Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23365 |
|---|---|
| ensemblid | ENSG00000196914.9 |
| hgncid | 14193 |
| symbol | ARHGEF12 |
| name | Rho guanine nucleotide exchange factor 12 |
| refseq_nuc | NM_015313.3 |
| refseq_prot | NP_056128.1 |
| ensembl_nuc | ENST00000397843.7 |
| ensembl_prot | ENSP00000380942.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 120336413 |
| end | 120489937 |
| strand | + |
| ver | v1.2 |
| region | chr11:120336413-120489937 |
| region5000 | chr11:120331413-120494937 |
| regionname0 | ARHGEF12_chr11_120336413_120489937 |
| regionname5000 | ARHGEF12_chr11_120331413_120494937 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1544 | 267 | 72 | 57 | 89 | 16 | 31 | 66 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0002 | 0/0 | 1544 | 26 | 0 | 0 | 20 | 0 | 6 | 16 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0003 | 0/0 | 1544 | 7 | 0 | 7 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0004 | 0/0 | 1544 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0005 | 0/0 | 1544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0006 | 0/0 | 1544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0007 | 0/0 | 1544 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0008 | 0/0 | 1544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0009 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0010 | 0/0 | 1544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4635 | 200 | 53 | 37 | 76 | 8 | 24 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0002 | 0/0 | 4635 | 37 | 15 | 14 | 0 | 6 | 2 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0003 | 0/0 | 4635 | 26 | 0 | 0 | 20 | 0 | 6 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0004 | 0/0 | 4635 | 16 | 0 | 0 | 11 | 0 | 5 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0005 | 0/0 | 4635 | 7 | 0 | 7 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0006 | 0/0 | 4635 | 6 | 0 | 5 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0007 | 0/0 | 4635 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0008 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0009 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0010 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0011 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0012 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0013 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0014 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0015 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0016 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0017 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| c0018 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 5692 | 115 | 28 | 27 | 37 | 8 | 13 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0002 | 0/0 | 5689 | 55 | 6 | 13 | 27 | 1 | 8 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0003 | 0/0 | 5692 | 25 | 5 | 12 | 0 | 6 | 2 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0004 | 0/0 | 5692 | 21 | 0 | 0 | 21 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0005 | 0/0 | 5692 | 11 | 0 | 0 | 6 | 0 | 5 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0006 | 0/0 | 5689 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0007 | 0/0 | 5690 | 8 | 7 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0008 | 0/0 | 5689 | 7 | 0 | 0 | 4 | 0 | 3 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0009 | 0/0 | 5692 | 6 | 0 | 2 | 3 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0010 | 0/0 | 5690 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0011 | 0/0 | 5692 | 5 | 0 | 2 | 0 | 1 | 2 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0012 | 0/0 | 5692 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0013 | 0/0 | 5692 | 3 | 1 | 2 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0014 | 0/0 | 5692 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0015 | 0/0 | 5687 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0016 | 0/0 | 5692 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0017 | 0/0 | 5689 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0018 | 0/0 | 5692 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0019 | 0/0 | 5692 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0020 | 0/0 | 5692 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0021 | 0/0 | 5692 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0022 | 0/0 | 5692 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0023 | 0/0 | 5692 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0024 | 0/0 | 5692 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0025 | 0/0 | 5692 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0026 | 0/0 | 5692 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0027 | 0/0 | 5692 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0028 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0029 | 0/0 | 5692 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0030 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0031 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0032 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0033 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0034 | 0/0 | 5692 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0035 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| t0036 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| 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 | 0 | 0 | 2 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4635 | 200 | 53 | 37 | 76 | 8 | 24 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0002 | 0/0 | 4635 | 37 | 15 | 14 | 0 | 6 | 2 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0004 | 0/0 | 4635 | 16 | 0 | 0 | 11 | 0 | 5 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0006 | 0/0 | 4635 | 6 | 0 | 5 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0007 | 0/0 | 4635 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0008 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0010 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0012 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0018 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0002c0003 | 0/0 | 4635 | 26 | 0 | 0 | 20 | 0 | 6 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0003c0005 | 0/0 | 4635 | 7 | 0 | 7 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0004c0009 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0005c0016 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0006c0013 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0007c0011 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0008c0014 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0009c0015 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0010c0017 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 10326 | 104 | 27 | 20 | 36 | 7 | 12 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0002 | 0/0 | 10323 | 25 | 4 | 8 | 11 | 0 | 2 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0004 | 0/0 | 10326 | 19 | 0 | 0 | 19 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0006 | 0/0 | 10323 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0007 | 0/0 | 10324 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0008 | 0/0 | 10323 | 7 | 0 | 0 | 4 | 0 | 3 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0009 | 0/0 | 10326 | 6 | 0 | 2 | 3 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0010 | 0/0 | 10324 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0011 | 0/0 | 10326 | 5 | 0 | 2 | 0 | 1 | 2 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0013 | 0/0 | 10326 | 3 | 1 | 2 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0014 | 0/0 | 10326 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0018 | 0/0 | 10326 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0021 | 0/0 | 10326 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0022 | 0/0 | 10326 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0023 | 0/0 | 10326 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0024 | 0/0 | 10326 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0025 | 0/0 | 10326 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0026 | 0/0 | 10326 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0027 | 0/0 | 10326 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0029 | 0/0 | 10326 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0031 | 0/0 | 10323 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0033 | 0/0 | 10323 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0035 | 0/0 | 10323 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0001t0036 | 0/0 | 10323 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0002t0002 | 0/0 | 10323 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0002t0003 | 0/0 | 10326 | 25 | 5 | 12 | 0 | 6 | 2 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0002t0007 | 0/0 | 10324 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0002t0016 | 0/0 | 10326 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0002t0019 | 0/0 | 10326 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0002t0034 | 0/0 | 10326 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0004t0005 | 0/0 | 10326 | 11 | 0 | 0 | 6 | 0 | 5 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0004t0012 | 0/0 | 10326 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0006t0002 | 0/0 | 10323 | 6 | 0 | 5 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0007t0015 | 0/0 | 10321 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0008t0020 | 0/0 | 10326 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0010t0001 | 0/0 | 10326 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0012t0001 | 0/0 | 10326 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0001c0018t0004 | 0/0 | 10326 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0002c0003t0002 | 0/0 | 10323 | 22 | 0 | 0 | 16 | 0 | 6 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0002c0003t0017 | 0/0 | 10323 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0002c0003t0028 | 0/0 | 10323 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0002c0003t0030 | 0/0 | 10323 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0003c0005t0001 | 0/0 | 10326 | 7 | 0 | 7 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0004c0009t0010 | 0/0 | 10324 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0005c0016t0032 | 0/0 | 10323 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0006c0013t0001 | 0/0 | 10326 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0007c0011t0001 | 0/0 | 10326 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0008c0014t0019 | 0/0 | 10326 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0009c0015t0004 | 0/0 | 10326 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| a0010c0017t0010 | 0/0 | 10324 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | copy fasta | chr11 | 120331413 | 120494937 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0008g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0008g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0008g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0008g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0008g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0009g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0009g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0009g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0010g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0010g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0011g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0011g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0011g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0011g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0011g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0013g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0013g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0014g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0014g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0014g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0018g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0018g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0021g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0022g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0023g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0024g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0025g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0026g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0027g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0029g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0031g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0033g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0035g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0001t0036g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0007g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0016g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0016g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0016g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0019g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0002t0034g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0005g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0005g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0012g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0012g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0012g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0012g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0004t0012g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0006t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0006t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0006t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0006t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0006t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0006t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0007t0015g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0007t0015g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0007t0015g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0008t0020g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0008t0020g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0010t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0012t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0001c0018t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0017g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0017g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0028g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0002c0003t0030g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0003c0005t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0003c0005t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0003c0005t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0003c0005t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0003c0005t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0003c0005t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0004c0009t0010g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0004c0009t0010g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0005c0016t0032g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0006c0013t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0007c0011t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0008c0014t0019g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0009c0015t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| a0010c0017t0010g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0001 | EUR | GBR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | GBR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | GBR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0065 | EUR | GBR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0040 | EUR | FIN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0036 | EUR | FIN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0283 | EAS | CHS | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00438 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | CHS | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00597 | hp2 | a0001 | c0004 | t0005 | g0048 | EAS | CHS | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00621 | hp1 | a0009 | c0015 | t0004 | g0229 | EAS | CHS | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0129 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0031 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00735 | hp2 | a0001 | c0006 | t0002 | g0301 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00738 | hp1 | a0001 | c0006 | t0002 | g0305 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00741 | hp1 | a0001 | c0001 | t0024 | g0214 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0034 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01069 | hp2 | a0001 | c0001 | t0013 | g0202 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0032 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01074 | hp2 | a0001 | c0007 | t0015 | g0126 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01081 | hp1 | a0003 | c0005 | t0001 | g0002 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01081 | hp2 | a0001 | c0001 | t0027 | g0270 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01099 | hp1 | a0001 | c0002 | t0034 | g0013 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0033 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01109 | hp1 | a0001 | c0002 | t0003 | g0027 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01167 | hp2 | a0001 | c0006 | t0002 | g0304 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01243 | hp1 | a0001 | c0001 | t0026 | g0230 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01243 | hp2 | a0001 | c0001 | t0011 | g0300 | AMR | PUR | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0039 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01255 | hp2 | a0001 | c0001 | t0013 | g0200 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0045 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0038 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0030 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01496 | hp1 | a0001 | c0006 | t0002 | g0303 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01496 | hp2 | a0003 | c0005 | t0001 | g0168 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | IBS | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0064 | EUR | IBS | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0001 | EUR | IBS | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01884 | hp1 | a0001 | c0002 | t0007 | g0041 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01934 | hp1 | a0001 | c0001 | t0011 | g0199 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01943 | hp2 | a0003 | c0005 | t0001 | g0002 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01952 | hp1 | a0003 | c0005 | t0001 | g0159 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01952 | hp2 | a0001 | c0001 | t0009 | g0007 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01975 | hp2 | a0003 | c0005 | t0001 | g0169 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01993 | hp2 | a0003 | c0005 | t0001 | g0165 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02027 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02040 | hp1 | a0001 | c0004 | t0005 | g0055 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02056 | hp2 | a0002 | c0003 | t0002 | g0137 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02083 | hp2 | a0002 | c0003 | t0030 | g0075 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0119 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02135 | hp2 | a0002 | c0003 | t0017 | g0282 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0062 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02148 | hp1 | a0001 | c0002 | t0003 | g0029 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02155 | hp1 | a0001 | c0004 | t0005 | g0054 | EAS | CDX | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | CDX | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CDX | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02165 | hp2 | a0002 | c0003 | t0017 | g0284 | EAS | CDX | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02258 | hp2 | a0001 | c0002 | t0016 | g0025 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02273 | hp1 | a0001 | c0001 | t0009 | g0006 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02273 | hp2 | a0003 | c0005 | t0001 | g0167 | AMR | PEL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0297 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02572 | hp2 | a0008 | c0014 | t0019 | g0011 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02602 | hp2 | a0001 | c0004 | t0005 | g0047 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0094 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02647 | hp1 | a0001 | c0007 | t0015 | g0127 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0096 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02683 | hp1 | a0002 | c0003 | t0002 | g0072 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02683 | hp2 | a0001 | c0001 | t0011 | g0192 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02698 | hp2 | a0001 | c0004 | t0005 | g0053 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02723 | hp1 | a0001 | c0001 | t0029 | g0190 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0134 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02735 | hp2 | a0002 | c0003 | t0002 | g0078 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0136 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02897 | hp1 | a0001 | c0002 | t0007 | g0042 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0063 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02922 | hp2 | a0001 | c0001 | t0018 | g0281 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02965 | hp1 | a0005 | c0016 | t0032 | g0100 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02965 | hp2 | a0001 | c0002 | t0016 | g0014 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02970 | hp1 | a0001 | c0001 | t0033 | g0131 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02976 | hp1 | a0001 | c0002 | t0007 | g0123 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02976 | hp2 | a0010 | c0017 | t0010 | g0298 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0122 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0294 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0118 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03195 | hp1 | a0001 | c0001 | t0018 | g0280 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03195 | hp2 | a0004 | c0009 | t0010 | g0276 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03209 | hp1 | a0001 | c0007 | t0015 | g0125 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03225 | hp1 | a0001 | c0002 | t0007 | g0044 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03239 | hp2 | a0001 | c0001 | t0022 | g0158 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03453 | hp2 | a0001 | c0001 | t0031 | g0090 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03486 | hp1 | a0001 | c0001 | t0035 | g0088 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03490 | hp1 | a0001 | c0001 | t0025 | g0235 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03490 | hp2 | a0002 | c0003 | t0002 | g0071 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03492 | hp1 | a0002 | c0003 | t0002 | g0081 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0089 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0138 | AFR | GWD | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0103 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03669 | hp1 | a0001 | c0002 | t0003 | g0028 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03704 | hp2 | a0001 | c0004 | t0005 | g0057 | SAS | PJL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03834 | hp2 | a0002 | c0003 | t0002 | g0083 | SAS | BEB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03942 | hp1 | a0001 | c0001 | t0009 | g0010 | SAS | BEB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03942 | hp2 | a0001 | c0004 | t0005 | g0056 | SAS | BEB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG04115 | hp1 | a0001 | c0001 | t0023 | g0178 | SAS | STU | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG04115 | hp2 | a0001 | c0001 | t0008 | g0092 | SAS | STU | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG04184 | hp1 | a0001 | c0001 | t0008 | g0130 | SAS | BEB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG04184 | hp2 | a0001 | c0004 | t0005 | g0049 | SAS | BEB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG04204 | hp1 | a0001 | c0001 | t0008 | g0104 | SAS | STU | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG04204 | hp2 | a0001 | c0001 | t0011 | g0286 | SAS | STU | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG04228 | hp1 | a0001 | c0001 | t0021 | g0162 | SAS | STU | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG04228 | hp2 | a0002 | c0003 | t0002 | g0082 | SAS | STU | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0101 | AFR | YRI | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18906 | hp1 | a0001 | c0002 | t0019 | g0012 | AFR | YRI | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18942 | hp2 | a0002 | c0003 | t0002 | g0084 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18945 | hp2 | a0001 | c0001 | t0014 | g0265 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18946 | hp1 | a0001 | c0001 | t0008 | g0020 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18946 | hp2 | a0001 | c0010 | t0001 | g0262 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18959 | hp1 | a0002 | c0003 | t0002 | g0067 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18959 | hp2 | a0001 | c0004 | t0012 | g0059 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18960 | hp1 | a0002 | c0003 | t0002 | g0086 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18965 | hp1 | a0001 | c0001 | t0014 | g0254 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18965 | hp2 | a0001 | c0001 | t0008 | g0111 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18967 | hp1 | a0002 | c0003 | t0002 | g0073 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18973 | hp1 | a0002 | c0003 | t0002 | g0076 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18977 | hp2 | a0002 | c0003 | t0002 | g0079 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18979 | hp2 | a0002 | c0003 | t0002 | g0016 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18982 | hp2 | a0001 | c0004 | t0005 | g0046 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18983 | hp1 | a0001 | c0004 | t0005 | g0051 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18984 | hp1 | a0001 | c0001 | t0008 | g0112 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18998 | hp1 | a0002 | c0003 | t0002 | g0077 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18999 | hp1 | a0002 | c0003 | t0002 | g0068 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19005 | hp2 | a0002 | c0003 | t0002 | g0080 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19011 | hp2 | a0002 | c0003 | t0002 | g0074 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19030 | hp1 | a0006 | c0013 | t0001 | g0293 | AFR | LWK | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19054 | hp2 | a0002 | c0003 | t0002 | g0070 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19056 | hp1 | a0001 | c0004 | t0012 | g0058 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19066 | hp1 | a0001 | c0004 | t0012 | g0050 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19066 | hp2 | a0001 | c0001 | t0014 | g0221 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19067 | hp1 | a0001 | c0004 | t0005 | g0061 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19070 | hp1 | a0001 | c0001 | t0009 | g0005 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19079 | hp2 | a0001 | c0018 | t0004 | g0239 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19080 | hp1 | a0001 | c0004 | t0012 | g0060 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19081 | hp1 | a0001 | c0004 | t0012 | g0052 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19083 | hp2 | a0002 | c0003 | t0002 | g0069 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19084 | hp1 | a0002 | c0003 | t0028 | g0066 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19086 | hp2 | a0002 | c0003 | t0002 | g0017 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19089 | hp1 | a0002 | c0003 | t0002 | g0085 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19240 | hp1 | a0001 | c0002 | t0016 | g0026 | AFR | YRI | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA19240 | hp2 | a0004 | c0009 | t0010 | g0299 | AFR | YRI | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0035 | AFR | ASW | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ASW | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA20752 | hp1 | a0001 | c0001 | t0011 | g0195 | EUR | TSI | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA20752 | hp2 | a0001 | c0006 | t0002 | g0302 | EUR | TSI | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA20805 | hp2 | a0001 | c0012 | t0001 | g0296 | EUR | TSI | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0037 | SAS | GIH | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA20905 | hp2 | a0007 | c0011 | t0001 | g0187 | SAS | GIH | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01123 | hp1 | a0001 | c0006 | t0002 | g0306 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG01123 | hp2 | a0001 | c0002 | t0007 | g0043 | AMR | CLM | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0023 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02109 | hp2 | a0001 | c0008 | t0020 | g0009 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02559 | hp1 | a0001 | c0008 | t0020 | g0008 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG03471 | hp2 | a0001 | c0001 | t0036 | g0087 | AFR | MSL | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | USA | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | USA | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0135 | AFR | USA | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0099 | AFR | USA | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA21309 | hp1 | a0001 | c0001 | t0013 | g0197 | AFR | LWK | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| NA21309 | hp2 | a0001 | c0002 | t0003 | g0128 | AFR | LWK | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0240 | REF | REF | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0248 | REF | REF | ARHGEF12_chr11_120331413_120494937 | ARHGEF12 | chr11 | 120331413 | 120494937 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:120429739
|
C | T | 1 | a0010 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.691C>T | p.Pro231Ser | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/41 | 1522/10326 | 691/4635 | 231/1544 | chr11 | 120429739 | ||
| chr11:120431897
|
A | G | 1 | a0005 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.910A>G | p.Ser304Gly | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/41 | 1741/10326 | 910/4635 | 304/1544 | chr11 | 120431897 | ||
| chr11:120440213
|
C | T | 1 | a0009 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1084C>T | p.His362Tyr | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/41 | 1915/10326 | 1084/4635 | 362/1544 | chr11 | 120440213 | ||
| chr11:120451664
|
A | G | 1 | a0008 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1996A>G | p.Met666Val | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/41 | 2827/10326 | 1996/4635 | 666/1544 | chr11 | 120451664 | ||
| chr11:120469351
|
A | T | 1 | a0002 | 26 | HG02056.hp2 HG02083.hp2 HG02135.hp2 others(23): Show |
missense_variant | MODERATE | c.2918A>T | p.Tyr973Phe | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/41 | 3749/10326 | 2918/4635 | 973/1544 | chr11 | 120469351 | ||
| chr11:120477467
|
A | T | 1 | a0007 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.3473A>T | p.Asp1158Val | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 36/41 | 4304/10326 | 3473/4635 | 1158/1544 | chr11 | 120477467 | ||
| chr11:120477485
|
A | C | 1 | a0006 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.3491A>C | p.Glu1164Ala | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 36/41 | 4322/10326 | 3491/4635 | 1164/1544 | chr11 | 120477485 | ||
| chr11:120478263
|
C | G | 1 | a0004 | 2 | HG03195.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.3640C>G | p.Gln1214Glu | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/41 | 4471/10326 | 3640/4635 | 1214/1544 | chr11 | 120478263 | ||
| chr11:120480110
|
A | G | 1 | a0003 | 7 | HG01081.hp1 HG01496.hp2 HG01943.hp2 others(4): Show |
missense_variant | MODERATE | c.3917A>G | p.Tyr1306Cys | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 38/41 | 4748/10326 | 3917/4635 | 1306/1544 | chr11 | 120480110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:120407768
|
A | G | 1 | a0001c0006 | 6 | HG00735.hp2 HG00738.hp1 HG01123.hp1 others(3): Show |
synonymous_variant | LOW | c.87A>G | p.Pro29Pro | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/41 | 918/10326 | 87/4635 | 29/1544 | chr11 | 120407768 | ||
| chr11:120420769
|
C | T | 1 | a0001c0018 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.216C>T | p.Cys72Cys | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/41 | 1047/10326 | 216/4635 | 72/1544 | chr11 | 120420769 | ||
| chr11:120458149
|
T | C | 2 | a0001c0002a0008c0014 | 38 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
synonymous_variant | LOW | c.2295T>C | p.Asp765Asp | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 25/41 | 3126/10326 | 2295/4635 | 765/1544 | chr11 | 120458149 | ||
| chr11:120458185
|
G | A | 1 | a0001c0008 | 2 | HG02109.hp2 HG02559.hp1 |
synonymous_variant | LOW | c.2331G>A | p.Val777Val | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 25/41 | 3162/10326 | 2331/4635 | 777/1544 | chr11 | 120458185 | ||
| chr11:120459310
|
T | G | 1 | a0001c0004 | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
synonymous_variant | LOW | c.2517T>G | p.Leu839Leu | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/41 | 3348/10326 | 2517/4635 | 839/1544 | chr11 | 120459310 | ||
| chr11:120475461
|
C | T | 2 | a0001c0012a0006c0013 | 2 | NA19030.hp1 NA20805.hp2 |
synonymous_variant | LOW | c.3231C>T | p.Ser1077Ser | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/41 | 4062/10326 | 3231/4635 | 1077/1544 | chr11 | 120475461 | ||
| chr11:120477231
|
A | G | 1 | a0001c0004 | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
synonymous_variant | LOW | c.3378A>G | p.Leu1126Leu | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 35/41 | 4209/10326 | 3378/4635 | 1126/1544 | chr11 | 120477231 | ||
| chr11:120478205
|
T | G | 1 | a0001c0010 | 1 | NA18946.hp2 | synonymous_variant | LOW | c.3582T>G | p.Ser1194Ser | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/41 | 4413/10326 | 3582/4635 | 1194/1544 | chr11 | 120478205 | ||
| chr11:120481372
|
C | T | 1 | a0001c0007 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.4350C>T | p.Ser1450Ser | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/41 | 5181/10326 | 4350/4635 | 1450/1544 | chr11 | 120481372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:120336464
|
C | T | 1 | a0001c0004t0012 | 5 | NA18959.hp2 NA19056.hp1 NA19066.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-780C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/41 | chr11 | 120336464 | ||||||
| chr11:120336609
|
T | C | 1 | a0001c0001t0021 | 1 | HG04228.hp1 | 5_prime_UTR_variant | MODIFIER | c.-635T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/41 | 635 | chr11 | 120336609 | |||||
| chr11:120336696
|
A | G | 26 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(23): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
5_prime_UTR_variant | MODIFIER | c.-548A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/41 | 548 | chr11 | 120336696 | |||||
| chr11:120336742
|
G | A | 1 | a0002c0003t0028 | 1 | NA19084.hp1 | 5_prime_UTR_variant | MODIFIER | c.-502G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/41 | 502 | chr11 | 120336742 | |||||
| chr11:120336774
|
C | G | 1 | a0001c0001t0027 | 1 | HG01081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-470C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/41 | 470 | chr11 | 120336774 | |||||
| chr11:120336799
|
G | C | 1 | a0001c0001t0029 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-445G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/41 | 445 | chr11 | 120336799 | |||||
| chr11:120336838
|
A | C | 2 | a0001c0001t0035a0001c0001t0036 | 2 | HG03471.hp2 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-406A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/41 | 406 | chr11 | 120336838 | |||||
| chr11:120336847
|
C | G | 1 | a0001c0002t0016 | 3 | HG02258.hp2 HG02965.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-397C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/41 | 397 | chr11 | 120336847 | |||||
| chr11:120485082
|
G | T | 2 | a0001c0002t0003a0001c0002t0016 | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 5 | chr11 | 120485082 | |||||
| chr11:120485248
|
A | G | 1 | a0001c0008t0020 | 2 | HG02109.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*171A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 171 | chr11 | 120485248 | |||||
| chr11:120485350
|
G | A | 2 | a0001c0001t0022a0001c0001t0023 | 2 | HG03239.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*273G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 273 | chr11 | 120485350 | |||||
| chr11:120485358
|
C | G | 2 | a0001c0004t0005a0001c0004t0012 | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*281C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 281 | chr11 | 120485358 | |||||
| chr11:120485608
|
C | G | 2 | a0001c0002t0003a0001c0002t0016 | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*531C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 531 | chr11 | 120485608 | |||||
| chr11:120485764
|
G | A | 1 | a0002c0003t0030 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*687G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 687 | chr11 | 120485764 | |||||
| chr11:120485872
|
G | A | 1 | a0001c0001t0013 | 3 | HG01069.hp2 HG01255.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*795G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 795 | chr11 | 120485872 | |||||
| chr11:120485874
|
C | T | 1 | a0001c0001t0014 | 3 | NA18945.hp2 NA18965.hp1 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*797C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 797 | chr11 | 120485874 | |||||
| chr11:120485949
|
T | C | 2 | a0001c0001t0031a0005c0016t0032 | 2 | HG02965.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*872T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 872 | chr11 | 120485949 | |||||
| chr11:120486123
|
A | G | 1 | a0001c0001t0008 | 7 | HG02129.hp2 HG04115.hp2 HG04184.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1046A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 1046 | chr11 | 120486123 | |||||
| chr11:120486309
|
T | C | 1 | a0001c0001t0035 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1232T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 1232 | chr11 | 120486309 | |||||
| chr11:120486367
|
C | T | 3 | a0001c0002t0019a0001c0002t0034a0008c0014t0019 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1290C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 1290 | chr11 | 120486367 | |||||
| chr11:120486464
|
G | A | 1 | a0001c0001t0022 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1387G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 1387 | chr11 | 120486464 | |||||
| chr11:120486511
|
A | G | 3 | a0001c0001t0004a0001c0018t0004a0009c0015t0004 | 21 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1434A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 1434 | chr11 | 120486511 | |||||
| chr11:120486525
|
A | G | 1 | a0001c0001t0018 | 2 | HG02922.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1448A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 1448 | chr11 | 120486525 | |||||
| chr11:120486632
|
G | A | 2 | a0001c0001t0006a0001c0001t0008 | 16 | HG02129.hp2 HG02615.hp1 HG02647.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1555G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 1555 | chr11 | 120486632 | |||||
| chr11:120486716
|
AT | A | 14 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(11): Show | 80 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1645delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 1645 | INFO_REALIGN_3_PRIME | chr11 | 120486716 | ||||
| chr11:120486827
|
T | C | 1 | a0001c0002t0034 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1750T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 1750 | chr11 | 120486827 | |||||
| chr11:120486838
|
G | A | 2 | a0001c0002t0003a0001c0002t0016 | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1761G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 1761 | chr11 | 120486838 | |||||
| chr11:120487133
|
CTT | C | 20 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(17): Show | 96 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2058_*2059delTT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 2058 | INFO_REALIGN_3_PRIME | chr11 | 120487133 | ||||
| chr11:120487300
|
G | T | 1 | a0005c0016t0032 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2223G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 2223 | chr11 | 120487300 | |||||
| chr11:120487436
|
C | T | 1 | a0001c0008t0020 | 2 | HG02109.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2359C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 2359 | chr11 | 120487436 | |||||
| chr11:120488036
|
A | G | 2 | a0001c0001t0031a0005c0016t0032 | 2 | HG02965.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2959A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 2959 | chr11 | 120488036 | |||||
| chr11:120488043
|
A | G | 1 | a0001c0001t0026 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2966A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 2966 | chr11 | 120488043 | |||||
| chr11:120488062
|
AGTT | A | 1 | a0001c0007t0015 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3001_*3003delGTT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 3001 | INFO_REALIGN_3_PRIME | chr11 | 120488062 | ||||
| chr11:120488468
|
T | C | 1 | a0001c0001t0033 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3391T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 3391 | chr11 | 120488468 | |||||
| chr11:120488474
|
A | G | 1 | a0001c0001t0029 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3397A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 3397 | chr11 | 120488474 | |||||
| chr11:120488601
|
C | G | 1 | a0001c0001t0025 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3524C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 3524 | chr11 | 120488601 | |||||
| chr11:120489247
|
T | C | 1 | a0001c0001t0011 | 5 | HG01243.hp2 HG01934.hp1 HG02683.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4170T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 4170 | chr11 | 120489247 | |||||
| chr11:120489562
|
G | A | 2 | a0001c0002t0003a0001c0002t0016 | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4485G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 4485 | chr11 | 120489562 | |||||
| chr11:120489668
|
C | T | 1 | a0001c0001t0024 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4591C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 41/41 | 4591 | chr11 | 120489668 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:120337293
|
CTTCG | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+23_32+26delTTCG | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120337293 | |||||
| chr11:120337476
|
A | G | 6 | a0001c0006t0002g0301a0001c0006t0002g0302a0001c0006t0002g0303others(3): Show | 6 | HG00735.hp2 HG00738.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+201A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120337476 | ||||||
| chr11:120337548
|
T | G | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.32+273T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120337548 | ||||||
| chr11:120338025
|
C | T | 1 | a0001c0001t0006g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+750C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120338025 | ||||||
| chr11:120338597
|
C | T | 1 | a0002c0003t0002g0137 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.32+1322C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120338597 | ||||||
| chr11:120338677
|
G | A | 51 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(48): Show | 52 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.32+1402G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120338677 | ||||||
| chr11:120338720
|
G | T | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.32+1445G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120338720 | ||||||
| chr11:120339005
|
C | CT | 145 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(142): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.32+1748dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120339005 | |||||
| chr11:120339005
|
C | CTT | 7 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0008g0130others(4): Show | 7 | HG00733.hp1 HG01952.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+1747_32+1748dup others(2): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120339005 | |||||
| chr11:120339010
|
T | G | 1 | a0001c0001t0001g0189 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.32+1735T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120339010 | ||||||
| chr11:120339103
|
T | G | 2 | a0001c0001t0006g0138a0001c0001t0029g0190 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.32+1828T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120339103 | ||||||
| chr11:120339189
|
T | A | 4 | a0001c0001t0006g0138a0001c0001t0029g0190a0001c0008t0020g0008others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+1914T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120339189 | ||||||
| chr11:120339226
|
G | A | 1 | a0001c0001t0001g0288 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.32+1951G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120339226 | ||||||
| chr11:120339453
|
G | C | 1 | a0001c0001t0009g0010 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.32+2178G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120339453 | ||||||
| chr11:120340229
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.32+2954C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120340229 | ||||||
| chr11:120340503
|
G | A | 140 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(137): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.32+3228G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120340503 | ||||||
| chr11:120340654
|
A | C | 1 | a0001c0001t0011g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.32+3379A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120340654 | ||||||
| chr11:120340894
|
A | G | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.32+3619A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120340894 | ||||||
| chr11:120341052
|
A | G | 4 | a0001c0001t0004g0283a0001c0001t0004g0285a0002c0003t0017g0282others(1): Show | 4 | HG00438.hp1 HG02135.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+3777A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120341052 | ||||||
| chr11:120341307
|
C | CTCGGCCT others(31): Show |
144 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(141): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.32+4049_32+4050ins others(38): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120341307 | |||||
| chr11:120341523
|
T | C | 3 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0023 | 3 | HG02109.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.32+4248T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120341523 | ||||||
| chr11:120341714
|
A | G | 77 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(74): Show | 77 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.32+4439A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120341714 | ||||||
| chr11:120341715
|
C | A | 1 | a0001c0001t0006g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+4440C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120341715 | ||||||
| chr11:120341892
|
T | C | 24 | a0002c0003t0002g0016a0002c0003t0002g0017a0002c0003t0002g0067others(21): Show | 24 | HG02056.hp2 HG02083.hp2 HG02683.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+4617T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120341892 | ||||||
| chr11:120341901
|
TTTGAG | T | 15 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0194others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.32+4628_32+4632del others(5): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120341901 | |||||
| chr11:120342585
|
C | T | 3 | a0001c0002t0003g0001a0001c0002t0003g0064a0001c0002t0003g0065 | 4 | HG00099.hp1 HG00140.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+5310C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120342585 | ||||||
| chr11:120342651
|
A | T | 144 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(141): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.32+5376A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120342651 | ||||||
| chr11:120343007
|
T | C | 2 | a0001c0001t0006g0138a0001c0001t0029g0190 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.32+5732T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120343007 | ||||||
| chr11:120343040
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.32+5765G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120343040 | ||||||
| chr11:120343061
|
AT | A | 144 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(141): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.32+5796delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120343061 | |||||
| chr11:120343398
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+6123A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120343398 | ||||||
| chr11:120343444
|
A | G | 2 | a0001c0002t0003g0062a0001c0002t0003g0063 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.32+6169A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120343444 | ||||||
| chr11:120343557
|
G | A | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.32+6282G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120343557 | ||||||
| chr11:120343575
|
G | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+6300G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120343575 | ||||||
| chr11:120343682
|
G | A | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+6407G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120343682 | ||||||
| chr11:120343819
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32+6544A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120343819 | ||||||
| chr11:120344057
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+6782A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120344057 | ||||||
| chr11:120344153
|
C | G | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+6878C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120344153 | ||||||
| chr11:120344265
|
C | CA | 35 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(32): Show | 35 | HG00621.hp1 HG00673.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.32+7019dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120344265 | |||||
| chr11:120344265
|
C | CAA | 12 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(9): Show | 12 | HG01433.hp1 HG02027.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+7018_32+7019dup others(2): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120344265 | |||||
| chr11:120344265
|
C | CAAAAAAA others(12): Show |
1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.32+7001_32+7019dup others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120344265 | |||||
| chr11:120344265
|
CA | C | 28 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(25): Show | 28 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.32+7019delA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120344265 | |||||
| chr11:120344265
|
CAA | C | 56 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(53): Show | 57 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.32+7018_32+7019del others(2): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120344265 | |||||
| chr11:120344265
|
CAAA | C | 96 | a0001c0001t0001g0177a0001c0001t0002g0018a0001c0001t0002g0019others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.32+7017_32+7019del others(3): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120344265 | |||||
| chr11:120344265
|
CAAAA | C | 8 | a0001c0001t0002g0133a0001c0001t0006g0122a0001c0002t0003g0045others(5): Show | 8 | HG01257.hp2 HG02451.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+7016_32+7019del others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120344265 | |||||
| chr11:120344265
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0018g0280a0001c0001t0018g0281 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.32+7007_32+7019del others(13): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120344265 | |||||
| chr11:120344285
|
A | C | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.32+7010A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120344285 | ||||||
| chr11:120344545
|
C | A | 1 | a0001c0001t0002g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.32+7270C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120344545 | ||||||
| chr11:120344553
|
T | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+7278T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120344553 | ||||||
| chr11:120344714
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+7439A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120344714 | ||||||
| chr11:120344795
|
A | C | 3 | a0001c0002t0007g0041a0001c0002t0007g0042a0001c0002t0007g0043 | 3 | HG01123.hp2 HG01884.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.32+7520A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120344795 | ||||||
| chr11:120345134
|
C | G | 116 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(113): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.32+7859C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120345134 | ||||||
| chr11:120345202
|
C | T | 1 | a0001c0001t0009g0004 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.32+7927C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120345202 | ||||||
| chr11:120345551
|
A | C | 144 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(141): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.32+8276A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120345551 | ||||||
| chr11:120345559
|
C | T | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+8284C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120345559 | ||||||
| chr11:120345685
|
G | A | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+8410G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120345685 | ||||||
| chr11:120345701
|
C | CA | 133 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.32+8446dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120345701 | |||||
| chr11:120345701
|
C | CAA | 44 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0146others(41): Show | 44 | HG00280.hp2 HG00597.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.32+8445_32+8446dup others(2): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120345701 | |||||
| chr11:120345701
|
C | CAAA | 7 | a0001c0001t0022g0158a0001c0004t0005g0046a0001c0004t0005g0047others(4): Show | 7 | HG00597.hp2 HG02602.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+8444_32+8446dup others(3): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120345701 | |||||
| chr11:120345716
|
A | C | 1 | a0009c0015t0004g0229 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.32+8441A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120345716 | ||||||
| chr11:120345747
|
A | AAT | 7 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 7 | HG00597.hp1 HG01099.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+8486_32+8487dup others(2): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120345747 | |||||
| chr11:120345902
|
C | G | 1 | a0001c0002t0034g0013 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.32+8627C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120345902 | ||||||
| chr11:120345959
|
C | T | 1 | a0010c0017t0010g0298 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.32+8684C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120345959 | ||||||
| chr11:120346197
|
T | A | 140 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(137): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.32+8922T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120346197 | ||||||
| chr11:120346289
|
T | A | 3 | a0001c0002t0016g0014a0001c0002t0016g0025a0001c0002t0016g0026 | 3 | HG02258.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.32+9014T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120346289 | ||||||
| chr11:120346551
|
G | T | 1 | a0009c0015t0004g0229 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.32+9276G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120346551 | ||||||
| chr11:120346746
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.32+9471A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120346746 | ||||||
| chr11:120347132
|
T | C | 3 | a0001c0001t0001g0209a0001c0001t0001g0232a0001c0001t0001g0245 | 3 | HG00639.hp2 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.32+9857T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347132 | ||||||
| chr11:120347132
|
TTTCC | T | 9 | a0001c0001t0001g0146a0001c0001t0001g0255a0001c0001t0001g0287others(6): Show | 10 | HG00099.hp1 HG00735.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.32+9908_32+9911del others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347132 | |||||
| chr11:120347141
|
TTCCTTCC others(20): Show |
T | 1 | a0001c0001t0002g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.32+9868_32+9894del others(27): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347141 | |||||
| chr11:120347143
|
C | CCTTTCCT others(6): Show |
1 | a0001c0002t0002g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.32+9871_32+9872ins others(13): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347143 | |||||
| chr11:120347143
|
C | CCTTTCCT others(10): Show |
1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.32+9871_32+9872ins others(17): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347143 | |||||
| chr11:120347143
|
C | CCTTTCTT others(1): Show |
5 | a0001c0002t0003g0036a0001c0002t0003g0037a0001c0002t0003g0038others(2): Show | 5 | HG00323.hp1 HG01255.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+9871_32+9872ins others(8): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347143 | |||||
| chr11:120347143
|
C | CCTTTCTT others(5): Show |
2 | a0001c0002t0003g0040a0001c0002t0003g0129 | 2 | HG00280.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.32+9871_32+9872ins others(12): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347143 | |||||
| chr11:120347144
|
C | CT | 22 | a0001c0001t0006g0138a0001c0001t0007g0136a0001c0001t0009g0003others(19): Show | 22 | HG00438.hp2 HG01099.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.32+9871dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347144 | |||||
| chr11:120347145
|
TTCC | T | 5 | a0001c0004t0005g0048a0001c0004t0005g0057a0001c0004t0012g0058others(2): Show | 5 | HG00597.hp2 HG03704.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+9872_32+9874del others(3): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347145 | |||||
| chr11:120347145
|
TTCCTTCC others(4): Show |
T | 10 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0049others(7): Show | 10 | HG02040.hp1 HG02155.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+9872_32+9882del others(11): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347145 | |||||
| chr11:120347145
|
TTCCTTCC others(8): Show |
T | 3 | a0001c0006t0002g0306a0002c0003t0002g0017a0002c0003t0002g0084 | 3 | HG01123.hp1 NA18942.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.32+9872_32+9886del others(15): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347145 | |||||
| chr11:120347145
|
TTCCTTCC others(12): Show |
T | 13 | a0001c0001t0002g0120a0001c0001t0006g0118a0001c0001t0008g0119others(10): Show | 13 | HG00735.hp2 HG00738.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.32+9872_32+9890del others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347145 | |||||
| chr11:120347145
|
TTCCTTCC others(16): Show |
T | 58 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(55): Show | 58 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.32+9872_32+9894del others(23): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347145 | |||||
| chr11:120347145
|
TTCCTTCC others(20): Show |
T | 1 | a0001c0001t0002g0097 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.32+9872_32+9898del others(27): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347145 | |||||
| chr11:120347145
|
TTCCTTCC others(24): Show |
T | 3 | a0001c0001t0033g0131a0001c0002t0007g0123a0001c0007t0015g0125 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.32+9872_32+9902del others(31): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347145 | |||||
| chr11:120347147
|
C | T | 23 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0009g0005others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.32+9872C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347147 | ||||||
| chr11:120347149
|
T | C | 6 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0009g0005others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+9874T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347149 | ||||||
| chr11:120347151
|
C | CCTTTCTT others(9): Show |
1 | a0001c0002t0034g0013 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.32+9879_32+9880ins others(16): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347151 | |||||
| chr11:120347151
|
C | CTTT | 3 | a0001c0001t0007g0136a0001c0002t0003g0128a0001c0002t0007g0042 | 3 | HG02809.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.32+9876_32+9877ins others(3): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347151 | ||||||
| chr11:120347151
|
C | CTTTCTTT | 11 | a0001c0001t0006g0138a0001c0001t0009g0003a0001c0001t0009g0004others(8): Show | 11 | HG00438.hp2 HG01884.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+9876_32+9877ins others(7): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347151 | ||||||
| chr11:120347151
|
C | CTTTCTTT others(4): Show |
4 | a0001c0002t0003g0063a0001c0002t0007g0043a0001c0002t0007g0044others(1): Show | 4 | HG01123.hp2 HG02922.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+9876_32+9877ins others(11): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347151 | ||||||
| chr11:120347151
|
C | CTTTCTTT others(8): Show |
1 | a0001c0002t0003g0027 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.32+9876_32+9877ins others(15): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347151 | ||||||
| chr11:120347151
|
C | CTTTCTTT others(12): Show |
2 | a0001c0001t0009g0007a0001c0002t0003g0028 | 2 | HG01952.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.32+9876_32+9877ins others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347151 | ||||||
| chr11:120347151
|
C | T | 27 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0009g0005others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.32+9876C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347151 | ||||||
| chr11:120347152
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.32+9877C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347152 | ||||||
| chr11:120347154
|
TC | T | 5 | a0001c0004t0005g0048a0001c0004t0005g0057a0001c0004t0012g0058others(2): Show | 5 | HG00597.hp2 HG03704.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+9881delC | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347154 | |||||
| chr11:120347155
|
C | T | 49 | a0001c0001t0006g0138a0001c0001t0007g0134a0001c0001t0007g0135others(46): Show | 50 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.32+9880C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347155 | ||||||
| chr11:120347159
|
C | T | 54 | a0001c0001t0006g0138a0001c0001t0007g0134a0001c0001t0007g0135others(51): Show | 55 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.32+9884C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347159 | ||||||
| chr11:120347162
|
TC | T | 10 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0049others(7): Show | 10 | HG02040.hp1 HG02155.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+9889delC | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347162 | |||||
| chr11:120347163
|
C | T | 55 | a0001c0001t0006g0138a0001c0001t0007g0134a0001c0001t0007g0135others(52): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.32+9888C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347163 | ||||||
| chr11:120347166
|
TC | T | 3 | a0001c0006t0002g0306a0002c0003t0002g0017a0002c0003t0002g0084 | 3 | HG01123.hp1 NA18942.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.32+9893delC | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347166 | |||||
| chr11:120347167
|
C | T | 65 | a0001c0001t0006g0138a0001c0001t0007g0134a0001c0001t0007g0135others(62): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.32+9892C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347167 | ||||||
| chr11:120347170
|
TC | T | 13 | a0001c0001t0002g0120a0001c0001t0006g0118a0001c0001t0008g0119others(10): Show | 13 | HG00735.hp2 HG00738.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.32+9897delC | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347170 | |||||
| chr11:120347171
|
C | T | 68 | a0001c0001t0006g0138a0001c0001t0007g0134a0001c0001t0007g0135others(65): Show | 69 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.32+9896C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347171 | ||||||
| chr11:120347174
|
TC | T | 59 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(56): Show | 59 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.32+9901delC | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347174 | |||||
| chr11:120347175
|
C | CCTTTCTT others(1): Show |
8 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(5): Show | 8 | HG00140.hp1 HG01943.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+9903_32+9904ins others(8): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347175 | |||||
| chr11:120347175
|
C | CCTTTCTT others(5): Show |
3 | a0001c0001t0001g0228a0001c0001t0027g0270a0002c0003t0017g0282 | 3 | HG01081.hp2 HG02135.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.32+9903_32+9904ins others(12): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347175 | |||||
| chr11:120347175
|
C | CCTTTCTT others(9): Show |
2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.32+9903_32+9904ins others(16): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347175 | |||||
| chr11:120347175
|
C | CCTTTCTT others(13): Show |
1 | a0001c0001t0001g0271 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.32+9903_32+9904ins others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347175 | |||||
| chr11:120347175
|
C | T | 83 | a0001c0001t0001g0292a0001c0001t0002g0120a0001c0001t0004g0272others(80): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.32+9900C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347175 | ||||||
| chr11:120347179
|
C | CCTTGCTT others(25): Show |
1 | a0006c0013t0001g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.32+9907_32+9908ins others(32): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347179 | |||||
| chr11:120347179
|
C | CCTTT | 8 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0153others(5): Show | 8 | HG00597.hp1 HG00673.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+9907_32+9908ins others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347179 | |||||
| chr11:120347179
|
C | CCTTTCTT others(8): Show |
1 | a0001c0001t0014g0254 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.32+9907_32+9908ins others(15): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347179 | |||||
| chr11:120347179
|
C | CCTTTCTT others(1): Show |
5 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0241others(2): Show | 5 | NA18947.hp1 NA18999.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+9907_32+9908ins others(8): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347179 | |||||
| chr11:120347179
|
C | CCTTTCTT others(5): Show |
21 | a0001c0001t0001g0140a0001c0001t0001g0201a0001c0001t0001g0205others(18): Show | 21 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+9907_32+9908ins others(12): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347179 | |||||
| chr11:120347179
|
C | CCTTTCTT others(9): Show |
11 | a0001c0001t0001g0259a0001c0001t0001g0278a0001c0001t0004g0243others(8): Show | 11 | HG00621.hp1 HG01069.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+9907_32+9908ins others(16): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347179 | |||||
| chr11:120347179
|
C | CCTTTCTT others(13): Show |
3 | a0001c0001t0001g0194a0001c0001t0001g0207a0001c0001t0001g0289 | 3 | HG00280.hp2 HG02027.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.32+9907_32+9908ins others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347179 | |||||
| chr11:120347179
|
C | CCTTTCTT others(21): Show |
1 | a0001c0001t0001g0275 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.32+9907_32+9908ins others(28): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347179 | |||||
| chr11:120347179
|
C | T | 176 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0146others(173): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.32+9904C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347179 | ||||||
| chr11:120347182
|
TC | T | 3 | a0001c0001t0033g0131a0001c0002t0007g0123a0001c0007t0015g0125 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.32+9909delC | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347182 | |||||
| chr11:120347183
|
C | CCTTCCTT others(33): Show |
1 | a0001c0001t0001g0191 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.32+9911_32+9912ins others(40): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTCCTT others(25): Show |
1 | a0001c0001t0026g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.32+9911_32+9912ins others(32): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTCCTT others(17): Show |
1 | a0001c0001t0011g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.32+9911_32+9912ins others(24): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTCCTT others(33): Show |
1 | a0001c0001t0011g0195 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.32+9911_32+9912ins others(40): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTCCTT others(5): Show |
1 | a0001c0001t0001g0196 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.32+9911_32+9912ins others(12): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTCCTT others(9): Show |
1 | a0001c0012t0001g0296 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.32+9911_32+9912ins others(16): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTCCTT others(17): Show |
3 | a0001c0001t0001g0233a0001c0001t0018g0280a0001c0001t0018g0281 | 3 | HG02922.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.32+9911_32+9912ins others(24): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTCCTT others(21): Show |
2 | a0001c0001t0001g0210a0001c0001t0011g0286 | 2 | HG01433.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.32+9911_32+9912ins others(28): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTCCTT others(25): Show |
2 | a0001c0001t0001g0211a0001c0001t0001g0232 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.32+9911_32+9912ins others(32): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTCCTT others(33): Show |
1 | a0001c0001t0001g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.32+9911_32+9912ins others(40): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTCCTT others(13): Show |
3 | a0001c0001t0001g0234a0001c0001t0004g0246a0001c0001t0004g0247 | 3 | HG01515.hp1 HG02040.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.32+9911_32+9912ins others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTCCTT others(17): Show |
3 | a0001c0001t0001g0198a0001c0001t0011g0192a0001c0001t0013g0197 | 3 | HG01993.hp1 HG02683.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.32+9911_32+9912ins others(24): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTCCTT others(21): Show |
2 | a0001c0001t0001g0213a0001c0001t0011g0199 | 2 | HG01934.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.32+9911_32+9912ins others(28): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTT | 9 | a0001c0001t0001g0148a0001c0001t0001g0166a0003c0005t0001g0002others(6): Show | 10 | HG00738.hp2 HG01081.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+9927_32+9930dup others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTTCTT others(1): Show |
3 | a0001c0001t0001g0160a0001c0001t0001g0170a0001c0001t0001g0188 | 3 | HG02698.hp1 NA18942.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.32+9923_32+9930dup others(8): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTTCTT others(5): Show |
2 | a0001c0001t0001g0209a0001c0001t0001g0273 | 2 | HG01256.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.32+9919_32+9930dup others(12): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTTCTT others(9): Show |
4 | a0001c0001t0001g0290a0001c0001t0004g0250a0001c0001t0004g0251others(1): Show | 4 | HG03540.hp1 NA19070.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+9915_32+9930dup others(16): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTTCTT others(13): Show |
9 | a0001c0001t0001g0231a0001c0001t0001g0236a0001c0001t0001g0237others(6): Show | 9 | HG00099.hp2 HG00741.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+9911_32+9930dup others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTTCTT others(17): Show |
1 | a0001c0001t0001g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.32+9930_32+9931ins others(24): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | CCTTTCTT others(25): Show |
2 | a0001c0001t0001g0240a0001c0018t0004g0239 | 2 | NA19079.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.32+9930_32+9931ins others(32): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347183 | |||||
| chr11:120347183
|
C | T | 246 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(243): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.32+9908C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347183 | ||||||
| chr11:120347198
|
T | TTC | 12 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0143others(9): Show | 12 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+9925_32+9926dup others(2): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347198 | |||||
| chr11:120347204
|
C | CTTTCTTT others(7): Show |
1 | a0001c0001t0001g0288 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.32+9930_32+9931ins others(14): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347204 | |||||
| chr11:120347262
|
CTCTCTGT others(3): Show |
C | 3 | a0001c0002t0016g0014a0001c0002t0016g0025a0001c0002t0016g0026 | 3 | HG02258.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.32+9989_32+9998del others(10): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347262 | |||||
| chr11:120347264
|
CTCTG | C | 4 | a0001c0002t0003g0035a0001c0002t0007g0041a0001c0002t0007g0043others(1): Show | 4 | HG00597.hp2 HG01123.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+9995_32+9998del others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347264 | |||||
| chr11:120347266
|
C | CTCTCTCT others(3): Show |
1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.32+9992_32+9993ins others(10): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347266 | |||||
| chr11:120347266
|
C | CTCTGTGT others(1): Show |
9 | a0001c0004t0005g0049a0001c0004t0005g0051a0001c0004t0005g0053others(6): Show | 9 | HG02040.hp1 HG02155.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+9992_32+9993ins others(8): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347266 | |||||
| chr11:120347266
|
C | CTCTGTGT others(3): Show |
4 | a0001c0004t0005g0046a0001c0004t0005g0056a0001c0004t0012g0052others(1): Show | 4 | HG03942.hp2 NA18959.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+9992_32+9993ins others(10): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347266 | |||||
| chr11:120347266
|
C | CTCTGTGT others(9): Show |
1 | a0001c0004t0012g0060 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.32+9992_32+9993ins others(16): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347266 | |||||
| chr11:120347266
|
C | G | 7 | a0001c0001t0006g0138a0001c0001t0009g0003a0001c0001t0009g0004others(4): Show | 7 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+9991C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347266 | ||||||
| chr11:120347266
|
CTGTCTG | C | 26 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(23): Show | 27 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.32+9995_32+10000de others(7): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347266 | |||||
| chr11:120347266
|
CTGTCTGT others(3): Show |
C | 6 | a0001c0001t0002g0021a0001c0001t0002g0093a0001c0001t0002g0114others(3): Show | 6 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+9995_32+10004de others(11): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347266 | |||||
| chr11:120347266
|
CTGTCTGT others(5): Show |
C | 24 | a0001c0001t0002g0018a0001c0001t0002g0091a0001c0001t0002g0095others(21): Show | 24 | HG01074.hp2 HG01256.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+9995_32+10006de others(13): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347266 | |||||
| chr11:120347266
|
CTGTCTGT others(7): Show |
C | 53 | a0001c0001t0002g0019a0001c0001t0002g0102a0001c0001t0002g0124others(50): Show | 53 | HG00735.hp2 HG00738.hp1 HG01123.hp1 others(50): Show |
intron_variant | MODIFIER | c.32+9995_32+10008de others(15): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347266 | |||||
| chr11:120347268
|
G | C | 2 | a0001c0002t0007g0042a0001c0002t0034g0013 | 2 | HG01099.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.32+9993G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347268 | ||||||
| chr11:120347270
|
C | CTG | 43 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0148others(40): Show | 44 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.32+10031_32+10032d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347270 | |||||
| chr11:120347270
|
C | CTGTG | 4 | a0001c0001t0001g0176a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | HG01934.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+10029_32+10032d others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347270 | |||||
| chr11:120347270
|
C | CTGTGTGT others(1): Show |
3 | a0001c0001t0010g0294a0001c0001t0010g0297a0010c0017t0010g0298 | 3 | HG02451.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32+10025_32+10032d others(10): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347270 | |||||
| chr11:120347270
|
C | CTGTGTGT others(7): Show |
2 | a0004c0009t0010g0276a0004c0009t0010g0299 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.32+10019_32+10032d others(16): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120347270 | |||||
| chr11:120347270
|
C | G | 26 | a0001c0001t0006g0138a0001c0001t0009g0003a0001c0001t0009g0004others(23): Show | 26 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.32+9995C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347270 | ||||||
| chr11:120347272
|
G | C | 1 | a0001c0004t0005g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.32+9997G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347272 | ||||||
| chr11:120347274
|
G | C | 1 | a0001c0012t0001g0296 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.32+9999G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347274 | ||||||
| chr11:120347278
|
G | C | 1 | a0001c0001t0002g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.32+10003G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347278 | ||||||
| chr11:120347280
|
G | C | 1 | a0001c0001t0002g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.32+10005G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347280 | ||||||
| chr11:120347282
|
G | C | 1 | a0001c0001t0008g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.32+10007G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347282 | ||||||
| chr11:120347531
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.32+10256C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347531 | ||||||
| chr11:120347534
|
T | C | 144 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(141): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.32+10259T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347534 | ||||||
| chr11:120347742
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.32+10467C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347742 | ||||||
| chr11:120347968
|
G | T | 1 | a0001c0001t0004g0244 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.32+10693G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347968 | ||||||
| chr11:120347972
|
A | G | 2 | a0002c0003t0002g0071a0002c0003t0002g0081 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.32+10697A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120347972 | ||||||
| chr11:120348012
|
C | T | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+10737C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120348012 | ||||||
| chr11:120348024
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0237 | 2 | HG00099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.32+10749A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120348024 | ||||||
| chr11:120348148
|
C | T | 4 | a0001c0002t0007g0041a0001c0002t0007g0042a0001c0002t0007g0043others(1): Show | 4 | HG01123.hp2 HG01884.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+10873C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120348148 | ||||||
| chr11:120348313
|
G | C | 4 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | HG02615.hp2 HG02970.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+11038G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120348313 | ||||||
| chr11:120348428
|
A | G | 2 | a0004c0009t0010g0276a0004c0009t0010g0299 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.32+11153A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120348428 | ||||||
| chr11:120348616
|
C | T | 1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.32+11341C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120348616 | ||||||
| chr11:120348837
|
G | A | 36 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0149others(33): Show | 37 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.32+11562G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120348837 | ||||||
| chr11:120349034
|
A | G | 2 | a0001c0001t0002g0113a0001c0001t0002g0132 | 2 | NA18940.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.32+11759A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120349034 | ||||||
| chr11:120349381
|
A | AT | 7 | a0001c0001t0008g0020a0001c0001t0008g0092a0001c0001t0008g0104others(4): Show | 7 | HG02129.hp2 HG04115.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+12112dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120349381 | |||||
| chr11:120349420
|
G | T | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+12145G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120349420 | ||||||
| chr11:120349463
|
GTATT | G | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.32+12196_32+12199d others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120349463 | |||||
| chr11:120349477
|
A | C | 1 | a0001c0001t0001g0191 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.32+12202A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120349477 | ||||||
| chr11:120349559
|
T | C | 144 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(141): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.32+12284T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120349559 | ||||||
| chr11:120349568
|
T | G | 1 | a0001c0002t0003g0028 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.32+12293T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120349568 | ||||||
| chr11:120349712
|
G | A | 3 | a0001c0001t0014g0221a0001c0001t0014g0254a0001c0001t0014g0265 | 3 | NA18945.hp2 NA18965.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.32+12437G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120349712 | ||||||
| chr11:120349823
|
G | A | 1 | a0001c0002t0034g0013 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.32+12548G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120349823 | ||||||
| chr11:120349848
|
T | A | 1 | a0001c0002t0007g0041 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.32+12573T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120349848 | ||||||
| chr11:120349979
|
C | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+12704C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120349979 | ||||||
| chr11:120350069
|
T | C | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+12794T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120350069 | ||||||
| chr11:120350359
|
C | T | 84 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(81): Show | 84 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.32+13084C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120350359 | ||||||
| chr11:120350514
|
C | CA | 19 | a0001c0001t0001g0146a0001c0001t0001g0274a0001c0001t0009g0006others(16): Show | 19 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.32+13254dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120350514 | |||||
| chr11:120350631
|
ACTGT | A | 31 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.32+13359_32+13362d others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120350631 | |||||
| chr11:120350712
|
G | A | 6 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(3): Show | 6 | HG01074.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+13437G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120350712 | ||||||
| chr11:120350721
|
G | C | 1 | a0001c0001t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.32+13446G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120350721 | ||||||
| chr11:120350909
|
A | G | 144 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(141): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.32+13634A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120350909 | ||||||
| chr11:120350943
|
G | A | 204 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(201): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.32+13668G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120350943 | ||||||
| chr11:120351088
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32+13813G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351088 | ||||||
| chr11:120351092
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+13817A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351092 | ||||||
| chr11:120351146
|
G | A | 1 | a0001c0002t0003g0035 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.32+13871G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351146 | ||||||
| chr11:120351186
|
A | G | 4 | a0002c0003t0002g0070a0002c0003t0002g0079a0002c0003t0002g0080others(1): Show | 4 | NA18960.hp1 NA18977.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+13911A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351186 | ||||||
| chr11:120351193
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.32+13918C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351193 | ||||||
| chr11:120351234
|
C | T | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32+13959C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351234 | ||||||
| chr11:120351244
|
G | A | 1 | a0001c0002t0007g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.32+13969G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351244 | ||||||
| chr11:120351278
|
C | T | 77 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(74): Show | 77 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.32+14003C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351278 | ||||||
| chr11:120351279
|
G | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+14004G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351279 | ||||||
| chr11:120351341
|
C | CA | 29 | a0001c0001t0024g0214a0001c0001t0031g0090a0001c0002t0003g0001others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.32+14089dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351341 | |||||
| chr11:120351341
|
C | CAA | 66 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(63): Show | 66 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.32+14088_32+14089d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351341 | |||||
| chr11:120351341
|
C | CAAA | 32 | a0001c0001t0002g0097a0001c0001t0002g0105a0001c0001t0002g0114others(29): Show | 32 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.32+14087_32+14089d others(5): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351341 | |||||
| chr11:120351341
|
C | CAAAA | 11 | a0001c0001t0006g0094a0001c0001t0006g0138a0001c0001t0009g0006others(8): Show | 11 | HG02155.hp1 HG02273.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+14086_32+14089d others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351341 | |||||
| chr11:120351341
|
CA | C | 119 | a0001c0001t0001g0140a0001c0001t0001g0144a0001c0001t0001g0147others(116): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.32+14089delA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351341 | |||||
| chr11:120351398
|
GTAGGAAA others(26): Show |
G | 1 | a0001c0001t0001g0279 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.32+14126_32+14158d others(35): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351398 | |||||
| chr11:120351408
|
AATATATA others(1): Show |
A | 4 | a0001c0001t0001g0207a0001c0001t0001g0245a0001c0001t0001g0249others(1): Show | 4 | HG00639.hp2 HG01099.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+14174_32+14181d others(10): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351408 | |||||
| chr11:120351408
|
AATATATA others(3): Show |
A | 14 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(11): Show | 14 | HG00733.hp2 NA18945.hp2 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.32+14172_32+14181d others(12): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351408 | |||||
| chr11:120351408
|
AATATATA others(11): Show |
A | 6 | a0001c0004t0005g0049a0001c0004t0005g0053a0001c0004t0005g0056others(3): Show | 6 | HG02698.hp2 HG03942.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+14164_32+14181d others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351408 | |||||
| chr11:120351408
|
AATATATA others(13): Show |
A | 1 | a0001c0004t0005g0057 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.32+14162_32+14181d others(22): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351408 | |||||
| chr11:120351408
|
AATATATA others(19): Show |
A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+14156_32+14181d others(28): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351408 | |||||
| chr11:120351419
|
ATATATAT others(33): Show |
A | 1 | a0001c0012t0001g0296 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.32+14146_32+14185d others(42): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351419 | |||||
| chr11:120351421
|
ATATATAT others(31): Show |
A | 3 | a0001c0001t0008g0020a0001c0001t0008g0112a0001c0002t0003g0034 | 3 | HG00741.hp2 NA18946.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.32+14148_32+14185d others(40): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351421 | |||||
| chr11:120351423
|
ATATATAT others(29): Show |
A | 3 | a0001c0001t0002g0105a0001c0001t0002g0121a0001c0001t0006g0103 | 3 | HG03579.hp2 NA18947.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.32+14150_32+14185d others(38): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351423 | |||||
| chr11:120351423
|
ATATATAT others(30): Show |
A | 40 | a0001c0001t0002g0019a0001c0001t0002g0021a0001c0001t0002g0091others(37): Show | 40 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.32+14150_32+14186d others(39): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351423 | |||||
| chr11:120351423
|
ATATATAT others(31): Show |
A | 32 | a0001c0001t0008g0104a0001c0001t0008g0111a0001c0001t0008g0119others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.32+14150_32+14187d others(40): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351423 | |||||
| chr11:120351423
|
ATATATAT others(32): Show |
A | 4 | a0001c0002t0003g0030a0001c0002t0003g0031a0001c0002t0003g0035others(1): Show | 4 | HG00735.hp1 HG01358.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+14150_32+14188d others(41): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351423 | |||||
| chr11:120351425
|
ATATATAT others(29): Show |
A | 1 | a0001c0001t0002g0108 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.32+14152_32+14187d others(38): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351425 | |||||
| chr11:120351425
|
ATATATAT others(30): Show |
A | 11 | a0001c0001t0002g0018a0001c0001t0002g0106a0001c0001t0002g0107others(8): Show | 11 | HG01109.hp1 HG01123.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+14152_32+14188d others(39): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351425 | |||||
| chr11:120351425
|
ATATATAT others(31): Show |
A | 13 | a0001c0002t0003g0015a0001c0002t0003g0032a0001c0002t0003g0036others(10): Show | 13 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.32+14152_32+14189d others(40): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351425 | |||||
| chr11:120351426
|
TATATATA others(22): Show |
T | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+14152_32+14180d others(31): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351426 | ||||||
| chr11:120351427
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0001g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.32+14154_32+14182d others(31): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351427 | |||||
| chr11:120351427
|
ATATATAT others(23): Show |
A | 10 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0152others(7): Show | 10 | HG00621.hp2 HG01074.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.32+14154_32+14183d others(32): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351427 | |||||
| chr11:120351427
|
ATATATAT others(24): Show |
A | 33 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0143others(30): Show | 34 | HG00597.hp1 HG00738.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.32+14154_32+14184d others(33): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351427 | |||||
| chr11:120351427
|
ATATATAT others(25): Show |
A | 1 | a0001c0001t0001g0149 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.32+14154_32+14185d others(34): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351427 | |||||
| chr11:120351427
|
ATATATAT others(29): Show |
A | 1 | a0001c0001t0031g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.32+14154_32+14189d others(38): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351427 | |||||
| chr11:120351427
|
ATATATAT others(30): Show |
A | 4 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127others(1): Show | 4 | HG01074.hp2 HG02083.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+14154_32+14190d others(39): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351427 | |||||
| chr11:120351429
|
ATATATAT others(22): Show |
A | 4 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+14156_32+14184d others(31): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351429 | |||||
| chr11:120351429
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0001g0171 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.32+14156_32+14185d others(32): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351429 | |||||
| chr11:120351429
|
ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.32+14156_32+14186d others(33): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351429 | |||||
| chr11:120351429
|
ATATATAT others(25): Show |
A | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32+14156_32+14187d others(34): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351429 | |||||
| chr11:120351429
|
ATATATAT others(29): Show |
A | 1 | a0005c0016t0032g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.32+14156_32+14191d others(38): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351429 | |||||
| chr11:120351430
|
TATATATA others(10): Show |
T | 2 | a0001c0004t0005g0054a0001c0004t0005g0055 | 2 | HG02040.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.32+14156_32+14172d others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351430 | ||||||
| chr11:120351432
|
TATATATA others(12): Show |
T | 6 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0051others(3): Show | 6 | HG02602.hp2 NA18959.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+14158_32+14176d others(21): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351432 | ||||||
| chr11:120351433
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0006g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+14160_32+14184d others(27): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351433 | |||||
| chr11:120351433
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0025g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.32+14160_32+14187d others(30): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351433 | |||||
| chr11:120351433
|
ATATATAT others(26): Show |
A | 2 | a0001c0001t0007g0134a0001c0001t0007g0135 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.32+14160_32+14192d others(35): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351433 | |||||
| chr11:120351434
|
TATATATA others(10): Show |
T | 1 | a0001c0004t0005g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.32+14160_32+14176d others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351434 | ||||||
| chr11:120351436
|
TATATATA others(10): Show |
T | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.32+14162_32+14178d others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351436 | ||||||
| chr11:120351436
|
TATATATA others(12): Show |
T | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+14162_32+14180d others(21): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351436 | ||||||
| chr11:120351437
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0027g0270 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.32+14164_32+14183d others(22): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351437 | |||||
| chr11:120351437
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0007g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.32+14164_32+14192d others(31): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351437 | |||||
| chr11:120351437
|
ATATATAT others(23): Show |
A | 1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.32+14164_32+14193d others(32): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351437 | |||||
| chr11:120351438
|
TATATATA others(6): Show |
T | 1 | a0001c0002t0034g0013 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.32+14164_32+14176d others(15): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351438 | ||||||
| chr11:120351439
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0013g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.32+14166_32+14186d others(23): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351439 | |||||
| chr11:120351441
|
ATATATAT others(13): Show |
A | 2 | a0001c0001t0013g0202a0010c0017t0010g0298 | 2 | HG01069.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.32+14168_32+14187d others(22): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351441 | |||||
| chr11:120351441
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0013g0200 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.32+14168_32+14188d others(23): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351441 | |||||
| chr11:120351443
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0240 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.32+14170_32+14188d others(21): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351443 | |||||
| chr11:120351443
|
ATATATAT others(14): Show |
A | 2 | a0001c0001t0010g0294a0001c0001t0010g0297 | 2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32+14170_32+14190d others(23): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351443 | |||||
| chr11:120351445
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0238 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.32+14172_32+14182d others(13): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351445 | |||||
| chr11:120351446
|
TATATATA others(2): Show |
T | 3 | a0001c0001t0001g0223a0001c0001t0004g0220a0001c0001t0004g0260 | 3 | NA18979.hp1 NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.32+14172_32+14180d others(11): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351446 | ||||||
| chr11:120351447
|
ATATATAT others(2): Show |
A | 7 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0275others(4): Show | 7 | HG00673.hp1 HG02135.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+14174_32+14182d others(11): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351447 | |||||
| chr11:120351447
|
ATATATAT others(3): Show |
A | 11 | a0001c0001t0001g0189a0001c0001t0001g0227a0001c0001t0001g0241others(8): Show | 11 | HG00140.hp1 HG01433.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+14174_32+14183d others(12): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351447 | |||||
| chr11:120351448
|
TATATATA | T | 3 | a0001c0001t0001g0219a0001c0001t0001g0236a0001c0001t0001g0259 | 3 | HG01517.hp2 NA19012.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.32+14174_32+14180d others(9): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351448 | ||||||
| chr11:120351449
|
A | T | 2 | a0001c0004t0005g0054a0001c0004t0005g0055 | 2 | HG02040.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.32+14174A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351449 | ||||||
| chr11:120351449
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0014g0254 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.32+14176_32+14185d others(12): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351449 | |||||
| chr11:120351449
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.32+14176_32+14187d others(14): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351449 | |||||
| chr11:120351449
|
ATATATAT others(9): Show |
A | 2 | a0004c0009t0010g0276a0004c0009t0010g0299 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.32+14176_32+14191d others(18): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351449 | |||||
| chr11:120351451
|
A | T | 8 | a0001c0004t0005g0049a0001c0004t0005g0053a0001c0004t0005g0054others(5): Show | 8 | HG00621.hp1 HG02040.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+14176A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351451 | ||||||
| chr11:120351451
|
ATATATTT others(5): Show |
A | 1 | a0001c0001t0001g0295 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.32+14178_32+14189d others(14): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351451 | |||||
| chr11:120351453
|
A | T | 20 | a0001c0001t0001g0255a0001c0001t0011g0300a0001c0002t0034g0013others(17): Show | 20 | HG00597.hp2 HG00621.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.32+14178A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351453 | ||||||
| chr11:120351455
|
A | T | 25 | a0001c0001t0001g0217a0001c0001t0001g0249a0001c0001t0001g0255others(22): Show | 25 | HG00597.hp2 HG00621.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+14180A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351455 | ||||||
| chr11:120351455
|
ATTTTTT | A | 6 | a0001c0001t0001g0198a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG01993.hp1 HG03453.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+14201_32+14206d others(8): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120351455 | |||||
| chr11:120351457
|
T | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0266 | 2 | HG01515.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.32+14182T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351457 | ||||||
| chr11:120351459
|
T | A | 2 | a0001c0001t0001g0231a0001c0001t0011g0199 | 2 | HG01346.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.32+14184T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351459 | ||||||
| chr11:120351461
|
T | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0231a0001c0001t0011g0199 | 3 | HG01346.hp2 HG01934.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.32+14186T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351461 | ||||||
| chr11:120351463
|
T | A | 1 | a0001c0001t0001g0231 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.32+14188T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351463 | ||||||
| chr11:120351482
|
G | T | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+14207G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351482 | ||||||
| chr11:120351502
|
T | C | 144 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(141): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.32+14227T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351502 | ||||||
| chr11:120351504
|
C | T | 1 | a0001c0002t0003g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.32+14229C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351504 | ||||||
| chr11:120351506
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.32+14231C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351506 | ||||||
| chr11:120351554
|
T | G | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.32+14279T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351554 | ||||||
| chr11:120351557
|
A | G | 204 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(201): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.32+14282A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351557 | ||||||
| chr11:120351636
|
A | G | 1 | a0006c0013t0001g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.32+14361A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351636 | ||||||
| chr11:120351766
|
C | T | 20 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0028others(17): Show | 21 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(18): Show |
intron_variant | MODIFIER | c.32+14491C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351766 | ||||||
| chr11:120351771
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0021g0162 | 2 | HG04228.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.32+14496G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120351771 | ||||||
| chr11:120352002
|
G | A | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+14727G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120352002 | ||||||
| chr11:120352251
|
T | C | 1 | a0001c0001t0010g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.32+14976T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120352251 | ||||||
| chr11:120352293
|
C | G | 1 | a0001c0001t0008g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.32+15018C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120352293 | ||||||
| chr11:120352416
|
T | C | 3 | a0001c0001t0001g0194a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | HG00280.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.32+15141T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120352416 | ||||||
| chr11:120352506
|
A | G | 2 | a0001c0002t0002g0022a0001c0002t0002g0024 | 2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.32+15231A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120352506 | ||||||
| chr11:120352551
|
T | A | 1 | a0001c0001t0008g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.32+15276T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120352551 | ||||||
| chr11:120352666
|
C | T | 1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.32+15391C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120352666 | ||||||
| chr11:120352690
|
C | T | 144 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(141): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.32+15415C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120352690 | ||||||
| chr11:120352804
|
G | A | 3 | a0001c0002t0016g0014a0001c0002t0016g0025a0001c0002t0016g0026 | 3 | HG02258.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.32+15529G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120352804 | ||||||
| chr11:120353360
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.32+16085T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120353360 | ||||||
| chr11:120353497
|
C | T | 1 | a0001c0001t0011g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.32+16222C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120353497 | ||||||
| chr11:120353610
|
A | G | 1 | a0001c0001t0002g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.32+16335A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120353610 | ||||||
| chr11:120353833
|
T | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+16558T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120353833 | ||||||
| chr11:120353835
|
T | C | 145 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(142): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.32+16560T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120353835 | ||||||
| chr11:120353882
|
T | C | 4 | a0001c0001t0006g0138a0001c0001t0029g0190a0001c0008t0020g0008others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+16607T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120353882 | ||||||
| chr11:120353941
|
A | G | 142 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.32+16666A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120353941 | ||||||
| chr11:120354080
|
G | A | 80 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(77): Show | 80 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.32+16805G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120354080 | ||||||
| chr11:120354180
|
G | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+16905G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120354180 | ||||||
| chr11:120354364
|
G | A | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32+17089G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120354364 | ||||||
| chr11:120354414
|
G | GGA | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+17146_32+17147d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120354414 | |||||
| chr11:120354877
|
C | T | 1 | a0001c0001t0004g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.32+17602C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120354877 | ||||||
| chr11:120355005
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.32+17730A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120355005 | ||||||
| chr11:120355016
|
C | T | 1 | a0001c0002t0003g0035 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.32+17741C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120355016 | ||||||
| chr11:120355052
|
C | T | 6 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(3): Show | 6 | HG01074.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+17777C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120355052 | ||||||
| chr11:120355175
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+17900A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120355175 | ||||||
| chr11:120355247
|
G | A | 2 | a0001c0002t0003g0034a0001c0002t0003g0035 | 2 | HG00741.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.32+17972G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120355247 | ||||||
| chr11:120355384
|
G | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152 | 3 | HG00597.hp1 HG02071.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.32+18109G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120355384 | ||||||
| chr11:120355406
|
T | G | 2 | a0001c0001t0006g0138a0001c0001t0029g0190 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.32+18131T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120355406 | ||||||
| chr11:120355441
|
A | G | 1 | a0001c0002t0003g0027 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.32+18166A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120355441 | ||||||
| chr11:120355592
|
A | C | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+18317A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120355592 | ||||||
| chr11:120355789
|
T | A | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32+18514T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120355789 | ||||||
| chr11:120356135
|
G | T | 1 | a0001c0002t0003g0033 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.32+18860G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120356135 | ||||||
| chr11:120356224
|
A | T | 1 | a0001c0001t0009g0005 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.32+18949A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120356224 | ||||||
| chr11:120356423
|
T | G | 1 | a0001c0002t0003g0023 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.32+19148T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120356423 | ||||||
| chr11:120356536
|
A | T | 1 | a0001c0001t0004g0272 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.32+19261A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120356536 | ||||||
| chr11:120356692
|
G | T | 1 | a0006c0013t0001g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.32+19417G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120356692 | ||||||
| chr11:120356733
|
T | C | 21 | a0001c0001t0002g0018a0001c0001t0002g0021a0001c0001t0002g0091others(18): Show | 21 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+19458T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120356733 | ||||||
| chr11:120356821
|
A | C | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.32+19546A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120356821 | ||||||
| chr11:120357014
|
G | GT | 6 | a0001c0001t0001g0290a0003c0005t0001g0002a0003c0005t0001g0159others(3): Show | 7 | HG01081.hp1 HG01496.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+19750dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120357014 | |||||
| chr11:120357021
|
T | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0172 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.32+19746T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120357021 | ||||||
| chr11:120357026
|
G | T | 4 | a0001c0001t0006g0138a0001c0001t0029g0190a0001c0008t0020g0008others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+19751G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120357026 | ||||||
| chr11:120357027
|
T | G | 4 | a0001c0001t0006g0138a0001c0001t0029g0190a0001c0008t0020g0008others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+19752T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120357027 | ||||||
| chr11:120357367
|
G | A | 1 | a0001c0001t0011g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.32+20092G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120357367 | ||||||
| chr11:120357409
|
T | A | 3 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0251 | 3 | HG02040.hp2 NA18977.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.32+20134T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120357409 | ||||||
| chr11:120357577
|
C | G | 115 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(112): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.32+20302C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120357577 | ||||||
| chr11:120357849
|
C | T | 8 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+20574C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120357849 | ||||||
| chr11:120357954
|
A | G | 3 | a0001c0002t0003g0001a0001c0002t0003g0064a0001c0002t0003g0065 | 4 | HG00099.hp1 HG00140.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+20679A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120357954 | ||||||
| chr11:120358073
|
G | C | 3 | a0001c0002t0016g0014a0001c0002t0016g0025a0001c0002t0016g0026 | 3 | HG02258.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.32+20798G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120358073 | ||||||
| chr11:120358100
|
C | T | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+20825C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120358100 | ||||||
| chr11:120358280
|
A | G | 78 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(75): Show | 78 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+21005A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120358280 | ||||||
| chr11:120358354
|
G | C | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.32+21079G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120358354 | ||||||
| chr11:120358691
|
T | G | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32+21416T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120358691 | ||||||
| chr11:120358698
|
A | T | 1 | a0001c0001t0011g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.32+21423A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120358698 | ||||||
| chr11:120358851
|
A | G | 4 | a0001c0001t0006g0138a0001c0001t0029g0190a0001c0008t0020g0008others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+21576A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120358851 | ||||||
| chr11:120359147
|
A | C | 1 | a0001c0001t0001g0219 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.32+21872A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120359147 | ||||||
| chr11:120359471
|
G | A | 3 | a0001c0002t0003g0129a0002c0003t0017g0282a0002c0003t0017g0284 | 3 | HG00733.hp1 HG02135.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.32+22196G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120359471 | ||||||
| chr11:120359549
|
G | C | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+22274G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120359549 | ||||||
| chr11:120359580
|
T | A | 4 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0006others(1): Show | 4 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+22305T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120359580 | ||||||
| chr11:120359683
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.32+22408A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120359683 | ||||||
| chr11:120359919
|
C | T | 1 | a0004c0009t0010g0299 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.32+22644C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120359919 | ||||||
| chr11:120359997
|
T | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+22722T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120359997 | ||||||
| chr11:120360209
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.32+22934G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120360209 | ||||||
| chr11:120360565
|
T | C | 1 | a0002c0003t0002g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.32+23290T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120360565 | ||||||
| chr11:120360578
|
G | C | 1 | a0010c0017t0010g0298 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.32+23303G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120360578 | ||||||
| chr11:120360644
|
C | T | 5 | a0001c0001t0010g0294a0001c0001t0010g0297a0004c0009t0010g0276others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+23369C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120360644 | ||||||
| chr11:120360645
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.32+23370G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120360645 | ||||||
| chr11:120360757
|
A | G | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32+23482A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120360757 | ||||||
| chr11:120360818
|
G | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+23543G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120360818 | ||||||
| chr11:120360909
|
T | G | 2 | a0001c0001t0006g0138a0001c0001t0029g0190 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.32+23634T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120360909 | ||||||
| chr11:120361157
|
G | C | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.32+23882G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120361157 | ||||||
| chr11:120361363
|
G | A | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+24088G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120361363 | ||||||
| chr11:120361401
|
C | T | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+24126C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120361401 | ||||||
| chr11:120361472
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.32+24197G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120361472 | ||||||
| chr11:120361634
|
G | C | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+24359G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120361634 | ||||||
| chr11:120361770
|
C | T | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+24495C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120361770 | ||||||
| chr11:120361800
|
T | A | 1 | a0001c0002t0003g0030 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.32+24525T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120361800 | ||||||
| chr11:120361820
|
G | T | 1 | a0003c0005t0001g0169 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.32+24545G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120361820 | ||||||
| chr11:120361921
|
A | T | 3 | a0001c0001t0014g0221a0001c0001t0014g0254a0001c0001t0014g0265 | 3 | NA18945.hp2 NA18965.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.32+24646A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120361921 | ||||||
| chr11:120362041
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.32+24766T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362041 | ||||||
| chr11:120362057
|
A | G | 19 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0028others(16): Show | 20 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(17): Show |
intron_variant | MODIFIER | c.32+24782A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362057 | ||||||
| chr11:120362081
|
A | C | 1 | a0001c0001t0006g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.32+24806A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362081 | ||||||
| chr11:120362083
|
A | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+24808A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362083 | ||||||
| chr11:120362088
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.32+24813A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362088 | ||||||
| chr11:120362325
|
T | C | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.32+25050T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362325 | ||||||
| chr11:120362343
|
T | G | 1 | a0001c0001t0001g0219 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.32+25068T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362343 | ||||||
| chr11:120362436
|
A | G | 2 | a0001c0001t0006g0138a0001c0001t0029g0190 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.32+25161A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362436 | ||||||
| chr11:120362449
|
G | A | 141 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(138): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.32+25174G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362449 | ||||||
| chr11:120362702
|
C | T | 2 | a0001c0001t0031g0090a0005c0016t0032g0100 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.32+25427C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362702 | ||||||
| chr11:120362827
|
G | A | 141 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(138): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.32+25552G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362827 | ||||||
| chr11:120362855
|
G | C | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.32+25580G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362855 | ||||||
| chr11:120362885
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.32+25610G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362885 | ||||||
| chr11:120362917
|
A | G | 117 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(114): Show | 118 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.32+25642A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120362917 | ||||||
| chr11:120363032
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.32+25757A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120363032 | ||||||
| chr11:120363055
|
G | A | 1 | a0001c0001t0006g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+25780G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120363055 | ||||||
| chr11:120363060
|
A | C | 1 | a0001c0008t0020g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.32+25785A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120363060 | ||||||
| chr11:120363086
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.32+25811C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120363086 | ||||||
| chr11:120363154
|
C | G | 1 | a0001c0002t0003g0035 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.32+25879C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120363154 | ||||||
| chr11:120363199
|
G | A | 117 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(114): Show | 118 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.32+25924G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120363199 | ||||||
| chr11:120363310
|
G | T | 3 | a0001c0001t0009g0005a0001c0001t0009g0006a0001c0001t0009g0007 | 3 | HG01952.hp2 HG02273.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.32+26035G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120363310 | ||||||
| chr11:120363587
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.32+26312G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120363587 | ||||||
| chr11:120363961
|
T | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+26686T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120363961 | ||||||
| chr11:120364091
|
G | A | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+26816G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120364091 | ||||||
| chr11:120364101
|
G | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+26826G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120364101 | ||||||
| chr11:120364413
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+27138A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120364413 | ||||||
| chr11:120364543
|
G | T | 3 | a0001c0001t0002g0019a0001c0001t0002g0102a0001c0001t0002g0124 | 3 | HG02486.hp2 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.32+27268G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120364543 | ||||||
| chr11:120364762
|
T | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+27487T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120364762 | ||||||
| chr11:120364816
|
A | AT | 55 | a0001c0001t0001g0145a0001c0001t0001g0154a0001c0001t0001g0189others(52): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.32+27561dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120364816 | |||||
| chr11:120364816
|
A | ATT | 72 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0091others(69): Show | 72 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.32+27560_32+27561d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120364816 | |||||
| chr11:120364816
|
A | ATTT | 8 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0121others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+27559_32+27561d others(5): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120364816 | |||||
| chr11:120364851
|
T | C | 87 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(84): Show | 87 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.32+27576T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120364851 | ||||||
| chr11:120364865
|
T | C | 34 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.32+27590T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120364865 | ||||||
| chr11:120364994
|
C | T | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.32+27719C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120364994 | ||||||
| chr11:120365047
|
G | A | 4 | a0001c0001t0002g0021a0001c0001t0002g0114a0001c0001t0002g0116others(1): Show | 4 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+27772G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120365047 | ||||||
| chr11:120365165
|
T | A | 61 | a0001c0001t0001g0189a0001c0001t0001g0205a0001c0001t0001g0206others(58): Show | 61 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.32+27890T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120365165 | ||||||
| chr11:120365410
|
A | G | 1 | a0001c0002t0003g0045 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.32+28135A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120365410 | ||||||
| chr11:120365570
|
A | G | 1 | a0001c0002t0003g0027 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.32+28295A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120365570 | ||||||
| chr11:120365624
|
G | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+28349G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120365624 | ||||||
| chr11:120365682
|
A | G | 4 | a0001c0001t0001g0194a0001c0001t0001g0201a0001c0001t0001g0203others(1): Show | 4 | HG00280.hp2 HG00323.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+28407A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120365682 | ||||||
| chr11:120365755
|
C | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+28480C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120365755 | ||||||
| chr11:120365772
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.32+28497G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120365772 | ||||||
| chr11:120365780
|
T | A | 2 | a0001c0002t0003g0062a0001c0002t0003g0063 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.32+28505T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120365780 | ||||||
| chr11:120365890
|
C | CA | 27 | a0001c0001t0002g0018a0001c0001t0002g0021a0001c0001t0002g0091others(24): Show | 27 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.32+28622dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120365890 | |||||
| chr11:120366081
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.32+28806G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120366081 | ||||||
| chr11:120366084
|
C | T | 1 | a0001c0001t0008g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.32+28809C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120366084 | ||||||
| chr11:120366129
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32+28854G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120366129 | ||||||
| chr11:120366210
|
T | G | 1 | a0001c0001t0002g0019 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.32+28935T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120366210 | ||||||
| chr11:120366301
|
T | C | 1 | a0001c0001t0013g0200 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.32+29026T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120366301 | ||||||
| chr11:120366532
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+29257A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120366532 | ||||||
| chr11:120366831
|
A | G | 4 | a0001c0001t0001g0209a0001c0001t0001g0232a0001c0001t0001g0233others(1): Show | 4 | HG01243.hp1 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+29556A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120366831 | ||||||
| chr11:120366889
|
G | A | 2 | a0001c0002t0003g0015a0001c0002t0003g0032 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.32+29614G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120366889 | ||||||
| chr11:120367014
|
TA | T | 33 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.32+29751delA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367014 | |||||
| chr11:120367049
|
C | T | 4 | a0001c0002t0003g0023a0001c0002t0016g0014a0001c0002t0016g0025others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+29774C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367049 | ||||||
| chr11:120367143
|
A | G | 1 | a0001c0001t0002g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.32+29868A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367143 | ||||||
| chr11:120367144
|
G | C | 8 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+29869G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367144 | ||||||
| chr11:120367241
|
GTTTTGGG others(5): Show |
G | 1 | a0001c0001t0011g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.32+29970_32+29981d others(14): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367241 | |||||
| chr11:120367262
|
C | T | 6 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0021g0162others(3): Show | 6 | HG03239.hp2 HG03704.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+29987C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367262 | ||||||
| chr11:120367282
|
G | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+30007G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367282 | ||||||
| chr11:120367353
|
C | CT | 59 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0144others(56): Show | 60 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.32+30108dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTT | 24 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(21): Show | 24 | HG00738.hp2 HG01109.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.32+30107_32+30108d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTT | 9 | a0001c0001t0001g0148a0001c0001t0001g0155a0001c0001t0001g0161others(6): Show | 9 | HG01978.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+30106_32+30108d others(5): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(3): Show |
8 | a0001c0001t0008g0020a0001c0001t0008g0104a0001c0001t0008g0112others(5): Show | 8 | HG01074.hp2 HG02698.hp2 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+30099_32+30108d others(12): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(4): Show |
12 | a0001c0001t0008g0092a0001c0002t0019g0012a0001c0004t0005g0049others(9): Show | 12 | HG02040.hp1 HG02155.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+30098_32+30108d others(13): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(5): Show |
7 | a0001c0001t0006g0094a0001c0001t0006g0118a0001c0001t0006g0138others(4): Show | 7 | HG02602.hp2 HG02615.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+30097_32+30108d others(14): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(6): Show |
12 | a0001c0001t0002g0018a0001c0001t0002g0021a0001c0001t0002g0097others(9): Show | 12 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.32+30096_32+30108d others(15): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(7): Show |
13 | a0001c0001t0002g0093a0001c0001t0002g0095a0001c0001t0002g0105others(10): Show | 13 | HG00735.hp2 HG01071.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.32+30095_32+30108d others(16): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(8): Show |
5 | a0001c0001t0002g0109a0001c0001t0002g0110a0001c0001t0002g0124others(2): Show | 5 | HG02486.hp2 HG03471.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+30094_32+30108d others(17): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(9): Show |
4 | a0001c0001t0002g0121a0001c0001t0035g0088a0001c0004t0005g0048others(1): Show | 4 | HG00597.hp2 HG00738.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+30093_32+30108d others(18): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(10): Show |
1 | a0002c0003t0002g0086 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.32+30092_32+30108d others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0002g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.32+30091_32+30108d others(20): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0033g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.32+30090_32+30108d others(21): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0002g0091a0001c0006t0002g0306 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.32+30089_32+30108d others(22): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0002g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.32+30088_32+30108d others(23): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(16): Show |
5 | a0002c0003t0002g0067a0002c0003t0002g0068a0002c0003t0002g0076others(2): Show | 5 | HG02165.hp2 NA18959.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+30086_32+30108d others(25): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(17): Show |
5 | a0002c0003t0002g0016a0002c0003t0002g0017a0002c0003t0002g0073others(2): Show | 5 | HG02135.hp2 NA18942.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+30085_32+30108d others(26): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(18): Show |
2 | a0001c0001t0031g0090a0002c0003t0002g0069 | 2 | HG03453.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.32+30084_32+30108d others(27): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0006g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.32+30082_32+30108d others(29): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(22): Show |
1 | a0002c0003t0002g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.32+30080_32+30108d others(31): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(24): Show |
1 | a0002c0003t0002g0070 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.32+30108_32+30109i others(33): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(26): Show |
1 | a0002c0003t0002g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.32+30108_32+30109i others(35): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
C | CTTTTTTT others(31): Show |
1 | a0002c0003t0002g0080 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.32+30108_32+30109i others(40): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
CTTTTTT | C | 29 | a0001c0002t0002g0022a0001c0002t0003g0001a0001c0002t0003g0015others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.32+30103_32+30108d others(8): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367353
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0012g0058 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.32+30097_32+30108d others(14): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120367353 | |||||
| chr11:120367368
|
T | C | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+30093T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367368 | ||||||
| chr11:120367396
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.32+30121C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367396 | ||||||
| chr11:120367404
|
C | T | 1 | a0001c0001t0007g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.32+30129C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367404 | ||||||
| chr11:120367526
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.32+30251C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367526 | ||||||
| chr11:120367701
|
T | C | 1 | a0001c0001t0004g0285 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.32+30426T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367701 | ||||||
| chr11:120367704
|
T | C | 206 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(203): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.32+30429T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367704 | ||||||
| chr11:120367741
|
C | T | 1 | a0002c0003t0002g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.32+30466C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367741 | ||||||
| chr11:120367825
|
G | A | 153 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.32+30550G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367825 | ||||||
| chr11:120367946
|
A | G | 140 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(137): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.32+30671A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120367946 | ||||||
| chr11:120368012
|
C | A | 142 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.32+30737C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368012 | ||||||
| chr11:120368115
|
T | C | 142 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.32+30840T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368115 | ||||||
| chr11:120368132
|
C | T | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+30857C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368132 | ||||||
| chr11:120368190
|
G | A | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32+30915G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368190 | ||||||
| chr11:120368253
|
T | C | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+30978T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368253 | ||||||
| chr11:120368342
|
T | C | 142 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.32+31067T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368342 | ||||||
| chr11:120368371
|
G | T | 2 | a0001c0001t0011g0195a0001c0001t0011g0199 | 2 | HG01934.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.32+31096G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368371 | ||||||
| chr11:120368379
|
G | A | 118 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.32+31104G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368379 | ||||||
| chr11:120368478
|
G | C | 6 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(3): Show | 6 | HG01074.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+31203G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368478 | ||||||
| chr11:120368640
|
G | A | 1 | a0001c0012t0001g0296 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.32+31365G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368640 | ||||||
| chr11:120368692
|
T | G | 2 | a0004c0009t0010g0276a0004c0009t0010g0299 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.32+31417T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368692 | ||||||
| chr11:120368747
|
C | G | 142 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.32+31472C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368747 | ||||||
| chr11:120368901
|
A | G | 6 | a0001c0006t0002g0301a0001c0006t0002g0302a0001c0006t0002g0303others(3): Show | 6 | HG00735.hp2 HG00738.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+31626A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120368901 | ||||||
| chr11:120369099
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.32+31824A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120369099 | ||||||
| chr11:120369125
|
CT | C | 7 | a0001c0001t0002g0133a0001c0001t0014g0265a0001c0007t0015g0125others(4): Show | 7 | HG01074.hp2 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+31869delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120369125 | |||||
| chr11:120369128
|
T | C | 1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.32+31853T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120369128 | ||||||
| chr11:120369177
|
G | GT | 54 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(51): Show | 55 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.32+31902_32+31903i others(3): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120369177 | ||||||
| chr11:120369228
|
A | G | 80 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(77): Show | 80 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.32+31953A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120369228 | ||||||
| chr11:120369369
|
T | C | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+32094T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120369369 | ||||||
| chr11:120369389
|
A | G | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.32+32114A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120369389 | ||||||
| chr11:120369437
|
T | A | 1 | a0001c0012t0001g0296 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.32+32162T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120369437 | ||||||
| chr11:120369456
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+32181A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120369456 | ||||||
| chr11:120369634
|
A | T | 3 | a0001c0001t0006g0089a0001c0001t0006g0101a0001c0001t0006g0103 | 3 | HG03516.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.32+32359A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120369634 | ||||||
| chr11:120369672
|
A | C | 1 | a0001c0001t0004g0244 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.32+32397A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120369672 | ||||||
| chr11:120370016
|
C | T | 1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.32+32741C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120370016 | ||||||
| chr11:120370166
|
A | T | 2 | a0001c0002t0003g0038a0001c0002t0003g0039 | 2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.32+32891A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120370166 | ||||||
| chr11:120370185
|
G | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+32910G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120370185 | ||||||
| chr11:120370211
|
G | A | 1 | a0001c0001t0011g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.32+32936G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120370211 | ||||||
| chr11:120370370
|
A | G | 1 | a0002c0003t0002g0068 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.32+33095A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120370370 | ||||||
| chr11:120370419
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.32+33144G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120370419 | ||||||
| chr11:120370583
|
T | C | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32+33308T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120370583 | ||||||
| chr11:120370825
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.32+33550C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120370825 | ||||||
| chr11:120371085
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.32+33810A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120371085 | ||||||
| chr11:120371214
|
T | C | 142 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.32+33939T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120371214 | ||||||
| chr11:120371297
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.32+34022T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120371297 | ||||||
| chr11:120371357
|
G | A | 1 | a0001c0001t0008g0020 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.32+34082G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120371357 | ||||||
| chr11:120371623
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32+34348A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120371623 | ||||||
| chr11:120371639
|
G | A | 78 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(75): Show | 78 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+34364G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120371639 | ||||||
| chr11:120371657
|
T | C | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32+34382T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120371657 | ||||||
| chr11:120371905
|
A | G | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.33-34213A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120371905 | ||||||
| chr11:120372041
|
T | C | 3 | a0001c0001t0002g0019a0001c0001t0002g0102a0001c0001t0002g0124 | 3 | HG02486.hp2 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.33-34077T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120372041 | ||||||
| chr11:120372103
|
A | T | 1 | a0001c0001t0008g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.33-34015A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120372103 | ||||||
| chr11:120372109
|
A | G | 1 | a0001c0002t0007g0042 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.33-34009A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120372109 | ||||||
| chr11:120372295
|
T | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-33823T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120372295 | ||||||
| chr11:120372459
|
A | G | 1 | a0010c0017t0010g0298 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.33-33659A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120372459 | ||||||
| chr11:120372762
|
T | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-33356T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120372762 | ||||||
| chr11:120372797
|
T | C | 11 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-33321T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120372797 | ||||||
| chr11:120372811
|
C | T | 2 | a0001c0001t0018g0280a0001c0001t0018g0281 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.33-33307C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120372811 | ||||||
| chr11:120372823
|
T | C | 8 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-33295T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120372823 | ||||||
| chr11:120372913
|
A | G | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.33-33205A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120372913 | ||||||
| chr11:120372992
|
G | A | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.33-33126G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120372992 | ||||||
| chr11:120373023
|
A | AT | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.33-33089dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120373023 | |||||
| chr11:120373263
|
T | G | 1 | a0001c0001t0001g0208 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.33-32855T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120373263 | ||||||
| chr11:120373427
|
C | G | 1 | a0001c0001t0033g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.33-32691C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120373427 | ||||||
| chr11:120373483
|
A | G | 139 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.33-32635A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120373483 | ||||||
| chr11:120373596
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.33-32522C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120373596 | ||||||
| chr11:120373856
|
G | A | 2 | a0001c0002t0003g0015a0001c0002t0003g0032 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.33-32262G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120373856 | ||||||
| chr11:120373868
|
C | T | 142 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.33-32250C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120373868 | ||||||
| chr11:120374019
|
T | G | 2 | a0001c0001t0010g0294a0001c0001t0010g0297 | 2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.33-32099T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120374019 | ||||||
| chr11:120374027
|
G | A | 13 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(10): Show | 14 | HG00597.hp1 HG00621.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-32091G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120374027 | ||||||
| chr11:120374105
|
C | G | 1 | a0001c0002t0003g0027 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.33-32013C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120374105 | ||||||
| chr11:120374220
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-31898A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120374220 | ||||||
| chr11:120374405
|
G | T | 1 | a0001c0002t0034g0013 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.33-31713G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120374405 | ||||||
| chr11:120374682
|
T | C | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-31436T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120374682 | ||||||
| chr11:120374745
|
T | C | 2 | a0001c0002t0002g0022a0001c0002t0002g0024 | 2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.33-31373T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120374745 | ||||||
| chr11:120374746
|
T | C | 2 | a0001c0004t0005g0049a0001c0004t0005g0053 | 2 | HG02698.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.33-31372T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120374746 | ||||||
| chr11:120374831
|
T | C | 1 | a0001c0001t0008g0119 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.33-31287T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120374831 | ||||||
| chr11:120374881
|
A | C | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-31237A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120374881 | ||||||
| chr11:120374984
|
G | C | 1 | a0001c0001t0002g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.33-31134G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120374984 | ||||||
| chr11:120375092
|
C | A | 1 | a0001c0001t0004g0272 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.33-31026C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120375092 | ||||||
| chr11:120375550
|
CT | C | 7 | a0001c0001t0008g0020a0001c0001t0009g0003a0001c0001t0009g0004others(4): Show | 7 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-30553delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120375550 | |||||
| chr11:120375714
|
A | G | 5 | a0001c0001t0002g0019a0001c0001t0002g0102a0001c0001t0002g0124others(2): Show | 5 | HG02486.hp2 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-30404A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120375714 | ||||||
| chr11:120375817
|
C | T | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-30301C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120375817 | ||||||
| chr11:120375829
|
C | T | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.33-30289C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120375829 | ||||||
| chr11:120376145
|
T | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-29973T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120376145 | ||||||
| chr11:120376194
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-29924A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120376194 | ||||||
| chr11:120376222
|
AT | A | 152 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.33-29885delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120376222 | |||||
| chr11:120376233
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.33-29885T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120376233 | ||||||
| chr11:120376273
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-29845A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120376273 | ||||||
| chr11:120376324
|
C | T | 62 | a0001c0001t0001g0189a0001c0001t0001g0205a0001c0001t0001g0206others(59): Show | 62 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.33-29794C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120376324 | ||||||
| chr11:120376452
|
T | A | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-29666T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120376452 | ||||||
| chr11:120376643
|
A | G | 1 | a0001c0004t0005g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.33-29475A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120376643 | ||||||
| chr11:120376690
|
C | A | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.33-29428C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120376690 | ||||||
| chr11:120376727
|
C | T | 34 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.33-29391C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120376727 | ||||||
| chr11:120376793
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.33-29325C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120376793 | ||||||
| chr11:120376902
|
C | T | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-29216C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120376902 | ||||||
| chr11:120376945
|
A | G | 3 | a0001c0001t0008g0020a0001c0001t0008g0111a0001c0001t0008g0112 | 3 | NA18946.hp1 NA18965.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.33-29173A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120376945 | ||||||
| chr11:120377314
|
G | T | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.33-28804G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120377314 | ||||||
| chr11:120377534
|
G | C | 2 | a0001c0001t0018g0280a0001c0001t0018g0281 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.33-28584G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120377534 | ||||||
| chr11:120377540
|
T | G | 150 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(147): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.33-28578T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120377540 | ||||||
| chr11:120377633
|
C | T | 85 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(82): Show | 85 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.33-28485C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120377633 | ||||||
| chr11:120377784
|
A | G | 34 | a0001c0001t0002g0133a0001c0001t0008g0020a0001c0001t0008g0092others(31): Show | 34 | HG02056.hp2 HG02083.hp2 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.33-28334A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120377784 | ||||||
| chr11:120378142
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.33-27976G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120378142 | ||||||
| chr11:120378161
|
ACAT | A | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-27955_33-27953d others(5): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120378161 | |||||
| chr11:120378168
|
C | T | 5 | a0001c0002t0007g0041a0001c0002t0007g0042a0001c0002t0007g0043others(2): Show | 5 | HG01123.hp2 HG01884.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-27950C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120378168 | ||||||
| chr11:120378562
|
A | G | 1 | a0001c0006t0002g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.33-27556A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120378562 | ||||||
| chr11:120378578
|
C | T | 153 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.33-27540C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120378578 | ||||||
| chr11:120378686
|
C | T | 32 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.33-27432C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120378686 | ||||||
| chr11:120378739
|
G | A | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.33-27379G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120378739 | ||||||
| chr11:120378784
|
G | A | 153 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.33-27334G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120378784 | ||||||
| chr11:120378861
|
T | C | 1 | a0003c0005t0001g0159 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.33-27257T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120378861 | ||||||
| chr11:120379129
|
A | G | 1 | a0001c0002t0003g0023 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.33-26989A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120379129 | ||||||
| chr11:120379375
|
G | T | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-26743G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120379375 | ||||||
| chr11:120379420
|
G | T | 1 | a0001c0001t0002g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.33-26698G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120379420 | ||||||
| chr11:120379490
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0144 | 2 | HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.33-26628A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120379490 | ||||||
| chr11:120379518
|
AT | A | 10 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0007g0134others(7): Show | 10 | HG00741.hp1 HG01074.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.33-26588delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120379518 | |||||
| chr11:120379543
|
A | T | 1 | a0001c0001t0001g0170 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.33-26575A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120379543 | ||||||
| chr11:120379778
|
A | T | 1 | a0001c0004t0005g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.33-26340A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120379778 | ||||||
| chr11:120379780
|
A | G | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.33-26338A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120379780 | ||||||
| chr11:120379862
|
T | G | 3 | a0001c0001t0008g0020a0001c0001t0008g0111a0001c0001t0008g0112 | 3 | NA18946.hp1 NA18965.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.33-26256T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120379862 | ||||||
| chr11:120379990
|
A | G | 152 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.33-26128A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120379990 | ||||||
| chr11:120380039
|
T | C | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.33-26079T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120380039 | ||||||
| chr11:120380060
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.33-26058C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120380060 | ||||||
| chr11:120380490
|
C | T | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-25628C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120380490 | ||||||
| chr11:120380997
|
G | A | 1 | a0001c0004t0005g0057 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.33-25121G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120380997 | ||||||
| chr11:120381024
|
T | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-25094T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120381024 | ||||||
| chr11:120381027
|
T | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-25091T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120381027 | ||||||
| chr11:120381096
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33-25022A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120381096 | ||||||
| chr11:120381155
|
CAG | C | 21 | a0001c0001t0002g0018a0001c0001t0002g0021a0001c0001t0002g0091others(18): Show | 21 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-24962_33-24961d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120381155 | ||||||
| chr11:120381511
|
C | T | 6 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(3): Show | 6 | HG01074.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-24607C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120381511 | ||||||
| chr11:120381512
|
G | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-24606G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120381512 | ||||||
| chr11:120381603
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0287 | 2 | HG02148.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.33-24515G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120381603 | ||||||
| chr11:120381642
|
T | A | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.33-24476T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120381642 | ||||||
| chr11:120381903
|
A | C | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-24215A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120381903 | ||||||
| chr11:120382086
|
C | T | 3 | a0001c0001t0002g0019a0001c0001t0002g0102a0001c0001t0002g0124 | 3 | HG02486.hp2 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.33-24032C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120382086 | ||||||
| chr11:120382119
|
G | A | 206 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(203): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.33-23999G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120382119 | ||||||
| chr11:120382128
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-23990A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120382128 | ||||||
| chr11:120382212
|
A | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG00597.hp1 HG02071.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-23906A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120382212 | ||||||
| chr11:120382404
|
T | C | 1 | a0006c0013t0001g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.33-23714T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120382404 | ||||||
| chr11:120382438
|
C | T | 1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.33-23680C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120382438 | ||||||
| chr11:120382522
|
T | C | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-23596T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120382522 | ||||||
| chr11:120382616
|
C | T | 1 | a0001c0002t0003g0029 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.33-23502C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120382616 | ||||||
| chr11:120382620
|
G | A | 6 | a0001c0006t0002g0301a0001c0006t0002g0302a0001c0006t0002g0303others(3): Show | 6 | HG00735.hp2 HG00738.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-23498G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120382620 | ||||||
| chr11:120382879
|
G | A | 3 | a0001c0001t0002g0105a0001c0001t0002g0110a0001c0001t0002g0120 | 3 | NA18945.hp1 NA18947.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.33-23239G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120382879 | ||||||
| chr11:120383008
|
G | A | 6 | a0003c0005t0001g0002a0003c0005t0001g0159a0003c0005t0001g0165others(3): Show | 7 | HG01081.hp1 HG01496.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-23110G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383008 | ||||||
| chr11:120383012
|
G | A | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.33-23106G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383012 | ||||||
| chr11:120383048
|
G | C | 1 | a0001c0001t0035g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.33-23070G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383048 | ||||||
| chr11:120383049
|
G | T | 1 | a0001c0001t0035g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.33-23069G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383049 | ||||||
| chr11:120383056
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33-23062G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383056 | ||||||
| chr11:120383057
|
C | T | 4 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0251others(1): Show | 4 | HG02040.hp2 NA18977.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-23061C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383057 | ||||||
| chr11:120383058
|
G | C | 13 | a0002c0003t0002g0016a0002c0003t0002g0017a0002c0003t0002g0067others(10): Show | 13 | HG02135.hp2 HG02165.hp2 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-23060G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383058 | ||||||
| chr11:120383481
|
C | G | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.33-22637C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383481 | ||||||
| chr11:120383542
|
A | G | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.33-22576A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383542 | ||||||
| chr11:120383610
|
G | C | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.33-22508G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383610 | ||||||
| chr11:120383779
|
C | T | 4 | a0001c0004t0005g0049a0001c0004t0005g0053a0001c0004t0005g0056others(1): Show | 4 | HG02698.hp2 HG03704.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-22339C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383779 | ||||||
| chr11:120383797
|
CT | C | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.33-22320delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383797 | ||||||
| chr11:120383837
|
G | A | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.33-22281G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383837 | ||||||
| chr11:120383975
|
C | T | 139 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.33-22143C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120383975 | ||||||
| chr11:120384075
|
C | T | 16 | a0001c0001t0002g0018a0001c0001t0002g0021a0001c0001t0002g0091others(13): Show | 16 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.33-22043C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120384075 | ||||||
| chr11:120384193
|
G | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-21925G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120384193 | ||||||
| chr11:120384195
|
G | A | 1 | a0001c0001t0010g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.33-21923G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120384195 | ||||||
| chr11:120384388
|
A | C | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.33-21730A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120384388 | ||||||
| chr11:120384545
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.33-21573G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120384545 | ||||||
| chr11:120384546
|
C | A | 1 | a0001c0001t0001g0241 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.33-21572C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120384546 | ||||||
| chr11:120384732
|
A | G | 1 | a0001c0001t0026g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33-21386A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120384732 | ||||||
| chr11:120384753
|
G | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-21365G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120384753 | ||||||
| chr11:120384830
|
T | A | 14 | a0002c0003t0002g0016a0002c0003t0002g0017a0002c0003t0002g0067others(11): Show | 14 | HG02056.hp2 HG02135.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-21288T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120384830 | ||||||
| chr11:120384878
|
AT | A | 90 | a0001c0001t0001g0234a0001c0001t0002g0018a0001c0001t0002g0019others(87): Show | 90 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-21223delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120384878 | |||||
| chr11:120384973
|
G | A | 1 | a0006c0013t0001g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.33-21145G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120384973 | ||||||
| chr11:120385200
|
A | G | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.33-20918A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120385200 | ||||||
| chr11:120385477
|
G | C | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.33-20641G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120385477 | ||||||
| chr11:120385592
|
G | A | 298 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(295): Show | 300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.33-20526G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120385592 | ||||||
| chr11:120385628
|
T | C | 86 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(83): Show | 86 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.33-20490T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120385628 | ||||||
| chr11:120385713
|
C | T | 1 | a0001c0001t0024g0214 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.33-20405C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120385713 | ||||||
| chr11:120385768
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.33-20350A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120385768 | ||||||
| chr11:120385788
|
A | G | 1 | a0001c0001t0011g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.33-20330A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120385788 | ||||||
| chr11:120385877
|
T | A | 2 | a0001c0001t0010g0294a0001c0001t0010g0297 | 2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.33-20241T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120385877 | ||||||
| chr11:120386136
|
G | A | 272 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(269): Show | 274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.33-19982G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120386136 | ||||||
| chr11:120386786
|
A | G | 80 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(77): Show | 80 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.33-19332A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120386786 | ||||||
| chr11:120386906
|
A | G | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-19212A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120386906 | ||||||
| chr11:120387632
|
T | C | 7 | a0001c0001t0006g0089a0001c0001t0006g0094a0001c0001t0006g0099others(4): Show | 7 | HG02615.hp1 HG03041.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-18486T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120387632 | ||||||
| chr11:120387854
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.33-18264C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120387854 | ||||||
| chr11:120388017
|
A | G | 1 | a0001c0001t0002g0107 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.33-18101A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388017 | ||||||
| chr11:120388058
|
T | C | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-18060T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388058 | ||||||
| chr11:120388084
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.33-18034C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388084 | ||||||
| chr11:120388085
|
G | A | 3 | a0001c0001t0001g0273a0001c0008t0020g0008a0001c0008t0020g0009 | 3 | HG01256.hp2 HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.33-18033G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388085 | ||||||
| chr11:120388113
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-18005A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388113 | ||||||
| chr11:120388212
|
G | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-17906G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388212 | ||||||
| chr11:120388353
|
G | A | 1 | a0001c0001t0013g0202 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.33-17765G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388353 | ||||||
| chr11:120388388
|
G | C | 2 | a0001c0001t0001g0249a0001c0001t0001g0255 | 2 | HG01099.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.33-17730G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388388 | ||||||
| chr11:120388412
|
A | G | 5 | a0001c0002t0007g0041a0001c0002t0007g0042a0001c0002t0007g0043others(2): Show | 5 | HG01123.hp2 HG01884.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-17706A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388412 | ||||||
| chr11:120388546
|
C | T | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.33-17572C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388546 | ||||||
| chr11:120388721
|
T | A | 153 | a0001c0001t0001g0147a0001c0001t0002g0018a0001c0001t0002g0019others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.33-17397T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388721 | ||||||
| chr11:120388748
|
C | A | 1 | a0001c0001t0004g0247 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.33-17370C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388748 | ||||||
| chr11:120388853
|
T | A | 1 | a0001c0007t0015g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.33-17265T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388853 | ||||||
| chr11:120388860
|
T | A | 8 | a0001c0001t0001g0189a0001c0001t0001g0227a0001c0001t0001g0271others(5): Show | 8 | HG00733.hp2 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-17258T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388860 | ||||||
| chr11:120388864
|
T | A | 1 | a0001c0007t0015g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.33-17254T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388864 | ||||||
| chr11:120388919
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-17199A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388919 | ||||||
| chr11:120388927
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.33-17191A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120388927 | ||||||
| chr11:120389090
|
C | T | 1 | a0003c0005t0001g0165 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.33-17028C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120389090 | ||||||
| chr11:120389733
|
G | A | 1 | a0001c0001t0001g0240 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.33-16385G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120389733 | ||||||
| chr11:120389863
|
C | CT | 5 | a0001c0001t0010g0294a0001c0001t0010g0297a0004c0009t0010g0276others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-16249dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120389863 | |||||
| chr11:120390202
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.33-15916C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120390202 | ||||||
| chr11:120390478
|
A | G | 145 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(142): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.33-15640A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120390478 | ||||||
| chr11:120390776
|
G | GGGTTCTA others(8): Show |
1 | a0001c0001t0002g0110 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.33-15340_33-15326d others(17): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120390776 | |||||
| chr11:120390833
|
A | G | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-15285A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120390833 | ||||||
| chr11:120390924
|
T | A | 1 | a0001c0004t0012g0060 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.33-15194T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120390924 | ||||||
| chr11:120390967
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.33-15151A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120390967 | ||||||
| chr11:120391082
|
C | T | 153 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.33-15036C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120391082 | ||||||
| chr11:120391225
|
C | G | 32 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.33-14893C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120391225 | ||||||
| chr11:120391395
|
T | A | 2 | a0001c0004t0005g0054a0001c0004t0005g0055 | 2 | HG02040.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.33-14723T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120391395 | ||||||
| chr11:120391400
|
G | C | 1 | a0001c0002t0003g0034 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.33-14718G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120391400 | ||||||
| chr11:120391759
|
G | T | 5 | a0001c0001t0010g0294a0001c0001t0010g0297a0004c0009t0010g0276others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-14359G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120391759 | ||||||
| chr11:120391947
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.33-14171T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120391947 | ||||||
| chr11:120392094
|
G | A | 1 | a0010c0017t0010g0298 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.33-14024G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120392094 | ||||||
| chr11:120392213
|
G | A | 126 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(123): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.33-13905G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120392213 | ||||||
| chr11:120392243
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-13875A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120392243 | ||||||
| chr11:120392262
|
C | T | 1 | a0001c0004t0005g0057 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.33-13856C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120392262 | ||||||
| chr11:120392313
|
A | G | 19 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0028others(16): Show | 20 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(17): Show |
intron_variant | MODIFIER | c.33-13805A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120392313 | ||||||
| chr11:120392336
|
A | T | 1 | a0001c0001t0002g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.33-13782A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120392336 | ||||||
| chr11:120392359
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33-13759C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120392359 | ||||||
| chr11:120392615
|
C | T | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-13503C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120392615 | ||||||
| chr11:120392842
|
A | G | 2 | a0002c0003t0002g0071a0002c0003t0002g0081 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.33-13276A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120392842 | ||||||
| chr11:120392891
|
A | G | 1 | a0005c0016t0032g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.33-13227A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120392891 | ||||||
| chr11:120392942
|
G | A | 1 | a0001c0001t0025g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.33-13176G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120392942 | ||||||
| chr11:120393000
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-13118A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120393000 | ||||||
| chr11:120393258
|
A | ATAATT | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.33-12856_33-12852d others(7): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120393258 | |||||
| chr11:120393614
|
A | G | 1 | a0001c0002t0003g0023 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.33-12504A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120393614 | ||||||
| chr11:120393824
|
C | T | 1 | a0001c0001t0011g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.33-12294C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120393824 | ||||||
| chr11:120393912
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33-12206C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120393912 | ||||||
| chr11:120394101
|
T | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-12017T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120394101 | ||||||
| chr11:120394244
|
G | A | 5 | a0001c0001t0010g0294a0001c0001t0010g0297a0004c0009t0010g0276others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-11874G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120394244 | ||||||
| chr11:120394447
|
C | T | 5 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(2): Show | 5 | HG02723.hp2 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-11671C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120394447 | ||||||
| chr11:120394485
|
C | T | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-11633C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120394485 | ||||||
| chr11:120394615
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-11503A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120394615 | ||||||
| chr11:120394836
|
T | A | 2 | a0001c0001t0006g0099a0001c0001t0006g0122 | 2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.33-11282T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120394836 | ||||||
| chr11:120394914
|
C | T | 4 | a0001c0001t0029g0190a0001c0002t0019g0012a0001c0002t0034g0013others(1): Show | 4 | HG01099.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-11204C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120394914 | ||||||
| chr11:120394927
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.33-11191C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120394927 | ||||||
| chr11:120394928
|
G | T | 1 | a0001c0001t0036g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.33-11190G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120394928 | ||||||
| chr11:120394971
|
C | T | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-11147C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120394971 | ||||||
| chr11:120394996
|
G | A | 1 | a0001c0001t0035g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.33-11122G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120394996 | ||||||
| chr11:120395019
|
T | C | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-11099T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120395019 | ||||||
| chr11:120395021
|
C | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-11097C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120395021 | ||||||
| chr11:120395056
|
C | CA | 35 | a0001c0001t0001g0140a0001c0001t0001g0154a0001c0001t0001g0179others(32): Show | 35 | HG00438.hp2 HG00621.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.33-11038dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120395056 | |||||
| chr11:120395056
|
CA | C | 19 | a0001c0001t0001g0170a0001c0001t0001g0228a0001c0001t0001g0234others(16): Show | 19 | HG01070.hp1 HG01255.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.33-11038delA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120395056 | |||||
| chr11:120395189
|
A | T | 3 | a0001c0001t0031g0090a0001c0001t0033g0131a0005c0016t0032g0100 | 3 | HG02965.hp1 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.33-10929A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120395189 | ||||||
| chr11:120395763
|
C | A | 1 | a0001c0001t0011g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.33-10355C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120395763 | ||||||
| chr11:120395763
|
C | G | 1 | a0001c0001t0026g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33-10355C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120395763 | ||||||
| chr11:120395767
|
C | A | 17 | a0001c0001t0001g0241a0001c0004t0005g0046a0001c0004t0005g0047others(14): Show | 17 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.33-10351C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120395767 | ||||||
| chr11:120395768
|
C | T | 32 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.33-10350C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120395768 | ||||||
| chr11:120395802
|
C | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-10316C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120395802 | ||||||
| chr11:120395872
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-10246A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120395872 | ||||||
| chr11:120395878
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.33-10240A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120395878 | ||||||
| chr11:120396429
|
G | A | 1 | a0001c0001t0002g0105 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.33-9689G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120396429 | ||||||
| chr11:120396547
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.33-9571A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120396547 | ||||||
| chr11:120396828
|
A | G | 37 | a0001c0001t0001g0140a0001c0001t0001g0146a0001c0001t0001g0148others(34): Show | 38 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.33-9290A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120396828 | ||||||
| chr11:120396837
|
A | G | 1 | a0001c0002t0034g0013 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.33-9281A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120396837 | ||||||
| chr11:120396946
|
A | T | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-9172A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120396946 | ||||||
| chr11:120397134
|
T | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-8984T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120397134 | ||||||
| chr11:120397313
|
A | G | 80 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(77): Show | 80 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.33-8805A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120397313 | ||||||
| chr11:120397340
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.33-8778C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120397340 | ||||||
| chr11:120397348
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0172 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.33-8770T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120397348 | ||||||
| chr11:120397782
|
G | A | 32 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.33-8336G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120397782 | ||||||
| chr11:120397901
|
A | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-8217A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120397901 | ||||||
| chr11:120398030
|
A | G | 11 | a0001c0001t0006g0089a0001c0001t0006g0094a0001c0001t0006g0096others(8): Show | 11 | HG02615.hp1 HG02647.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.33-8088A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120398030 | ||||||
| chr11:120398069
|
C | T | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.33-8049C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120398069 | ||||||
| chr11:120398121
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-7997A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120398121 | ||||||
| chr11:120398308
|
A | T | 3 | a0001c0002t0016g0014a0001c0002t0016g0025a0001c0002t0016g0026 | 3 | HG02258.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.33-7810A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120398308 | ||||||
| chr11:120398448
|
G | A | 1 | a0007c0011t0001g0187 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.33-7670G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120398448 | ||||||
| chr11:120398599
|
G | A | 153 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.33-7519G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120398599 | ||||||
| chr11:120399321
|
C | CA | 35 | a0001c0001t0001g0143a0001c0001t0001g0146a0001c0001t0001g0148others(32): Show | 35 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.33-6767dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAA | 12 | a0001c0001t0001g0208a0001c0001t0001g0217a0001c0001t0001g0223others(9): Show | 12 | HG01106.hp1 HG01243.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.33-6768_33-6767dup others(2): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAA | 14 | a0001c0001t0001g0166a0001c0001t0002g0098a0001c0001t0002g0115others(11): Show | 14 | HG00738.hp2 HG01123.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-6769_33-6767dup others(3): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAA | 11 | a0001c0001t0001g0249a0001c0001t0002g0097a0001c0001t0002g0110others(8): Show | 11 | HG01099.hp2 HG02056.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.33-6770_33-6767dup others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAA | 12 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0113others(9): Show | 12 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-6771_33-6767dup others(5): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAA | 9 | a0001c0001t0002g0021a0001c0001t0002g0091a0001c0001t0002g0106others(6): Show | 9 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-6772_33-6767dup others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA | 14 | a0001c0001t0002g0095a0001c0001t0002g0102a0001c0001t0002g0114others(11): Show | 14 | HG00639.hp1 HG01358.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-6773_33-6767dup others(7): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(1): Show |
7 | a0001c0001t0002g0093a0001c0001t0006g0089a0001c0001t0006g0103others(4): Show | 7 | HG01123.hp2 HG01978.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-6774_33-6767dup others(8): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(3): Show |
3 | a0001c0002t0003g0015a0001c0002t0003g0032a0001c0002t0019g0012 | 3 | HG01070.hp1 HG01071.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-6776_33-6767dup others(10): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0002g0109a0001c0002t0003g0001a0001c0002t0003g0062others(3): Show | 7 | HG00099.hp1 HG01515.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-6777_33-6767dup others(11): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(5): Show |
4 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0033others(1): Show | 4 | HG01106.hp2 HG02148.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-6778_33-6767dup others(12): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(6): Show |
1 | a0001c0002t0003g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.33-6779_33-6767dup others(13): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(7): Show |
3 | a0001c0002t0003g0038a0001c0002t0003g0040a0001c0002t0016g0026 | 3 | HG00280.hp1 HG01346.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.33-6780_33-6767dup others(14): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(10): Show |
1 | a0001c0002t0003g0065 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.33-6783_33-6767dup others(17): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(12): Show |
1 | a0001c0002t0003g0036 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.33-6785_33-6767dup others(19): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(15): Show |
1 | a0001c0002t0003g0035 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.33-6788_33-6767dup others(22): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(17): Show |
1 | a0001c0002t0003g0034 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.33-6790_33-6767dup others(24): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(18): Show |
1 | a0001c0002t0003g0037 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.33-6791_33-6767dup others(25): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(26): Show |
1 | a0001c0002t0003g0045 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.33-6767_33-6766ins others(33): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(31): Show |
1 | a0001c0002t0003g0030 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.33-6767_33-6766ins others(38): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
C | CAAAAAAA others(33): Show |
1 | a0001c0002t0003g0129 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.33-6767_33-6766ins others(40): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
CA | C | 22 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0182others(19): Show | 22 | HG00280.hp2 HG01256.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.33-6767delA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
CAA | C | 27 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0196others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.33-6768_33-6767del others(2): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
CAAAAAA | C | 15 | a0001c0001t0029g0190a0001c0004t0005g0046a0001c0004t0005g0047others(12): Show | 15 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.33-6772_33-6767del others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-6776_33-6767del others(10): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0003g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.33-6777_33-6767del others(11): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
CAAAAAAA others(5): Show |
C | 7 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(4): Show | 7 | HG01074.hp2 HG01109.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-6778_33-6767del others(12): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0002g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.33-6779_33-6767del others(13): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0002g0018 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.33-6781_33-6767del others(15): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399321
|
CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.33-6784_33-6767del others(18): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399321 | |||||
| chr11:120399343
|
A | G | 5 | a0001c0001t0010g0294a0001c0001t0010g0297a0004c0009t0010g0276others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-6775A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120399343 | ||||||
| chr11:120399352
|
G | A | 2 | a0001c0002t0003g0037a0001c0002t0003g0045 | 2 | HG01257.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.33-6766G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120399352 | ||||||
| chr11:120399372
|
C | G | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-6746C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120399372 | ||||||
| chr11:120399389
|
G | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-6729G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120399389 | ||||||
| chr11:120399461
|
A | G | 86 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(83): Show | 86 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.33-6657A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120399461 | ||||||
| chr11:120399540
|
A | G | 78 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(75): Show | 78 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.33-6578A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120399540 | ||||||
| chr11:120399544
|
A | G | 142 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.33-6574A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120399544 | ||||||
| chr11:120399911
|
ATAT | A | 78 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(75): Show | 78 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.33-6201_33-6199del others(3): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120399911 | |||||
| chr11:120400000
|
C | T | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.33-6118C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120400000 | ||||||
| chr11:120400012
|
C | A | 2 | a0002c0003t0002g0072a0002c0003t0002g0082 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.33-6106C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120400012 | ||||||
| chr11:120400201
|
G | A | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.33-5917G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120400201 | ||||||
| chr11:120400374
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.33-5744T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120400374 | ||||||
| chr11:120400916
|
G | A | 1 | a0001c0002t0003g0033 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.33-5202G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120400916 | ||||||
| chr11:120401009
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.33-5109C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120401009 | ||||||
| chr11:120401031
|
G | A | 2 | a0001c0001t0009g0003a0001c0001t0009g0004 | 2 | HG00438.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.33-5087G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120401031 | ||||||
| chr11:120401731
|
T | C | 1 | a0001c0001t0001g0259 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.33-4387T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120401731 | ||||||
| chr11:120402515
|
C | G | 153 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.33-3603C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120402515 | ||||||
| chr11:120402571
|
C | T | 2 | a0001c0004t0005g0049a0001c0004t0005g0053 | 2 | HG02698.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.33-3547C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120402571 | ||||||
| chr11:120402592
|
A | G | 34 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.33-3526A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120402592 | ||||||
| chr11:120402607
|
G | A | 121 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(118): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.33-3511G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120402607 | ||||||
| chr11:120402644
|
G | A | 206 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(203): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.33-3474G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120402644 | ||||||
| chr11:120402657
|
A | G | 4 | a0002c0003t0002g0070a0002c0003t0002g0079a0002c0003t0002g0080others(1): Show | 4 | NA18960.hp1 NA18977.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-3461A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120402657 | ||||||
| chr11:120402816
|
AG | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-3300delG | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120402816 | |||||
| chr11:120402888
|
G | A | 116 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(113): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.33-3230G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120402888 | ||||||
| chr11:120402977
|
A | G | 34 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.33-3141A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120402977 | ||||||
| chr11:120402998
|
A | G | 1 | a0001c0001t0006g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.33-3120A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120402998 | ||||||
| chr11:120403156
|
G | A | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.33-2962G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120403156 | ||||||
| chr11:120403232
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.33-2886C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120403232 | ||||||
| chr11:120403238
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.33-2880G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120403238 | ||||||
| chr11:120403299
|
G | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-2819G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120403299 | ||||||
| chr11:120403323
|
A | G | 4 | a0001c0001t0002g0093a0001c0001t0002g0095a0001c0001t0002g0106others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-2795A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120403323 | ||||||
| chr11:120403494
|
G | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-2624G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120403494 | ||||||
| chr11:120403502
|
A | G | 153 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.33-2616A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120403502 | ||||||
| chr11:120403505
|
G | A | 4 | a0001c0001t0002g0021a0001c0001t0002g0114a0001c0001t0002g0116others(1): Show | 4 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-2613G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120403505 | ||||||
| chr11:120403629
|
G | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-2489G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120403629 | ||||||
| chr11:120403644
|
C | A | 121 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(118): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.33-2474C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120403644 | ||||||
| chr11:120403792
|
G | T | 153 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.33-2326G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120403792 | ||||||
| chr11:120404184
|
T | C | 20 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0028others(17): Show | 21 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-1934T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120404184 | ||||||
| chr11:120404330
|
C | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0092a0001c0001t0008g0104others(4): Show | 7 | HG02129.hp2 HG04115.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-1788C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120404330 | ||||||
| chr11:120404424
|
A | G | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.33-1694A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120404424 | ||||||
| chr11:120404525
|
T | G | 39 | a0001c0001t0002g0018a0001c0001t0002g0021a0001c0001t0002g0091others(36): Show | 39 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.33-1593T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120404525 | ||||||
| chr11:120404686
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.33-1432G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120404686 | ||||||
| chr11:120404908
|
C | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-1210C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120404908 | ||||||
| chr11:120405103
|
T | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-1015T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120405103 | ||||||
| chr11:120405417
|
T | TG | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-700dupG | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | 120405417 | |||||
| chr11:120405505
|
G | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-613G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120405505 | ||||||
| chr11:120405699
|
G | A | 1 | a0001c0001t0025g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.33-419G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120405699 | ||||||
| chr11:120405793
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33-325A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120405793 | ||||||
| chr11:120406087
|
T | G | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.33-31T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | 120406087 | ||||||
| chr11:120406194
|
T | C | 34 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.56+53T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120406194 | ||||||
| chr11:120406366
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.56+225A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120406366 | ||||||
| chr11:120406397
|
T | A | 1 | a0001c0001t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.56+256T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120406397 | ||||||
| chr11:120406401
|
T | C | 2 | a0001c0006t0002g0301a0001c0006t0002g0304 | 2 | HG00735.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.56+260T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120406401 | ||||||
| chr11:120406482
|
T | G | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.56+341T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120406482 | ||||||
| chr11:120406550
|
TTTTTA | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+429_56+433delAT others(3): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | INFO_REALIGN_3_PRIME | chr11 | 120406550 | |||||
| chr11:120406679
|
C | G | 34 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.56+538C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120406679 | ||||||
| chr11:120406683
|
C | A | 34 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.56+542C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120406683 | ||||||
| chr11:120406692
|
G | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0289 | 2 | NA18992.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.56+551G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120406692 | ||||||
| chr11:120406713
|
C | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.56+572C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120406713 | ||||||
| chr11:120406791
|
C | A | 1 | a0001c0001t0033g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.56+650C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120406791 | ||||||
| chr11:120406801
|
G | T | 1 | a0001c0001t0006g0118 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.56+660G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120406801 | ||||||
| chr11:120407032
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.57-706G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120407032 | ||||||
| chr11:120407086
|
C | G | 1 | a0001c0002t0034g0013 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.57-652C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120407086 | ||||||
| chr11:120407238
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.57-500G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120407238 | ||||||
| chr11:120407316
|
G | T | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.57-422G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120407316 | ||||||
| chr11:120407333
|
C | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-405C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120407333 | ||||||
| chr11:120407457
|
G | C | 34 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.57-281G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120407457 | ||||||
| chr11:120407575
|
A | G | 1 | a0001c0001t0008g0119 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.57-163A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120407575 | ||||||
| chr11:120407650
|
T | C | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.57-88T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 2/40 | chr11 | 120407650 | ||||||
| chr11:120407979
|
T | C | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.142+156T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120407979 | ||||||
| chr11:120408342
|
C | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.142+519C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120408342 | ||||||
| chr11:120408423
|
G | C | 34 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(31): Show | 35 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.142+600G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120408423 | ||||||
| chr11:120408424
|
G | C | 1 | a0001c0001t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.142+601G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120408424 | ||||||
| chr11:120408461
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.142+638A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120408461 | ||||||
| chr11:120408646
|
T | A | 1 | a0001c0001t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.143-748T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120408646 | ||||||
| chr11:120408650
|
A | T | 1 | a0001c0001t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.143-744A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120408650 | ||||||
| chr11:120408674
|
T | G | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.143-720T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120408674 | ||||||
| chr11:120408792
|
G | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-602G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120408792 | ||||||
| chr11:120408911
|
G | T | 32 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.143-483G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120408911 | ||||||
| chr11:120408953
|
C | G | 1 | a0001c0001t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.143-441C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120408953 | ||||||
| chr11:120409033
|
T | C | 4 | a0001c0004t0005g0049a0001c0004t0005g0053a0001c0004t0005g0056others(1): Show | 4 | HG02698.hp2 HG03704.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-361T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120409033 | ||||||
| chr11:120409152
|
T | C | 2 | a0001c0001t0018g0280a0001c0001t0018g0281 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.143-242T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120409152 | ||||||
| chr11:120409382
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-12G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3/40 | chr11 | 120409382 | ||||||
| chr11:120409751
|
C | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+301C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120409751 | ||||||
| chr11:120409788
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.199+338C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120409788 | ||||||
| chr11:120409910
|
C | T | 1 | a0001c0001t0004g0285 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.199+460C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120409910 | ||||||
| chr11:120409982
|
G | C | 1 | a0001c0001t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.199+532G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120409982 | ||||||
| chr11:120410293
|
GT | G | 195 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(192): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.199+856delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | 120410293 | |||||
| chr11:120410298
|
T | G | 1 | a0001c0001t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.199+848T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120410298 | ||||||
| chr11:120410350
|
T | G | 1 | a0001c0001t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.199+900T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120410350 | ||||||
| chr11:120410351
|
G | T | 1 | a0001c0001t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.199+901G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120410351 | ||||||
| chr11:120410364
|
T | C | 1 | a0001c0001t0007g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.199+914T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120410364 | ||||||
| chr11:120410733
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.199+1283G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120410733 | ||||||
| chr11:120410783
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.199+1333C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120410783 | ||||||
| chr11:120411060
|
T | A | 1 | a0001c0010t0001g0262 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.199+1610T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120411060 | ||||||
| chr11:120411316
|
A | G | 2 | a0001c0001t0011g0195a0001c0001t0011g0199 | 2 | HG01934.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.199+1866A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120411316 | ||||||
| chr11:120411505
|
C | T | 5 | a0001c0001t0006g0089a0001c0001t0006g0094a0001c0001t0006g0101others(2): Show | 5 | HG02615.hp1 HG03139.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+2055C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120411505 | ||||||
| chr11:120411581
|
C | CT | 81 | a0001c0001t0001g0189a0001c0001t0001g0207a0001c0001t0001g0210others(78): Show | 81 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.199+2157dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | 120411581 | |||||
| chr11:120411581
|
C | CTT | 9 | a0001c0001t0002g0093a0001c0001t0002g0095a0001c0001t0002g0121others(6): Show | 9 | HG01123.hp1 HG01358.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.199+2156_199+2157d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | 120411581 | |||||
| chr11:120411581
|
C | CTTTTT | 12 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(9): Show | 12 | HG00597.hp2 HG02602.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.199+2153_199+2157d others(7): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | 120411581 | |||||
| chr11:120411581
|
CT | C | 80 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0143others(77): Show | 82 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.199+2157delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | 120411581 | |||||
| chr11:120411581
|
CTT | C | 14 | a0001c0001t0001g0175a0001c0001t0009g0003a0001c0001t0009g0004others(11): Show | 14 | HG00323.hp1 HG00438.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.199+2156_199+2157d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | 120411581 | |||||
| chr11:120411690
|
A | T | 1 | a0001c0001t0004g0285 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.199+2240A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120411690 | ||||||
| chr11:120411857
|
G | A | 32 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.199+2407G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120411857 | ||||||
| chr11:120411910
|
AT | A | 6 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(3): Show | 6 | HG01074.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+2461delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120411910 | ||||||
| chr11:120412055
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.199+2605T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120412055 | ||||||
| chr11:120412253
|
G | A | 1 | a0002c0003t0002g0137 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.199+2803G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120412253 | ||||||
| chr11:120412253
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.199+2803G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120412253 | ||||||
| chr11:120412505
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.199+3055A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120412505 | ||||||
| chr11:120412820
|
T | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.199+3370T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120412820 | ||||||
| chr11:120412929
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.199+3479G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120412929 | ||||||
| chr11:120412997
|
T | A | 1 | a0001c0001t0001g0268 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.199+3547T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120412997 | ||||||
| chr11:120413094
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.199+3644G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120413094 | ||||||
| chr11:120413192
|
T | C | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.199+3742T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120413192 | ||||||
| chr11:120413436
|
T | G | 5 | a0001c0001t0010g0294a0001c0001t0010g0297a0004c0009t0010g0276others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+3986T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120413436 | ||||||
| chr11:120413641
|
C | T | 1 | a0001c0001t0009g0010 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.199+4191C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120413641 | ||||||
| chr11:120413980
|
A | C | 2 | a0001c0001t0035g0088a0001c0001t0036g0087 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.199+4530A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120413980 | ||||||
| chr11:120413993
|
C | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.199+4543C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120413993 | ||||||
| chr11:120414016
|
A | G | 1 | a0001c0001t0004g0260 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.199+4566A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120414016 | ||||||
| chr11:120414060
|
G | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.199+4610G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120414060 | ||||||
| chr11:120414349
|
G | A | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.199+4899G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120414349 | ||||||
| chr11:120414427
|
T | TG | 152 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.199+4977_199+4978i others(3): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120414427 | ||||||
| chr11:120414449
|
G | A | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.199+4999G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120414449 | ||||||
| chr11:120414491
|
C | A | 1 | a0001c0001t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.199+5041C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120414491 | ||||||
| chr11:120414791
|
T | C | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.199+5341T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120414791 | ||||||
| chr11:120414796
|
T | A | 7 | a0001c0001t0001g0208a0001c0001t0001g0215a0001c0001t0001g0222others(4): Show | 7 | HG00673.hp1 NA18963.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+5346T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120414796 | ||||||
| chr11:120414884
|
G | C | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.199+5434G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120414884 | ||||||
| chr11:120414894
|
C | T | 300 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(297): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.199+5444C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120414894 | ||||||
| chr11:120414927
|
T | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.199+5477T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120414927 | ||||||
| chr11:120414996
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.199+5546A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120414996 | ||||||
| chr11:120415722
|
C | T | 1 | a0001c0008t0020g0009 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.200-5031C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120415722 | ||||||
| chr11:120415888
|
C | A | 1 | a0001c0001t0009g0010 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.200-4865C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120415888 | ||||||
| chr11:120416129
|
A | T | 1 | a0001c0001t0002g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.200-4624A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120416129 | ||||||
| chr11:120416259
|
C | T | 1 | a0002c0003t0030g0075 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.200-4494C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120416259 | ||||||
| chr11:120416601
|
T | A | 1 | a0001c0001t0002g0105 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.200-4152T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120416601 | ||||||
| chr11:120416605
|
A | G | 1 | a0001c0001t0009g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.200-4148A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120416605 | ||||||
| chr11:120417094
|
A | G | 32 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.200-3659A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120417094 | ||||||
| chr11:120417095
|
T | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.200-3658T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120417095 | ||||||
| chr11:120417147
|
G | T | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.200-3606G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120417147 | ||||||
| chr11:120417162
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.200-3591C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120417162 | ||||||
| chr11:120417266
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.200-3487A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120417266 | ||||||
| chr11:120417351
|
C | T | 21 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0027others(18): Show | 22 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.200-3402C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120417351 | ||||||
| chr11:120417505
|
A | AT | 89 | a0001c0001t0001g0207a0001c0001t0001g0288a0001c0001t0001g0290others(86): Show | 89 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(86): Show |
intron_variant | MODIFIER | c.200-3228dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | 120417505 | |||||
| chr11:120417505
|
AT | A | 10 | a0001c0001t0001g0147a0001c0001t0001g0177a0001c0001t0001g0201others(7): Show | 10 | HG00323.hp2 HG00639.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.200-3228delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | 120417505 | |||||
| chr11:120417659
|
T | C | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.200-3094T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120417659 | ||||||
| chr11:120417663
|
T | C | 145 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(142): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.200-3090T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120417663 | ||||||
| chr11:120417694
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.200-3059A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120417694 | ||||||
| chr11:120418011
|
G | A | 1 | a0001c0001t0024g0214 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.200-2742G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120418011 | ||||||
| chr11:120418031
|
G | T | 13 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(10): Show | 14 | HG00597.hp1 HG00621.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.200-2722G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120418031 | ||||||
| chr11:120418207
|
A | G | 2 | a0001c0001t0022g0158a0001c0001t0023g0178 | 2 | HG03239.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.200-2546A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120418207 | ||||||
| chr11:120418235
|
G | C | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.200-2518G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120418235 | ||||||
| chr11:120418652
|
G | A | 6 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(3): Show | 6 | HG01074.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.200-2101G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120418652 | ||||||
| chr11:120418769
|
C | T | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.200-1984C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120418769 | ||||||
| chr11:120418808
|
C | T | 2 | a0001c0001t0011g0195a0001c0001t0011g0199 | 2 | HG01934.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.200-1945C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120418808 | ||||||
| chr11:120418819
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.200-1934T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120418819 | ||||||
| chr11:120418990
|
T | C | 86 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(83): Show | 86 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.200-1763T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120418990 | ||||||
| chr11:120419143
|
G | A | 1 | a0001c0001t0035g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.200-1610G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120419143 | ||||||
| chr11:120419203
|
G | A | 5 | a0001c0001t0002g0021a0001c0001t0002g0114a0001c0001t0002g0115others(2): Show | 5 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.200-1550G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120419203 | ||||||
| chr11:120419229
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0002g0095 | 2 | HG01358.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.200-1524C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120419229 | ||||||
| chr11:120419237
|
G | GGCGTGAG others(7): Show |
1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.200-1514_200-1513i others(16): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | 120419237 | |||||
| chr11:120419279
|
T | G | 1 | a0001c0001t0001g0240 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.200-1474T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120419279 | ||||||
| chr11:120419465
|
G | GT | 142 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.200-1287dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | 120419465 | |||||
| chr11:120419949
|
G | A | 1 | a0002c0003t0002g0078 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.200-804G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120419949 | ||||||
| chr11:120420051
|
AAC | A | 6 | a0001c0006t0002g0301a0001c0006t0002g0302a0001c0006t0002g0303others(3): Show | 6 | HG00735.hp2 HG00738.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.200-698_200-697del others(2): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | INFO_REALIGN_3_PRIME | chr11 | 120420051 | |||||
| chr11:120420085
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.200-668A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120420085 | ||||||
| chr11:120420287
|
G | C | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.200-466G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120420287 | ||||||
| chr11:120420375
|
A | G | 3 | a0001c0001t0004g0243a0001c0001t0004g0260a0001c0001t0004g0264 | 3 | NA19011.hp1 NA19056.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.200-378A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120420375 | ||||||
| chr11:120420427
|
A | G | 1 | a0001c0002t0003g0027 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.200-326A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120420427 | ||||||
| chr11:120420428
|
C | G | 79 | a0001c0001t0002g0018a0001c0001t0002g0021a0001c0001t0002g0091others(76): Show | 79 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.200-325C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120420428 | ||||||
| chr11:120420564
|
T | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.200-189T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 4/40 | chr11 | 120420564 | ||||||
| chr11:120421141
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.298+290A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421141 | ||||||
| chr11:120421152
|
G | A | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.298+301G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421152 | ||||||
| chr11:120421251
|
A | G | 8 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+400A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421251 | ||||||
| chr11:120421331
|
T | C | 35 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(32): Show | 36 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.299-472T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421331 | ||||||
| chr11:120421382
|
G | A | 1 | a0001c0001t0004g0244 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.299-421G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421382 | ||||||
| chr11:120421388
|
C | T | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.299-415C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421388 | ||||||
| chr11:120421429
|
G | GT | 25 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0150others(22): Show | 25 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.299-362dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | INFO_REALIGN_3_PRIME | chr11 | 120421429 | |||||
| chr11:120421429
|
G | GTTTTTTT others(3): Show |
3 | a0001c0004t0005g0049a0001c0004t0005g0056a0001c0004t0005g0057 | 3 | HG03704.hp2 HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.299-371_299-362dup others(10): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | INFO_REALIGN_3_PRIME | chr11 | 120421429 | |||||
| chr11:120421429
|
G | GTTTTTTT others(6): Show |
1 | a0001c0004t0005g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.299-362_299-361ins others(13): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | INFO_REALIGN_3_PRIME | chr11 | 120421429 | |||||
| chr11:120421438
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.299-365T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421438 | ||||||
| chr11:120421440
|
TTG | T | 33 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0193others(30): Show | 33 | HG00099.hp2 HG00323.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.299-361_299-360del others(2): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | INFO_REALIGN_3_PRIME | chr11 | 120421440 | |||||
| chr11:120421441
|
TG | T | 42 | a0001c0001t0001g0181a0001c0001t0001g0194a0001c0001t0001g0196others(39): Show | 42 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.299-361delG | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421441 | ||||||
| chr11:120421442
|
G | T | 225 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(222): Show | 227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.299-361G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421442 | ||||||
| chr11:120421455
|
T | G | 86 | a0001c0001t0001g0238a0001c0001t0002g0018a0001c0001t0002g0019others(83): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.299-348T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421455 | ||||||
| chr11:120421455
|
T | TG | 33 | a0001c0001t0001g0213a0001c0001t0002g0093a0001c0001t0002g0106others(30): Show | 33 | HG00735.hp1 HG00735.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.299-346dupG | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | INFO_REALIGN_3_PRIME | chr11 | 120421455 | |||||
| chr11:120421657
|
C | T | 7 | a0001c0001t0010g0294a0001c0001t0010g0297a0001c0012t0001g0296others(4): Show | 7 | HG02451.hp2 HG02976.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-146C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421657 | ||||||
| chr11:120421674
|
G | A | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.299-129G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421674 | ||||||
| chr11:120421768
|
T | C | 33 | a0001c0001t0008g0020a0001c0001t0008g0092a0001c0001t0008g0104others(30): Show | 33 | HG02056.hp2 HG02083.hp2 HG02129.hp2 others(30): Show |
intron_variant | MODIFIER | c.299-35T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421768 | ||||||
| chr11:120421771
|
A | G | 1 | a0001c0006t0002g0306 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.299-32A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421771 | ||||||
| chr11:120421787
|
T | C | 3 | a0001c0001t0009g0005a0001c0001t0009g0006a0001c0001t0009g0007 | 3 | HG01952.hp2 HG02273.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.299-16T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 5/40 | chr11 | 120421787 | ||||||
| chr11:120421861
|
T | A | 300 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(297): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.348+9T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120421861 | ||||||
| chr11:120421965
|
T | C | 1 | a0001c0002t0034g0013 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.348+113T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120421965 | ||||||
| chr11:120422016
|
C | T | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.348+164C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120422016 | ||||||
| chr11:120422429
|
G | A | 33 | a0001c0001t0008g0020a0001c0001t0008g0092a0001c0001t0008g0104others(30): Show | 33 | HG02056.hp2 HG02083.hp2 HG02129.hp2 others(30): Show |
intron_variant | MODIFIER | c.348+577G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120422429 | ||||||
| chr11:120422433
|
C | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.348+581C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120422433 | ||||||
| chr11:120422469
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348+617C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120422469 | ||||||
| chr11:120422781
|
A | G | 118 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.348+929A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120422781 | ||||||
| chr11:120422811
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.348+959A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120422811 | ||||||
| chr11:120422859
|
G | A | 1 | a0001c0004t0005g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.348+1007G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120422859 | ||||||
| chr11:120422934
|
C | G | 1 | a0001c0001t0002g0109 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.348+1082C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120422934 | ||||||
| chr11:120423072
|
A | C | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.348+1220A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120423072 | ||||||
| chr11:120423085
|
A | C | 1 | a0001c0001t0009g0005 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.348+1233A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120423085 | ||||||
| chr11:120423249
|
A | T | 62 | a0001c0001t0001g0157a0001c0001t0001g0205a0001c0001t0001g0206others(59): Show | 62 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.349-1109A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120423249 | ||||||
| chr11:120423295
|
G | A | 78 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(75): Show | 78 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.349-1063G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120423295 | ||||||
| chr11:120423438
|
C | T | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.349-920C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120423438 | ||||||
| chr11:120423441
|
G | A | 4 | a0001c0002t0003g0015a0001c0002t0003g0032a0001c0002t0003g0036others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-917G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120423441 | ||||||
| chr11:120423508
|
T | G | 1 | a0007c0011t0001g0187 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.349-850T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120423508 | ||||||
| chr11:120423714
|
C | T | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.349-644C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120423714 | ||||||
| chr11:120423765
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.349-593A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120423765 | ||||||
| chr11:120423926
|
T | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.349-432T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120423926 | ||||||
| chr11:120424152
|
G | A | 117 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(114): Show | 118 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.349-206G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 6/40 | chr11 | 120424152 | ||||||
| chr11:120424457
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0184 | 3 | HG02258.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.406+42C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120424457 | ||||||
| chr11:120424551
|
G | C | 1 | a0001c0004t0005g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.406+136G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120424551 | ||||||
| chr11:120424952
|
A | G | 5 | a0001c0001t0001g0213a0001c0001t0001g0238a0001c0001t0001g0241others(2): Show | 5 | NA18961.hp2 NA18973.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.406+537A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120424952 | ||||||
| chr11:120425063
|
C | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.406+648C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120425063 | ||||||
| chr11:120425145
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.406+730A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120425145 | ||||||
| chr11:120425335
|
C | T | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.406+920C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120425335 | ||||||
| chr11:120425339
|
G | GT | 6 | a0001c0001t0001g0150a0001c0001t0001g0156a0001c0001t0001g0176others(3): Show | 6 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+940dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | INFO_REALIGN_3_PRIME | chr11 | 120425339 | |||||
| chr11:120425348
|
T | G | 19 | a0001c0001t0006g0099a0001c0001t0009g0003a0001c0001t0009g0004others(16): Show | 19 | HG00438.hp2 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.406+933T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120425348 | ||||||
| chr11:120425352
|
T | G | 157 | a0001c0001t0001g0147a0001c0001t0001g0160a0001c0001t0001g0163others(154): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.406+937T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120425352 | ||||||
| chr11:120425352
|
T | TG | 4 | a0001c0001t0001g0288a0001c0001t0006g0096a0001c0004t0005g0048others(1): Show | 4 | HG00597.hp2 HG02647.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+937_406+938ins others(1): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120425352 | ||||||
| chr11:120425353
|
T | G | 9 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+938T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120425353 | ||||||
| chr11:120425588
|
T | C | 2 | a0001c0002t0002g0022a0001c0002t0002g0024 | 2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.406+1173T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120425588 | ||||||
| chr11:120425754
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.406+1339A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120425754 | ||||||
| chr11:120425760
|
T | TA | 7 | a0001c0001t0001g0155a0001c0001t0001g0172a0001c0001t0001g0268others(4): Show | 7 | HG02165.hp1 HG02615.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.406+1362dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | INFO_REALIGN_3_PRIME | chr11 | 120425760 | |||||
| chr11:120425760
|
TA | T | 156 | a0001c0001t0001g0173a0001c0001t0001g0179a0001c0001t0001g0180others(153): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.406+1362delA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | INFO_REALIGN_3_PRIME | chr11 | 120425760 | |||||
| chr11:120425760
|
TAA | T | 11 | a0001c0001t0002g0019a0001c0001t0002g0021a0001c0001t0002g0102others(8): Show | 11 | HG00438.hp2 HG01070.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.406+1361_406+1362d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | INFO_REALIGN_3_PRIME | chr11 | 120425760 | |||||
| chr11:120426475
|
T | G | 1 | a0002c0003t0017g0282 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.407-1594T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120426475 | ||||||
| chr11:120426613
|
G | C | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.407-1456G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120426613 | ||||||
| chr11:120426864
|
T | TG | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.407-1205_407-1204i others(3): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120426864 | ||||||
| chr11:120426864
|
TTTTTTGT others(5): Show |
T | 86 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(83): Show | 86 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.407-1187_407-1176d others(14): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | INFO_REALIGN_3_PRIME | chr11 | 120426864 | |||||
| chr11:120426886
|
T | C | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.407-1183T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120426886 | ||||||
| chr11:120426972
|
G | C | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.407-1097G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120426972 | ||||||
| chr11:120427145
|
A | C | 9 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.407-924A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120427145 | ||||||
| chr11:120427258
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.407-811C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120427258 | ||||||
| chr11:120427537
|
T | TA | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.407-520dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | INFO_REALIGN_3_PRIME | chr11 | 120427537 | |||||
| chr11:120427822
|
T | C | 1 | a0001c0001t0009g0010 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.407-247T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120427822 | ||||||
| chr11:120427846
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.407-223A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120427846 | ||||||
| chr11:120427946
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.407-123G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120427946 | ||||||
| chr11:120428030
|
T | TTTCCC | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.407-26_407-22dupCC others(3): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | INFO_REALIGN_3_PRIME | chr11 | 120428030 | |||||
| chr11:120428040
|
C | G | 1 | a0001c0002t0003g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.407-29C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 7/40 | chr11 | 120428040 | ||||||
| chr11:120428451
|
A | G | 1 | a0001c0001t0033g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.585+204A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 8/40 | chr11 | 120428451 | ||||||
| chr11:120428723
|
G | T | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.585+476G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 8/40 | chr11 | 120428723 | ||||||
| chr11:120428986
|
A | T | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.586-454A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 8/40 | chr11 | 120428986 | ||||||
| chr11:120428998
|
T | C | 80 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(77): Show | 80 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.586-442T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 8/40 | chr11 | 120428998 | ||||||
| chr11:120429251
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.586-189G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 8/40 | chr11 | 120429251 | ||||||
| chr11:120429360
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.586-80A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 8/40 | chr11 | 120429360 | ||||||
| chr11:120429618
|
A | C | 32 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.664-94A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 9/40 | chr11 | 120429618 | ||||||
| chr11:120429850
|
G | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.783+19G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120429850 | ||||||
| chr11:120429898
|
A | T | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.783+67A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120429898 | ||||||
| chr11:120429986
|
A | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | HG00280.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.783+155A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120429986 | ||||||
| chr11:120430095
|
T | A | 80 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(77): Show | 80 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.783+264T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120430095 | ||||||
| chr11:120430145
|
T | C | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.783+314T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120430145 | ||||||
| chr11:120430328
|
A | G | 1 | a0001c0002t0002g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.783+497A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120430328 | ||||||
| chr11:120430666
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.783+835C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120430666 | ||||||
| chr11:120431146
|
C | T | 5 | a0001c0001t0010g0294a0001c0001t0010g0297a0004c0009t0010g0276others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-625C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120431146 | ||||||
| chr11:120431195
|
C | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0210 | 2 | HG01433.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.784-576C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120431195 | ||||||
| chr11:120431418
|
C | T | 1 | a0001c0001t0002g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.784-353C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120431418 | ||||||
| chr11:120431446
|
C | T | 1 | a0001c0004t0005g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.784-325C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120431446 | ||||||
| chr11:120431482
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.784-289A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120431482 | ||||||
| chr11:120431530
|
C | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.784-241C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120431530 | ||||||
| chr11:120431590
|
G | A | 1 | a0001c0001t0033g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.784-181G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120431590 | ||||||
| chr11:120431620
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.784-151G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120431620 | ||||||
| chr11:120431757
|
T | C | 1 | a0001c0002t0003g0033 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.784-14T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120431757 | ||||||
| chr11:120431758
|
T | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG00597.hp1 HG02071.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-13T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 10/40 | chr11 | 120431758 | ||||||
| chr11:120431918
|
T | A | 4 | a0001c0001t0002g0019a0001c0001t0002g0102a0001c0001t0002g0124others(1): Show | 4 | HG02486.hp2 HG02723.hp1 HG02897.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.924+7T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120431918 | ||||||
| chr11:120431920
|
T | C | 19 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(16): Show | 19 | HG00597.hp2 HG01074.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.924+9T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120431920 | ||||||
| chr11:120432020
|
C | T | 52 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(49): Show | 53 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.924+109C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120432020 | ||||||
| chr11:120432093
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.924+182A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120432093 | ||||||
| chr11:120432170
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.924+259C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120432170 | ||||||
| chr11:120432390
|
A | C | 1 | a0001c0001t0006g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.924+479A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120432390 | ||||||
| chr11:120432407
|
T | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.924+496T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120432407 | ||||||
| chr11:120432427
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.924+516A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120432427 | ||||||
| chr11:120432597
|
C | T | 1 | a0001c0001t0009g0010 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.924+686C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120432597 | ||||||
| chr11:120432661
|
G | C | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.924+750G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120432661 | ||||||
| chr11:120432793
|
G | A | 1 | a0002c0003t0002g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.924+882G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120432793 | ||||||
| chr11:120432807
|
T | A | 3 | a0001c0001t0004g0250a0001c0001t0004g0253a0001c0001t0004g0277 | 3 | NA18960.hp2 NA19070.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.924+896T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120432807 | ||||||
| chr11:120433054
|
C | T | 6 | a0001c0001t0001g0213a0001c0001t0001g0238a0001c0001t0001g0241others(3): Show | 6 | NA18961.hp2 NA18973.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.924+1143C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120433054 | ||||||
| chr11:120433230
|
G | T | 153 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.924+1319G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120433230 | ||||||
| chr11:120433685
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.924+1774G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120433685 | ||||||
| chr11:120433733
|
G | A | 2 | a0001c0002t0003g0015a0001c0002t0003g0032 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.924+1822G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120433733 | ||||||
| chr11:120433906
|
C | A | 1 | a0001c0001t0006g0094 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.924+1995C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120433906 | ||||||
| chr11:120433990
|
T | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0257 | 2 | HG02071.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.924+2079T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120433990 | ||||||
| chr11:120434022
|
A | T | 1 | a0001c0001t0011g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.924+2111A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120434022 | ||||||
| chr11:120434030
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.924+2119A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120434030 | ||||||
| chr11:120434069
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.924+2158A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120434069 | ||||||
| chr11:120434112
|
A | G | 3 | a0001c0001t0001g0148a0001c0001t0001g0175a0001c0001t0001g0177 | 3 | HG01074.hp1 HG01109.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.924+2201A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120434112 | ||||||
| chr11:120434283
|
T | G | 1 | a0001c0001t0008g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.924+2372T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120434283 | ||||||
| chr11:120434562
|
G | A | 1 | a0001c0001t0009g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.924+2651G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120434562 | ||||||
| chr11:120434870
|
A | G | 1 | a0001c0001t0026g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.925-2438A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120434870 | ||||||
| chr11:120435078
|
A | G | 34 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.925-2230A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120435078 | ||||||
| chr11:120435164
|
A | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0092a0001c0001t0008g0104others(4): Show | 7 | HG02129.hp2 HG04115.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.925-2144A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120435164 | ||||||
| chr11:120435342
|
C | T | 1 | a0001c0004t0005g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.925-1966C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120435342 | ||||||
| chr11:120435512
|
C | CT | 67 | a0001c0001t0001g0152a0001c0001t0001g0205a0001c0001t0001g0206others(64): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.925-1776dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | INFO_REALIGN_3_PRIME | chr11 | 120435512 | |||||
| chr11:120435578
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.925-1730A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120435578 | ||||||
| chr11:120435583
|
C | T | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.925-1725C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120435583 | ||||||
| chr11:120435873
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.925-1435T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120435873 | ||||||
| chr11:120436036
|
C | A | 1 | a0001c0012t0001g0296 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.925-1272C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120436036 | ||||||
| chr11:120436050
|
T | C | 59 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(56): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.925-1258T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120436050 | ||||||
| chr11:120436092
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.925-1216A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120436092 | ||||||
| chr11:120436103
|
G | T | 1 | a0001c0004t0005g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.925-1205G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120436103 | ||||||
| chr11:120436420
|
G | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.925-888G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120436420 | ||||||
| chr11:120436664
|
A | G | 5 | a0001c0001t0010g0294a0001c0001t0010g0297a0004c0009t0010g0276others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.925-644A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120436664 | ||||||
| chr11:120436799
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.925-509C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120436799 | ||||||
| chr11:120436823
|
T | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.925-485T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120436823 | ||||||
| chr11:120436887
|
A | G | 21 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(18): Show | 21 | HG00438.hp2 HG00597.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.925-421A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120436887 | ||||||
| chr11:120436910
|
T | C | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.925-398T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120436910 | ||||||
| chr11:120436983
|
T | TAAATA | 59 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(56): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.925-323_925-322ins others(5): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | INFO_REALIGN_3_PRIME | chr11 | 120436983 | |||||
| chr11:120437033
|
A | G | 59 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(56): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.925-275A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120437033 | ||||||
| chr11:120437182
|
G | A | 2 | a0001c0001t0029g0190a0002c0003t0017g0282 | 2 | HG02135.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.925-126G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120437182 | ||||||
| chr11:120437277
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.925-31A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 11/40 | chr11 | 120437277 | ||||||
| chr11:120437394
|
A | T | 1 | a0001c0001t0008g0119 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.999+12A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120437394 | ||||||
| chr11:120437581
|
A | G | 153 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.999+199A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120437581 | ||||||
| chr11:120437700
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+318A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120437700 | ||||||
| chr11:120437710
|
C | T | 6 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(3): Show | 6 | HG01074.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+328C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120437710 | ||||||
| chr11:120438293
|
C | CT | 86 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(83): Show | 86 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.999+919dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | INFO_REALIGN_3_PRIME | chr11 | 120438293 | |||||
| chr11:120438327
|
A | G | 152 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.999+945A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120438327 | ||||||
| chr11:120438447
|
T | A | 14 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(11): Show | 14 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.999+1065T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120438447 | ||||||
| chr11:120438734
|
C | T | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.999+1352C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120438734 | ||||||
| chr11:120438751
|
C | T | 27 | a0001c0001t0002g0018a0001c0001t0002g0021a0001c0001t0002g0091others(24): Show | 27 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.999+1369C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120438751 | ||||||
| chr11:120438886
|
CAG | C | 4 | a0002c0003t0002g0070a0002c0003t0002g0079a0002c0003t0002g0080others(1): Show | 4 | NA18960.hp1 NA18977.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-1240_1000-123 others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | INFO_REALIGN_3_PRIME | chr11 | 120438886 | |||||
| chr11:120439142
|
C | T | 96 | a0001c0001t0001g0157a0001c0001t0001g0189a0001c0001t0001g0191others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1000-987C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120439142 | ||||||
| chr11:120439239
|
T | C | 2 | a0001c0001t0001g0249a0001c0001t0001g0255 | 2 | HG01099.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1000-890T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120439239 | ||||||
| chr11:120439508
|
A | G | 2 | a0001c0002t0003g0062a0001c0002t0003g0063 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1000-621A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120439508 | ||||||
| chr11:120439613
|
T | C | 37 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(34): Show | 38 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1000-516T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120439613 | ||||||
| chr11:120439623
|
C | A | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1000-506C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120439623 | ||||||
| chr11:120439952
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.1000-177A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 12/40 | chr11 | 120439952 | ||||||
| chr11:120440250
|
G | A | 57 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(54): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1092+29G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120440250 | ||||||
| chr11:120440269
|
A | C | 51 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(48): Show | 52 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1092+48A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120440269 | ||||||
| chr11:120440345
|
A | G | 37 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(34): Show | 38 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1092+124A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120440345 | ||||||
| chr11:120440448
|
A | G | 1 | a0002c0003t0002g0078 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1092+227A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120440448 | ||||||
| chr11:120440481
|
G | A | 2 | a0001c0001t0011g0195a0001c0001t0011g0199 | 2 | HG01934.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1092+260G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120440481 | ||||||
| chr11:120440489
|
A | T | 86 | a0001c0001t0001g0217a0001c0001t0001g0290a0001c0001t0002g0018others(83): Show | 86 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.1092+268A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120440489 | ||||||
| chr11:120440513
|
A | C | 1 | a0001c0001t0001g0287 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1092+292A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120440513 | ||||||
| chr11:120440700
|
T | A | 34 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.1092+479T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120440700 | ||||||
| chr11:120440752
|
A | G | 2 | a0001c0004t0005g0054a0001c0004t0005g0055 | 2 | HG02040.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1092+531A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120440752 | ||||||
| chr11:120440962
|
T | C | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1092+741T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120440962 | ||||||
| chr11:120440979
|
A | G | 5 | a0001c0001t0010g0294a0001c0001t0010g0297a0004c0009t0010g0276others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-728A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120440979 | ||||||
| chr11:120441395
|
T | G | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1093-312T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120441395 | ||||||
| chr11:120441449
|
G | C | 2 | a0001c0002t0003g0062a0001c0002t0003g0063 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1093-258G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120441449 | ||||||
| chr11:120441477
|
C | T | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1093-230C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 13/40 | chr11 | 120441477 | ||||||
| chr11:120442037
|
G | A | 152 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1204-67G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 14/40 | chr11 | 120442037 | ||||||
| chr11:120442259
|
C | T | 2 | a0001c0002t0003g0015a0001c0002t0003g0032 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1302+57C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442259 | ||||||
| chr11:120442346
|
C | CT | 12 | a0001c0001t0008g0020a0001c0001t0009g0003a0001c0001t0009g0004others(9): Show | 12 | HG00438.hp2 HG01099.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1302+156dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442346 | |||||
| chr11:120442346
|
CT | C | 63 | a0001c0001t0001g0157a0001c0001t0001g0189a0001c0001t0001g0205others(60): Show | 63 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1302+156delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442346 | |||||
| chr11:120442358
|
T | C | 1 | a0002c0003t0028g0066 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1302+156T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442358 | ||||||
| chr11:120442412
|
T | TTA | 10 | a0001c0001t0002g0021a0001c0001t0002g0113a0001c0001t0002g0114others(7): Show | 10 | HG00639.hp1 HG00733.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.1302+225_1302+226d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442412 | |||||
| chr11:120442412
|
T | TTATATA | 6 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0009g0003others(3): Show | 6 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302+221_1302+226d others(8): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442412 | |||||
| chr11:120442427
|
T | C | 4 | a0001c0001t0001g0144a0001c0001t0001g0174a0001c0001t0004g0220others(1): Show | 4 | HG02257.hp2 HG02523.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+225T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442427 | ||||||
| chr11:120442427
|
T | TAC | 6 | a0001c0001t0001g0141a0001c0001t0001g0166a0001c0001t0001g0189others(3): Show | 6 | HG00738.hp2 HG01123.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+253_1302+254d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442427 | |||||
| chr11:120442427
|
TAC | T | 38 | a0001c0001t0001g0173a0001c0001t0001g0279a0001c0001t0008g0020others(35): Show | 38 | HG00735.hp2 HG01167.hp1 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.1302+253_1302+254d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442427 | |||||
| chr11:120442427
|
TACAC | T | 7 | a0001c0001t0001g0148a0001c0001t0001g0161a0001c0001t0001g0175others(4): Show | 7 | HG01074.hp1 HG01109.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+251_1302+254d others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442427 | |||||
| chr11:120442427
|
TACACACA others(3): Show |
T | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+245_1302+254d others(12): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442427 | |||||
| chr11:120442427
|
TACACACA others(5): Show |
T | 6 | a0001c0001t0001g0198a0001c0001t0011g0192a0001c0001t0011g0195others(3): Show | 6 | HG01243.hp2 HG01934.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+243_1302+254d others(14): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442427 | |||||
| chr11:120442429
|
C | T | 78 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(75): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1302+227C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442429 | ||||||
| chr11:120442431
|
C | T | 33 | a0001c0001t0008g0020a0001c0001t0008g0111a0001c0001t0008g0112others(30): Show | 33 | HG01074.hp2 HG02056.hp2 HG02083.hp2 others(30): Show |
intron_variant | MODIFIER | c.1302+229C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442431 | ||||||
| chr11:120442433
|
C | T | 1 | a0002c0003t0002g0017 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1302+231C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442433 | ||||||
| chr11:120442437
|
CACACACA others(19): Show |
C | 1 | a0001c0001t0002g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1302+258_1302+283d others(28): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442437 | |||||
| chr11:120442439
|
C | T | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+237C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442439 | ||||||
| chr11:120442453
|
CACAT | C | 4 | a0001c0001t0035g0088a0001c0002t0019g0012a0001c0012t0001g0296others(1): Show | 4 | HG03486.hp1 NA18906.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+253_1302+256d others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442453 | |||||
| chr11:120442455
|
C | T | 1 | a0001c0001t0022g0158 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1302+253C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442455 | ||||||
| chr11:120442455
|
CAT | C | 4 | a0001c0001t0031g0090a0001c0001t0033g0131a0001c0001t0036g0087others(1): Show | 4 | HG02965.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+261_1302+262d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442455 | |||||
| chr11:120442457
|
T | C | 1 | a0001c0002t0003g0129 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1302+255T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442457 | ||||||
| chr11:120442463
|
T | C | 2 | a0001c0001t0002g0133a0001c0001t0022g0158 | 2 | HG02451.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1302+261T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442463 | ||||||
| chr11:120442463
|
T | TAC | 27 | a0001c0001t0001g0213a0001c0001t0001g0238a0001c0001t0001g0241others(24): Show | 27 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.1302+279_1302+280d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442463 | |||||
| chr11:120442463
|
TAC | T | 35 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(32): Show | 36 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.1302+279_1302+280d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120442463 | |||||
| chr11:120442465
|
C | T | 10 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(7): Show | 10 | HG00438.hp2 HG00733.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+263C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442465 | ||||||
| chr11:120442550
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1302+348A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442550 | ||||||
| chr11:120442673
|
A | G | 1 | a0001c0001t0025g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1302+471A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442673 | ||||||
| chr11:120442830
|
C | T | 43 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(40): Show | 44 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.1302+628C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442830 | ||||||
| chr11:120442973
|
A | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0164a0001c0001t0001g0174others(1): Show | 4 | HG00673.hp2 HG01934.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+771A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120442973 | ||||||
| chr11:120443021
|
C | CT | 13 | a0001c0001t0001g0177a0001c0001t0001g0287a0001c0001t0010g0294others(10): Show | 13 | HG00597.hp2 HG01099.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1302+837dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120443021 | |||||
| chr11:120443021
|
C | CTT | 31 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1302+836_1302+837d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | 120443021 | |||||
| chr11:120443190
|
T | G | 34 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.1302+988T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120443190 | ||||||
| chr11:120443218
|
C | T | 1 | a0001c0001t0010g0294 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1302+1016C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120443218 | ||||||
| chr11:120443290
|
G | A | 1 | a0001c0001t0008g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1302+1088G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120443290 | ||||||
| chr11:120443422
|
C | G | 1 | a0001c0001t0006g0094 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1302+1220C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120443422 | ||||||
| chr11:120443469
|
C | G | 43 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(40): Show | 44 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.1302+1267C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120443469 | ||||||
| chr11:120443569
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+1367A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120443569 | ||||||
| chr11:120443663
|
A | G | 1 | a0001c0002t0007g0042 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1302+1461A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120443663 | ||||||
| chr11:120443999
|
G | A | 1 | a0001c0002t0003g0045 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1303-1423G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120443999 | ||||||
| chr11:120444062
|
A | G | 1 | a0001c0001t0006g0094 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1303-1360A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120444062 | ||||||
| chr11:120444134
|
G | A | 1 | a0001c0001t0011g0195 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1303-1288G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120444134 | ||||||
| chr11:120444268
|
G | C | 1 | a0001c0002t0034g0013 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1303-1154G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120444268 | ||||||
| chr11:120444327
|
A | G | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1303-1095A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120444327 | ||||||
| chr11:120444329
|
A | C | 1 | a0002c0003t0002g0078 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1303-1093A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120444329 | ||||||
| chr11:120444577
|
C | T | 14 | a0001c0001t0010g0297a0002c0003t0002g0016a0002c0003t0002g0017others(11): Show | 14 | HG02135.hp2 HG02165.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1303-845C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120444577 | ||||||
| chr11:120444587
|
T | C | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1303-835T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120444587 | ||||||
| chr11:120444625
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1303-797T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120444625 | ||||||
| chr11:120444928
|
T | C | 37 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(34): Show | 38 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1303-494T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120444928 | ||||||
| chr11:120444938
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1303-484T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120444938 | ||||||
| chr11:120444975
|
T | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1303-447T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120444975 | ||||||
| chr11:120445149
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1303-273A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120445149 | ||||||
| chr11:120445302
|
T | C | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.1303-120T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | chr11 | 120445302 | ||||||
| chr11:120445702
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1345+238C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | chr11 | 120445702 | ||||||
| chr11:120445746
|
A | G | 11 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1345+282A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | chr11 | 120445746 | ||||||
| chr11:120445778
|
A | G | 1 | a0001c0007t0015g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1345+314A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | chr11 | 120445778 | ||||||
| chr11:120445794
|
A | C | 1 | a0001c0001t0006g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1345+330A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | chr11 | 120445794 | ||||||
| chr11:120445880
|
T | C | 57 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(54): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1345+416T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | chr11 | 120445880 | ||||||
| chr11:120445891
|
C | T | 1 | a0001c0004t0012g0052 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1345+427C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | chr11 | 120445891 | ||||||
| chr11:120446008
|
G | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-395G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | chr11 | 120446008 | ||||||
| chr11:120446055
|
G | T | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1346-348G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | chr11 | 120446055 | ||||||
| chr11:120446083
|
A | C | 1 | a0001c0001t0002g0113 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1346-320A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | chr11 | 120446083 | ||||||
| chr11:120446198
|
A | AAAT | 24 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0179others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.1346-167_1346-165d others(5): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | 120446198 | |||||
| chr11:120446198
|
A | AAATAAT | 3 | a0001c0001t0029g0190a0001c0002t0034g0013a0001c0008t0020g0008 | 3 | HG01099.hp1 HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1346-170_1346-165d others(8): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | 120446198 | |||||
| chr11:120446198
|
A | AAATAATA others(5): Show |
3 | a0001c0001t0026g0230a0001c0002t0019g0012a0001c0008t0020g0009 | 3 | HG01243.hp1 HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1346-176_1346-165d others(14): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | 120446198 | |||||
| chr11:120446198
|
AAAT | A | 163 | a0001c0001t0001g0143a0001c0001t0001g0146a0001c0001t0001g0148others(160): Show | 164 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1346-167_1346-165d others(5): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | 120446198 | |||||
| chr11:120446198
|
AAATAAT | A | 7 | a0001c0001t0004g0243a0001c0001t0004g0260a0001c0001t0004g0264others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1346-170_1346-165d others(8): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | 120446198 | |||||
| chr11:120446198
|
AAATAATA others(2): Show |
A | 33 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0027others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.1346-173_1346-165d others(11): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | 120446198 | |||||
| chr11:120446198
|
AAATAATA others(8): Show |
A | 1 | a0001c0001t0002g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1346-179_1346-165d others(17): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | 120446198 | |||||
| chr11:120446237
|
T | TAATAATA others(2): Show |
3 | a0001c0004t0005g0047a0001c0004t0005g0048a0001c0004t0012g0052 | 3 | HG00597.hp2 HG02602.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1346-165_1346-164i others(11): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | 120446237 | |||||
| chr11:120446237
|
T | TAATAATA others(5): Show |
7 | a0001c0004t0005g0046a0001c0004t0005g0051a0001c0004t0005g0054others(4): Show | 7 | HG02040.hp1 HG02155.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.1346-165_1346-164i others(14): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | 120446237 | |||||
| chr11:120446237
|
T | TAATAATA others(8): Show |
6 | a0001c0004t0005g0049a0001c0004t0005g0053a0001c0004t0005g0056others(3): Show | 6 | HG02698.hp2 HG03704.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-165_1346-164i others(17): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | INFO_REALIGN_3_PRIME | chr11 | 120446237 | |||||
| chr11:120446274
|
C | T | 5 | a0001c0001t0010g0294a0001c0001t0010g0297a0004c0009t0010g0276others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346-129C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 16/40 | chr11 | 120446274 | ||||||
| chr11:120446616
|
G | A | 1 | a0001c0002t0034g0013 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1451+108G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 17/40 | chr11 | 120446616 | ||||||
| chr11:120446670
|
A | G | 1 | a0001c0001t0006g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1451+162A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 17/40 | chr11 | 120446670 | ||||||
| chr11:120447591
|
G | A | 1 | a0001c0001t0011g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1590-283G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 18/40 | chr11 | 120447591 | ||||||
| chr11:120447718
|
A | G | 1 | a0006c0013t0001g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1590-156A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 18/40 | chr11 | 120447718 | ||||||
| chr11:120447810
|
T | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1590-64T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 18/40 | chr11 | 120447810 | ||||||
| chr11:120448188
|
C | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1623-46C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 19/40 | chr11 | 120448188 | ||||||
| chr11:120448192
|
C | T | 1 | a0001c0001t0011g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1623-42C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 19/40 | chr11 | 120448192 | ||||||
| chr11:120448355
|
A | C | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
splice_region_variant&intron_variant | LOW | c.1737+7A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 20/40 | chr11 | 120448355 | ||||||
| chr11:120448526
|
A | G | 1 | a0002c0003t0002g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1737+178A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 20/40 | chr11 | 120448526 | ||||||
| chr11:120448641
|
C | T | 1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1737+293C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 20/40 | chr11 | 120448641 | ||||||
| chr11:120448701
|
T | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+353T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 20/40 | chr11 | 120448701 | ||||||
| chr11:120449036
|
G | T | 1 | a0001c0001t0001g0287 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1738-73G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 20/40 | chr11 | 120449036 | ||||||
| chr11:120449037
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1738-72C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 20/40 | chr11 | 120449037 | ||||||
| chr11:120449080
|
A | G | 2 | a0001c0002t0003g0038a0001c0002t0003g0039 | 2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1738-29A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 20/40 | chr11 | 120449080 | ||||||
| chr11:120449265
|
C | T | 2 | a0001c0001t0006g0099a0001c0001t0006g0122 | 2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1843+51C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120449265 | ||||||
| chr11:120449339
|
A | G | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1843+125A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120449339 | ||||||
| chr11:120449381
|
C | G | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1843+167C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120449381 | ||||||
| chr11:120449461
|
G | A | 1 | a0001c0001t0006g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1843+247G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120449461 | ||||||
| chr11:120449475
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1843+261C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120449475 | ||||||
| chr11:120449496
|
C | G | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1843+282C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120449496 | ||||||
| chr11:120449648
|
G | A | 1 | a0001c0002t0003g0063 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1843+434G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120449648 | ||||||
| chr11:120449681
|
A | G | 1 | a0001c0001t0026g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1843+467A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120449681 | ||||||
| chr11:120449834
|
T | TA | 37 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0003g0001others(34): Show | 38 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1843+631dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | INFO_REALIGN_3_PRIME | chr11 | 120449834 | |||||
| chr11:120449956
|
C | T | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1843+742C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120449956 | ||||||
| chr11:120449973
|
A | G | 1 | a0001c0001t0026g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1843+759A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120449973 | ||||||
| chr11:120450098
|
C | T | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.1843+884C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120450098 | ||||||
| chr11:120450249
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1843+1035G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120450249 | ||||||
| chr11:120450370
|
C | CA | 178 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0151others(175): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.1844-1119dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | INFO_REALIGN_3_PRIME | chr11 | 120450370 | |||||
| chr11:120450370
|
C | CAA | 31 | a0001c0001t0001g0198a0001c0001t0001g0209a0001c0001t0001g0213others(28): Show | 31 | HG00140.hp1 HG00597.hp2 HG01993.hp1 others(28): Show |
intron_variant | MODIFIER | c.1844-1120_1844-111 others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | INFO_REALIGN_3_PRIME | chr11 | 120450370 | |||||
| chr11:120450370
|
CA | C | 7 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0002t0007g0041others(4): Show | 7 | HG01123.hp2 HG01884.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1844-1119delA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | INFO_REALIGN_3_PRIME | chr11 | 120450370 | |||||
| chr11:120450492
|
G | C | 21 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0027others(18): Show | 22 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1844-1020G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120450492 | ||||||
| chr11:120450824
|
A | C | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1844-688A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120450824 | ||||||
| chr11:120450938
|
C | A | 1 | a0001c0001t0001g0196 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1844-574C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120450938 | ||||||
| chr11:120450944
|
C | T | 32 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.1844-568C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120450944 | ||||||
| chr11:120451035
|
C | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1844-477C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120451035 | ||||||
| chr11:120451131
|
T | G | 3 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02486.hp1 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1844-381T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120451131 | ||||||
| chr11:120451164
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1844-348A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120451164 | ||||||
| chr11:120451370
|
G | A | 79 | a0001c0001t0001g0157a0001c0001t0001g0189a0001c0001t0001g0191others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1844-142G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120451370 | ||||||
| chr11:120451467
|
G | A | 14 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(11): Show | 14 | HG00673.hp1 HG02027.hp1 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.1844-45G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 21/40 | chr11 | 120451467 | ||||||
| chr11:120452041
|
A | G | 1 | a0007c0011t0001g0187 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2056+317A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120452041 | ||||||
| chr11:120452287
|
G | A | 1 | a0001c0001t0002g0018 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2056+563G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120452287 | ||||||
| chr11:120452313
|
G | C | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2056+589G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120452313 | ||||||
| chr11:120452497
|
A | G | 21 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(18): Show | 21 | HG00438.hp2 HG00597.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.2056+773A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120452497 | ||||||
| chr11:120452505
|
G | A | 95 | a0001c0001t0001g0157a0001c0001t0001g0189a0001c0001t0001g0191others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.2056+781G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120452505 | ||||||
| chr11:120452681
|
C | T | 15 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(12): Show | 15 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.2056+957C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120452681 | ||||||
| chr11:120452939
|
G | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.2056+1215G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120452939 | ||||||
| chr11:120452944
|
G | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.2056+1220G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120452944 | ||||||
| chr11:120452945
|
A | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.2056+1221A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120452945 | ||||||
| chr11:120453012
|
C | CA | 6 | a0001c0001t0001g0191a0001c0001t0001g0218a0001c0001t0001g0288others(3): Show | 6 | HG01243.hp2 HG02056.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.2056+1293dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | INFO_REALIGN_3_PRIME | chr11 | 120453012 | |||||
| chr11:120453016
|
A | C | 10 | a0001c0001t0001g0279a0001c0001t0009g0003a0001c0001t0009g0004others(7): Show | 10 | HG00438.hp2 HG01099.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.2056+1292A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453016 | ||||||
| chr11:120453017
|
A | C | 5 | a0001c0001t0001g0245a0001c0001t0001g0249a0001c0001t0001g0255others(2): Show | 5 | HG00639.hp2 HG01099.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.2056+1293A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453017 | ||||||
| chr11:120453017
|
AC | A | 5 | a0001c0001t0010g0294a0001c0001t0010g0297a0001c0007t0015g0125others(2): Show | 5 | HG01074.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2056+1294delC | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453017 | ||||||
| chr11:120453018
|
C | A | 125 | a0001c0001t0001g0157a0001c0001t0001g0189a0001c0001t0001g0191others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2056+1294C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453018 | ||||||
| chr11:120453018
|
C | CA | 30 | a0001c0001t0001g0152a0001c0002t0002g0022a0001c0002t0002g0024others(27): Show | 30 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.2056+1303dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | INFO_REALIGN_3_PRIME | chr11 | 120453018 | |||||
| chr11:120453018
|
C | CAA | 5 | a0001c0002t0003g0001a0001c0002t0003g0034a0001c0002t0003g0035others(2): Show | 6 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.2056+1302_2056+130 others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | INFO_REALIGN_3_PRIME | chr11 | 120453018 | |||||
| chr11:120453200
|
A | G | 59 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(56): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.2056+1476A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453200 | ||||||
| chr11:120453325
|
C | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2056+1601C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453325 | ||||||
| chr11:120453371
|
G | A | 153 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.2056+1647G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453371 | ||||||
| chr11:120453378
|
C | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.2056+1654C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453378 | ||||||
| chr11:120453478
|
G | A | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2056+1754G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453478 | ||||||
| chr11:120453547
|
G | C | 1 | a0001c0001t0011g0192 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2056+1823G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453547 | ||||||
| chr11:120453717
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2056+1993C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453717 | ||||||
| chr11:120453808
|
C | G | 1 | a0001c0001t0001g0173 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2056+2084C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453808 | ||||||
| chr11:120453875
|
G | C | 1 | a0001c0001t0002g0109 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2056+2151G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453875 | ||||||
| chr11:120453987
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2056+2263A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120453987 | ||||||
| chr11:120454404
|
T | G | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2056+2680T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120454404 | ||||||
| chr11:120454456
|
A | C | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2057-2662A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120454456 | ||||||
| chr11:120454613
|
G | A | 3 | a0001c0001t0010g0294a0001c0001t0010g0297a0010c0017t0010g0298 | 3 | HG02451.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2057-2505G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120454613 | ||||||
| chr11:120454817
|
C | T | 1 | a0001c0008t0020g0009 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2057-2301C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120454817 | ||||||
| chr11:120454839
|
G | A | 84 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(81): Show | 84 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.2057-2279G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120454839 | ||||||
| chr11:120454850
|
C | A | 84 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(81): Show | 84 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.2057-2268C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120454850 | ||||||
| chr11:120455265
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2057-1853A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120455265 | ||||||
| chr11:120455568
|
G | A | 248 | a0001c0001t0001g0157a0001c0001t0001g0189a0001c0001t0001g0191others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2057-1550G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120455568 | ||||||
| chr11:120455748
|
A | G | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2057-1370A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120455748 | ||||||
| chr11:120456005
|
A | G | 1 | a0001c0001t0001g0240 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2057-1113A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120456005 | ||||||
| chr11:120456071
|
A | G | 1 | a0001c0002t0003g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2057-1047A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120456071 | ||||||
| chr11:120456439
|
G | A | 1 | a0001c0001t0004g0220 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2057-679G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120456439 | ||||||
| chr11:120456477
|
CAG | C | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2057-638_2057-637d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | INFO_REALIGN_3_PRIME | chr11 | 120456477 | |||||
| chr11:120456585
|
G | A | 1 | a0001c0002t0003g0023 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2057-533G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120456585 | ||||||
| chr11:120457108
|
T | C | 2 | a0001c0001t0001g0160a0001c0001t0021g0162 | 2 | HG04228.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2057-10T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 22/40 | chr11 | 120457108 | ||||||
| chr11:120457332
|
T | A | 1 | a0001c0001t0001g0259 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2189+82T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 23/40 | chr11 | 120457332 | ||||||
| chr11:120457654
|
A | G | 1 | a0001c0001t0011g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2190-67A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 23/40 | chr11 | 120457654 | ||||||
| chr11:120457675
|
A | T | 21 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(18): Show | 21 | HG00438.hp2 HG00597.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.2190-46A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 23/40 | chr11 | 120457675 | ||||||
| chr11:120457926
|
A | T | 1 | a0001c0001t0026g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2226-154A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 24/40 | chr11 | 120457926 | ||||||
| chr11:120457990
|
G | A | 1 | a0001c0001t0004g0252 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2226-90G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 24/40 | chr11 | 120457990 | ||||||
| chr11:120458707
|
C | A | 1 | a0001c0001t0014g0221 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2381-467C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 25/40 | chr11 | 120458707 | ||||||
| chr11:120459353
|
A | G | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2527+33A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | chr11 | 120459353 | ||||||
| chr11:120459440
|
G | C | 144 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(141): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2527+120G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | chr11 | 120459440 | ||||||
| chr11:120459729
|
G | T | 1 | a0001c0002t0003g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2527+409G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | chr11 | 120459729 | ||||||
| chr11:120459760
|
G | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2527+440G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | chr11 | 120459760 | ||||||
| chr11:120459918
|
G | A | 1 | a0001c0001t0027g0270 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2527+598G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | chr11 | 120459918 | ||||||
| chr11:120459954
|
C | T | 2 | a0001c0001t0035g0088a0001c0001t0036g0087 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2527+634C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | chr11 | 120459954 | ||||||
| chr11:120460005
|
C | T | 3 | a0001c0001t0002g0105a0001c0001t0002g0110a0001c0001t0002g0120 | 3 | NA18945.hp1 NA18947.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2528-667C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | chr11 | 120460005 | ||||||
| chr11:120460019
|
A | G | 57 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(54): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.2528-653A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | chr11 | 120460019 | ||||||
| chr11:120460179
|
C | T | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2528-493C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | chr11 | 120460179 | ||||||
| chr11:120460195
|
A | G | 3 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0021g0162 | 3 | HG03704.hp1 HG04228.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2528-477A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | chr11 | 120460195 | ||||||
| chr11:120460428
|
C | A | 3 | a0001c0001t0014g0221a0001c0001t0014g0254a0001c0001t0014g0265 | 3 | NA18945.hp2 NA18965.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2528-244C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | chr11 | 120460428 | ||||||
| chr11:120460576
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2528-96G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | chr11 | 120460576 | ||||||
| chr11:120460583
|
TA | T | 53 | a0001c0001t0002g0098a0001c0001t0029g0190a0001c0002t0003g0001others(50): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.2528-77delA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 26/40 | INFO_REALIGN_3_PRIME | chr11 | 120460583 | |||||
| chr11:120460842
|
T | C | 1 | a0001c0001t0002g0097 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2613+85T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120460842 | ||||||
| chr11:120460992
|
C | A | 86 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(83): Show | 86 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.2613+235C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120460992 | ||||||
| chr11:120461033
|
C | A | 1 | a0001c0001t0001g0213 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2613+276C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120461033 | ||||||
| chr11:120461200
|
C | T | 1 | a0001c0001t0008g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2613+443C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120461200 | ||||||
| chr11:120461207
|
A | C | 51 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(48): Show | 52 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.2613+450A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120461207 | ||||||
| chr11:120461369
|
G | A | 1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2613+612G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120461369 | ||||||
| chr11:120461510
|
G | A | 4 | a0001c0002t0003g0023a0001c0002t0016g0014a0001c0002t0016g0025others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2613+753G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120461510 | ||||||
| chr11:120461735
|
G | A | 3 | a0001c0001t0011g0195a0001c0001t0011g0199a0001c0001t0011g0300 | 3 | HG01243.hp2 HG01934.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2613+978G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120461735 | ||||||
| chr11:120461848
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2613+1091C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120461848 | ||||||
| chr11:120461853
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.2613+1096A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120461853 | ||||||
| chr11:120461984
|
C | CCATTCAA others(16): Show |
35 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(32): Show | 36 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.2613+1227_2613+122 others(27): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120461984 | ||||||
| chr11:120461984
|
C | CCATTCAA others(16): Show |
17 | a0001c0001t0029g0190a0001c0004t0005g0046a0001c0004t0005g0047others(14): Show | 17 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.2613+1227_2613+122 others(27): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120461984 | ||||||
| chr11:120461985
|
T | C | 52 | a0001c0001t0029g0190a0001c0002t0003g0001a0001c0002t0003g0015others(49): Show | 53 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.2613+1228T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120461985 | ||||||
| chr11:120462505
|
C | T | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2613+1748C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120462505 | ||||||
| chr11:120462817
|
A | C | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.2613+2060A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120462817 | ||||||
| chr11:120463019
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2614-2218A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463019 | ||||||
| chr11:120463092
|
A | G | 145 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(142): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2614-2145A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463092 | ||||||
| chr11:120463241
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2614-1996A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463241 | ||||||
| chr11:120463417
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2614-1820C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463417 | ||||||
| chr11:120463440
|
G | A | 32 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.2614-1797G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463440 | ||||||
| chr11:120463458
|
G | A | 1 | a0001c0002t0003g0035 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2614-1779G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463458 | ||||||
| chr11:120463480
|
G | A | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2614-1757G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463480 | ||||||
| chr11:120463525
|
C | CA | 18 | a0001c0001t0001g0146a0001c0001t0001g0171a0001c0001t0001g0205others(15): Show | 18 | HG00438.hp1 HG00438.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.2614-1691dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | INFO_REALIGN_3_PRIME | chr11 | 120463525 | |||||
| chr11:120463525
|
C | CAAA | 11 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0049others(8): Show | 11 | HG02040.hp1 HG02602.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.2614-1693_2614-169 others(7): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | INFO_REALIGN_3_PRIME | chr11 | 120463525 | |||||
| chr11:120463525
|
CA | C | 79 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(76): Show | 79 | HG00323.hp2 HG00639.hp1 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.2614-1691delA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | INFO_REALIGN_3_PRIME | chr11 | 120463525 | |||||
| chr11:120463525
|
CAA | C | 38 | a0001c0001t0006g0096a0001c0001t0006g0138a0001c0002t0002g0022others(35): Show | 39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.2614-1692_2614-169 others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | INFO_REALIGN_3_PRIME | chr11 | 120463525 | |||||
| chr11:120463546
|
AC | A | 6 | a0001c0006t0002g0301a0001c0006t0002g0302a0001c0006t0002g0303others(3): Show | 6 | HG00735.hp2 HG00738.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.2614-1689delC | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | INFO_REALIGN_3_PRIME | chr11 | 120463546 | |||||
| chr11:120463547
|
C | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.2614-1690C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463547 | ||||||
| chr11:120463779
|
T | C | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.2614-1458T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463779 | ||||||
| chr11:120463793
|
C | A | 1 | a0001c0002t0007g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2614-1444C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463793 | ||||||
| chr11:120463799
|
A | G | 1 | a0001c0001t0002g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2614-1438A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463799 | ||||||
| chr11:120463905
|
C | G | 5 | a0001c0001t0010g0294a0001c0001t0010g0297a0004c0009t0010g0276others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2614-1332C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463905 | ||||||
| chr11:120463971
|
T | G | 35 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(32): Show | 36 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.2614-1266T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120463971 | ||||||
| chr11:120464056
|
T | G | 2 | a0001c0002t0007g0041a0001c0002t0007g0043 | 2 | HG01123.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2614-1181T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120464056 | ||||||
| chr11:120464154
|
A | C | 35 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(32): Show | 36 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.2614-1083A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120464154 | ||||||
| chr11:120464163
|
T | C | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2614-1074T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120464163 | ||||||
| chr11:120464366
|
G | GTCAGGAG others(4): Show |
1 | a0001c0001t0029g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2614-870_2614-860d others(13): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | INFO_REALIGN_3_PRIME | chr11 | 120464366 | |||||
| chr11:120464501
|
G | A | 1 | a0001c0001t0002g0115 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2614-736G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120464501 | ||||||
| chr11:120464598
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.2614-639A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120464598 | ||||||
| chr11:120464958
|
A | G | 2 | a0001c0002t0003g0062a0001c0002t0003g0063 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2614-279A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120464958 | ||||||
| chr11:120465003
|
C | CA | 33 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.2614-226dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | INFO_REALIGN_3_PRIME | chr11 | 120465003 | |||||
| chr11:120465012
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2614-225G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120465012 | ||||||
| chr11:120465015
|
A | G | 2 | a0001c0002t0003g0062a0001c0002t0003g0063 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2614-222A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120465015 | ||||||
| chr11:120465023
|
G | A | 2 | a0001c0002t0003g0062a0001c0002t0003g0063 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2614-214G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 27/40 | chr11 | 120465023 | ||||||
| chr11:120465866
|
A | G | 2 | a0001c0001t0035g0088a0001c0001t0036g0087 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2739+504A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 28/40 | chr11 | 120465866 | ||||||
| chr11:120465980
|
G | A | 1 | a0001c0001t0026g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2739+618G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 28/40 | chr11 | 120465980 | ||||||
| chr11:120466080
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2739+718G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 28/40 | chr11 | 120466080 | ||||||
| chr11:120466193
|
G | T | 142 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.2739+831G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 28/40 | chr11 | 120466193 | ||||||
| chr11:120466201
|
C | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.2739+839C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 28/40 | chr11 | 120466201 | ||||||
| chr11:120466364
|
G | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.2740-830G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 28/40 | chr11 | 120466364 | ||||||
| chr11:120466681
|
G | A | 1 | a0001c0001t0026g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2740-513G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 28/40 | chr11 | 120466681 | ||||||
| chr11:120466794
|
T | C | 1 | a0002c0003t0030g0075 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2740-400T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 28/40 | chr11 | 120466794 | ||||||
| chr11:120466810
|
A | C | 142 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.2740-384A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 28/40 | chr11 | 120466810 | ||||||
| chr11:120466996
|
A | G | 144 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(141): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2740-198A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 28/40 | chr11 | 120466996 | ||||||
| chr11:120467003
|
G | A | 1 | a0002c0003t0002g0078 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2740-191G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 28/40 | chr11 | 120467003 | ||||||
| chr11:120467331
|
A | G | 36 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(33): Show | 37 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.2854+23A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120467331 | ||||||
| chr11:120467353
|
C | T | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2854+45C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120467353 | ||||||
| chr11:120467433
|
C | CT | 14 | a0001c0001t0001g0144a0001c0001t0001g0180a0001c0001t0001g0189others(11): Show | 14 | HG00741.hp2 HG01109.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2854+144dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | INFO_REALIGN_3_PRIME | chr11 | 120467433 | |||||
| chr11:120467433
|
CT | C | 7 | a0001c0001t0002g0097a0001c0001t0009g0003a0001c0001t0009g0004others(4): Show | 7 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.2854+144delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | INFO_REALIGN_3_PRIME | chr11 | 120467433 | |||||
| chr11:120467490
|
TGGA | T | 3 | a0001c0001t0002g0019a0001c0001t0002g0102a0001c0001t0002g0124 | 3 | HG02486.hp2 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2854+184_2854+186d others(5): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | INFO_REALIGN_3_PRIME | chr11 | 120467490 | |||||
| chr11:120467553
|
C | A | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2854+245C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120467553 | ||||||
| chr11:120467590
|
A | G | 1 | a0001c0001t0006g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2854+282A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120467590 | ||||||
| chr11:120467606
|
C | CT | 95 | a0001c0001t0001g0182a0001c0001t0001g0185a0001c0001t0001g0186others(92): Show | 95 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.2854+317dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | INFO_REALIGN_3_PRIME | chr11 | 120467606 | |||||
| chr11:120467606
|
C | CTT | 58 | a0001c0001t0006g0089a0001c0001t0007g0134a0001c0001t0007g0135others(55): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.2854+316_2854+317d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | INFO_REALIGN_3_PRIME | chr11 | 120467606 | |||||
| chr11:120467799
|
T | C | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.2854+491T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120467799 | ||||||
| chr11:120468211
|
ACTGAAAT others(35): Show |
A | 1 | a0001c0001t0001g0255 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2854+905_2854+946d others(44): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | INFO_REALIGN_3_PRIME | chr11 | 120468211 | |||||
| chr11:120468293
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2854+985T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120468293 | ||||||
| chr11:120468323
|
T | G | 1 | a0010c0017t0010g0298 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2855-965T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120468323 | ||||||
| chr11:120468428
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2855-860C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120468428 | ||||||
| chr11:120468429
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2855-859G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120468429 | ||||||
| chr11:120468479
|
C | T | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2855-809C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120468479 | ||||||
| chr11:120468637
|
A | G | 1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2855-651A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120468637 | ||||||
| chr11:120468676
|
C | T | 1 | a0001c0001t0006g0103 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2855-612C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120468676 | ||||||
| chr11:120469104
|
G | A | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2855-184G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 29/40 | chr11 | 120469104 | ||||||
| chr11:120469521
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2955+133A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120469521 | ||||||
| chr11:120469653
|
A | G | 1 | a0001c0001t0001g0278 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2955+265A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120469653 | ||||||
| chr11:120469674
|
G | A | 80 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(77): Show | 80 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.2955+286G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120469674 | ||||||
| chr11:120469813
|
C | T | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.2955+425C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120469813 | ||||||
| chr11:120469873
|
A | T | 1 | a0001c0001t0001g0236 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2955+485A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120469873 | ||||||
| chr11:120470256
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.2955+868A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120470256 | ||||||
| chr11:120470262
|
C | T | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2955+874C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120470262 | ||||||
| chr11:120470447
|
A | G | 2 | a0001c0002t0003g0062a0001c0002t0003g0063 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2955+1059A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120470447 | ||||||
| chr11:120470457
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2955+1069C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120470457 | ||||||
| chr11:120470542
|
G | C | 3 | a0001c0001t0008g0020a0001c0001t0008g0111a0001c0001t0008g0112 | 3 | NA18946.hp1 NA18965.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.2955+1154G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120470542 | ||||||
| chr11:120470579
|
C | T | 1 | a0001c0002t0003g0028 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2955+1191C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120470579 | ||||||
| chr11:120471014
|
T | C | 38 | a0001c0001t0002g0019a0001c0001t0002g0102a0001c0001t0002g0124others(35): Show | 39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.2955+1626T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120471014 | ||||||
| chr11:120471135
|
A | G | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2955+1747A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120471135 | ||||||
| chr11:120471229
|
T | C | 48 | a0001c0001t0002g0018a0001c0001t0002g0021a0001c0001t0002g0091others(45): Show | 48 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.2956-1821T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120471229 | ||||||
| chr11:120471248
|
A | G | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2956-1802A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120471248 | ||||||
| chr11:120471285
|
G | A | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2956-1765G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120471285 | ||||||
| chr11:120471444
|
A | T | 1 | a0001c0001t0001g0275 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2956-1606A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120471444 | ||||||
| chr11:120471710
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2956-1340G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120471710 | ||||||
| chr11:120471817
|
C | G | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2956-1233C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120471817 | ||||||
| chr11:120471857
|
T | C | 1 | a0001c0001t0002g0115 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2956-1193T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120471857 | ||||||
| chr11:120472002
|
G | A | 1 | a0010c0017t0010g0298 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2956-1048G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120472002 | ||||||
| chr11:120472095
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0234a0001c0001t0001g0236 | 3 | HG01433.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2956-955G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120472095 | ||||||
| chr11:120472146
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0021g0162 | 2 | HG04228.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2956-904A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120472146 | ||||||
| chr11:120472245
|
TA | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | HG00280.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2956-799delA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | INFO_REALIGN_3_PRIME | chr11 | 120472245 | |||||
| chr11:120472324
|
T | G | 6 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0021g0162others(3): Show | 6 | HG03239.hp2 HG03704.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.2956-726T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120472324 | ||||||
| chr11:120472398
|
G | T | 6 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136others(3): Show | 6 | HG01074.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2956-652G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120472398 | ||||||
| chr11:120472562
|
C | T | 151 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2956-488C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120472562 | ||||||
| chr11:120472601
|
C | G | 1 | a0001c0002t0003g0029 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2956-449C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120472601 | ||||||
| chr11:120472694
|
G | A | 1 | a0006c0013t0001g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2956-356G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120472694 | ||||||
| chr11:120472745
|
C | G | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2956-305C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120472745 | ||||||
| chr11:120472941
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0021g0162 | 2 | HG04228.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2956-109C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 30/40 | chr11 | 120472941 | ||||||
| chr11:120473211
|
A | G | 1 | a0001c0001t0027g0270 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3033+84A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120473211 | ||||||
| chr11:120473243
|
A | T | 1 | a0001c0001t0002g0120 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3033+116A>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120473243 | ||||||
| chr11:120473257
|
T | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.3033+130T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120473257 | ||||||
| chr11:120473730
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3033+603T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120473730 | ||||||
| chr11:120473740
|
C | A | 5 | a0001c0002t0007g0041a0001c0002t0007g0042a0001c0002t0007g0043others(2): Show | 5 | HG01123.hp2 HG01884.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3033+613C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120473740 | ||||||
| chr11:120473751
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.3033+624A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120473751 | ||||||
| chr11:120473817
|
C | T | 151 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.3033+690C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120473817 | ||||||
| chr11:120473842
|
A | G | 35 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(32): Show | 36 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.3033+715A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120473842 | ||||||
| chr11:120473967
|
C | A | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3034-593C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120473967 | ||||||
| chr11:120474065
|
T | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.3034-495T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120474065 | ||||||
| chr11:120474103
|
T | C | 1 | a0001c0001t0026g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3034-457T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120474103 | ||||||
| chr11:120474293
|
T | G | 35 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(32): Show | 36 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.3034-267T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120474293 | ||||||
| chr11:120474295
|
A | G | 35 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(32): Show | 36 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.3034-265A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 31/40 | chr11 | 120474295 | ||||||
| chr11:120475610
|
T | G | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3277+103T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | chr11 | 120475610 | ||||||
| chr11:120475651
|
G | A | 80 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(77): Show | 80 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.3277+144G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | chr11 | 120475651 | ||||||
| chr11:120475705
|
AAC | A | 27 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.3277+200_3277+201d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | INFO_REALIGN_3_PRIME | chr11 | 120475705 | |||||
| chr11:120475726
|
ATT | A | 51 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(48): Show | 52 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.3277+223_3277+224d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | INFO_REALIGN_3_PRIME | chr11 | 120475726 | |||||
| chr11:120475749
|
C | T | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3277+242C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | chr11 | 120475749 | ||||||
| chr11:120475778
|
A | G | 1 | a0002c0003t0002g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3277+271A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | chr11 | 120475778 | ||||||
| chr11:120475970
|
C | A | 1 | a0001c0001t0001g0266 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3277+463C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | chr11 | 120475970 | ||||||
| chr11:120476146
|
C | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.3278-515C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | chr11 | 120476146 | ||||||
| chr11:120476183
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3278-478A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | chr11 | 120476183 | ||||||
| chr11:120476355
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3278-306G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | chr11 | 120476355 | ||||||
| chr11:120476491
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3278-170G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | chr11 | 120476491 | ||||||
| chr11:120476507
|
G | A | 1 | a0001c0001t0011g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3278-154G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | chr11 | 120476507 | ||||||
| chr11:120476528
|
C | G | 1 | a0001c0001t0002g0019 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3278-133C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 33/40 | chr11 | 120476528 | ||||||
| chr11:120476803
|
G | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.3365+55G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | chr11 | 120476803 | ||||||
| chr11:120476877
|
C | T | 9 | a0001c0001t0008g0020a0001c0001t0008g0092a0001c0001t0008g0104others(6): Show | 9 | HG02129.hp2 HG04115.hp2 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.3365+129C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | chr11 | 120476877 | ||||||
| chr11:120477006
|
C | T | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3366-213C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | chr11 | 120477006 | ||||||
| chr11:120477081
|
T | TTTG | 12 | a0001c0001t0001g0170a0001c0001t0001g0194a0001c0001t0001g0203others(9): Show | 12 | HG00280.hp2 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3366-101_3366-99du others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | INFO_REALIGN_3_PRIME | chr11 | 120477081 | |||||
| chr11:120477081
|
TTTG | T | 51 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0143others(48): Show | 52 | HG00438.hp2 HG00597.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.3366-101_3366-99de others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | INFO_REALIGN_3_PRIME | chr11 | 120477081 | |||||
| chr11:120477081
|
TTTGTTG | T | 13 | a0001c0001t0006g0118a0001c0002t0003g0023a0001c0002t0003g0027others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.3366-104_3366-99de others(7): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | INFO_REALIGN_3_PRIME | chr11 | 120477081 | |||||
| chr11:120477081
|
TTTGTTGT others(2): Show |
T | 22 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0030others(19): Show | 23 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.3366-107_3366-99de others(10): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | INFO_REALIGN_3_PRIME | chr11 | 120477081 | |||||
| chr11:120477081
|
TTTGTTGT others(5): Show |
T | 3 | a0001c0002t0019g0012a0001c0002t0034g0013a0008c0014t0019g0011 | 3 | HG01099.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3366-110_3366-99de others(13): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | INFO_REALIGN_3_PRIME | chr11 | 120477081 | |||||
| chr11:120477118
|
T | G | 1 | a0001c0001t0018g0280 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3366-101T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | chr11 | 120477118 | ||||||
| chr11:120477133
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3366-86T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | chr11 | 120477133 | ||||||
| chr11:120477177
|
T | TTGTTG | 143 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.3366-41_3366-40ins others(5): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 34/40 | INFO_REALIGN_3_PRIME | chr11 | 120477177 | |||||
| chr11:120477419
|
G | GT | 8 | a0001c0001t0001g0180a0001c0001t0001g0191a0001c0001t0001g0289others(5): Show | 8 | HG00621.hp1 HG02056.hp1 HG02145.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.3453-9dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 35/40 | INFO_REALIGN_3_PRIME | chr11 | 120477419 | |||||
| chr11:120477423
|
T | G | 1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3453-24T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 35/40 | chr11 | 120477423 | ||||||
| chr11:120477428
|
T | G | 2 | a0001c0001t0026g0230a0001c0001t0029g0190 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3453-19T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 35/40 | chr11 | 120477428 | ||||||
| chr11:120477735
|
A | G | 204 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(201): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.3532+209A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 36/40 | chr11 | 120477735 | ||||||
| chr11:120477845
|
C | T | 3 | a0001c0001t0007g0134a0001c0001t0007g0135a0001c0001t0007g0136 | 3 | HG02723.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3533-311C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 36/40 | chr11 | 120477845 | ||||||
| chr11:120477862
|
C | CA | 30 | a0001c0001t0002g0113a0001c0001t0002g0132a0001c0001t0009g0004others(27): Show | 30 | HG00597.hp2 HG01099.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.3533-282dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 36/40 | INFO_REALIGN_3_PRIME | chr11 | 120477862 | |||||
| chr11:120477874
|
AG | A | 4 | a0001c0002t0003g0128a0001c0007t0015g0125a0001c0007t0015g0126others(1): Show | 4 | HG01074.hp2 HG03209.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.3533-281delG | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 36/40 | chr11 | 120477874 | ||||||
| chr11:120477875
|
G | A | 147 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(144): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.3533-281G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 36/40 | chr11 | 120477875 | ||||||
| chr11:120477888
|
A | G | 53 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(50): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.3533-268A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 36/40 | chr11 | 120477888 | ||||||
| chr11:120477892
|
G | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.3533-264G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 36/40 | chr11 | 120477892 | ||||||
| chr11:120477892
|
G | T | 129 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(126): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.3533-264G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 36/40 | chr11 | 120477892 | ||||||
| chr11:120477893
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.3533-263A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 36/40 | chr11 | 120477893 | ||||||
| chr11:120478062
|
G | GT | 19 | a0001c0001t0001g0288a0001c0002t0003g0062a0001c0002t0003g0063others(16): Show | 19 | HG00597.hp2 HG02040.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.3533-82dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 36/40 | INFO_REALIGN_3_PRIME | chr11 | 120478062 | |||||
| chr11:120478407
|
C | T | 4 | a0001c0002t0003g0023a0001c0002t0016g0014a0001c0002t0016g0025others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3766+18C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120478407 | ||||||
| chr11:120478433
|
A | G | 53 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(50): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.3766+44A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120478433 | ||||||
| chr11:120478529
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.3766+140A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120478529 | ||||||
| chr11:120478555
|
A | G | 3 | a0001c0001t0010g0294a0001c0001t0010g0297a0010c0017t0010g0298 | 3 | HG02451.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3766+166A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120478555 | ||||||
| chr11:120478601
|
A | C | 53 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(50): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.3766+212A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120478601 | ||||||
| chr11:120478616
|
A | G | 1 | a0001c0004t0005g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3766+227A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120478616 | ||||||
| chr11:120478744
|
G | A | 3 | a0001c0001t0001g0194a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | HG00280.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3766+355G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120478744 | ||||||
| chr11:120478822
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.3766+433A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120478822 | ||||||
| chr11:120479385
|
G | A | 1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3767-575G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120479385 | ||||||
| chr11:120479423
|
G | A | 1 | a0001c0001t0002g0109 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3767-537G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120479423 | ||||||
| chr11:120479474
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3767-486T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120479474 | ||||||
| chr11:120479494
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3767-466C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120479494 | ||||||
| chr11:120479570
|
G | A | 3 | a0001c0001t0010g0294a0001c0001t0010g0297a0010c0017t0010g0298 | 3 | HG02451.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3767-390G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120479570 | ||||||
| chr11:120479634
|
T | C | 1 | a0002c0003t0002g0085 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3767-326T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120479634 | ||||||
| chr11:120479684
|
T | G | 53 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(50): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.3767-276T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120479684 | ||||||
| chr11:120479834
|
T | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.3767-126T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 37/40 | chr11 | 120479834 | ||||||
| chr11:120480520
|
G | GGT | 36 | a0001c0001t0001g0236a0001c0001t0009g0003a0001c0001t0009g0004others(33): Show | 37 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.4237+109_4237+110d others(4): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 38/40 | INFO_REALIGN_3_PRIME | chr11 | 120480520 | |||||
| chr11:120480721
|
T | A | 27 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.4237+291T>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 38/40 | chr11 | 120480721 | ||||||
| chr11:120480722
|
A | AAGTCT | 27 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.4237+292_4237+293i others(7): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 38/40 | chr11 | 120480722 | ||||||
| chr11:120480800
|
G | A | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.4237+370G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 38/40 | chr11 | 120480800 | ||||||
| chr11:120481165
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.4238-95A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 38/40 | chr11 | 120481165 | ||||||
| chr11:120481602
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4554+26G>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120481602 | ||||||
| chr11:120481667
|
A | G | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.4554+91A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120481667 | ||||||
| chr11:120481686
|
T | G | 1 | a0006c0013t0001g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4554+110T>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120481686 | ||||||
| chr11:120481694
|
A | G | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.4554+118A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120481694 | ||||||
| chr11:120481760
|
C | CT | 6 | a0001c0001t0001g0140a0001c0001t0001g0180a0001c0001t0001g0203others(3): Show | 6 | HG01257.hp1 HG01258.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.4554+201dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | INFO_REALIGN_3_PRIME | chr11 | 120481760 | |||||
| chr11:120481798
|
C | G | 3 | a0001c0007t0015g0125a0001c0007t0015g0126a0001c0007t0015g0127 | 3 | HG01074.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4554+222C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120481798 | ||||||
| chr11:120481995
|
G | A | 16 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0048others(13): Show | 16 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.4554+419G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120481995 | ||||||
| chr11:120482034
|
C | T | 1 | a0001c0001t0025g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4554+458C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482034 | ||||||
| chr11:120482048
|
C | T | 1 | a0001c0002t0003g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4554+472C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482048 | ||||||
| chr11:120482049
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4554+473G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482049 | ||||||
| chr11:120482060
|
G | A | 1 | a0001c0002t0019g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4554+484G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482060 | ||||||
| chr11:120482080
|
A | G | 1 | a0001c0001t0002g0018 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.4554+504A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482080 | ||||||
| chr11:120482225
|
T | C | 1 | a0001c0001t0002g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4554+649T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482225 | ||||||
| chr11:120482235
|
C | G | 2 | a0001c0004t0005g0054a0001c0004t0005g0055 | 2 | HG02040.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.4554+659C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482235 | ||||||
| chr11:120482327
|
C | T | 1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4554+751C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482327 | ||||||
| chr11:120482332
|
G | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(2): Show | 5 | HG00438.hp2 HG01952.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.4554+756G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482332 | ||||||
| chr11:120482363
|
C | A | 23 | a0001c0001t0009g0003a0001c0001t0009g0004a0001c0001t0009g0005others(20): Show | 23 | HG00438.hp2 HG00597.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.4554+787C>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482363 | ||||||
| chr11:120482407
|
A | C | 1 | a0001c0001t0001g0189 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4554+831A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482407 | ||||||
| chr11:120482444
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0021g0162 | 2 | HG04228.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.4554+868A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482444 | ||||||
| chr11:120482528
|
G | A | 27 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.4554+952G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482528 | ||||||
| chr11:120482589
|
A | C | 142 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.4554+1013A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482589 | ||||||
| chr11:120482675
|
G | A | 1 | a0001c0001t0009g0006 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4554+1099G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482675 | ||||||
| chr11:120482676
|
C | T | 2 | a0001c0008t0020g0008a0001c0008t0020g0009 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.4554+1100C>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482676 | ||||||
| chr11:120482729
|
A | C | 1 | a0002c0003t0002g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4554+1153A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482729 | ||||||
| chr11:120482744
|
C | CA | 21 | a0001c0001t0002g0105a0001c0001t0008g0104a0001c0004t0005g0046others(18): Show | 21 | HG00597.hp2 HG02040.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.4554+1184dupA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | INFO_REALIGN_3_PRIME | chr11 | 120482744 | |||||
| chr11:120482744
|
CA | C | 96 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0157others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.4554+1184delA | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | INFO_REALIGN_3_PRIME | chr11 | 120482744 | |||||
| chr11:120482826
|
A | G | 1 | a0001c0004t0005g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4554+1250A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120482826 | ||||||
| chr11:120483241
|
A | G | 1 | a0008c0014t0019g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4555-1197A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120483241 | ||||||
| chr11:120483250
|
A | C | 1 | a0001c0001t0001g0269 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4555-1188A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120483250 | ||||||
| chr11:120483258
|
C | CT | 137 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(134): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.4555-1158dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | INFO_REALIGN_3_PRIME | chr11 | 120483258 | |||||
| chr11:120483258
|
C | CTT | 16 | a0001c0001t0001g0149a0001c0001t0001g0155a0001c0001t0001g0164others(13): Show | 16 | HG00673.hp2 HG01993.hp2 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.4555-1159_4555-115 others(6): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | INFO_REALIGN_3_PRIME | chr11 | 120483258 | |||||
| chr11:120483258
|
CT | C | 9 | a0001c0001t0001g0182a0001c0001t0001g0201a0001c0001t0001g0225others(6): Show | 9 | HG00323.hp2 HG01069.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.4555-1158delT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | INFO_REALIGN_3_PRIME | chr11 | 120483258 | |||||
| chr11:120483338
|
G | A | 1 | a0001c0001t0013g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4555-1100G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120483338 | ||||||
| chr11:120483340
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4555-1098A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120483340 | ||||||
| chr11:120483354
|
A | C | 2 | a0001c0001t0001g0249a0001c0001t0001g0255 | 2 | HG01099.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.4555-1084A>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120483354 | ||||||
| chr11:120483427
|
A | AT | 27 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0023others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.4555-996dupT | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | INFO_REALIGN_3_PRIME | chr11 | 120483427 | |||||
| chr11:120483452
|
C | G | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.4555-986C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120483452 | ||||||
| chr11:120483466
|
C | G | 1 | a0001c0001t0026g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4555-972C>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120483466 | ||||||
| chr11:120483606
|
T | C | 2 | a0001c0001t0013g0197a0001c0001t0013g0202 | 2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4555-832T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120483606 | ||||||
| chr11:120483651
|
G | T | 1 | a0001c0001t0001g0269 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4555-787G>T | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120483651 | ||||||
| chr11:120483654
|
G | A | 1 | a0001c0001t0006g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4555-784G>A | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120483654 | ||||||
| chr11:120484364
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4555-74T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 39/40 | chr11 | 120484364 | ||||||
| chr11:120484521
|
A | G | 98 | a0001c0001t0001g0157a0001c0001t0001g0164a0001c0001t0001g0189others(95): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.4624+14A>G | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 40/40 | chr11 | 120484521 | ||||||
| chr11:120485047
|
T | C | 2 | a0001c0012t0001g0296a0006c0013t0001g0293 | 2 | NA19030.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.4625-20T>C | ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 40/40 | chr11 | 120485047 |