Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9828 |
|---|---|
| ensemblid | ENSG00000110237.5 |
| hgncid | 21726 |
| symbol | ARHGEF17 |
| name | Rho guanine nucleotide exchange factor 17 |
| refseq_nuc | NM_014786.4 |
| refseq_prot | NP_055601.2 |
| ensembl_nuc | ENST00000263674.4 |
| ensembl_prot | ENSP00000263674.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 73308276 |
| end | 73369388 |
| strand | + |
| ver | v1.2 |
| region | chr11:73308276-73369388 |
| region5000 | chr11:73303276-73374388 |
| regionname0 | ARHGEF17_chr11_73308276_73369388 |
| regionname5000 | ARHGEF17_chr11_73303276_73374388 |
| 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 | 2063 | 111 | 17 | 28 | 45 | 9 | 10 | 29 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002 | 0/0 | 2064 | 52 | 39 | 9 | 0 | 3 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003 | 0/0 | 2064 | 32 | 26 | 0 | 6 | 0 | 0 | 4 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0004 | 0/0 | 2064 | 8 | 0 | 3 | 0 | 1 | 4 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0005 | 0/0 | 2063 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0006 | 0/0 | 2063 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0007 | 0/0 | 2063 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0008 | 0/0 | 2063 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0009 | 0/0 | 2064 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0010 | 0/0 | 2063 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0011 | 0/0 | 2063 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0012 | 0/0 | 2063 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0013 | 0/0 | 2063 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0014 | 0/0 | 2063 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0015 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0016 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0017 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0018 | 0/0 | 2063 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0019 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0020 | 0/0 | 2063 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| 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 | 6192 | 104 | 15 | 28 | 42 | 8 | 9 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0002 | 0/0 | 6195 | 23 | 22 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0003 | 0/0 | 6195 | 22 | 16 | 0 | 6 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0004 | 0/0 | 6195 | 10 | 0 | 6 | 0 | 3 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0005 | 0/0 | 6195 | 7 | 0 | 3 | 0 | 1 | 3 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0006 | 0/0 | 6195 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0007 | 0/0 | 6195 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0008 | 0/0 | 6195 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0009 | 0/0 | 6192 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0010 | 0/0 | 6192 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0011 | 0/0 | 6192 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0012 | 0/0 | 6195 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0013 | 0/0 | 6192 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0014 | 0/0 | 6195 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0015 | 0/0 | 6195 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0016 | 0/0 | 6195 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0017 | 0/0 | 6192 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0018 | 0/0 | 6192 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0019 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0020 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0021 | 0/0 | 6192 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0022 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0023 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0024 | 0/0 | 6192 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0025 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0026 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0027 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0028 | 0/0 | 6192 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0029 | 0/0 | 6192 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0030 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0031 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0032 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0033 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0034 | 0/0 | 6195 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0035 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0036 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0037 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0038 | 0/0 | 6195 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0039 | 0/0 | 6192 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0040 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0041 | 0/0 | 6195 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| c0042 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| 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 | 1972 | 142 | 40 | 26 | 53 | 10 | 11 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0002 | 0/0 | 1972 | 30 | 24 | 0 | 6 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0003 | 0/0 | 1972 | 18 | 8 | 6 | 0 | 3 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0004 | 0/0 | 1972 | 13 | 7 | 5 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0005 | 0/0 | 1972 | 6 | 0 | 3 | 0 | 0 | 3 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0006 | 0/0 | 1972 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0007 | 0/0 | 1972 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0008 | 0/0 | 1972 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0009 | 0/0 | 1972 | 2 | 0 | 0 | 0 | 1 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0010 | 0/0 | 1972 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0011 | 0/0 | 1972 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0012 | 0/0 | 1972 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0013 | 0/0 | 1972 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0014 | 0/0 | 1972 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0015 | 0/0 | 1972 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0016 | 0/0 | 1972 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0017 | 0/0 | 1972 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| t0018 | 0/0 | 1972 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| 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 | 6192 | 104 | 15 | 28 | 42 | 8 | 9 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0020 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0021 | 0/0 | 6192 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0023 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0024 | 0/0 | 6192 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0027 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0028 | 0/0 | 6192 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0029 | 0/0 | 6192 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0002 | 0/0 | 6195 | 23 | 22 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0004 | 0/0 | 6195 | 10 | 0 | 6 | 0 | 3 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0006 | 0/0 | 6195 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0008 | 0/0 | 6195 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0012 | 0/0 | 6195 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0016 | 0/0 | 6195 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0034 | 0/0 | 6195 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0035 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0036 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0037 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0003 | 0/0 | 6195 | 22 | 16 | 0 | 6 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0007 | 0/0 | 6195 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0015 | 0/0 | 6195 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0030 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0031 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0032 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0004c0005 | 0/0 | 6195 | 7 | 0 | 3 | 0 | 1 | 3 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0004c0038 | 0/0 | 6195 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0005c0009 | 0/0 | 6192 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0006c0011 | 0/0 | 6192 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0007c0010 | 0/0 | 6192 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0008c0013 | 0/0 | 6192 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0009c0014 | 0/0 | 6195 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0010c0025 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0011c0019 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0012c0022 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0013c0026 | 0/0 | 6192 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0014c0018 | 0/0 | 6192 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0015c0042 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0016c0033 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0017c0040 | 0/0 | 6195 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0018c0039 | 0/0 | 6192 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0019c0041 | 0/0 | 6195 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0020c0017 | 0/0 | 6192 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 8163 | 98 | 15 | 25 | 39 | 8 | 9 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0001t0004 | 0/0 | 8163 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0001t0010 | 0/0 | 8163 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0001t0015 | 0/0 | 8163 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0001t0017 | 0/0 | 8163 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0020t0001 | 0/0 | 8163 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0021t0001 | 0/0 | 8163 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0023t0001 | 0/0 | 8163 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0024t0001 | 0/0 | 8163 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0027t0001 | 0/0 | 8163 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0028t0001 | 0/0 | 8163 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0001c0029t0001 | 0/0 | 8163 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0002t0001 | 0/0 | 8166 | 19 | 18 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0002t0004 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0002t0008 | 0/0 | 8166 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0002t0012 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0004t0003 | 0/0 | 8166 | 10 | 0 | 6 | 0 | 3 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0006t0003 | 0/0 | 8166 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0008t0001 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0008t0002 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0008t0006 | 0/0 | 8166 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0008t0018 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0012t0007 | 0/0 | 8166 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0016t0003 | 0/0 | 8166 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0034t0004 | 0/0 | 8166 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0035t0006 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0036t0004 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0002c0037t0013 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0003t0002 | 0/0 | 8166 | 20 | 14 | 0 | 6 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0003t0004 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0003t0011 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0007t0002 | 0/0 | 8166 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0015t0004 | 0/0 | 8166 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0030t0014 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0031t0004 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0003c0032t0004 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0004c0005t0005 | 0/0 | 8166 | 5 | 0 | 3 | 0 | 0 | 2 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0004c0005t0009 | 0/0 | 8166 | 2 | 0 | 0 | 0 | 1 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0004c0038t0005 | 0/0 | 8166 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0005c0009t0001 | 0/0 | 8163 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0006c0011t0001 | 0/0 | 8163 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0007c0010t0001 | 0/0 | 8163 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0008c0013t0004 | 0/0 | 8163 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0009c0014t0002 | 0/0 | 8166 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0010c0025t0001 | 0/0 | 8163 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0011c0019t0001 | 0/0 | 8163 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0012c0022t0001 | 0/0 | 8163 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0013c0026t0001 | 0/0 | 8163 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0014c0018t0001 | 0/0 | 8163 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0015c0042t0002 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0016c0033t0002 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0017c0040t0001 | 0/0 | 8166 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0018c0039t0001 | 0/0 | 8163 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0019c0041t0016 | 0/0 | 8166 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| a0020c0017t0004 | 0/0 | 8163 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | copy fasta | chr11 | 73303276 | 73374388 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0010g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0010g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0015g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0001t0017g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0020t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0021t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0023t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0024t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0027t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0028t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0001c0029t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0002t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0004t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0004t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0004t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0004t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0004t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0004t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0004t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0004t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0006t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0006t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0006t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0006t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0006t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0006t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0008t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0008t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0008t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0008t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0008t0018g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0012t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0012t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0016t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0016t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0034t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0035t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0036t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0002c0037t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0003t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0007t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0007t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0007t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0007t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0007t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0015t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0015t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0030t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0031t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0003c0032t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0004c0005t0005g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0004c0005t0005g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0004c0005t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0004c0005t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0004c0005t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0004c0005t0009g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0004c0005t0009g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0004c0038t0005g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0005c0009t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0005c0009t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0005c0009t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0005c0009t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0006c0011t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0006c0011t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0006c0011t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0007c0010t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0007c0010t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0007c0010t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0008c0013t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0008c0013t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0009c0014t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0009c0014t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0010c0025t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0011c0019t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0012c0022t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0013c0026t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0014c0018t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0015c0042t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0016c0033t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0017c0040t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0018c0039t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0019c0041t0016g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| a0020c0017t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00140 | hp2 | a0004 | c0005 | t0009 | g0016 | EUR | GBR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00280 | hp1 | a0014 | c0018 | t0001 | g0138 | EUR | FIN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | FIN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00323 | hp2 | a0002 | c0004 | t0003 | g0145 | EUR | FIN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00438 | hp2 | a0003 | c0003 | t0002 | g0052 | EAS | CHS | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00621 | hp2 | a0007 | c0010 | t0001 | g0194 | EAS | CHS | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00738 | hp2 | a0002 | c0004 | t0003 | g0147 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0098 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01071 | hp2 | a0020 | c0017 | t0004 | g0097 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01074 | hp1 | a0002 | c0034 | t0004 | g0133 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01106 | hp2 | a0002 | c0008 | t0006 | g0142 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01167 | hp2 | a0004 | c0005 | t0005 | g0018 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01168 | hp1 | a0002 | c0004 | t0003 | g0146 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0099 | AMR | PUR | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01255 | hp1 | a0004 | c0005 | t0005 | g0017 | AMR | CLM | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01261 | hp1 | a0002 | c0004 | t0003 | g0005 | AMR | CLM | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0148 | AMR | CLM | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01346 | hp1 | a0001 | c0001 | t0017 | g0193 | AMR | CLM | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01346 | hp2 | a0008 | c0013 | t0004 | g0095 | AMR | CLM | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01433 | hp2 | a0002 | c0004 | t0003 | g0149 | AMR | CLM | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01515 | hp1 | a0001 | c0028 | t0001 | g0107 | EUR | IBS | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01515 | hp2 | a0002 | c0004 | t0003 | g0004 | EUR | IBS | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | IBS | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01517 | hp2 | a0002 | c0004 | t0003 | g0004 | EUR | IBS | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01884 | hp1 | a0003 | c0003 | t0002 | g0050 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01884 | hp2 | a0002 | c0035 | t0006 | g0141 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01891 | hp2 | a0001 | c0029 | t0001 | g0079 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01928 | hp1 | a0002 | c0004 | t0003 | g0144 | AMR | PEL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01934 | hp2 | a0004 | c0005 | t0005 | g0021 | AMR | PEL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02004 | hp2 | a0002 | c0004 | t0003 | g0005 | AMR | PEL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02027 | hp1 | a0003 | c0003 | t0002 | g0150 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02055 | hp1 | a0009 | c0014 | t0002 | g0045 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02055 | hp2 | a0003 | c0003 | t0002 | g0043 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02074 | hp1 | a0007 | c0010 | t0001 | g0189 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02080 | hp2 | a0005 | c0009 | t0001 | g0039 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02083 | hp2 | a0005 | c0009 | t0001 | g0105 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02132 | hp2 | a0005 | c0009 | t0001 | g0106 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02258 | hp1 | a0002 | c0012 | t0007 | g0131 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02258 | hp2 | a0002 | c0006 | t0003 | g0012 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02280 | hp1 | a0003 | c0003 | t0004 | g0058 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02280 | hp2 | a0003 | c0007 | t0002 | g0038 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02451 | hp1 | a0003 | c0003 | t0002 | g0055 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02572 | hp2 | a0002 | c0006 | t0003 | g0009 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02615 | hp1 | a0003 | c0015 | t0004 | g0047 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02615 | hp2 | a0002 | c0016 | t0003 | g0221 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02622 | hp1 | a0003 | c0003 | t0002 | g0220 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02622 | hp2 | a0006 | c0011 | t0001 | g0214 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0159 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02647 | hp1 | a0009 | c0014 | t0002 | g0044 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02647 | hp2 | a0002 | c0006 | t0003 | g0011 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02683 | hp1 | a0004 | c0005 | t0005 | g0015 | SAS | PJL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0158 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02717 | hp2 | a0002 | c0037 | t0013 | g0155 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0168 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02723 | hp2 | a0002 | c0006 | t0003 | g0013 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0162 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02886 | hp1 | a0017 | c0040 | t0001 | g0028 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02886 | hp2 | a0003 | c0007 | t0002 | g0037 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02895 | hp1 | a0003 | c0003 | t0002 | g0064 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02896 | hp1 | a0002 | c0002 | t0008 | g0024 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0157 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02897 | hp1 | a0003 | c0003 | t0002 | g0061 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0170 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0164 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02965 | hp1 | a0003 | c0007 | t0002 | g0034 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02965 | hp2 | a0006 | c0011 | t0001 | g0215 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02970 | hp1 | a0003 | c0003 | t0002 | g0060 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02970 | hp2 | a0002 | c0002 | t0008 | g0025 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02976 | hp1 | a0002 | c0036 | t0004 | g0134 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0165 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03041 | hp2 | a0003 | c0003 | t0002 | g0062 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03098 | hp2 | a0002 | c0008 | t0018 | g0007 | AFR | MSL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03130 | hp1 | a0002 | c0008 | t0001 | g0042 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03130 | hp2 | a0003 | c0003 | t0002 | g0049 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03139 | hp1 | a0003 | c0003 | t0011 | g0136 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03139 | hp2 | a0002 | c0002 | t0004 | g0156 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03195 | hp1 | a0002 | c0012 | t0007 | g0132 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03209 | hp2 | a0003 | c0032 | t0004 | g0057 | AFR | MSL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03225 | hp1 | a0003 | c0031 | t0004 | g0056 | AFR | MSL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03239 | hp2 | a0004 | c0005 | t0005 | g0014 | SAS | PJL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03453 | hp1 | a0002 | c0008 | t0006 | g0140 | AFR | MSL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03453 | hp2 | a0002 | c0002 | t0012 | g0163 | AFR | MSL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03490 | hp1 | a0019 | c0041 | t0016 | g0154 | SAS | PJL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0167 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03516 | hp2 | a0006 | c0011 | t0001 | g0183 | AFR | ESN | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03579 | hp1 | a0003 | c0003 | t0002 | g0054 | AFR | MSL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03669 | hp1 | a0004 | c0038 | t0005 | g0019 | SAS | PJL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03669 | hp2 | a0018 | c0039 | t0001 | g0078 | SAS | PJL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03688 | hp1 | a0008 | c0013 | t0004 | g0096 | SAS | STU | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03831 | hp2 | a0002 | c0004 | t0003 | g0143 | SAS | BEB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03942 | hp1 | a0001 | c0024 | t0001 | g0196 | SAS | BEB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18522 | hp1 | a0003 | c0003 | t0002 | g0063 | AFR | YRI | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18522 | hp2 | a0003 | c0030 | t0014 | g0031 | AFR | YRI | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18612 | hp1 | a0007 | c0010 | t0001 | g0187 | EAS | CHB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18906 | hp1 | a0015 | c0042 | t0002 | g0040 | AFR | YRI | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18906 | hp2 | a0003 | c0015 | t0004 | g0048 | AFR | YRI | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18939 | hp1 | a0012 | c0022 | t0001 | g0003 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18952 | hp2 | a0001 | c0001 | t0015 | g0202 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18965 | hp1 | a0013 | c0026 | t0001 | g0070 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18965 | hp2 | a0003 | c0003 | t0002 | g0046 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18970 | hp2 | a0005 | c0009 | t0001 | g0065 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18981 | hp1 | a0010 | c0025 | t0001 | g0125 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18981 | hp2 | a0003 | c0003 | t0002 | g0152 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18984 | hp1 | a0001 | c0001 | t0010 | g0213 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18984 | hp2 | a0011 | c0019 | t0001 | g0041 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18985 | hp2 | a0003 | c0003 | t0002 | g0059 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19002 | hp2 | a0001 | c0001 | t0010 | g0217 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19007 | hp2 | a0001 | c0027 | t0001 | g0088 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0160 | AFR | LWK | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | LWK | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19060 | hp1 | a0001 | c0020 | t0001 | g0083 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19060 | hp2 | a0003 | c0003 | t0002 | g0151 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19085 | hp1 | a0001 | c0023 | t0001 | g0127 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | YRI | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA20129 | hp1 | a0003 | c0003 | t0002 | g0051 | AFR | ASW | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA20129 | hp2 | a0001 | c0021 | t0001 | g0077 | AFR | ASW | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | TSI | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | GIH | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA20905 | hp2 | a0004 | c0005 | t0009 | g0020 | SAS | GIH | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02109 | hp1 | a0002 | c0016 | t0003 | g0222 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02486 | hp1 | a0003 | c0007 | t0002 | g0036 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02486 | hp2 | a0003 | c0003 | t0002 | g0137 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG02559 | hp2 | a0003 | c0003 | t0002 | g0223 | AFR | ACB | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | MSL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG03471 | hp2 | a0003 | c0007 | t0002 | g0035 | AFR | MSL | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG06807 | hp1 | a0002 | c0006 | t0003 | g0010 | AFR | USA | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| HG06807 | hp2 | a0002 | c0008 | t0002 | g0139 | AFR | USA | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA20300 | hp1 | a0002 | c0006 | t0003 | g0008 | AFR | USA | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | USA | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| NA21309 | hp2 | a0016 | c0033 | t0002 | g0053 | AFR | LWK | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0094 | REF | REF | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0216 | REF | REF | ARHGEF17_chr11_73303276_73374388 | ARHGEF17 | chr11 | 73303276 | 73374388 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:73308769
|
G | A | 1 | a0020 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.131G>A | p.Cys44Tyr | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 494/8163 | 131/6192 | 44/2063 | chr11 | 73308769 | ||
| chr11:73308937
|
G | A | 1 | a0008 | 2 | HG01346.hp2 HG03688.hp1 |
missense_variant | MODERATE | c.299G>A | p.Gly100Glu | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 662/8163 | 299/6192 | 100/2063 | chr11 | 73308937 | ||
| chr11:73308982
|
C | T | 1 | a0019 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.344C>T | p.Ala115Val | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 707/8163 | 344/6192 | 115/2063 | chr11 | 73308982 | ||
| chr11:73309030
|
A | G | 1 | a0018 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.392A>G | p.Lys131Arg | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 755/8163 | 392/6192 | 131/2063 | chr11 | 73309030 | ||
| chr11:73309330
|
G | GCTC | 8 | a0002a0003a0004others(5): Show | 98 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
conservative_inframe_insertion | MODERATE | c.703_705dupTCC | p.Ser235dup | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 1069/8163 | 706/6192 | 236/2063 | INFO_REALIGN_3_PRIME | chr11 | 73309330 | |
| chr11:73309354
|
C | A | 1 | a0009 | 2 | HG02055.hp1 HG02647.hp1 |
missense_variant | MODERATE | c.716C>A | p.Ser239Tyr | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 1079/8163 | 716/6192 | 239/2063 | chr11 | 73309354 | ||
| chr11:73309377
|
G | A | 1 | a0017 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.739G>A | p.Ala247Thr | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 1102/8163 | 739/6192 | 247/2063 | chr11 | 73309377 | ||
| chr11:73309588
|
G | C | 3 | a0003a0009a0016 | 35 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(32): Show |
missense_variant | MODERATE | c.950G>C | p.Ser317Thr | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 1313/8163 | 950/6192 | 317/2063 | chr11 | 73309588 | ||
| chr11:73309801
|
G | T | 1 | a0004 | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
missense_variant | MODERATE | c.1163G>T | p.Arg388Leu | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 1526/8163 | 1163/6192 | 388/2063 | chr11 | 73309801 | ||
| chr11:73310373
|
G | A | 1 | a0007 | 3 | HG00621.hp2 HG02074.hp1 NA18612.hp1 |
missense_variant | MODERATE | c.1735G>A | p.Glu579Lys | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 2098/8163 | 1735/6192 | 579/2063 | chr11 | 73310373 | ||
| chr11:73310962
|
T | C | 1 | a0014 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.2324T>C | p.Met775Thr | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 2687/8163 | 2324/6192 | 775/2063 | chr11 | 73310962 | ||
| chr11:73310965
|
A | G | 1 | a0016 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2327A>G | p.Asp776Gly | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 2690/8163 | 2327/6192 | 776/2063 | chr11 | 73310965 | ||
| chr11:73311441
|
C | T | 1 | a0013 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.2803C>T | p.Arg935Trp | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 3166/8163 | 2803/6192 | 935/2063 | chr11 | 73311441 | ||
| chr11:73311474
|
A | T | 1 | a0010 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.2836A>T | p.Ser946Cys | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 3199/8163 | 2836/6192 | 946/2063 | chr11 | 73311474 | ||
| chr11:73311682
|
A | T | 1 | a0015 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.3044A>T | p.His1015Leu | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 3407/8163 | 3044/6192 | 1015/2063 | chr11 | 73311682 | ||
| chr11:73311744
|
C | G | 1 | a0010 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.3106C>G | p.Pro1036Ala | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 3469/8163 | 3106/6192 | 1036/2063 | chr11 | 73311744 | ||
| chr11:73357119
|
G | A | 1 | a0011 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.3986G>A | p.Arg1329His | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 8/21 | 4349/8163 | 3986/6192 | 1329/2063 | chr11 | 73357119 | ||
| chr11:73360507
|
C | A | 1 | a0005 | 4 | HG02080.hp2 HG02083.hp2 HG02132.hp2 others(1): Show |
missense_variant | MODERATE | c.4394C>A | p.Ala1465Asp | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 11/21 | 4757/8163 | 4394/6192 | 1465/2063 | chr11 | 73360507 | ||
| chr11:73365442
|
A | T | 1 | a0012 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.5603A>T | p.Asp1868Val | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 19/21 | 5966/8163 | 5603/6192 | 1868/2063 | chr11 | 73365442 | ||
| chr11:73367640
|
G | A | 1 | a0006 | 3 | HG02622.hp2 HG02965.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.6052G>A | p.Ala2018Thr | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 6415/8163 | 6052/6192 | 2018/2063 | chr11 | 73367640 | ||
| chr11:73369386
|
G | A | 1 | a0002 | 3 | HG01106.hp2 HG01884.hp2 HG03453.hp1 |
splice_region_variant | LOW | c.*1606G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | chr11 | 73369386 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:73308731
|
G | A | 1 | a0002c0012 | 2 | HG02258.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.93G>A | p.Glu31Glu | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 456/8163 | 93/6192 | 31/2063 | chr11 | 73308731 | ||
| chr11:73308833
|
C | T | 1 | a0015c0042 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.195C>T | p.Pro65Pro | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 558/8163 | 195/6192 | 65/2063 | chr11 | 73308833 | ||
| chr11:73309013
|
C | T | 3 | a0002c0002a0002c0004a0017c0040 | 34 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(31): Show |
synonymous_variant | LOW | c.375C>T | p.Ser125Ser | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 738/8163 | 375/6192 | 125/2063 | chr11 | 73309013 | ||
| chr11:73310021
|
C | T | 1 | a0001c0029 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1383C>T | p.Ser461Ser | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 1746/8163 | 1383/6192 | 461/2063 | chr11 | 73310021 | ||
| chr11:73310039
|
C | T | 13 | a0002c0016a0002c0037a0003c0003others(10): Show | 47 | HG00140.hp2 HG00438.hp2 HG01167.hp2 others(44): Show |
synonymous_variant | LOW | c.1401C>T | p.Ile467Ile | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 1764/8163 | 1401/6192 | 467/2063 | chr11 | 73310039 | ||
| chr11:73310078
|
A | G | 1 | a0001c0028 | 1 | HG01515.hp1 | synonymous_variant | LOW | c.1440A>G | p.Ser480Ser | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 1803/8163 | 1440/6192 | 480/2063 | chr11 | 73310078 | ||
| chr11:73310165
|
C | T | 1 | a0001c0027 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.1527C>T | p.Ser509Ser | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 1890/8163 | 1527/6192 | 509/2063 | chr11 | 73310165 | ||
| chr11:73311071
|
G | T | 1 | a0002c0036 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.2433G>T | p.Gly811Gly | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 2796/8163 | 2433/6192 | 811/2063 | chr11 | 73311071 | ||
| chr11:73311233
|
C | A | 2 | a0002c0034a0002c0036 | 2 | HG01074.hp1 HG02976.hp1 |
synonymous_variant | LOW | c.2595C>A | p.Ile865Ile | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 2958/8163 | 2595/6192 | 865/2063 | chr11 | 73311233 | ||
| chr11:73311617
|
A | G | 1 | a0003c0015 | 2 | HG02615.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.2979A>G | p.Arg993Arg | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 3342/8163 | 2979/6192 | 993/2063 | chr11 | 73311617 | ||
| chr11:73311644
|
G | A | 1 | a0003c0030 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.3006G>A | p.Ser1002Ser | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 3369/8163 | 3006/6192 | 1002/2063 | chr11 | 73311644 | ||
| chr11:73311678
|
C | T | 1 | a0003c0007 | 5 | HG02280.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.3040C>T | p.Leu1014Leu | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 3403/8163 | 3040/6192 | 1014/2063 | chr11 | 73311678 | ||
| chr11:73311743
|
G | C | 1 | a0010c0025 | 1 | NA18981.hp1 | synonymous_variant | LOW | c.3105G>C | p.Pro1035Pro | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 3468/8163 | 3105/6192 | 1035/2063 | chr11 | 73311743 | ||
| chr11:73356186
|
G | A | 1 | a0003c0031 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.3675G>A | p.Lys1225Lys | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 6/21 | 4038/8163 | 3675/6192 | 1225/2063 | chr11 | 73356186 | ||
| chr11:73356231
|
G | A | 1 | a0002c0037 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.3720G>A | p.Ala1240Ala | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 6/21 | 4083/8163 | 3720/6192 | 1240/2063 | chr11 | 73356231 | ||
| chr11:73360397
|
G | A | 1 | a0002c0035 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.4284G>A | p.Ala1428Ala | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 11/21 | 4647/8163 | 4284/6192 | 1428/2063 | chr11 | 73360397 | ||
| chr11:73360484
|
C | T | 1 | a0001c0024 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.4371C>T | p.Asp1457Asp | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 11/21 | 4734/8163 | 4371/6192 | 1457/2063 | chr11 | 73360484 | ||
| chr11:73360508
|
C | T | 1 | a0001c0023 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.4395C>T | p.Ala1465Ala | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 11/21 | 4758/8163 | 4395/6192 | 1465/2063 | chr11 | 73360508 | ||
| chr11:73362075
|
G | A | 1 | a0001c0020 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.4530G>A | p.Pro1510Pro | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 13/21 | 4893/8163 | 4530/6192 | 1510/2063 | chr11 | 73362075 | ||
| chr11:73362213
|
G | T | 1 | a0019c0041 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.4668G>T | p.Val1556Val | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 13/21 | 5031/8163 | 4668/6192 | 1556/2063 | chr11 | 73362213 | ||
| chr11:73362481
|
C | T | 2 | a0003c0031a0003c0032 | 2 | HG03209.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.4743C>T | p.Pro1581Pro | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 14/21 | 5106/8163 | 4743/6192 | 1581/2063 | chr11 | 73362481 | ||
| chr11:73362517
|
C | T | 1 | a0002c0006 | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
synonymous_variant | LOW | c.4779C>T | p.Asp1593Asp | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 14/21 | 5142/8163 | 4779/6192 | 1593/2063 | chr11 | 73362517 | ||
| chr11:73362535
|
C | T | 2 | a0004c0005a0004c0038 | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
synonymous_variant | LOW | c.4797C>T | p.Leu1599Leu | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 14/21 | 5160/8163 | 4797/6192 | 1599/2063 | chr11 | 73362535 | ||
| chr11:73365545
|
C | T | 1 | a0002c0004 | 10 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(7): Show |
synonymous_variant | LOW | c.5706C>T | p.Pro1902Pro | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 19/21 | 6069/8163 | 5706/6192 | 1902/2063 | chr11 | 73365545 | ||
| chr11:73365682
|
G | A | 1 | a0001c0021 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.5730G>A | p.Ser1910Ser | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/21 | 6093/8163 | 5730/6192 | 1910/2063 | chr11 | 73365682 | ||
| chr11:73367738
|
T | C | 1 | a0004c0038 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.6150T>C | p.Gly2050Gly | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 6513/8163 | 6150/6192 | 2050/2063 | chr11 | 73367738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:73308366
|
C | T | 1 | a0002c0008t0018 | 1 | HG03098.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-273C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | chr11 | 73308366 | ||||||
| chr11:73308438
|
C | T | 2 | a0004c0005t0005a0004c0038t0005 | 6 | HG01167.hp2 HG01255.hp1 HG01934.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-201C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/21 | 201 | chr11 | 73308438 | |||||
| chr11:73367882
|
G | T | 1 | a0002c0008t0018 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 102 | chr11 | 73367882 | |||||
| chr11:73367920
|
C | T | 1 | a0001c0001t0017 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*140C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 140 | chr11 | 73367920 | |||||
| chr11:73367958
|
G | T | 1 | a0002c0008t0018 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*178G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 178 | chr11 | 73367958 | |||||
| chr11:73367976
|
C | A | 1 | a0002c0012t0007 | 2 | HG02258.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*196C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 196 | chr11 | 73367976 | |||||
| chr11:73368008
|
C | T | 1 | a0019c0041t0016 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*228C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 228 | chr11 | 73368008 | |||||
| chr11:73368100
|
G | A | 1 | a0002c0002t0008 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*320G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 320 | chr11 | 73368100 | |||||
| chr11:73368105
|
G | T | 1 | a0001c0001t0015 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*325G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 325 | chr11 | 73368105 | |||||
| chr11:73368147
|
G | A | 1 | a0003c0003t0011 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*367G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 367 | chr11 | 73368147 | |||||
| chr11:73368451
|
C | T | 1 | a0003c0030t0014 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*671C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 671 | chr11 | 73368451 | |||||
| chr11:73368689
|
T | C | 1 | a0002c0012t0007 | 2 | HG02258.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*909T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 909 | chr11 | 73368689 | |||||
| chr11:73368830
|
C | T | 2 | a0002c0008t0018a0002c0037t0013 | 2 | HG02717.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1050C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 1050 | chr11 | 73368830 | |||||
| chr11:73368899
|
T | G | 1 | a0003c0030t0014 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1119T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 1119 | chr11 | 73368899 | |||||
| chr11:73368934
|
G | C | 4 | a0002c0004t0003a0002c0006t0003a0002c0016t0003others(1): Show | 19 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1154G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 1154 | chr11 | 73368934 | |||||
| chr11:73369159
|
G | A | 1 | a0002c0002t0012 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1379G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 1379 | chr11 | 73369159 | |||||
| chr11:73369248
|
G | A | 1 | a0002c0012t0007 | 2 | HG02258.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1468G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 1468 | chr11 | 73369248 | |||||
| chr11:73369265
|
A | G | 7 | a0002c0008t0002a0003c0003t0002a0003c0007t0002others(4): Show | 31 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1485A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 1485 | chr11 | 73369265 | |||||
| chr11:73369291
|
G | A | 3 | a0004c0005t0005a0004c0005t0009a0004c0038t0005 | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1511G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 1511 | chr11 | 73369291 | |||||
| chr11:73369360
|
A | G | 30 | a0001c0001t0004a0002c0002t0004a0002c0004t0003others(27): Show | 79 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1580A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 1580 | chr11 | 73369360 | |||||
| chr11:73369373
|
G | T | 1 | a0001c0001t0010 | 2 | NA18984.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1593G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 21/21 | 1593 | chr11 | 73369373 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:73311884
|
C | T | 1 | a0003c0003t0002g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3192+54C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73311884 | ||||||
| chr11:73312011
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3192+181T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73312011 | ||||||
| chr11:73312113
|
C | T | 2 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3192+283C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73312113 | ||||||
| chr11:73312227
|
C | T | 1 | a0003c0003t0002g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3192+397C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73312227 | ||||||
| chr11:73312308
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.3192+478G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73312308 | ||||||
| chr11:73312371
|
C | A | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3192+541C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73312371 | ||||||
| chr11:73312403
|
T | A | 6 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3192+573T>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73312403 | ||||||
| chr11:73312487
|
T | C | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3192+657T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73312487 | ||||||
| chr11:73312655
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3192+825T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73312655 | ||||||
| chr11:73312710
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3192+880G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73312710 | ||||||
| chr11:73313155
|
C | T | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG02523.hp2 NA18612.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.3192+1325C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313155 | ||||||
| chr11:73313177
|
C | T | 15 | a0002c0002t0001g0157a0002c0002t0001g0158a0002c0002t0001g0159others(12): Show | 15 | HG02630.hp1 HG02717.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.3192+1347C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313177 | ||||||
| chr11:73313278
|
C | T | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3192+1448C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313278 | ||||||
| chr11:73313313
|
G | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3192+1483G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313313 | ||||||
| chr11:73313337
|
T | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG02027.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.3192+1507T>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313337 | ||||||
| chr11:73313458
|
T | C | 8 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(5): Show | 8 | HG02451.hp2 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3192+1628T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313458 | ||||||
| chr11:73313488
|
T | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG00423.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.3192+1658T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313488 | ||||||
| chr11:73313543
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3192+1713C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313543 | ||||||
| chr11:73313557
|
C | T | 1 | a0002c0016t0003g0222 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3192+1727C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313557 | ||||||
| chr11:73313586
|
G | A | 1 | a0003c0030t0014g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3192+1756G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313586 | ||||||
| chr11:73313694
|
A | G | 10 | a0002c0016t0003g0221a0002c0016t0003g0222a0004c0005t0005g0014others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.3192+1864A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313694 | ||||||
| chr11:73313730
|
A | G | 6 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3192+1900A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313730 | ||||||
| chr11:73313841
|
C | T | 2 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3192+2011C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313841 | ||||||
| chr11:73313869
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3192+2039G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73313869 | ||||||
| chr11:73314245
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3192+2415G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73314245 | ||||||
| chr11:73314271
|
G | A | 6 | a0003c0007t0002g0034a0003c0007t0002g0035a0003c0007t0002g0036others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3192+2441G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73314271 | ||||||
| chr11:73314525
|
G | T | 3 | a0003c0003t0002g0150a0003c0003t0002g0151a0003c0003t0002g0152 | 3 | HG02027.hp1 NA18981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3192+2695G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73314525 | ||||||
| chr11:73314547
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3192+2717C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73314547 | ||||||
| chr11:73314690
|
C | T | 36 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(33): Show | 38 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.3192+2860C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73314690 | ||||||
| chr11:73314707
|
G | T | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3192+2877G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73314707 | ||||||
| chr11:73314790
|
T | C | 1 | a0005c0009t0001g0039 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3192+2960T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73314790 | ||||||
| chr11:73314890
|
G | A | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3192+3060G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73314890 | ||||||
| chr11:73314926
|
G | A | 37 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(34): Show | 39 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3192+3096G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73314926 | ||||||
| chr11:73315020
|
G | A | 37 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(34): Show | 39 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3192+3190G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73315020 | ||||||
| chr11:73315054
|
A | C | 36 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(33): Show | 38 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.3192+3224A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73315054 | ||||||
| chr11:73315356
|
A | C | 1 | a0014c0018t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3192+3526A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73315356 | ||||||
| chr11:73315479
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3192+3649C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73315479 | ||||||
| chr11:73315570
|
A | G | 1 | a0003c0003t0002g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3192+3740A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73315570 | ||||||
| chr11:73315606
|
C | T | 37 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(34): Show | 39 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3192+3776C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73315606 | ||||||
| chr11:73315633
|
C | T | 37 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(34): Show | 39 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3192+3803C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73315633 | ||||||
| chr11:73315748
|
G | T | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3192+3918G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73315748 | ||||||
| chr11:73315905
|
C | G | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3192+4075C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73315905 | ||||||
| chr11:73315971
|
T | G | 1 | a0015c0042t0002g0040 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3192+4141T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73315971 | ||||||
| chr11:73316060
|
C | T | 8 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(5): Show | 8 | HG02451.hp2 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3192+4230C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73316060 | ||||||
| chr11:73316065
|
G | A | 9 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(6): Show | 9 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.3192+4235G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73316065 | ||||||
| chr11:73316196
|
A | G | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3192+4366A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73316196 | ||||||
| chr11:73316301
|
C | A | 1 | a0001c0001t0001g0175 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3192+4471C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73316301 | ||||||
| chr11:73316395
|
T | TC | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3192+4565_3192+456 others(5): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73316395 | ||||||
| chr11:73316556
|
G | A | 1 | a0011c0019t0001g0041 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3192+4726G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73316556 | ||||||
| chr11:73316792
|
G | C | 2 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3192+4962G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73316792 | ||||||
| chr11:73317021
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3192+5191A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73317021 | ||||||
| chr11:73317023
|
A | T | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3192+5193A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73317023 | ||||||
| chr11:73317026
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3192+5196T>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73317026 | ||||||
| chr11:73317027
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3192+5197T>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73317027 | ||||||
| chr11:73317033
|
A | G | 37 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(34): Show | 39 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3192+5203A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73317033 | ||||||
| chr11:73317175
|
G | A | 1 | a0002c0008t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3192+5345G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73317175 | ||||||
| chr11:73317398
|
G | A | 8 | a0003c0003t0002g0043a0003c0003t0002g0223a0003c0007t0002g0034others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3192+5568G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73317398 | ||||||
| chr11:73317595
|
A | C | 1 | a0001c0001t0001g0032 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3192+5765A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73317595 | ||||||
| chr11:73317704
|
G | A | 1 | a0002c0008t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3192+5874G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73317704 | ||||||
| chr11:73317743
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG00423.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.3192+5913G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73317743 | ||||||
| chr11:73318201
|
G | C | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3192+6371G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73318201 | ||||||
| chr11:73318224
|
C | G | 89 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(86): Show | 91 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.3192+6394C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73318224 | ||||||
| chr11:73318307
|
GT | G | 37 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(34): Show | 39 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3192+6478delT | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73318307 | ||||||
| chr11:73318309
|
C | A | 37 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(34): Show | 39 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3192+6479C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73318309 | ||||||
| chr11:73318488
|
A | G | 15 | a0002c0002t0001g0157a0002c0002t0001g0158a0002c0002t0001g0159others(12): Show | 15 | HG02630.hp1 HG02717.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.3192+6658A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73318488 | ||||||
| chr11:73318490
|
G | T | 4 | a0002c0012t0007g0131a0002c0012t0007g0132a0002c0034t0004g0133others(1): Show | 4 | HG01074.hp1 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3192+6660G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73318490 | ||||||
| chr11:73318580
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3192+6750T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73318580 | ||||||
| chr11:73318968
|
C | T | 1 | a0003c0030t0014g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3192+7138C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73318968 | ||||||
| chr11:73319065
|
C | CT | 18 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(15): Show | 18 | HG00280.hp2 HG00621.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.3192+7252dupT | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73319065 | |||||
| chr11:73319065
|
CT | C | 10 | a0001c0001t0001g0180a0002c0002t0001g0148a0002c0004t0003g0004others(7): Show | 12 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.3192+7252delT | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73319065 | |||||
| chr11:73319065
|
CTT | C | 28 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(25): Show | 28 | HG01106.hp2 HG01884.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.3192+7251_3192+725 others(6): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73319065 | |||||
| chr11:73319260
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG00140.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.3192+7430C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73319260 | ||||||
| chr11:73319269
|
G | T | 1 | a0002c0006t0003g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3192+7439G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73319269 | ||||||
| chr11:73319305
|
G | A | 1 | a0005c0009t0001g0065 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3192+7475G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73319305 | ||||||
| chr11:73319357
|
C | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3192+7527C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73319357 | ||||||
| chr11:73319476
|
T | C | 37 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(34): Show | 39 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3192+7646T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73319476 | ||||||
| chr11:73319497
|
C | T | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3192+7667C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73319497 | ||||||
| chr11:73319533
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 4 | HG00639.hp1 HG00741.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.3192+7703G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73319533 | ||||||
| chr11:73319733
|
G | A | 1 | a0013c0026t0001g0070 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3192+7903G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73319733 | ||||||
| chr11:73320083
|
A | AACTCCCT others(1): Show |
85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3192+8255_3192+825 others(12): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73320083 | |||||
| chr11:73320140
|
G | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3192+8310G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73320140 | ||||||
| chr11:73320368
|
T | G | 38 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(35): Show | 40 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.3192+8538T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73320368 | ||||||
| chr11:73320472
|
TA | T | 37 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(34): Show | 39 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3192+8657delA | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73320472 | |||||
| chr11:73320498
|
G | A | 1 | a0002c0006t0003g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3192+8668G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73320498 | ||||||
| chr11:73320508
|
C | T | 9 | a0002c0002t0001g0148a0002c0004t0003g0004a0002c0004t0003g0005others(6): Show | 11 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.3192+8678C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73320508 | ||||||
| chr11:73320628
|
C | CA | 44 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0072others(41): Show | 44 | HG00323.hp1 HG00438.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.3192+8820dupA | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73320628 | |||||
| chr11:73320628
|
CA | C | 49 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(46): Show | 51 | HG00140.hp2 HG00323.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.3192+8820delA | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73320628 | |||||
| chr11:73320660
|
GA | G | 26 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0029others(23): Show | 26 | HG01106.hp2 HG01884.hp2 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.3192+8831delA | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73320660 | ||||||
| chr11:73320661
|
A | AT | 8 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0001g0178others(5): Show | 8 | HG00423.hp2 HG01175.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.3192+8847dupT | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73320661 | |||||
| chr11:73320661
|
A | T | 1 | a0002c0002t0001g0170 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3192+8831A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73320661 | ||||||
| chr11:73320685
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.3192+8855G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73320685 | ||||||
| chr11:73320779
|
A | G | 1 | a0002c0036t0004g0134 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3192+8949A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73320779 | ||||||
| chr11:73320862
|
A | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00280.hp2 NA20752.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.3192+9032A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73320862 | ||||||
| chr11:73320909
|
G | A | 4 | a0002c0012t0007g0131a0002c0012t0007g0132a0002c0034t0004g0133others(1): Show | 4 | HG01074.hp1 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3192+9079G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73320909 | ||||||
| chr11:73321180
|
C | T | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.3192+9350C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73321180 | ||||||
| chr11:73321268
|
C | CTCT | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3192+9442_3192+944 others(7): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73321268 | |||||
| chr11:73321302
|
T | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.3192+9472T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73321302 | ||||||
| chr11:73321331
|
G | A | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(2): Show | 5 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.3192+9501G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73321331 | ||||||
| chr11:73321426
|
A | G | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3192+9596A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73321426 | ||||||
| chr11:73321493
|
G | A | 1 | a0015c0042t0002g0040 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3192+9663G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73321493 | ||||||
| chr11:73321538
|
A | C | 38 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(35): Show | 40 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.3192+9708A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73321538 | ||||||
| chr11:73321573
|
A | G | 1 | a0002c0002t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3192+9743A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73321573 | ||||||
| chr11:73321789
|
C | T | 7 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(4): Show | 7 | HG00621.hp1 HG02523.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.3192+9959C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73321789 | ||||||
| chr11:73322342
|
A | G | 11 | a0003c0031t0004g0056a0003c0032t0004g0057a0004c0005t0005g0014others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.3192+10512A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73322342 | ||||||
| chr11:73322454
|
C | T | 1 | a0002c0006t0003g0012 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3192+10624C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73322454 | ||||||
| chr11:73322483
|
C | A | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3192+10653C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73322483 | ||||||
| chr11:73322559
|
G | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3192+10729G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73322559 | ||||||
| chr11:73322593
|
G | A | 23 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(20): Show | 23 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(20): Show |
intron_variant | MODIFIER | c.3192+10763G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73322593 | ||||||
| chr11:73322805
|
G | A | 38 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(35): Show | 40 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.3192+10975G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73322805 | ||||||
| chr11:73322891
|
A | C | 28 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(25): Show | 28 | HG01106.hp2 HG01884.hp2 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.3192+11061A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73322891 | ||||||
| chr11:73322952
|
G | C | 2 | a0002c0012t0007g0131a0002c0012t0007g0132 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3192+11122G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73322952 | ||||||
| chr11:73323022
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3192+11192G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323022 | ||||||
| chr11:73323073
|
C | G | 1 | a0001c0001t0001g0179 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3192+11243C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323073 | ||||||
| chr11:73323085
|
C | G | 1 | a0002c0002t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3192+11255C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323085 | ||||||
| chr11:73323197
|
G | A | 1 | a0002c0008t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3192+11367G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323197 | ||||||
| chr11:73323243
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3192+11413C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323243 | ||||||
| chr11:73323356
|
G | C | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3192+11526G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323356 | ||||||
| chr11:73323476
|
C | G | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3192+11646C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323476 | ||||||
| chr11:73323481
|
G | C | 18 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(15): Show | 18 | HG01106.hp2 HG01884.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.3192+11651G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323481 | ||||||
| chr11:73323566
|
G | A | 4 | a0002c0012t0007g0131a0002c0012t0007g0132a0002c0034t0004g0133others(1): Show | 4 | HG01074.hp1 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3192+11736G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323566 | ||||||
| chr11:73323605
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0128 | 2 | HG01175.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3192+11775C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323605 | ||||||
| chr11:73323668
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3192+11838A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323668 | ||||||
| chr11:73323696
|
T | C | 2 | a0009c0014t0002g0044a0009c0014t0002g0045 | 2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3192+11866T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323696 | ||||||
| chr11:73323790
|
TAGG | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 5 | HG00738.hp1 HG01081.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.3192+11963_3192+11 others(9): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73323790 | |||||
| chr11:73323820
|
C | G | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3192+11990C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323820 | ||||||
| chr11:73323855
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3192+12025G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73323855 | ||||||
| chr11:73324016
|
G | A | 37 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(34): Show | 39 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3192+12186G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324016 | ||||||
| chr11:73324024
|
G | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3192+12194G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324024 | ||||||
| chr11:73324091
|
G | A | 1 | a0002c0002t0004g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3192+12261G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324091 | ||||||
| chr11:73324097
|
G | A | 4 | a0002c0012t0007g0131a0002c0012t0007g0132a0002c0034t0004g0133others(1): Show | 4 | HG01074.hp1 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3192+12267G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324097 | ||||||
| chr11:73324102
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3192+12272G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324102 | ||||||
| chr11:73324228
|
G | T | 1 | a0001c0001t0010g0213 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3192+12398G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324228 | ||||||
| chr11:73324251
|
C | T | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3192+12421C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324251 | ||||||
| chr11:73324273
|
G | T | 4 | a0002c0012t0007g0131a0002c0012t0007g0132a0002c0034t0004g0133others(1): Show | 4 | HG01074.hp1 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3192+12443G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324273 | ||||||
| chr11:73324315
|
C | T | 1 | a0001c0028t0001g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3192+12485C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324315 | ||||||
| chr11:73324404
|
A | T | 1 | a0001c0001t0010g0213 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3192+12574A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324404 | ||||||
| chr11:73324422
|
C | G | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3192+12592C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324422 | ||||||
| chr11:73324472
|
C | A | 1 | a0001c0001t0010g0213 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3192+12642C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324472 | ||||||
| chr11:73324473
|
A | G | 1 | a0001c0001t0010g0213 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3192+12643A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324473 | ||||||
| chr11:73324514
|
G | A | 1 | a0002c0008t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3192+12684G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324514 | ||||||
| chr11:73324518
|
C | T | 28 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(25): Show | 28 | HG01106.hp2 HG01884.hp2 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.3192+12688C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324518 | ||||||
| chr11:73324540
|
G | T | 1 | a0001c0001t0010g0213 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3192+12710G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324540 | ||||||
| chr11:73324754
|
T | C | 47 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(44): Show | 47 | HG00140.hp2 HG00438.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.3192+12924T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324754 | ||||||
| chr11:73324781
|
T | A | 1 | a0015c0042t0002g0040 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3192+12951T>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324781 | ||||||
| chr11:73324807
|
G | A | 38 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(35): Show | 40 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.3192+12977G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324807 | ||||||
| chr11:73324870
|
G | A | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3192+13040G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73324870 | ||||||
| chr11:73325084
|
A | G | 6 | a0001c0001t0001g0135a0005c0009t0001g0039a0005c0009t0001g0065others(3): Show | 6 | HG01175.hp2 HG02080.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.3192+13254A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73325084 | ||||||
| chr11:73325134
|
C | T | 47 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(44): Show | 47 | HG00140.hp2 HG00438.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.3192+13304C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73325134 | ||||||
| chr11:73325272
|
C | G | 2 | a0003c0003t0002g0043a0003c0003t0002g0223 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.3192+13442C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73325272 | ||||||
| chr11:73325326
|
G | T | 1 | a0005c0009t0001g0039 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3192+13496G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73325326 | ||||||
| chr11:73325436
|
G | A | 47 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(44): Show | 47 | HG00140.hp2 HG00438.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.3192+13606G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73325436 | ||||||
| chr11:73325519
|
G | A | 33 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(30): Show | 33 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.3192+13689G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73325519 | ||||||
| chr11:73325527
|
G | A | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3192+13697G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73325527 | ||||||
| chr11:73325550
|
A | T | 1 | a0003c0003t0004g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3192+13720A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73325550 | ||||||
| chr11:73325725
|
T | G | 2 | a0006c0011t0001g0214a0006c0011t0001g0215 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3192+13895T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73325725 | ||||||
| chr11:73325878
|
C | T | 23 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(20): Show | 23 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(20): Show |
intron_variant | MODIFIER | c.3192+14048C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73325878 | ||||||
| chr11:73326044
|
G | A | 9 | a0002c0002t0001g0148a0002c0004t0003g0004a0002c0004t0003g0005others(6): Show | 11 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.3192+14214G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73326044 | ||||||
| chr11:73326092
|
C | T | 2 | a0003c0003t0002g0043a0003c0003t0002g0223 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.3192+14262C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73326092 | ||||||
| chr11:73326377
|
C | G | 28 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(25): Show | 28 | HG01106.hp2 HG01884.hp2 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.3192+14547C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73326377 | ||||||
| chr11:73326378
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3192+14548G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73326378 | ||||||
| chr11:73326432
|
T | G | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3192+14602T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73326432 | ||||||
| chr11:73326485
|
C | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3192+14655C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73326485 | ||||||
| chr11:73326517
|
C | A | 2 | a0003c0003t0002g0046a0003c0003t0002g0059 | 2 | NA18965.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.3192+14687C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73326517 | ||||||
| chr11:73326593
|
G | A | 9 | a0002c0002t0001g0148a0002c0004t0003g0004a0002c0004t0003g0005others(6): Show | 11 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.3192+14763G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73326593 | ||||||
| chr11:73326635
|
G | T | 1 | a0003c0003t0004g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3192+14805G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73326635 | ||||||
| chr11:73326678
|
C | T | 2 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3192+14848C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73326678 | ||||||
| chr11:73326896
|
A | G | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3192+15066A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73326896 | ||||||
| chr11:73327036
|
T | A | 15 | a0002c0002t0001g0157a0002c0002t0001g0158a0002c0002t0001g0159others(12): Show | 15 | HG02630.hp1 HG02717.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.3192+15206T>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327036 | ||||||
| chr11:73327125
|
C | T | 33 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(30): Show | 33 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.3192+15295C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327125 | ||||||
| chr11:73327227
|
C | T | 2 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3192+15397C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327227 | ||||||
| chr11:73327261
|
C | T | 1 | a0003c0003t0002g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3192+15431C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327261 | ||||||
| chr11:73327262
|
G | A | 38 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(35): Show | 40 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.3192+15432G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327262 | ||||||
| chr11:73327264
|
TC | T | 38 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(35): Show | 40 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.3192+15437delC | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73327264 | |||||
| chr11:73327333
|
C | T | 2 | a0005c0009t0001g0105a0005c0009t0001g0106 | 2 | HG02083.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.3192+15503C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327333 | ||||||
| chr11:73327458
|
C | CT | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3192+15629dupT | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73327458 | |||||
| chr11:73327534
|
T | C | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3192+15704T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327534 | ||||||
| chr11:73327568
|
C | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3192+15738C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327568 | ||||||
| chr11:73327701
|
C | G | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3192+15871C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327701 | ||||||
| chr11:73327775
|
C | T | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3192+15945C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327775 | ||||||
| chr11:73327777
|
C | T | 30 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(27): Show | 30 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.3192+15947C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327777 | ||||||
| chr11:73327789
|
G | A | 38 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(35): Show | 40 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.3192+15959G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327789 | ||||||
| chr11:73327853
|
T | TG | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3192+16023_3192+16 others(7): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327853 | ||||||
| chr11:73327876
|
T | TA | 4 | a0002c0008t0002g0139a0002c0008t0006g0140a0002c0008t0006g0142others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3192+16047dupA | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73327876 | |||||
| chr11:73327908
|
T | C | 4 | a0002c0012t0007g0131a0002c0012t0007g0132a0002c0034t0004g0133others(1): Show | 4 | HG01074.hp1 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3192+16078T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73327908 | ||||||
| chr11:73328147
|
T | C | 4 | a0002c0008t0002g0139a0002c0008t0006g0140a0002c0008t0006g0142others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3192+16317T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328147 | ||||||
| chr11:73328155
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3192+16325A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328155 | ||||||
| chr11:73328184
|
G | A | 47 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(44): Show | 47 | HG00140.hp2 HG00438.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.3192+16354G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328184 | ||||||
| chr11:73328202
|
G | T | 38 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(35): Show | 40 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.3192+16372G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328202 | ||||||
| chr11:73328243
|
C | T | 17 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(14): Show | 17 | HG00140.hp1 HG01074.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.3192+16413C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328243 | ||||||
| chr11:73328249
|
G | A | 4 | a0002c0008t0002g0139a0002c0008t0006g0140a0002c0008t0006g0142others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3192+16419G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328249 | ||||||
| chr11:73328255
|
C | G | 6 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3192+16425C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328255 | ||||||
| chr11:73328300
|
G | A | 2 | a0003c0015t0004g0047a0003c0015t0004g0048 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3192+16470G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328300 | ||||||
| chr11:73328357
|
C | T | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3192+16527C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328357 | ||||||
| chr11:73328503
|
A | G | 5 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.3192+16673A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328503 | ||||||
| chr11:73328657
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3192+16827G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328657 | ||||||
| chr11:73328747
|
G | T | 2 | a0009c0014t0002g0044a0009c0014t0002g0045 | 2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3192+16917G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328747 | ||||||
| chr11:73328854
|
T | TCCGGGCT others(3): Show |
1 | a0001c0001t0001g0218 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3192+17025_3192+17 others(16): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73328854 | |||||
| chr11:73328926
|
C | T | 1 | a0003c0003t0002g0151 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3192+17096C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328926 | ||||||
| chr11:73328985
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3192+17155C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73328985 | ||||||
| chr11:73329049
|
A | T | 1 | a0002c0002t0001g0170 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3192+17219A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329049 | ||||||
| chr11:73329087
|
G | A | 1 | a0003c0003t0004g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3192+17257G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329087 | ||||||
| chr11:73329138
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3192+17308C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329138 | ||||||
| chr11:73329244
|
T | G | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3192+17414T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329244 | ||||||
| chr11:73329322
|
CAT | C | 3 | a0001c0001t0001g0205a0003c0003t0002g0054a0006c0011t0001g0215 | 3 | HG02965.hp2 HG03579.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.3193-17510_3193-17 others(8): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329322 | |||||
| chr11:73329322
|
CATAT | C | 2 | a0001c0001t0001g0207a0003c0003t0002g0052 | 2 | HG00438.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.3193-17512_3193-17 others(10): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329322 | |||||
| chr11:73329322
|
CATATAT | C | 11 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0219others(8): Show | 11 | HG01517.hp1 HG02027.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3193-17514_3193-17 others(12): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329322 | |||||
| chr11:73329322
|
CATATATA others(1): Show |
C | 4 | a0002c0034t0004g0133a0003c0003t0002g0062a0003c0003t0002g0063others(1): Show | 4 | HG01074.hp1 HG03041.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3193-17516_3193-17 others(14): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329322 | |||||
| chr11:73329322
|
CATATATA others(3): Show |
C | 3 | a0002c0012t0007g0131a0002c0012t0007g0132a0004c0005t0005g0014 | 3 | HG02258.hp1 HG03195.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.3193-17518_3193-17 others(16): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329322 | |||||
| chr11:73329322
|
CATATATA others(5): Show |
C | 4 | a0002c0016t0003g0222a0004c0005t0005g0018a0004c0005t0005g0021others(1): Show | 4 | HG01167.hp2 HG01934.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.3193-17520_3193-17 others(18): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329322 | |||||
| chr11:73329322
|
CATATATA others(7): Show |
C | 7 | a0001c0001t0001g0114a0001c0001t0001g0120a0001c0001t0001g0123others(4): Show | 7 | HG00140.hp2 HG03942.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.3193-17522_3193-17 others(20): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329322 | |||||
| chr11:73329322
|
CATATATA others(9): Show |
C | 14 | a0001c0001t0001g0032a0001c0001t0001g0108a0001c0001t0001g0110others(11): Show | 14 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.3193-17524_3193-17 others(22): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329322 | |||||
| chr11:73329322
|
CATATATA others(11): Show |
C | 41 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.3193-17526_3193-17 others(24): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329322 | |||||
| chr11:73329322
|
CATATATA others(15): Show |
C | 3 | a0002c0008t0002g0139a0002c0008t0006g0142a0002c0035t0006g0141 | 3 | HG01106.hp2 HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3192+17523_3193-17 others(28): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329322 | |||||
| chr11:73329323
|
A | G | 4 | a0003c0015t0004g0047a0003c0015t0004g0048a0003c0031t0004g0056others(1): Show | 4 | HG02615.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3192+17493A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329323 | ||||||
| chr11:73329325
|
A | G | 4 | a0003c0015t0004g0047a0003c0015t0004g0048a0003c0031t0004g0056others(1): Show | 4 | HG02615.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3192+17495A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329325 | ||||||
| chr11:73329346
|
TATATATA others(14): Show |
T | 1 | a0002c0008t0006g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3192+17517_3193-17 others(27): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329346 | ||||||
| chr11:73329348
|
TATATATA others(12): Show |
T | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3192+17519_3193-17 others(25): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329348 | ||||||
| chr11:73329350
|
TATATATA others(16): Show |
T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3192+17521_3193-17 others(29): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329350 | ||||||
| chr11:73329353
|
ATATATAT others(14): Show |
A | 3 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0218 | 3 | NA20752.hp1 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3192+17525_3193-17 others(27): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329353 | |||||
| chr11:73329353
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3192+17525_3193-17 others(29): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329353 | |||||
| chr11:73329354
|
TATATATA others(6): Show |
T | 1 | a0004c0005t0005g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3192+17525_3193-17 others(19): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329354 | ||||||
| chr11:73329354
|
TATATATA others(8): Show |
T | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3192+17525_3193-17 others(21): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329354 | ||||||
| chr11:73329354
|
TATATATA others(10): Show |
T | 2 | a0001c0001t0001g0104a0001c0001t0001g0118 | 2 | HG01074.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.3192+17525_3193-17 others(23): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329354 | ||||||
| chr11:73329354
|
TATATATA others(12): Show |
T | 1 | a0001c0001t0001g0102 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3192+17525_3193-17 others(25): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329354 | ||||||
| chr11:73329355
|
ATATATAT others(15): Show |
A | 2 | a0001c0001t0001g0080a0001c0029t0001g0079 | 2 | HG01891.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3193-17526_3193-17 others(28): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329355 | |||||
| chr11:73329356
|
TATATA | T | 5 | a0002c0002t0001g0029a0003c0003t0002g0043a0003c0003t0002g0046others(2): Show | 5 | HG02055.hp2 HG03195.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.3193-17526_3193-17 others(11): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329356 | ||||||
| chr11:73329356
|
TATATATA others(4): Show |
T | 1 | a0004c0005t0005g0015 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3193-17526_3193-17 others(17): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329356 | ||||||
| chr11:73329356
|
TATATATA others(8): Show |
T | 2 | a0001c0001t0001g0002a0001c0001t0001g0119 | 3 | HG00140.hp1 HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.3193-17526_3193-17 others(21): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329356 | ||||||
| chr11:73329356
|
TATATATA others(10): Show |
T | 9 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0084others(6): Show | 9 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.3193-17526_3193-17 others(23): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329356 | ||||||
| chr11:73329357
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0022 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3193-17524_3193-17 others(23): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329357 | |||||
| chr11:73329357
|
ATATATAT others(11): Show |
A | 1 | a0001c0021t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3193-17524_3193-17 others(24): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329357 | |||||
| chr11:73329358
|
TATATATA others(6): Show |
T | 1 | a0002c0036t0004g0134 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3193-17524_3193-17 others(19): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329358 | ||||||
| chr11:73329358
|
TATATATA others(8): Show |
T | 2 | a0001c0001t0001g0116a0001c0001t0001g0171 | 2 | HG02630.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.3193-17524_3193-17 others(21): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329358 | ||||||
| chr11:73329359
|
A | AT | 2 | a0002c0004t0003g0145a0002c0004t0003g0146 | 2 | HG00323.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.3193-17523dupT | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329359 | |||||
| chr11:73329359
|
A | T | 5 | a0002c0002t0001g0148a0002c0004t0003g0147a0003c0003t0002g0060others(2): Show | 5 | HG00738.hp2 HG01261.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3193-17524A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329359 | ||||||
| chr11:73329360
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0121 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3193-17522_3193-17 others(19): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329360 | ||||||
| chr11:73329361
|
A | ATT | 2 | a0002c0004t0003g0005a0003c0003t0002g0137 | 3 | HG01261.hp1 HG02004.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3193-17521_3193-17 others(8): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329361 | |||||
| chr11:73329361
|
A | T | 14 | a0002c0002t0001g0148a0002c0004t0003g0144a0002c0004t0003g0145others(11): Show | 14 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.3193-17522A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329361 | ||||||
| chr11:73329362
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0076 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3193-17520_3193-17 others(17): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329362 | ||||||
| chr11:73329363
|
A | T | 26 | a0002c0002t0001g0029a0002c0002t0001g0148a0002c0004t0003g0005others(23): Show | 27 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.3193-17520A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329363 | ||||||
| chr11:73329365
|
A | ATTTTTTT others(3): Show |
1 | a0002c0002t0001g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3193-17517_3193-17 others(16): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329365 | |||||
| chr11:73329365
|
A | T | 36 | a0002c0002t0001g0029a0002c0002t0001g0148a0002c0002t0001g0169others(33): Show | 38 | HG00323.hp2 HG00438.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.3193-17518A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329365 | ||||||
| chr11:73329367
|
A | ATTTTTTT others(4): Show |
1 | a0002c0002t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3193-17515_3193-17 others(17): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329367 | |||||
| chr11:73329367
|
A | T | 53 | a0001c0001t0001g0209a0002c0002t0001g0029a0002c0002t0001g0148others(50): Show | 55 | HG00323.hp2 HG00438.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.3193-17516A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329367 | ||||||
| chr11:73329367
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3193-17514_3193-17 others(16): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329367 | |||||
| chr11:73329369
|
A | ATTTTTTT others(3): Show |
1 | a0002c0002t0012g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3193-17513_3193-17 others(16): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329369 | |||||
| chr11:73329369
|
A | ATTTTTTT others(4): Show |
1 | a0002c0002t0001g0164 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3193-17513_3193-17 others(17): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329369 | |||||
| chr11:73329369
|
A | G | 1 | a0003c0032t0004g0057 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3193-17514A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329369 | ||||||
| chr11:73329369
|
A | T | 68 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(65): Show | 70 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.3193-17514A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329369 | ||||||
| chr11:73329370
|
TA | T | 2 | a0001c0001t0001g0178a0002c0006t0003g0011 | 2 | HG00423.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3193-17512delA | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329370 | ||||||
| chr11:73329371
|
A | ATTTTTTT others(3): Show |
1 | a0002c0002t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3193-17511_3193-17 others(16): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329371 | |||||
| chr11:73329371
|
A | ATTTTTTT others(4): Show |
1 | a0002c0002t0001g0160 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3193-17511_3193-17 others(17): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329371 | |||||
| chr11:73329371
|
A | ATTTTTTT others(6): Show |
1 | a0002c0002t0001g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3193-17511_3193-17 others(19): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329371 | |||||
| chr11:73329371
|
A | G | 1 | a0003c0031t0004g0056 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3193-17512A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329371 | ||||||
| chr11:73329371
|
A | T | 88 | a0001c0001t0001g0072a0001c0001t0001g0100a0001c0001t0001g0114others(85): Show | 90 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.3193-17512A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329371 | ||||||
| chr11:73329373
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(28): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0188a0007c0010t0001g0187 | 2 | HG01978.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.3193-17509_3193-17 others(22): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATAT others(7): Show |
1 | a0007c0010t0001g0189 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(20): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(26): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0191 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(16): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0181 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(17): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(22): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0017g0193 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(23): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATAT others(12): Show |
1 | a0002c0002t0008g0024 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(25): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0176a0001c0001t0001g0179 | 2 | HG00099.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.3193-17509_3193-17 others(17): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0174a0001c0001t0001g0177 | 2 | HG01106.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.3193-17509_3193-17 others(18): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATAT others(7): Show |
1 | a0007c0010t0001g0194 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(20): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATTT others(3): Show |
2 | a0001c0001t0001g0175a0001c0001t0001g0182 | 2 | HG02027.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.3193-17509_3193-17 others(16): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATTT others(5): Show |
1 | a0002c0008t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(18): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATTT others(9): Show |
1 | a0002c0002t0008g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(22): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATATTT others(14): Show |
1 | a0002c0002t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(27): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATTTTT others(7): Show |
1 | a0002c0002t0001g0170 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(20): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATATTTTT others(9): Show |
1 | a0002c0002t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(22): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATGTATTT others(3): Show |
1 | a0003c0015t0004g0047 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3193-17509_3193-17 others(16): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATTTTTTT others(6): Show |
1 | a0002c0002t0001g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3193-17506_3193-17 others(19): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | ATTTTTTT others(7): Show |
1 | a0002c0002t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3193-17507_3193-17 others(20): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329373 | |||||
| chr11:73329373
|
A | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(135): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.3193-17510A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329373 | ||||||
| chr11:73329390
|
G | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-17493G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329390 | ||||||
| chr11:73329392
|
A | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-17491A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329392 | ||||||
| chr11:73329404
|
TG | T | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3193-17478delG | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329404 | ||||||
| chr11:73329405
|
G | GT | 5 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3193-17466dupT | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73329405 | |||||
| chr11:73329409
|
T | TC | 35 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(32): Show | 35 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.3193-17474_3193-17 others(7): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329409 | ||||||
| chr11:73329422
|
C | T | 3 | a0002c0002t0008g0024a0002c0002t0008g0025a0003c0003t0002g0043 | 3 | HG02055.hp2 HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3193-17461C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329422 | ||||||
| chr11:73329453
|
G | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-17430G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329453 | ||||||
| chr11:73329495
|
G | A | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3193-17388G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329495 | ||||||
| chr11:73329556
|
C | T | 36 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(33): Show | 38 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.3193-17327C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329556 | ||||||
| chr11:73329582
|
T | C | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3193-17301T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329582 | ||||||
| chr11:73329611
|
G | C | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3193-17272G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329611 | ||||||
| chr11:73329648
|
C | T | 35 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(32): Show | 35 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.3193-17235C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329648 | ||||||
| chr11:73329696
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3193-17187G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329696 | ||||||
| chr11:73329782
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3193-17101T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329782 | ||||||
| chr11:73329962
|
G | A | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3193-16921G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73329962 | ||||||
| chr11:73330032
|
A | G | 46 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(43): Show | 46 | HG00140.hp2 HG00438.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.3193-16851A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73330032 | ||||||
| chr11:73330049
|
A | G | 2 | a0003c0015t0004g0047a0003c0015t0004g0048 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3193-16834A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73330049 | ||||||
| chr11:73330115
|
T | G | 1 | a0002c0008t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3193-16768T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73330115 | ||||||
| chr11:73330154
|
T | C | 1 | a0017c0040t0001g0028 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3193-16729T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73330154 | ||||||
| chr11:73330294
|
T | C | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3193-16589T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73330294 | ||||||
| chr11:73330376
|
C | T | 33 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(30): Show | 33 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.3193-16507C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73330376 | ||||||
| chr11:73330451
|
G | A | 1 | a0009c0014t0002g0045 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3193-16432G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73330451 | ||||||
| chr11:73330503
|
A | T | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3193-16380A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73330503 | ||||||
| chr11:73330560
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3193-16323G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73330560 | ||||||
| chr11:73330805
|
C | T | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3193-16078C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73330805 | ||||||
| chr11:73331002
|
C | T | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3193-15881C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73331002 | ||||||
| chr11:73331218
|
A | T | 27 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(24): Show | 27 | HG01106.hp2 HG01884.hp2 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.3193-15665A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73331218 | ||||||
| chr11:73331223
|
A | C | 1 | a0002c0002t0001g0148 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3193-15660A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73331223 | ||||||
| chr11:73331358
|
G | T | 28 | a0001c0001t0001g0101a0002c0002t0001g0023a0002c0002t0001g0026others(25): Show | 28 | HG01106.hp2 HG01884.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.3193-15525G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73331358 | ||||||
| chr11:73331647
|
G | C | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3193-15236G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73331647 | ||||||
| chr11:73331781
|
C | T | 47 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(44): Show | 47 | HG00140.hp2 HG00438.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.3193-15102C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73331781 | ||||||
| chr11:73331938
|
T | G | 1 | a0005c0009t0001g0105 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3193-14945T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73331938 | ||||||
| chr11:73332033
|
G | C | 1 | a0002c0002t0012g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3193-14850G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73332033 | ||||||
| chr11:73332191
|
T | G | 9 | a0002c0002t0001g0148a0002c0004t0003g0004a0002c0004t0003g0005others(6): Show | 11 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.3193-14692T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73332191 | ||||||
| chr11:73332350
|
C | CGT | 9 | a0001c0001t0001g0130a0001c0001t0001g0182a0001c0001t0001g0184others(6): Show | 9 | HG01243.hp1 HG02080.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3193-14476_3193-14 others(8): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
C | CGTGT | 5 | a0001c0001t0001g0178a0001c0001t0001g0190a0001c0001t0001g0191others(2): Show | 5 | HG00423.hp2 HG04204.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.3193-14478_3193-14 others(10): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
C | CGTGTGT | 7 | a0001c0001t0001g0174a0001c0001t0001g0177a0001c0001t0001g0204others(4): Show | 7 | HG01106.hp1 HG01255.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.3193-14480_3193-14 others(12): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
C | CGTGTGTG others(1): Show |
3 | a0001c0001t0001g0176a0001c0001t0010g0213a0004c0005t0005g0014 | 3 | HG03239.hp2 NA18971.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.3193-14482_3193-14 others(14): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
C | CGTGTGTG others(5): Show |
4 | a0001c0001t0001g0114a0001c0001t0001g0212a0003c0030t0014g0031others(1): Show | 4 | HG02683.hp1 NA18522.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.3193-14486_3193-14 others(18): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
C | CGTGTGTG others(7): Show |
2 | a0001c0001t0001g0210a0009c0014t0002g0045 | 2 | HG02055.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.3193-14488_3193-14 others(20): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
C | CGTGTGTG others(9): Show |
2 | a0001c0001t0001g0211a0001c0001t0010g0217 | 2 | NA18939.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.3193-14490_3193-14 others(22): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
CGT | C | 9 | a0001c0001t0001g0175a0001c0001t0001g0179a0001c0001t0001g0185others(6): Show | 9 | HG00099.hp2 HG00609.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.3193-14476_3193-14 others(8): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
CGTGT | C | 6 | a0001c0001t0001g0181a0001c0001t0001g0198a0003c0003t0002g0043others(3): Show | 6 | HG01255.hp1 HG02055.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.3193-14478_3193-14 others(10): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
CGTGTGT | C | 18 | a0001c0001t0001g0153a0001c0001t0001g0188a0001c0001t0001g0195others(15): Show | 18 | HG00738.hp2 HG01167.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.3193-14480_3193-14 others(12): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
CGTGTGTG others(1): Show |
C | 15 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0171others(12): Show | 15 | HG00621.hp2 HG01261.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.3193-14482_3193-14 others(14): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
CGTGTGTG others(3): Show |
C | 22 | a0001c0001t0001g0032a0001c0001t0001g0081a0001c0001t0001g0082others(19): Show | 22 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.3193-14484_3193-14 others(16): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
CGTGTGTG others(5): Show |
C | 11 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0001t0001g0172others(8): Show | 13 | HG01074.hp1 HG01106.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.3193-14486_3193-14 others(18): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
CGTGTGTG others(7): Show |
C | 25 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(22): Show | 25 | HG00323.hp2 HG01168.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.3193-14488_3193-14 others(20): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
CGTGTGTG others(9): Show |
C | 17 | a0001c0029t0001g0079a0002c0002t0001g0157a0002c0002t0001g0158others(14): Show | 17 | HG01891.hp2 HG02630.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.3193-14490_3193-14 others(22): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
CGTGTGTG others(11): Show |
C | 1 | a0002c0016t0003g0222 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3193-14492_3193-14 others(24): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
CGTGTGTG others(13): Show |
C | 3 | a0003c0003t0004g0058a0003c0031t0004g0056a0003c0032t0004g0057 | 3 | HG02280.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3193-14494_3193-14 others(26): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
CGTGTGTG others(17): Show |
C | 3 | a0002c0004t0003g0144a0004c0005t0009g0016a0004c0005t0009g0020 | 3 | HG00140.hp2 HG01928.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.3193-14498_3193-14 others(30): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332350
|
CGTGTGTG others(27): Show |
C | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3193-14508_3193-14 others(40): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332350 | |||||
| chr11:73332379
|
GTGTGTGT others(23): Show |
G | 1 | a0001c0001t0001g0113 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3193-14502_3193-14 others(36): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332379 | |||||
| chr11:73332391
|
GTGTGTGT others(11): Show |
G | 1 | a0020c0017t0004g0097 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3193-14490_3193-14 others(24): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332391 | |||||
| chr11:73332395
|
GTGTGTGT others(7): Show |
G | 4 | a0001c0001t0001g0100a0001c0001t0001g0121a0008c0013t0004g0095others(1): Show | 4 | HG00609.hp1 HG01346.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.3193-14486_3193-14 others(20): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332395 | |||||
| chr11:73332397
|
GTGTGTGT others(5): Show |
G | 9 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0068others(6): Show | 9 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.3193-14484_3193-14 others(18): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332397 | |||||
| chr11:73332399
|
GTGTGTGT others(3): Show |
G | 15 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0067others(12): Show | 15 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.3193-14482_3193-14 others(16): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332399 | |||||
| chr11:73332401
|
GTGTGTGT others(1): Show |
G | 8 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0094others(5): Show | 9 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.3193-14480_3193-14 others(14): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332401 | |||||
| chr11:73332401
|
GTGTGTGT others(2): Show |
G | 3 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0084 | 3 | HG00639.hp1 HG00639.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3193-14480_3193-14 others(15): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332401 | |||||
| chr11:73332401
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0001g0075 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3193-14480_3193-14 others(16): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332401 | |||||
| chr11:73332407
|
GTA | G | 2 | a0001c0001t0001g0002a0001c0027t0001g0088 | 3 | HG02083.hp1 HG02132.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.3193-14474_3193-14 others(8): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73332407 | |||||
| chr11:73332409
|
A | G | 3 | a0001c0001t0001g0076a0001c0020t0001g0083a0013c0026t0001g0070 | 3 | NA18965.hp1 NA19060.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.3193-14474A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73332409 | ||||||
| chr11:73332532
|
C | T | 1 | a0003c0032t0004g0057 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3193-14351C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73332532 | ||||||
| chr11:73332631
|
G | A | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3193-14252G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73332631 | ||||||
| chr11:73332668
|
C | T | 2 | a0003c0031t0004g0056a0003c0032t0004g0057 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3193-14215C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73332668 | ||||||
| chr11:73332690
|
C | T | 3 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222 | 3 | HG02109.hp1 HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3193-14193C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73332690 | ||||||
| chr11:73332718
|
G | A | 5 | a0001c0001t0004g0098a0001c0001t0004g0099a0008c0013t0004g0095others(2): Show | 5 | HG00741.hp2 HG01071.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.3193-14165G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73332718 | ||||||
| chr11:73333044
|
G | C | 4 | a0002c0008t0002g0139a0002c0008t0006g0140a0002c0008t0006g0142others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3193-13839G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333044 | ||||||
| chr11:73333089
|
G | A | 1 | a0011c0019t0001g0041 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3193-13794G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333089 | ||||||
| chr11:73333168
|
A | C | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3193-13715A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333168 | ||||||
| chr11:73333170
|
T | C | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3193-13713T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333170 | ||||||
| chr11:73333171
|
G | T | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3193-13712G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333171 | ||||||
| chr11:73333172
|
A | T | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3193-13711A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333172 | ||||||
| chr11:73333198
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.3193-13685A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333198 | ||||||
| chr11:73333268
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3193-13615G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333268 | ||||||
| chr11:73333306
|
T | C | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3193-13577T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333306 | ||||||
| chr11:73333372
|
G | A | 2 | a0002c0016t0003g0221a0019c0041t0016g0154 | 2 | HG02615.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.3193-13511G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333372 | ||||||
| chr11:73333405
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0212 | 2 | NA18997.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.3193-13478C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333405 | ||||||
| chr11:73333620
|
G | A | 2 | a0001c0027t0001g0088a0013c0026t0001g0070 | 2 | NA18965.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.3193-13263G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333620 | ||||||
| chr11:73333687
|
C | T | 2 | a0009c0014t0002g0044a0009c0014t0002g0045 | 2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3193-13196C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333687 | ||||||
| chr11:73333717
|
G | C | 5 | a0003c0003t0002g0060a0003c0003t0002g0061a0003c0003t0002g0062others(2): Show | 5 | HG02895.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3193-13166G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333717 | ||||||
| chr11:73333810
|
C | A | 2 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3193-13073C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73333810 | ||||||
| chr11:73334029
|
T | C | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3193-12854T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73334029 | ||||||
| chr11:73334084
|
C | T | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3193-12799C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73334084 | ||||||
| chr11:73334237
|
A | G | 30 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(27): Show | 30 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.3193-12646A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73334237 | ||||||
| chr11:73334455
|
C | T | 46 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(43): Show | 46 | HG00140.hp2 HG00438.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.3193-12428C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73334455 | ||||||
| chr11:73334456
|
G | C | 1 | a0006c0011t0001g0215 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3193-12427G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73334456 | ||||||
| chr11:73334545
|
A | G | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3193-12338A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73334545 | ||||||
| chr11:73334717
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3193-12166C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73334717 | ||||||
| chr11:73334834
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0192 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3193-12049C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73334834 | ||||||
| chr11:73335181
|
C | T | 1 | a0002c0004t0003g0144 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3193-11702C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73335181 | ||||||
| chr11:73335254
|
T | C | 86 | a0001c0001t0001g0111a0002c0002t0001g0023a0002c0002t0001g0026others(83): Show | 88 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.3193-11629T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73335254 | ||||||
| chr11:73335255
|
G | A | 30 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(27): Show | 30 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.3193-11628G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73335255 | ||||||
| chr11:73335322
|
C | G | 2 | a0002c0002t0001g0157a0002c0002t0001g0170 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3193-11561C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73335322 | ||||||
| chr11:73335517
|
G | A | 32 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(29): Show | 32 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.3193-11366G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73335517 | ||||||
| chr11:73335618
|
A | G | 46 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(43): Show | 46 | HG00140.hp2 HG00438.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.3193-11265A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73335618 | ||||||
| chr11:73335695
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3193-11188T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73335695 | ||||||
| chr11:73335761
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3193-11122T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73335761 | ||||||
| chr11:73335771
|
C | A | 4 | a0002c0012t0007g0131a0002c0012t0007g0132a0002c0034t0004g0133others(1): Show | 4 | HG01074.hp1 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3193-11112C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73335771 | ||||||
| chr11:73335785
|
T | C | 35 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(32): Show | 35 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.3193-11098T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73335785 | ||||||
| chr11:73335817
|
A | G | 7 | a0003c0003t0002g0049a0003c0003t0002g0050a0003c0003t0002g0051others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.3193-11066A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73335817 | ||||||
| chr11:73335881
|
G | A | 4 | a0002c0008t0002g0139a0002c0008t0006g0140a0002c0008t0006g0142others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3193-11002G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73335881 | ||||||
| chr11:73336621
|
T | G | 38 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(35): Show | 40 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.3193-10262T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73336621 | ||||||
| chr11:73336668
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3193-10215A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73336668 | ||||||
| chr11:73336685
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3193-10198C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73336685 | ||||||
| chr11:73336973
|
A | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-9910A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73336973 | ||||||
| chr11:73336983
|
A | G | 1 | a0001c0001t0001g0094 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3193-9900A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73336983 | ||||||
| chr11:73337149
|
G | A | 2 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3193-9734G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73337149 | ||||||
| chr11:73337192
|
G | A | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3193-9691G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73337192 | ||||||
| chr11:73337222
|
T | G | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3193-9661T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73337222 | ||||||
| chr11:73337321
|
C | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-9562C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73337321 | ||||||
| chr11:73337372
|
C | A | 2 | a0002c0012t0007g0131a0002c0012t0007g0132 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3193-9511C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73337372 | ||||||
| chr11:73337406
|
G | GA | 9 | a0001c0001t0001g0076a0001c0001t0001g0121a0001c0001t0001g0181others(6): Show | 9 | HG02055.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.3193-9459dupA | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73337406 | |||||
| chr11:73337406
|
GA | G | 9 | a0002c0002t0001g0169a0002c0002t0008g0024a0002c0008t0002g0139others(6): Show | 9 | HG01106.hp2 HG01884.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.3193-9459delA | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73337406 | |||||
| chr11:73337620
|
G | A | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3193-9263G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73337620 | ||||||
| chr11:73337634
|
G | T | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3193-9249G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73337634 | ||||||
| chr11:73337710
|
A | G | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3193-9173A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73337710 | ||||||
| chr11:73337724
|
TTTA | T | 6 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0116others(3): Show | 6 | HG00280.hp2 HG02630.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.3193-9150_3193-914 others(7): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73337724 | |||||
| chr11:73337774
|
C | G | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3193-9109C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73337774 | ||||||
| chr11:73338216
|
G | A | 1 | a0002c0002t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3193-8667G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73338216 | ||||||
| chr11:73338285
|
C | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-8598C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73338285 | ||||||
| chr11:73338307
|
A | G | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3193-8576A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73338307 | ||||||
| chr11:73338335
|
G | A | 1 | a0002c0016t0003g0221 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3193-8548G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73338335 | ||||||
| chr11:73338442
|
C | A | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3193-8441C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73338442 | ||||||
| chr11:73338538
|
C | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-8345C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73338538 | ||||||
| chr11:73338726
|
G | A | 38 | a0002c0008t0018g0007a0002c0016t0003g0222a0003c0003t0002g0043others(35): Show | 38 | HG00140.hp2 HG00438.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.3193-8157G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73338726 | ||||||
| chr11:73338832
|
T | C | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG02523.hp2 NA18612.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.3193-8051T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73338832 | ||||||
| chr11:73339070
|
G | A | 1 | a0003c0030t0014g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3193-7813G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73339070 | ||||||
| chr11:73339094
|
C | A | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3193-7789C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73339094 | ||||||
| chr11:73339128
|
C | T | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3193-7755C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73339128 | ||||||
| chr11:73339420
|
G | A | 2 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3193-7463G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73339420 | ||||||
| chr11:73339606
|
G | A | 1 | a0002c0008t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3193-7277G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73339606 | ||||||
| chr11:73339660
|
T | C | 1 | a0002c0008t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3193-7223T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73339660 | ||||||
| chr11:73339777
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00280.hp2 NA20752.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.3193-7106G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73339777 | ||||||
| chr11:73339850
|
T | C | 1 | a0004c0005t0005g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3193-7033T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73339850 | ||||||
| chr11:73340025
|
C | T | 35 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(32): Show | 35 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.3193-6858C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73340025 | ||||||
| chr11:73340056
|
G | A | 11 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010others(8): Show | 11 | HG01074.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3193-6827G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73340056 | ||||||
| chr11:73340219
|
C | T | 35 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(32): Show | 35 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.3193-6664C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73340219 | ||||||
| chr11:73340406
|
T | C | 1 | a0002c0002t0001g0167 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3193-6477T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73340406 | ||||||
| chr11:73340580
|
G | C | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3193-6303G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73340580 | ||||||
| chr11:73340640
|
G | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-6243G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73340640 | ||||||
| chr11:73340832
|
C | G | 27 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(24): Show | 27 | HG01106.hp2 HG01884.hp2 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.3193-6051C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73340832 | ||||||
| chr11:73340859
|
C | G | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3193-6024C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73340859 | ||||||
| chr11:73341015
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.3193-5868G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341015 | ||||||
| chr11:73341032
|
G | A | 1 | a0015c0042t0002g0040 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3193-5851G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341032 | ||||||
| chr11:73341266
|
A | G | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3193-5617A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341266 | ||||||
| chr11:73341321
|
G | C | 6 | a0003c0003t0002g0046a0003c0003t0002g0052a0003c0003t0002g0059others(3): Show | 6 | HG00438.hp2 HG02027.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3193-5562G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341321 | ||||||
| chr11:73341400
|
G | C | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3193-5483G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341400 | ||||||
| chr11:73341406
|
A | C | 1 | a0001c0001t0001g0201 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3193-5477A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341406 | ||||||
| chr11:73341495
|
A | G | 37 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(34): Show | 39 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3193-5388A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341495 | ||||||
| chr11:73341501
|
G | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-5382G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341501 | ||||||
| chr11:73341518
|
G | A | 37 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(34): Show | 39 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3193-5365G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341518 | ||||||
| chr11:73341528
|
T | G | 9 | a0002c0002t0001g0148a0002c0004t0003g0004a0002c0004t0003g0005others(6): Show | 11 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.3193-5355T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341528 | ||||||
| chr11:73341532
|
G | C | 2 | a0002c0002t0001g0026a0002c0002t0001g0030 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3193-5351G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341532 | ||||||
| chr11:73341591
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3193-5292C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341591 | ||||||
| chr11:73341794
|
A | T | 46 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(43): Show | 46 | HG00140.hp2 HG00438.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.3193-5089A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341794 | ||||||
| chr11:73341984
|
C | T | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3193-4899C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73341984 | ||||||
| chr11:73341991
|
CCT | C | 17 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0102others(14): Show | 17 | HG00140.hp1 HG01074.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.3193-4890_3193-488 others(6): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73341991 | |||||
| chr11:73342107
|
A | G | 1 | a0002c0036t0004g0134 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3193-4776A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73342107 | ||||||
| chr11:73342137
|
ATGGGAGC others(12): Show |
A | 83 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(80): Show | 85 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.3193-4709_3193-469 others(23): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73342137 | |||||
| chr11:73342155
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3193-4728G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73342155 | ||||||
| chr11:73342174
|
G | A | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3193-4709G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73342174 | ||||||
| chr11:73342390
|
T | C | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-4493T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73342390 | ||||||
| chr11:73342422
|
C | T | 36 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(33): Show | 38 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.3193-4461C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73342422 | ||||||
| chr11:73342433
|
G | A | 4 | a0003c0015t0004g0047a0003c0015t0004g0048a0003c0031t0004g0056others(1): Show | 4 | HG02615.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3193-4450G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73342433 | ||||||
| chr11:73342468
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3193-4415A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73342468 | ||||||
| chr11:73342669
|
T | C | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3193-4214T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73342669 | ||||||
| chr11:73342735
|
C | T | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3193-4148C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73342735 | ||||||
| chr11:73342806
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0209 | 2 | HG02683.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.3193-4077G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73342806 | ||||||
| chr11:73342962
|
C | CG | 5 | a0003c0003t0002g0060a0003c0003t0002g0061a0003c0003t0002g0062others(2): Show | 5 | HG02895.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3193-3918dupG | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73342962 | |||||
| chr11:73343023
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3193-3860C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343023 | ||||||
| chr11:73343090
|
C | A | 5 | a0003c0007t0002g0034a0003c0007t0002g0035a0003c0007t0002g0036others(2): Show | 5 | HG02280.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3193-3793C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343090 | ||||||
| chr11:73343096
|
GCCCCGCC others(4): Show |
G | 1 | a0003c0003t0002g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3193-3781_3193-377 others(15): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73343096 | |||||
| chr11:73343107
|
A | AC | 14 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0089others(11): Show | 14 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.3193-3772dupC | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 73343107 | |||||
| chr11:73343218
|
G | T | 2 | a0001c0001t0004g0098a0001c0001t0004g0099 | 2 | HG00741.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.3193-3665G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343218 | ||||||
| chr11:73343423
|
C | A | 84 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(81): Show | 86 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.3193-3460C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343423 | ||||||
| chr11:73343424
|
C | G | 84 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(81): Show | 86 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.3193-3459C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343424 | ||||||
| chr11:73343445
|
G | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-3438G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343445 | ||||||
| chr11:73343572
|
C | T | 1 | a0008c0013t0004g0096 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3193-3311C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343572 | ||||||
| chr11:73343646
|
A | G | 4 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3193-3237A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343646 | ||||||
| chr11:73343716
|
G | A | 2 | a0004c0005t0005g0014a0004c0005t0005g0015 | 2 | HG02683.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.3193-3167G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343716 | ||||||
| chr11:73343727
|
C | T | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3193-3156C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343727 | ||||||
| chr11:73343728
|
G | A | 6 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3193-3155G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343728 | ||||||
| chr11:73343842
|
A | G | 1 | a0003c0003t0002g0152 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3193-3041A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343842 | ||||||
| chr11:73343863
|
A | T | 92 | a0002c0002t0001g0026a0002c0002t0001g0030a0002c0002t0001g0148others(89): Show | 94 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.3193-3020A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343863 | ||||||
| chr11:73343864
|
A | G | 30 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(27): Show | 30 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.3193-3019A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343864 | ||||||
| chr11:73343957
|
G | A | 1 | a0002c0006t0003g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3193-2926G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73343957 | ||||||
| chr11:73344064
|
C | T | 3 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010 | 3 | HG02572.hp2 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3193-2819C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344064 | ||||||
| chr11:73344113
|
G | A | 2 | a0002c0034t0004g0133a0002c0036t0004g0134 | 2 | HG01074.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3193-2770G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344113 | ||||||
| chr11:73344278
|
G | A | 9 | a0002c0002t0001g0148a0002c0004t0003g0004a0002c0004t0003g0005others(6): Show | 11 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.3193-2605G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344278 | ||||||
| chr11:73344379
|
C | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0188a0001c0001t0001g0197others(5): Show | 8 | HG01978.hp2 HG02004.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.3193-2504C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344379 | ||||||
| chr11:73344379
|
C | T | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3193-2504C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344379 | ||||||
| chr11:73344389
|
A | C | 1 | a0004c0005t0005g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3193-2494A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344389 | ||||||
| chr11:73344453
|
G | C | 1 | a0002c0034t0004g0133 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3193-2430G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344453 | ||||||
| chr11:73344517
|
G | T | 2 | a0003c0031t0004g0056a0003c0032t0004g0057 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3193-2366G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344517 | ||||||
| chr11:73344539
|
C | T | 2 | a0002c0008t0018g0007a0003c0032t0004g0057 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3193-2344C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344539 | ||||||
| chr11:73344557
|
G | A | 1 | a0009c0014t0002g0045 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3193-2326G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344557 | ||||||
| chr11:73344569
|
G | A | 24 | a0003c0003t0002g0043a0003c0003t0002g0049a0003c0003t0002g0050others(21): Show | 24 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.3193-2314G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344569 | ||||||
| chr11:73344817
|
C | T | 1 | a0001c0024t0001g0196 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3193-2066C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344817 | ||||||
| chr11:73344872
|
G | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-2011G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344872 | ||||||
| chr11:73344954
|
C | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-1929C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344954 | ||||||
| chr11:73344977
|
G | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-1906G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73344977 | ||||||
| chr11:73345001
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3193-1882A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73345001 | ||||||
| chr11:73345057
|
G | A | 2 | a0002c0012t0007g0131a0002c0012t0007g0132 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3193-1826G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73345057 | ||||||
| chr11:73345132
|
C | T | 1 | a0001c0021t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3193-1751C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73345132 | ||||||
| chr11:73345468
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3193-1415G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73345468 | ||||||
| chr11:73345513
|
G | T | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3193-1370G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73345513 | ||||||
| chr11:73345942
|
A | T | 84 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(81): Show | 86 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.3193-941A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73345942 | ||||||
| chr11:73345968
|
A | G | 96 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(93): Show | 98 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.3193-915A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73345968 | ||||||
| chr11:73346006
|
G | A | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3193-877G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73346006 | ||||||
| chr11:73346222
|
A | G | 1 | a0003c0003t0002g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3193-661A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73346222 | ||||||
| chr11:73346257
|
C | T | 1 | a0002c0008t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3193-626C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73346257 | ||||||
| chr11:73346466
|
A | G | 85 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(82): Show | 87 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.3193-417A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73346466 | ||||||
| chr11:73346549
|
G | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG00642.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.3193-334G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73346549 | ||||||
| chr11:73346619
|
G | T | 2 | a0003c0015t0004g0047a0003c0015t0004g0048 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3193-264G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73346619 | ||||||
| chr11:73346656
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3193-227G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73346656 | ||||||
| chr11:73346743
|
C | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3193-140C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73346743 | ||||||
| chr11:73346744
|
G | A | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3193-139G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73346744 | ||||||
| chr11:73346764
|
G | T | 5 | a0001c0001t0001g0114a0001c0001t0001g0210a0001c0001t0001g0212others(2): Show | 5 | NA18984.hp1 NA18997.hp1 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.3193-119G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | chr11 | 73346764 | ||||||
| chr11:73347033
|
A | G | 1 | a0003c0003t0004g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3270+73A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73347033 | ||||||
| chr11:73347054
|
C | G | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3270+94C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73347054 | ||||||
| chr11:73347088
|
G | A | 1 | a0004c0005t0005g0018 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3270+128G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73347088 | ||||||
| chr11:73347964
|
G | A | 28 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(25): Show | 28 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.3270+1004G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73347964 | ||||||
| chr11:73348103
|
C | T | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0218 | 3 | HG00280.hp2 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3270+1143C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348103 | ||||||
| chr11:73348132
|
C | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3270+1172C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348132 | ||||||
| chr11:73348294
|
G | T | 34 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(31): Show | 34 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(31): Show |
intron_variant | MODIFIER | c.3270+1334G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348294 | ||||||
| chr11:73348296
|
G | A | 46 | a0002c0008t0018g0007a0002c0016t0003g0221a0002c0016t0003g0222others(43): Show | 46 | HG00140.hp2 HG00438.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.3270+1336G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348296 | ||||||
| chr11:73348330
|
C | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3270+1370C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348330 | ||||||
| chr11:73348386
|
G | A | 2 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3270+1426G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348386 | ||||||
| chr11:73348434
|
G | A | 1 | a0002c0006t0003g0008 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3270+1474G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348434 | ||||||
| chr11:73348434
|
G | C | 4 | a0003c0015t0004g0047a0003c0015t0004g0048a0003c0031t0004g0056others(1): Show | 4 | HG02615.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3270+1474G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348434 | ||||||
| chr11:73348459
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0130 | 2 | NA20752.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3270+1499A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348459 | ||||||
| chr11:73348469
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3270+1509A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348469 | ||||||
| chr11:73348608
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3270+1648G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348608 | ||||||
| chr11:73348795
|
C | T | 1 | a0001c0023t0001g0127 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3270+1835C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348795 | ||||||
| chr11:73348796
|
G | A | 1 | a0004c0038t0005g0019 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3270+1836G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348796 | ||||||
| chr11:73348876
|
G | T | 1 | a0003c0003t0002g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3270+1916G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348876 | ||||||
| chr11:73348910
|
G | A | 3 | a0002c0008t0002g0139a0002c0008t0006g0140a0002c0008t0006g0142 | 3 | HG01106.hp2 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3270+1950G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348910 | ||||||
| chr11:73348927
|
C | T | 1 | a0010c0025t0001g0125 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3270+1967C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348927 | ||||||
| chr11:73348938
|
G | A | 23 | a0003c0003t0002g0043a0003c0003t0002g0049a0003c0003t0002g0050others(20): Show | 23 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3270+1978G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73348938 | ||||||
| chr11:73349078
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3270+2118G>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73349078 | ||||||
| chr11:73349084
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3270+2124G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73349084 | ||||||
| chr11:73349129
|
A | G | 1 | a0003c0003t0002g0152 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3270+2169A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73349129 | ||||||
| chr11:73349249
|
A | G | 2 | a0002c0012t0007g0131a0002c0012t0007g0132 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3270+2289A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73349249 | ||||||
| chr11:73349408
|
A | T | 30 | a0002c0008t0001g0042a0003c0003t0002g0043a0003c0003t0002g0046others(27): Show | 30 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.3270+2448A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73349408 | ||||||
| chr11:73349430
|
C | T | 2 | a0002c0008t0001g0042a0019c0041t0016g0154 | 2 | HG03130.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.3270+2470C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73349430 | ||||||
| chr11:73349470
|
C | T | 41 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(38): Show | 43 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.3270+2510C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73349470 | ||||||
| chr11:73349539
|
C | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3270+2579C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73349539 | ||||||
| chr11:73349654
|
C | T | 20 | a0003c0003t0002g0046a0003c0003t0002g0049a0003c0003t0002g0050others(17): Show | 20 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.3270+2694C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73349654 | ||||||
| chr11:73349749
|
C | G | 1 | a0002c0002t0001g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3270+2789C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73349749 | ||||||
| chr11:73349817
|
G | A | 3 | a0003c0003t0004g0058a0003c0015t0004g0047a0003c0015t0004g0048 | 3 | HG02280.hp1 HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3270+2857G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73349817 | ||||||
| chr11:73349867
|
G | A | 1 | a0002c0006t0003g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3270+2907G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73349867 | ||||||
| chr11:73350057
|
A | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 4 | HG00639.hp1 HG00741.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.3271-2773A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350057 | ||||||
| chr11:73350085
|
C | G | 92 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(89): Show | 94 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.3271-2745C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350085 | ||||||
| chr11:73350187
|
A | T | 74 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(71): Show | 74 | HG00140.hp2 HG00438.hp2 HG01106.hp2 others(71): Show |
intron_variant | MODIFIER | c.3271-2643A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350187 | ||||||
| chr11:73350190
|
C | T | 8 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(5): Show | 8 | HG02451.hp2 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3271-2640C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350190 | ||||||
| chr11:73350198
|
C | T | 17 | a0002c0004t0003g0004a0002c0004t0003g0005a0002c0004t0003g0143others(14): Show | 19 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.3271-2632C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350198 | ||||||
| chr11:73350279
|
C | T | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3271-2551C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350279 | ||||||
| chr11:73350363
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3271-2467T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350363 | ||||||
| chr11:73350401
|
G | A | 7 | a0003c0003t0002g0046a0003c0003t0002g0052a0003c0003t0002g0059others(4): Show | 7 | HG00438.hp2 HG02027.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3271-2429G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350401 | ||||||
| chr11:73350466
|
C | T | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3271-2364C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350466 | ||||||
| chr11:73350593
|
C | T | 2 | a0004c0005t0005g0014a0004c0005t0005g0015 | 2 | HG02683.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.3271-2237C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350593 | ||||||
| chr11:73350689
|
T | C | 92 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(89): Show | 94 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.3271-2141T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350689 | ||||||
| chr11:73350731
|
G | A | 1 | a0002c0008t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3271-2099G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350731 | ||||||
| chr11:73350767
|
C | T | 23 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(20): Show | 23 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(20): Show |
intron_variant | MODIFIER | c.3271-2063C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350767 | ||||||
| chr11:73350811
|
G | A | 8 | a0002c0004t0003g0004a0002c0004t0003g0005a0002c0004t0003g0143others(5): Show | 10 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.3271-2019G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350811 | ||||||
| chr11:73350860
|
C | G | 74 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(71): Show | 74 | HG00140.hp2 HG00438.hp2 HG01106.hp2 others(71): Show |
intron_variant | MODIFIER | c.3271-1970C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73350860 | ||||||
| chr11:73351032
|
C | A | 1 | a0003c0031t0004g0056 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3271-1798C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73351032 | ||||||
| chr11:73351288
|
T | C | 1 | a0002c0036t0004g0134 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3271-1542T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73351288 | ||||||
| chr11:73351301
|
T | C | 2 | a0002c0012t0007g0131a0002c0012t0007g0132 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3271-1529T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73351301 | ||||||
| chr11:73351327
|
G | GT | 74 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(71): Show | 74 | HG00140.hp2 HG00438.hp2 HG01106.hp2 others(71): Show |
intron_variant | MODIFIER | c.3271-1495dupT | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | 73351327 | |||||
| chr11:73351429
|
T | G | 1 | a0001c0001t0001g0201 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3271-1401T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73351429 | ||||||
| chr11:73351454
|
C | T | 3 | a0002c0002t0001g0157a0002c0002t0001g0164a0002c0002t0001g0170 | 3 | HG02896.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3271-1376C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73351454 | ||||||
| chr11:73351527
|
T | C | 92 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(89): Show | 94 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.3271-1303T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73351527 | ||||||
| chr11:73351530
|
C | A | 17 | a0002c0004t0003g0004a0002c0004t0003g0005a0002c0004t0003g0143others(14): Show | 19 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.3271-1300C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73351530 | ||||||
| chr11:73351556
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3271-1274A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73351556 | ||||||
| chr11:73351928
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG00423.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.3271-902A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73351928 | ||||||
| chr11:73351973
|
G | T | 17 | a0002c0004t0003g0004a0002c0004t0003g0005a0002c0004t0003g0143others(14): Show | 19 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.3271-857G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73351973 | ||||||
| chr11:73351974
|
T | G | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3271-856T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73351974 | ||||||
| chr11:73352049
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3271-781G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73352049 | ||||||
| chr11:73352192
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3271-638C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73352192 | ||||||
| chr11:73352423
|
G | A | 8 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(5): Show | 8 | HG02451.hp2 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3271-407G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73352423 | ||||||
| chr11:73352563
|
GCT | G | 30 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(27): Show | 30 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.3271-264_3271-263d others(4): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr11 | 73352563 | |||||
| chr11:73352735
|
G | A | 18 | a0002c0004t0003g0004a0002c0004t0003g0005a0002c0004t0003g0143others(15): Show | 20 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.3271-95G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 2/20 | chr11 | 73352735 | ||||||
| chr11:73353028
|
G | A | 2 | a0002c0012t0007g0131a0002c0012t0007g0132 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3453+16G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73353028 | ||||||
| chr11:73353259
|
C | G | 2 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3453+247C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73353259 | ||||||
| chr11:73353302
|
C | T | 5 | a0003c0003t0004g0058a0003c0015t0004g0047a0003c0015t0004g0048others(2): Show | 5 | HG02280.hp1 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3453+290C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73353302 | ||||||
| chr11:73353315
|
C | T | 1 | a0014c0018t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3453+303C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73353315 | ||||||
| chr11:73353371
|
A | G | 61 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(58): Show | 61 | HG00438.hp2 HG01106.hp2 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.3453+359A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73353371 | ||||||
| chr11:73353553
|
G | A | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3453+541G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73353553 | ||||||
| chr11:73353668
|
C | G | 17 | a0002c0004t0003g0004a0002c0004t0003g0005a0002c0004t0003g0143others(14): Show | 19 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.3453+656C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73353668 | ||||||
| chr11:73353723
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG02027.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.3453+711C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73353723 | ||||||
| chr11:73353860
|
T | G | 3 | a0002c0006t0003g0011a0002c0006t0003g0012a0002c0006t0003g0013 | 3 | HG02258.hp2 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.3453+848T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73353860 | ||||||
| chr11:73354080
|
T | G | 1 | a0003c0003t0004g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3453+1068T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73354080 | ||||||
| chr11:73354288
|
C | G | 1 | a0003c0003t0002g0046 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3454-1245C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73354288 | ||||||
| chr11:73354438
|
G | A | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3454-1095G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73354438 | ||||||
| chr11:73354646
|
G | A | 17 | a0002c0004t0003g0004a0002c0004t0003g0005a0002c0004t0003g0143others(14): Show | 19 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.3454-887G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73354646 | ||||||
| chr11:73354663
|
G | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.3454-870G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73354663 | ||||||
| chr11:73354715
|
CA | C | 13 | a0001c0001t0001g0180a0002c0008t0001g0042a0002c0012t0007g0131others(10): Show | 13 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.3454-802delA | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr11 | 73354715 | |||||
| chr11:73354715
|
CAAA | C | 16 | a0002c0004t0003g0004a0002c0004t0003g0005a0002c0004t0003g0143others(13): Show | 18 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.3454-804_3454-802d others(5): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr11 | 73354715 | |||||
| chr11:73354864
|
G | A | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3454-669G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73354864 | ||||||
| chr11:73354872
|
C | T | 2 | a0002c0012t0007g0131a0002c0012t0007g0132 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3454-661C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73354872 | ||||||
| chr11:73354934
|
G | A | 70 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(67): Show | 70 | HG00140.hp2 HG00438.hp2 HG01106.hp2 others(67): Show |
intron_variant | MODIFIER | c.3454-599G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73354934 | ||||||
| chr11:73355030
|
A | T | 2 | a0002c0012t0007g0131a0002c0012t0007g0132 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3454-503A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73355030 | ||||||
| chr11:73355276
|
A | T | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3454-257A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73355276 | ||||||
| chr11:73355517
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3454-16G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3/20 | chr11 | 73355517 | ||||||
| chr11:73355726
|
G | A | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3570+77G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 4/20 | chr11 | 73355726 | ||||||
| chr11:73356129
|
C | T | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3664-46C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 5/20 | chr11 | 73356129 | ||||||
| chr11:73356520
|
G | A | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3840+169G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 6/20 | chr11 | 73356520 | ||||||
| chr11:73357149
|
C | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4001+15C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 8/20 | chr11 | 73357149 | ||||||
| chr11:73357169
|
CAG | C | 6 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4001+36_4001+37del others(2): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 8/20 | chr11 | 73357169 | ||||||
| chr11:73357434
|
CT | C | 6 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4087+111delT | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr11 | 73357434 | |||||
| chr11:73357446
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4087+119G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73357446 | ||||||
| chr11:73357511
|
T | C | 1 | a0004c0038t0005g0019 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4087+184T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73357511 | ||||||
| chr11:73357526
|
T | C | 92 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(89): Show | 94 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.4087+199T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73357526 | ||||||
| chr11:73357574
|
G | A | 1 | a0002c0034t0004g0133 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4087+247G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73357574 | ||||||
| chr11:73357724
|
A | C | 71 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(68): Show | 71 | HG00140.hp2 HG00438.hp2 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.4087+397A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73357724 | ||||||
| chr11:73357794
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4087+467C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73357794 | ||||||
| chr11:73357876
|
C | T | 4 | a0002c0008t0002g0139a0002c0008t0006g0140a0002c0008t0006g0142others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4087+549C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73357876 | ||||||
| chr11:73357970
|
C | T | 22 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(19): Show | 22 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(19): Show |
intron_variant | MODIFIER | c.4087+643C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73357970 | ||||||
| chr11:73358035
|
G | A | 1 | a0002c0002t0004g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4087+708G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73358035 | ||||||
| chr11:73358106
|
G | A | 3 | a0008c0013t0004g0095a0008c0013t0004g0096a0020c0017t0004g0097 | 3 | HG01071.hp2 HG01346.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.4087+779G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73358106 | ||||||
| chr11:73358274
|
G | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4087+947G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73358274 | ||||||
| chr11:73358292
|
A | G | 1 | a0002c0002t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4087+965A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73358292 | ||||||
| chr11:73358297
|
G | A | 1 | a0001c0001t0015g0202 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.4087+970G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73358297 | ||||||
| chr11:73358390
|
G | A | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4087+1063G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73358390 | ||||||
| chr11:73358453
|
C | CT | 75 | a0001c0001t0001g0087a0001c0001t0001g0172a0001c0001t0001g0205others(72): Show | 77 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.4087+1149dupT | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr11 | 73358453 | |||||
| chr11:73358453
|
C | CTT | 10 | a0002c0002t0001g0026a0002c0002t0001g0157a0002c0002t0001g0167others(7): Show | 10 | HG02027.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.4087+1148_4087+114 others(6): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr11 | 73358453 | |||||
| chr11:73358453
|
CT | C | 5 | a0001c0001t0001g0180a0001c0001t0001g0200a0001c0001t0017g0193others(2): Show | 5 | HG01346.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.4087+1149delT | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr11 | 73358453 | |||||
| chr11:73358481
|
C | T | 6 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4087+1154C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73358481 | ||||||
| chr11:73358493
|
C | G | 91 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(88): Show | 93 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.4087+1166C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73358493 | ||||||
| chr11:73358588
|
G | T | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.4088-1246G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73358588 | ||||||
| chr11:73358624
|
A | AT | 61 | a0001c0001t0001g0176a0002c0002t0001g0023a0002c0002t0001g0027others(58): Show | 61 | HG00438.hp2 HG01106.hp2 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.4088-1196dupT | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr11 | 73358624 | |||||
| chr11:73358699
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4088-1135T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73358699 | ||||||
| chr11:73358783
|
A | G | 1 | a0003c0003t0004g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4088-1051A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73358783 | ||||||
| chr11:73359039
|
G | T | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4088-795G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73359039 | ||||||
| chr11:73359172
|
T | G | 1 | a0002c0002t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4088-662T>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73359172 | ||||||
| chr11:73359313
|
A | C | 1 | a0009c0014t0002g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4088-521A>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73359313 | ||||||
| chr11:73359355
|
G | T | 5 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.4088-479G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73359355 | ||||||
| chr11:73359413
|
C | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4088-421C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73359413 | ||||||
| chr11:73359610
|
G | A | 1 | a0003c0030t0014g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4088-224G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73359610 | ||||||
| chr11:73359711
|
C | T | 1 | a0003c0003t0002g0152 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4088-123C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73359711 | ||||||
| chr11:73359735
|
C | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4088-99C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 9/20 | chr11 | 73359735 | ||||||
| chr11:73360218
|
T | C | 92 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(89): Show | 94 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.4207-102T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 10/20 | chr11 | 73360218 | ||||||
| chr11:73360630
|
G | A | 5 | a0003c0007t0002g0034a0003c0007t0002g0035a0003c0007t0002g0036others(2): Show | 5 | HG02280.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.4420+97G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 11/20 | chr11 | 73360630 | ||||||
| chr11:73360733
|
A | G | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4420+200A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 11/20 | chr11 | 73360733 | ||||||
| chr11:73360761
|
C | A | 6 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4420+228C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 11/20 | chr11 | 73360761 | ||||||
| chr11:73360833
|
A | G | 17 | a0002c0004t0003g0004a0002c0004t0003g0005a0002c0004t0003g0143others(14): Show | 19 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.4421-255A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 11/20 | chr11 | 73360833 | ||||||
| chr11:73360844
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG00423.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.4421-244C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 11/20 | chr11 | 73360844 | ||||||
| chr11:73360926
|
A | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4421-162A>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 11/20 | chr11 | 73360926 | ||||||
| chr11:73361198
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4494+37C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 12/20 | chr11 | 73361198 | ||||||
| chr11:73361247
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4494+86C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 12/20 | chr11 | 73361247 | ||||||
| chr11:73361269
|
T | A | 6 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4494+108T>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 12/20 | chr11 | 73361269 | ||||||
| chr11:73361375
|
T | C | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4494+214T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 12/20 | chr11 | 73361375 | ||||||
| chr11:73361445
|
G | A | 1 | a0003c0003t0011g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4494+284G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 12/20 | chr11 | 73361445 | ||||||
| chr11:73361476
|
A | G | 2 | a0003c0003t0002g0151a0003c0003t0002g0152 | 2 | NA18981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.4494+315A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 12/20 | chr11 | 73361476 | ||||||
| chr11:73361539
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4494+378C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 12/20 | chr11 | 73361539 | ||||||
| chr11:73361920
|
CCACA | C | 96 | a0001c0001t0004g0098a0001c0001t0004g0099a0002c0002t0001g0023others(93): Show | 98 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.4495-110_4495-107d others(6): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr11 | 73361920 | |||||
| chr11:73361934
|
C | T | 1 | a0019c0041t0016g0154 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4495-106C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 12/20 | chr11 | 73361934 | ||||||
| chr11:73362301
|
G | GCA | 2 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.4694+66_4694+67dup others(2): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr11 | 73362301 | |||||
| chr11:73362307
|
T | A | 1 | a0002c0034t0004g0133 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4694+68T>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 13/20 | chr11 | 73362307 | ||||||
| chr11:73362364
|
T | A | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.4695-69T>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 13/20 | chr11 | 73362364 | ||||||
| chr11:73362416
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4695-17A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 13/20 | chr11 | 73362416 | ||||||
| chr11:73362801
|
G | A | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.4996+67G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 14/20 | chr11 | 73362801 | ||||||
| chr11:73362864
|
A | G | 6 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4996+130A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 14/20 | chr11 | 73362864 | ||||||
| chr11:73362975
|
G | A | 5 | a0003c0007t0002g0034a0003c0007t0002g0035a0003c0007t0002g0036others(2): Show | 5 | HG02280.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.4997-231G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 14/20 | chr11 | 73362975 | ||||||
| chr11:73363013
|
A | G | 96 | a0001c0001t0004g0098a0001c0001t0004g0099a0002c0002t0001g0023others(93): Show | 98 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.4997-193A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 14/20 | chr11 | 73363013 | ||||||
| chr11:73363081
|
C | T | 1 | a0002c0037t0013g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4997-125C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 14/20 | chr11 | 73363081 | ||||||
| chr11:73363110
|
G | A | 2 | a0003c0003t0002g0043a0003c0003t0002g0223 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.4997-96G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 14/20 | chr11 | 73363110 | ||||||
| chr11:73363115
|
G | A | 5 | a0002c0004t0003g0004a0002c0004t0003g0005a0002c0004t0003g0143others(2): Show | 7 | HG00323.hp2 HG01168.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.4997-91G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 14/20 | chr11 | 73363115 | ||||||
| chr11:73363572
|
C | G | 1 | a0002c0008t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5246+117C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 15/20 | chr11 | 73363572 | ||||||
| chr11:73363582
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.5246+127G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 15/20 | chr11 | 73363582 | ||||||
| chr11:73363681
|
G | A | 5 | a0003c0003t0004g0058a0003c0015t0004g0047a0003c0015t0004g0048others(2): Show | 5 | HG02280.hp1 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.5247-66G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 15/20 | chr11 | 73363681 | ||||||
| chr11:73363706
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5247-41T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 15/20 | chr11 | 73363706 | ||||||
| chr11:73364166
|
A | G | 1 | a0003c0003t0002g0223 | 1 | HG02559.hp2 | splice_region_variant&intron_variant | LOW | c.5334-6A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 16/20 | chr11 | 73364166 | ||||||
| chr11:73364270
|
C | G | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5401+31C>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 17/20 | chr11 | 73364270 | ||||||
| chr11:73364972
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.5550+372C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 18/20 | chr11 | 73364972 | ||||||
| chr11:73365022
|
G | A | 2 | a0009c0014t0002g0044a0009c0014t0002g0045 | 2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.5551-368G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 18/20 | chr11 | 73365022 | ||||||
| chr11:73365258
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.5551-132C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 18/20 | chr11 | 73365258 | ||||||
| chr11:73365352
|
G | T | 1 | a0003c0003t0002g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5551-38G>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 18/20 | chr11 | 73365352 | ||||||
| chr11:73365611
|
C | T | 2 | a0002c0012t0007g0131a0002c0012t0007g0132 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5725+47C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 19/20 | chr11 | 73365611 | ||||||
| chr11:73366096
|
T | C | 1 | a0002c0008t0018g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5995+149T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73366096 | ||||||
| chr11:73366119
|
T | TTG | 11 | a0001c0001t0001g0190a0002c0004t0003g0004a0002c0004t0003g0005others(8): Show | 13 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.5995+193_5995+194d others(4): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr11 | 73366119 | |||||
| chr11:73366140
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0130 | 2 | NA20752.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.5995+193T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73366140 | ||||||
| chr11:73366140
|
TGC | T | 5 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0027others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.5995+196_5995+197d others(4): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr11 | 73366140 | |||||
| chr11:73366142
|
C | T | 57 | a0002c0002t0001g0157a0002c0002t0001g0158a0002c0002t0001g0159others(54): Show | 59 | HG00140.hp2 HG00323.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.5995+195C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73366142 | ||||||
| chr11:73366144
|
C | T | 8 | a0004c0005t0005g0014a0004c0005t0005g0015a0004c0005t0005g0017others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.5995+197C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73366144 | ||||||
| chr11:73366146
|
C | T | 2 | a0002c0008t0018g0007a0002c0037t0013g0155 | 2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5995+199C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73366146 | ||||||
| chr11:73366382
|
G | A | 10 | a0002c0004t0003g0004a0002c0004t0003g0005a0002c0004t0003g0143others(7): Show | 12 | HG00323.hp2 HG00738.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.5995+435G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73366382 | ||||||
| chr11:73366482
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5995+535A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73366482 | ||||||
| chr11:73366509
|
G | A | 5 | a0003c0003t0002g0060a0003c0003t0002g0061a0003c0003t0002g0062others(2): Show | 5 | HG02895.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.5995+562G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73366509 | ||||||
| chr11:73366750
|
A | G | 6 | a0002c0006t0003g0008a0002c0006t0003g0009a0002c0006t0003g0010others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.5995+803A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73366750 | ||||||
| chr11:73366751
|
A | G | 1 | a0005c0009t0001g0105 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.5995+804A>G | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73366751 | ||||||
| chr11:73366945
|
C | A | 30 | a0003c0003t0002g0043a0003c0003t0002g0046a0003c0003t0002g0049others(27): Show | 30 | HG00438.hp2 HG01884.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.5996-639C>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73366945 | ||||||
| chr11:73366972
|
G | A | 2 | a0002c0012t0007g0131a0002c0012t0007g0132 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5996-612G>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73366972 | ||||||
| chr11:73367360
|
T | C | 2 | a0002c0016t0003g0221a0002c0016t0003g0222 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.5996-224T>C | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73367360 | ||||||
| chr11:73367425
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5996-159C>T | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73367425 | ||||||
| chr11:73367565
|
T | A | 1 | a0003c0003t0002g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5996-19T>A | ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 20/20 | chr11 | 73367565 |