 84 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(81): Show | 84 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.32+2766T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041533 | ||||||
| chr1:157041635
|
G | A | 1 | a0002c0004t0005g0128 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.32+2664C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041635 | ||||||
| chr1:157041699
|
C | A | 1 | a0002c0004t0005g0129 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.32+2600G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041699 | ||||||
| chr1:157041768
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01099.hp1 HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.32+2531G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041768 | ||||||
| chr1:157041814
|
T | C | 1 | a0001c0001t0004g0182 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.32+2485A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041814 | ||||||
| chr1:157041822
|
C | G | 2 | a0003c0003t0006g0026a0003c0003t0006g0027 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.32+2477G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041822 | ||||||
| chr1:157041827
|
G | A | 2 | a0003c0003t0006g0026a0003c0003t0006g0027 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.32+2472C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041827 | ||||||
| chr1:157042224
|
T | C | 2 | a0003c0003t0003g0270a0003c0003t0003g0271 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.32+2075A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042224 | ||||||
| chr1:157042391
|
C | T | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+1908G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042391 | ||||||
| chr1:157042429
|
T | C | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+1870A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042429 | ||||||
| chr1:157042454
|
T | C | 1 | a0001c0001t0001g0345 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.32+1845A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042454 | ||||||
| chr1:157042666
|
T | C | 3 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0001g0348 | 3 | NA19009.hp2 NA19064.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.32+1633A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042666 | ||||||
| chr1:157042783
|
A | C | 85 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(82): Show | 85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+1516T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042783 | ||||||
| chr1:157042802
|
A | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+1497T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042802 | ||||||
| chr1:157042989
|
G | A | 2 | a0002c0002t0002g0098a0002c0002t0002g0099 | 2 | NA18977.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.32+1310C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042989 | ||||||
| chr1:157043183
|
A | G | 3 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+1116T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043183 | ||||||
| chr1:157043273
|
C | T | 1 | a0002c0002t0002g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.32+1026G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043273 | ||||||
| chr1:157043357
|
T | A | 5 | a0002c0002t0002g0100a0002c0002t0002g0101a0002c0002t0002g0102others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+942A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043357 | ||||||
| chr1:157043369
|
T | C | 90 | a0001c0001t0006g0088a0002c0002t0002g0001a0002c0002t0002g0005others(87): Show | 91 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.32+930A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043369 | ||||||
| chr1:157043498
|
C | G | 356 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(353): Show | 358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.32+801G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043498 | ||||||
| chr1:157043579
|
T | C | 1 | a0002c0004t0005g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+720A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043579 | ||||||
| chr1:157043669
|
C | G | 3 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0030g0209 | 3 | HG01884.hp2 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.32+630G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043669 | ||||||
| chr1:157043962
|
C | A | 1 | a0001c0001t0004g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+337G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043962 | ||||||
| chr1:157043981
|
C | G | 1 | a0002c0002t0002g0005 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.32+318G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043981 | ||||||
| chr1:157044157
|
C | A | 21 | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+142G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157044157 |