Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23229 |
|---|---|
| ensemblid | ENSG00000131089.17 |
| hgncid | 14561 |
| symbol | ARHGEF9 |
| name | Cdc42 guanine nucleotide exchange factor 9 |
| refseq_nuc | NM_001353921.2 |
| refseq_prot | NP_001340850.1 |
| ensembl_nuc | ENST00000671741.2 |
| ensembl_prot | ENSP00000500715.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 63634967 |
| end | 63785214 |
| strand | - |
| ver | v1.2 |
| region | chrX:63634967-63785214 |
| region5000 | chrX:63629967-63790214 |
| regionname0 | ARHGEF9_chrX_63634967_63785214 |
| regionname5000 | ARHGEF9_chrX_63629967_63790214 |
| 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 | 523 | 166 | 47 | 29 | 67 | 5 | 16 | 52 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0002 | 0/0 | 499 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0003 | 0/0 | 523 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| 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 | 1572 | 166 | 47 | 29 | 67 | 5 | 16 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| c0002 | 0/0 | 1573 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| c0003 | 0/0 | 1572 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| 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 | 3131 | 96 | 3 | 17 | 60 | 4 | 10 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0002 | 0/0 | 3129 | 29 | 21 | 2 | 5 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0003 | 0/0 | 3127 | 10 | 10 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0004 | 0/0 | 3133 | 5 | 1 | 3 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0005 | 0/0 | 3128 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0006 | 0/0 | 3122 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0007 | 0/0 | 3133 | 3 | 0 | 1 | 1 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0008 | 0/0 | 3130 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0009 | 0/0 | 3130 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0010 | 0/0 | 3135 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0011 | 0/0 | 3132 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0012 | 0/0 | 3131 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0013 | 0/0 | 3131 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0014 | 0/0 | 3130 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0015 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0016 | 0/0 | 3129 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0017 | 0/0 | 3130 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0018 | 0/0 | 3131 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0019 | 0/0 | 3129 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0020 | 0/0 | 3127 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0021 | 0/0 | 3127 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| t0022 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| 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 | 1572 | 166 | 47 | 29 | 67 | 5 | 16 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0002c0002 | 0/0 | 1573 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0003c0003 | 0/0 | 1572 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4702 | 96 | 3 | 17 | 60 | 4 | 10 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0002 | 0/0 | 4700 | 29 | 21 | 2 | 5 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0003 | 0/0 | 4698 | 10 | 10 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0004 | 0/0 | 4704 | 5 | 1 | 3 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0005 | 0/0 | 4699 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0006 | 0/0 | 4693 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0007 | 0/0 | 4704 | 3 | 0 | 1 | 1 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0008 | 0/0 | 4701 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0009 | 0/0 | 4701 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0010 | 0/0 | 4706 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0011 | 0/0 | 4703 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0012 | 0/0 | 4702 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0013 | 0/0 | 4702 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0014 | 0/0 | 4701 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0016 | 0/0 | 4700 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0017 | 0/0 | 4701 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0018 | 0/0 | 4702 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0019 | 0/0 | 4700 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0020 | 0/0 | 4698 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0001c0001t0021 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0002c0002t0015 | 0/0 | 4685 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| a0003c0003t0022 | 0/0 | 4699 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | copy fasta | chrX | 63629967 | 63790214 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0006g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0009g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0010g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0011g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0012g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0013g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0014g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0016g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0017g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0018g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0019g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0020g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0021g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0002c0002t0015g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0003c0003t0022g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0138 | EAS | CHS | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0109 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00735 | hp1 | a0001 | c0001 | t0017 | g0003 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00738 | hp1 | a0001 | c0001 | t0020 | g0012 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0019 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0088 | AMR | PEL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0058 | AMR | PEL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0087 | AMR | PEL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02723 | hp1 | a0001 | c0001 | t0019 | g0034 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02738 | hp1 | a0001 | c0001 | t0011 | g0048 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02809 | hp2 | a0003 | c0003 | t0022 | g0038 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0007 | AFR | ESN | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02965 | hp1 | a0001 | c0001 | t0016 | g0029 | AFR | ESN | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ESN | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03492 | hp1 | a0001 | c0001 | t0013 | g0066 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03688 | hp1 | a0001 | c0001 | t0012 | g0125 | SAS | STU | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG04115 | hp1 | a0001 | c0001 | t0010 | g0080 | SAS | STU | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | STU | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0091 | SAS | STU | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | YRI | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18965 | hp1 | a0001 | c0001 | t0014 | g0045 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19076 | hp1 | a0002 | c0002 | t0015 | g0011 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | YRI | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | YRI | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0056 | EUR | TSI | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | GIH | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02486 | hp1 | a0001 | c0001 | t0021 | g0096 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03471 | hp1 | a0001 | c0001 | t0018 | g0140 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | USA | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | USA | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0082 | REF | REF | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0079 | REF | REF | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:63638202
|
G | GT | 1 | a0002 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1397dupA | p.Asn466fs | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 1466/4702 | 1397/1572 | 466/523 | chrX | 63638202 | ||
| chrX:63724693
|
T | C | 1 | a0003 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.49A>G | p.Ile17Val | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/10 | 118/4702 | 49/1572 | 17/523 | chrX | 63724693 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:63635030
|
AT | A | 1 | a0002c0002t0015 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2997delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 2997 | chrX | 63635030 | |||||
| chrX:63635107
|
GA | G | 1 | a0001c0001t0014 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2920delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 2920 | chrX | 63635107 | |||||
| chrX:63635290
|
G | GA | 7 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(4): Show | 15 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2737dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 2737 | chrX | 63635290 | |||||
| chrX:63635832
|
TG | T | 1 | a0002c0002t0015 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2195delC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 2195 | chrX | 63635832 | |||||
| chrX:63635987
|
C | CG | 1 | a0002c0002t0015 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2040dupC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 2040 | chrX | 63635987 | |||||
| chrX:63636103
|
G | T | 1 | a0001c0001t0021 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1925C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 1925 | chrX | 63636103 | |||||
| chrX:63636431
|
G | T | 1 | a0001c0001t0010 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1597C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 1597 | chrX | 63636431 | |||||
| chrX:63636492
|
AG | A | 1 | a0002c0002t0015 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1535delC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 1535 | chrX | 63636492 | |||||
| chrX:63636504
|
C | T | 1 | a0001c0001t0013 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1524G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 1524 | chrX | 63636504 | |||||
| chrX:63636576
|
T | C | 1 | a0001c0001t0008 | 2 | HG02647.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1452A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 1452 | chrX | 63636576 | |||||
| chrX:63636604
|
C | T | 1 | a0001c0001t0020 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1424G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 1424 | chrX | 63636604 | |||||
| chrX:63637161
|
C | T | 1 | a0001c0001t0012 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*867G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 867 | chrX | 63637161 | |||||
| chrX:63637203
|
G | GA | 1 | a0001c0001t0018 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*824dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 824 | chrX | 63637203 | |||||
| chrX:63637250
|
CATCATCA others(9): Show |
C | 1 | a0002c0002t0015 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*762_*777delATCAGA others(10): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 762 | chrX | 63637250 | |||||
| chrX:63637716
|
A | AG | 1 | a0001c0001t0011 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*311dupC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 311 | chrX | 63637716 | |||||
| chrX:63637744
|
T | G | 1 | a0001c0001t0009 | 2 | HG02280.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*284A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 284 | chrX | 63637744 | |||||
| chrX:63637816
|
C | A | 1 | a0003c0003t0022 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*212G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 212 | chrX | 63637816 | |||||
| chrX:63637840
|
ATC | A | 1 | a0001c0001t0016 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186_*187delGA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 186 | chrX | 63637840 | |||||
| chrX:63637846
|
C | CTG | 1 | a0001c0001t0007 | 3 | HG00621.hp1 HG00642.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*180_*181dupCA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 181 | chrX | 63637846 | |||||
| chrX:63637846
|
C | CTGTG | 1 | a0001c0001t0010 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*178_*181dupCACA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 181 | chrX | 63637846 | |||||
| chrX:63637846
|
CTG | C | 6 | a0001c0001t0002a0001c0001t0008a0001c0001t0009others(3): Show | 36 | HG00735.hp1 HG01167.hp1 HG01255.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*180_*181delCA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 180 | chrX | 63637846 | |||||
| chrX:63637846
|
CTGTG | C | 5 | a0001c0001t0003a0001c0001t0005a0001c0001t0020others(2): Show | 18 | HG00738.hp1 HG01243.hp1 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*178_*181delCACA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 178 | chrX | 63637846 | |||||
| chrX:63637850
|
G | C | 1 | a0001c0001t0019 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*178C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 178 | chrX | 63637850 | |||||
| chrX:63637872
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0006 | 3 | HG00639.hp2 HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*146_*155delGACACA others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 146 | chrX | 63637872 | |||||
| chrX:63637918
|
C | CTG | 1 | a0001c0001t0004 | 5 | HG01928.hp1 HG01934.hp1 HG02300.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*108_*109dupCA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 109 | chrX | 63637918 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:63638625
|
G | A | 2 | a0001c0001t0008g0004a0001c0001t0008g0005 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1391-416C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63638625 | ||||||
| chrX:63638669
|
G | GT | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-461dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63638669 | ||||||
| chrX:63638992
|
TC | T | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-784delG | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63638992 | ||||||
| chrX:63638998
|
A | C | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1391-789T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63638998 | ||||||
| chrX:63639342
|
AG | A | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-1134delC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63639342 | ||||||
| chrX:63639368
|
A | AAT | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-1160_1391-115 others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63639368 | ||||||
| chrX:63639442
|
T | C | 3 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0022 | 3 | HG01243.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1391-1233A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63639442 | ||||||
| chrX:63639587
|
C | CT | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-1379dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63639587 | ||||||
| chrX:63640054
|
A | AG | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-1846dupC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63640054 | ||||||
| chrX:63640130
|
C | CA | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-1922dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63640130 | ||||||
| chrX:63640263
|
A | AT | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-2055dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63640263 | ||||||
| chrX:63640543
|
G | GT | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-2335dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63640543 | ||||||
| chrX:63640670
|
T | TG | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-2462dupC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63640670 | ||||||
| chrX:63640765
|
G | GT | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-2557dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63640765 | ||||||
| chrX:63640902
|
T | C | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1391-2693A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63640902 | ||||||
| chrX:63641073
|
T | TG | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-2865dupC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641073 | ||||||
| chrX:63641117
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1390+2863G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641117 | ||||||
| chrX:63641182
|
T | TC | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+2797dupG | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641182 | ||||||
| chrX:63641258
|
A | AG | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+2721dupC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641258 | ||||||
| chrX:63641288
|
G | GA | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+2691_1390+269 others(5): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641288 | ||||||
| chrX:63641340
|
G | GA | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+2639dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641340 | ||||||
| chrX:63641356
|
G | GA | 6 | a0001c0001t0001g0010a0001c0001t0001g0165a0001c0001t0002g0147others(3): Show | 6 | HG01358.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1390+2623dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641356 | ||||||
| chrX:63641356
|
GA | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0104a0001c0001t0002g0064 | 3 | HG01167.hp1 NA18944.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1390+2623delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641356 | ||||||
| chrX:63641357
|
A | G | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1390+2623T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641357 | ||||||
| chrX:63641380
|
AAGAC | A | 2 | a0001c0001t0002g0037a0001c0001t0019g0034 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1390+2596_1390+259 others(8): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641380 | ||||||
| chrX:63641635
|
T | TC | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+2344dupG | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641635 | ||||||
| chrX:63641772
|
AG | A | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+2207delC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641772 | ||||||
| chrX:63641821
|
A | AC | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+2158dupG | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641821 | ||||||
| chrX:63641821
|
AC | A | 1 | a0001c0001t0003g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1390+2158delG | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641821 | ||||||
| chrX:63641875
|
TA | T | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+2104delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641875 | ||||||
| chrX:63641898
|
G | GA | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+2081dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641898 | ||||||
| chrX:63641952
|
C | T | 2 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1390+2028G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641952 | ||||||
| chrX:63642093
|
C | CAT | 8 | a0001c0001t0001g0001a0001c0001t0001g0103a0001c0001t0001g0115others(5): Show | 10 | HG00621.hp1 HG02056.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1390+1885_1390+188 others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642093 | ||||||
| chrX:63642100
|
A | AT | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+1879dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642100 | ||||||
| chrX:63642112
|
C | A | 1 | a0001c0001t0002g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1390+1868G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642112 | ||||||
| chrX:63642118
|
A | AG | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+1861dupC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642118 | ||||||
| chrX:63642208
|
A | AG | 1 | a0002c0002t0015g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+1771dupC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642208 | ||||||
| chrX:63642392
|
T | C | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1390+1588A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642392 | ||||||
| chrX:63642411
|
A | C | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1390+1569T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642411 | ||||||
| chrX:63642579
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1390+1401G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642579 | ||||||
| chrX:63642806
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1390+1174G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642806 | ||||||
| chrX:63642934
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1390+1046A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642934 | ||||||
| chrX:63643360
|
C | CTT | 13 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1390+618_1390+619d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643360 | ||||||
| chrX:63643360
|
C | CTTT | 1 | a0001c0001t0005g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1390+617_1390+619d others(5): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643360 | ||||||
| chrX:63643360
|
CT | C | 5 | a0001c0001t0001g0113a0001c0001t0002g0064a0001c0001t0003g0041others(2): Show | 5 | HG01167.hp1 HG02109.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390+619delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643360 | ||||||
| chrX:63643461
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1390+519G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643461 | ||||||
| chrX:63643717
|
T | TA | 5 | a0001c0001t0001g0053a0001c0001t0001g0090a0001c0001t0001g0152others(2): Show | 5 | HG02647.hp1 NA18940.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390+262dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643717 | ||||||
| chrX:63643717
|
T | TAA | 12 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(9): Show | 12 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.1390+261_1390+262d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643717 | ||||||
| chrX:63643717
|
TA | T | 2 | a0001c0001t0001g0156a0001c0001t0002g0037 | 2 | HG01256.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1390+262delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643717 | ||||||
| chrX:63643756
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0161 | 2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1390+224G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643756 | ||||||
| chrX:63643799
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1390+181A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643799 | ||||||
| chrX:63643817
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1390+163C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643817 | ||||||
| chrX:63644097
|
A | C | 15 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(12): Show | 15 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1322-49T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644097 | ||||||
| chrX:63644146
|
CAT | C | 1 | a0001c0001t0001g0107 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1322-100_1322-99de others(3): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644146 | ||||||
| chrX:63644167
|
C | CA | 6 | a0001c0001t0001g0114a0001c0001t0005g0015a0001c0001t0005g0016others(3): Show | 6 | HG01243.hp1 HG02738.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1322-120dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644167 | ||||||
| chrX:63644167
|
C | CAA | 10 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0006g0019others(7): Show | 10 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1322-121_1322-120d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644167 | ||||||
| chrX:63644167
|
CA | C | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1322-120delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644167 | ||||||
| chrX:63644238
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1322-190G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644238 | ||||||
| chrX:63644637
|
T | TA | 1 | a0001c0001t0002g0009 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1322-590dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644637 | ||||||
| chrX:63644762
|
A | AT | 1 | a0001c0001t0001g0067 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1322-715dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644762 | ||||||
| chrX:63644762
|
A | T | 1 | a0001c0001t0013g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1322-714T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644762 | ||||||
| chrX:63644762
|
AT | A | 20 | a0001c0001t0001g0028a0001c0001t0001g0123a0001c0001t0001g0141others(17): Show | 20 | HG01167.hp1 HG01255.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.1322-715delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644762 | ||||||
| chrX:63644762
|
ATT | A | 7 | a0001c0001t0002g0026a0001c0001t0002g0030a0001c0001t0002g0032others(4): Show | 7 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1322-716_1322-715d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644762 | ||||||
| chrX:63644765
|
T | A | 9 | a0001c0001t0001g0070a0001c0001t0001g0104a0001c0001t0001g0133others(6): Show | 9 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1322-717A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644765 | ||||||
| chrX:63644871
|
T | A | 1 | a0001c0001t0020g0012 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1322-823A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644871 | ||||||
| chrX:63645012
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1322-964G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645012 | ||||||
| chrX:63645054
|
A | C | 16 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1322-1006T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645054 | ||||||
| chrX:63645214
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1322-1166A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645214 | ||||||
| chrX:63645221
|
A | AT | 1 | a0001c0001t0001g0164 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1322-1174dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645221 | ||||||
| chrX:63645221
|
AT | A | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1322-1174delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645221 | ||||||
| chrX:63645464
|
C | A | 1 | a0001c0001t0001g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1322-1416G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645464 | ||||||
| chrX:63645471
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1322-1423C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645471 | ||||||
| chrX:63645605
|
C | G | 5 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1322-1557G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645605 | ||||||
| chrX:63645677
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0002g0075 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1322-1629G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645677 | ||||||
| chrX:63645678
|
G | A | 1 | a0001c0001t0004g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1322-1630C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645678 | ||||||
| chrX:63645884
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1322-1836G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645884 | ||||||
| chrX:63645951
|
G | A | 1 | a0001c0001t0017g0003 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1322-1903C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645951 | ||||||
| chrX:63646116
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1322-2068T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646116 | ||||||
| chrX:63646130
|
G | C | 17 | a0001c0001t0002g0013a0001c0001t0003g0041a0001c0001t0003g0102others(14): Show | 17 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1322-2082C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646130 | ||||||
| chrX:63646278
|
A | G | 16 | a0001c0001t0001g0028a0001c0001t0002g0013a0001c0001t0002g0023others(13): Show | 16 | HG01255.hp1 HG02622.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.1322-2230T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646278 | ||||||
| chrX:63646361
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1322-2313T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646361 | ||||||
| chrX:63646593
|
C | G | 3 | a0001c0001t0002g0035a0001c0001t0002g0063a0001c0001t0002g0064 | 3 | HG01167.hp1 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1322-2545G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646593 | ||||||
| chrX:63646608
|
T | A | 1 | a0001c0001t0020g0012 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1322-2560A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646608 | ||||||
| chrX:63646992
|
A | C | 1 | a0001c0001t0001g0002 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1322-2944T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646992 | ||||||
| chrX:63647345
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1322-3297G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63647345 | ||||||
| chrX:63647412
|
T | C | 29 | a0001c0001t0002g0013a0001c0001t0002g0035a0001c0001t0003g0041others(26): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1322-3364A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63647412 | ||||||
| chrX:63647413
|
G | C | 29 | a0001c0001t0002g0013a0001c0001t0002g0035a0001c0001t0003g0041others(26): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1322-3365C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63647413 | ||||||
| chrX:63647443
|
G | T | 1 | a0001c0001t0004g0052 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1322-3395C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63647443 | ||||||
| chrX:63648283
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1322-4235C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63648283 | ||||||
| chrX:63648314
|
T | G | 1 | a0001c0001t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1322-4266A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63648314 | ||||||
| chrX:63648475
|
T | G | 29 | a0001c0001t0002g0013a0001c0001t0002g0035a0001c0001t0003g0041others(26): Show | 29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1322-4427A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63648475 | ||||||
| chrX:63649018
|
C | A | 1 | a0001c0001t0002g0110 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1322-4970G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63649018 | ||||||
| chrX:63649030
|
T | C | 1 | a0001c0001t0021g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1322-4982A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63649030 | ||||||
| chrX:63649042
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1322-4994G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63649042 | ||||||
| chrX:63649353
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1322-5305C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63649353 | ||||||
| chrX:63649410
|
T | C | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1322-5362A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63649410 | ||||||
| chrX:63650063
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1321+5431C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63650063 | ||||||
| chrX:63650206
|
T | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321+5288A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63650206 | ||||||
| chrX:63650342
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1321+5152G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63650342 | ||||||
| chrX:63650445
|
GA | G | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1321+5048delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63650445 | ||||||
| chrX:63650677
|
A | G | 1 | a0001c0001t0001g0002 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1321+4817T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63650677 | ||||||
| chrX:63651868
|
A | C | 1 | a0001c0001t0003g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1321+3626T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63651868 | ||||||
| chrX:63652170
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1321+3324T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63652170 | ||||||
| chrX:63652492
|
A | G | 1 | a0001c0001t0002g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1321+3002T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63652492 | ||||||
| chrX:63652594
|
CATA | C | 1 | a0001c0001t0001g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1321+2897_1321+289 others(7): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63652594 | ||||||
| chrX:63652827
|
TG | T | 1 | a0001c0001t0001g0162 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1321+2666delC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63652827 | ||||||
| chrX:63652917
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1321+2577G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63652917 | ||||||
| chrX:63653215
|
C | A | 1 | a0001c0001t0002g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1321+2279G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63653215 | ||||||
| chrX:63653351
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0116 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1321+2143C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63653351 | ||||||
| chrX:63653546
|
GTTAC | G | 1 | a0001c0001t0010g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1321+1944_1321+194 others(8): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63653546 | ||||||
| chrX:63653776
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1321+1718C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63653776 | ||||||
| chrX:63653928
|
C | T | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1321+1566G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63653928 | ||||||
| chrX:63654078
|
G | GT | 1 | a0001c0001t0002g0076 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1321+1415dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63654078 | ||||||
| chrX:63654078
|
GT | G | 11 | a0001c0001t0001g0044a0001c0001t0005g0015a0001c0001t0005g0016others(8): Show | 11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321+1415delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63654078 | ||||||
| chrX:63654159
|
C | CA | 6 | a0001c0001t0001g0008a0001c0001t0001g0135a0001c0001t0001g0155others(3): Show | 6 | HG00735.hp2 HG01109.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1321+1334dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63654159 | ||||||
| chrX:63654159
|
CA | C | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1321+1334delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63654159 | ||||||
| chrX:63654545
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1321+949G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63654545 | ||||||
| chrX:63655171
|
T | G | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1321+323A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63655171 | ||||||
| chrX:63655311
|
T | C | 2 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1321+183A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63655311 | ||||||
| chrX:63655835
|
T | C | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1078-98A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63655835 | ||||||
| chrX:63656061
|
G | T | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1078-324C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63656061 | ||||||
| chrX:63656519
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1078-782A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63656519 | ||||||
| chrX:63656868
|
A | G | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(3): Show | 6 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-1131T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63656868 | ||||||
| chrX:63657135
|
C | T | 4 | a0001c0001t0003g0043a0001c0001t0003g0074a0001c0001t0003g0101others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-1398G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63657135 | ||||||
| chrX:63657345
|
T | C | 13 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(10): Show | 13 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-1608A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63657345 | ||||||
| chrX:63657637
|
C | A | 1 | a0001c0001t0001g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1078-1900G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63657637 | ||||||
| chrX:63657849
|
C | T | 7 | a0001c0001t0003g0043a0001c0001t0003g0072a0001c0001t0003g0073others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078-2112G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63657849 | ||||||
| chrX:63658194
|
G | C | 1 | a0001c0001t0001g0040 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1078-2457C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63658194 | ||||||
| chrX:63660089
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1078-4352G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63660089 | ||||||
| chrX:63660765
|
G | T | 1 | a0001c0001t0017g0003 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1078-5028C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63660765 | ||||||
| chrX:63660901
|
A | G | 8 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(5): Show | 8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077+4985T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63660901 | ||||||
| chrX:63660906
|
A | T | 2 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1077+4980T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63660906 | ||||||
| chrX:63660993
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1077+4893G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63660993 | ||||||
| chrX:63661279
|
A | G | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+4607T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63661279 | ||||||
| chrX:63661497
|
C | T | 1 | a0001c0001t0004g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1077+4389G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63661497 | ||||||
| chrX:63661679
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1077+4207T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63661679 | ||||||
| chrX:63661755
|
CTT | C | 1 | a0001c0001t0002g0013 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1077+4129_1077+413 others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63661755 | ||||||
| chrX:63661758
|
T | TTC | 8 | a0001c0001t0002g0009a0001c0001t0002g0120a0001c0001t0002g0129others(5): Show | 8 | HG00735.hp1 HG02132.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077+4126_1077+412 others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63661758 | ||||||
| chrX:63661758
|
TTCTC | T | 1 | a0001c0001t0002g0024 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1077+4124_1077+412 others(8): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63661758 | ||||||
| chrX:63661871
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1077+4015A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63661871 | ||||||
| chrX:63662493
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1077+3393A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63662493 | ||||||
| chrX:63662724
|
T | C | 6 | a0001c0001t0001g0092a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG02015.hp1 HG02074.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+3162A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63662724 | ||||||
| chrX:63662932
|
G | C | 1 | a0001c0001t0007g0138 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1077+2954C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63662932 | ||||||
| chrX:63663141
|
C | A | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0013g0066 | 3 | HG00280.hp1 HG01099.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1077+2745G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63663141 | ||||||
| chrX:63663341
|
C | A | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+2545G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63663341 | ||||||
| chrX:63663355
|
G | A | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1077+2531C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63663355 | ||||||
| chrX:63663710
|
A | G | 1 | a0001c0001t0021g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1077+2176T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63663710 | ||||||
| chrX:63664895
|
G | GT | 1 | a0001c0001t0001g0160 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1077+990_1077+991i others(3): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63664895 | ||||||
| chrX:63664920
|
G | A | 27 | a0001c0001t0003g0041a0001c0001t0003g0043a0001c0001t0003g0072others(24): Show | 27 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1077+966C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63664920 | ||||||
| chrX:63665107
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1077+779A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665107 | ||||||
| chrX:63665166
|
AG | A | 1 | a0001c0001t0001g0160 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1077+719delC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665166 | ||||||
| chrX:63665198
|
G | A | 1 | a0001c0001t0017g0003 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1077+688C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665198 | ||||||
| chrX:63665341
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1077+545C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665341 | ||||||
| chrX:63665536
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1077+350A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665536 | ||||||
| chrX:63665558
|
T | G | 1 | a0001c0001t0002g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1077+328A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665558 | ||||||
| chrX:63665827
|
G | T | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1077+59C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665827 | ||||||
| chrX:63665834
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1077+52G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665834 | ||||||
| chrX:63666115
|
A | G | 1 | a0001c0001t0007g0109 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.946-98T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666115 | ||||||
| chrX:63666326
|
C | CCT | 2 | a0001c0001t0001g0085a0001c0001t0002g0098 | 2 | HG01952.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.946-311_946-310dup others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666326 | ||||||
| chrX:63666326
|
CCTCT | C | 1 | a0001c0001t0001g0053 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.946-313_946-310del others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666326 | ||||||
| chrX:63666402
|
T | TTA | 1 | a0001c0001t0001g0070 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.946-387_946-386dup others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666402 | ||||||
| chrX:63666402
|
TTA | T | 1 | a0001c0001t0001g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.946-387_946-386del others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666402 | ||||||
| chrX:63666417
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.946-400A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666417 | ||||||
| chrX:63666417
|
T | TAC | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-402_946-401dup others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666417 | ||||||
| chrX:63666447
|
T | TATATAC | 1 | a0001c0001t0001g0085 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.946-431_946-430ins others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666447 | ||||||
| chrX:63666449
|
T | TACACACA others(3): Show |
2 | a0001c0001t0002g0037a0001c0001t0019g0034 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.946-433_946-432ins others(10): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666449 | ||||||
| chrX:63666453
|
T | C | 2 | a0001c0001t0002g0037a0001c0001t0019g0034 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.946-436A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666453
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.946-436A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666453
|
T | TAC | 3 | a0001c0001t0006g0019a0001c0001t0006g0020a0001c0001t0006g0021 | 3 | HG00639.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.946-438_946-437dup others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666453
|
T | TACAC | 9 | a0001c0001t0001g0039a0001c0001t0002g0065a0001c0001t0002g0098others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.946-440_946-437dup others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666453
|
T | TACACAC | 5 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0002g0024others(2): Show | 5 | HG02809.hp2 HG02886.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.946-442_946-437dup others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666453
|
T | TACACACA others(1): Show |
83 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0028others(80): Show | 84 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.946-444_946-437dup others(8): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666453
|
T | TACACACA others(3): Show |
39 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0046others(36): Show | 41 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.946-446_946-437dup others(10): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666453
|
T | TACACACA others(5): Show |
5 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0119others(2): Show | 5 | HG03490.hp1 HG04115.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-448_946-437dup others(12): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666453
|
T | TACACACA others(7): Show |
5 | a0001c0001t0001g0126a0001c0001t0001g0137a0001c0001t0002g0009others(2): Show | 5 | HG00642.hp1 HG01099.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-450_946-437dup others(14): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666453
|
T | TACACACA others(9): Show |
2 | a0001c0001t0002g0035a0001c0001t0021g0096 | 2 | HG02486.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.946-452_946-437dup others(16): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666453
|
T | TACACACA others(19): Show |
1 | a0001c0001t0001g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.946-462_946-437dup others(26): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666453
|
TAC | T | 2 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.946-438_946-437del others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666453
|
TACAC | T | 3 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0017g0003 | 3 | HG00735.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.946-440_946-437del others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | ||||||
| chrX:63666487
|
C | CACAT | 1 | a0001c0001t0003g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.946-471_946-470ins others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666487 | ||||||
| chrX:63666489
|
T | C | 1 | a0001c0001t0010g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.946-472A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666489 | ||||||
| chrX:63666552
|
T | C | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.946-535A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666552 | ||||||
| chrX:63666700
|
T | G | 1 | a0001c0001t0003g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.946-683A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666700 | ||||||
| chrX:63667760
|
C | T | 1 | a0001c0001t0003g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.946-1743G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63667760 | ||||||
| chrX:63668133
|
A | AT | 2 | a0001c0001t0001g0156a0001c0001t0002g0026 | 2 | HG01256.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.946-2117dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63668133 | ||||||
| chrX:63668133
|
AT | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0119 | 2 | HG03490.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.946-2117delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63668133 | ||||||
| chrX:63668197
|
G | A | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.946-2180C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63668197 | ||||||
| chrX:63668262
|
T | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-2245A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63668262 | ||||||
| chrX:63668366
|
G | A | 1 | a0001c0001t0002g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.946-2349C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63668366 | ||||||
| chrX:63668383
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.946-2366G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63668383 | ||||||
| chrX:63668911
|
C | G | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.946-2894G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63668911 | ||||||
| chrX:63669012
|
C | T | 5 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-2995G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63669012 | ||||||
| chrX:63669128
|
G | A | 1 | a0001c0001t0002g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.946-3111C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63669128 | ||||||
| chrX:63669173
|
G | T | 1 | a0001c0001t0017g0003 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.946-3156C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63669173 | ||||||
| chrX:63669391
|
T | A | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.946-3374A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63669391 | ||||||
| chrX:63669538
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-3521G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63669538 | ||||||
| chrX:63670136
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.945+3902C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63670136 | ||||||
| chrX:63670286
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.945+3752A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63670286 | ||||||
| chrX:63671200
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.945+2838C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63671200 | ||||||
| chrX:63671545
|
G | A | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.945+2493C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63671545 | ||||||
| chrX:63671909
|
G | A | 7 | a0001c0001t0002g0026a0001c0001t0002g0030a0001c0001t0002g0032others(4): Show | 7 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.945+2129C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63671909 | ||||||
| chrX:63673109
|
A | G | 27 | a0001c0001t0003g0041a0001c0001t0003g0043a0001c0001t0003g0072others(24): Show | 27 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.945+929T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63673109 | ||||||
| chrX:63673686
|
G | C | 1 | a0001c0001t0001g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.945+352C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63673686 | ||||||
| chrX:63674168
|
CTG | C | 1 | a0001c0001t0004g0052 | 1 | NA20300.hp1 | splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.816-3_816-2delCA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63674168 | ||||||
| chrX:63674725
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.816-558C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63674725 | ||||||
| chrX:63676125
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0003g0041a0001c0001t0003g0102others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.816-1958G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63676125 | ||||||
| chrX:63676308
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.815+2032A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63676308 | ||||||
| chrX:63676435
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.815+1905G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63676435 | ||||||
| chrX:63676478
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.815+1862A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63676478 | ||||||
| chrX:63676560
|
G | A | 1 | a0001c0001t0021g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.815+1780C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63676560 | ||||||
| chrX:63676806
|
A | G | 1 | a0001c0001t0002g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.815+1534T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63676806 | ||||||
| chrX:63677242
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.815+1098A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63677242 | ||||||
| chrX:63677582
|
G | A | 4 | a0001c0001t0003g0043a0001c0001t0003g0074a0001c0001t0003g0101others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+758C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63677582 | ||||||
| chrX:63677616
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.815+724G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63677616 | ||||||
| chrX:63677853
|
A | C | 10 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(7): Show | 10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+487T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63677853 | ||||||
| chrX:63678031
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.815+309C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63678031 | ||||||
| chrX:63678038
|
G | A | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.815+302C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63678038 | ||||||
| chrX:63678105
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.815+235A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63678105 | ||||||
| chrX:63678704
|
G | T | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.583-132C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63678704 | ||||||
| chrX:63678763
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.583-191C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63678763 | ||||||
| chrX:63678934
|
A | G | 2 | a0001c0001t0002g0030a0001c0001t0002g0032 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.583-362T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63678934 | ||||||
| chrX:63679748
|
A | C | 1 | a0001c0001t0001g0145 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.583-1176T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63679748 | ||||||
| chrX:63680559
|
T | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-1987A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63680559 | ||||||
| chrX:63680787
|
C | T | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-2215G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63680787 | ||||||
| chrX:63680853
|
A | AAAAC | 1 | a0001c0001t0002g0024 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.583-2285_583-2282d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63680853 | ||||||
| chrX:63680866
|
A | AAAC | 3 | a0001c0001t0001g0107a0001c0001t0002g0075a0001c0001t0002g0100 | 3 | HG03540.hp1 HG03579.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.583-2297_583-2295d others(5): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63680866 | ||||||
| chrX:63681174
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.583-2602C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63681174 | ||||||
| chrX:63681326
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.583-2754C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63681326 | ||||||
| chrX:63681451
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(1): Show | 4 | HG00639.hp1 HG01070.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-2879G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63681451 | ||||||
| chrX:63681923
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.583-3351G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63681923 | ||||||
| chrX:63682133
|
C | CAATA | 8 | a0001c0001t0001g0095a0001c0001t0001g0118a0001c0001t0001g0135others(5): Show | 8 | HG00621.hp1 HG01106.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.583-3565_583-3562d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63682133 | ||||||
| chrX:63682133
|
CAATA | C | 15 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.583-3565_583-3562d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63682133 | ||||||
| chrX:63682133
|
CAATAAAT others(1): Show |
C | 3 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0022 | 3 | HG01243.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.583-3569_583-3562d others(10): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63682133 | ||||||
| chrX:63682461
|
G | A | 2 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.583-3889C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63682461 | ||||||
| chrX:63682512
|
C | CA | 1 | a0001c0001t0001g0057 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.583-3941dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63682512 | ||||||
| chrX:63682512
|
CA | C | 2 | a0001c0001t0001g0152a0002c0002t0015g0011 | 2 | NA19072.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.583-3941delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63682512 | ||||||
| chrX:63682525
|
GAAGAA | G | 1 | a0001c0001t0017g0003 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.583-3958_583-3954d others(7): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63682525 | ||||||
| chrX:63683092
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.583-4520G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63683092 | ||||||
| chrX:63683156
|
C | CA | 1 | a0001c0001t0001g0115 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.583-4585dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63683156 | ||||||
| chrX:63684163
|
C | CA | 1 | a0001c0001t0002g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.583-5592dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63684163 | ||||||
| chrX:63684202
|
G | A | 1 | a0001c0001t0005g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.583-5630C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63684202 | ||||||
| chrX:63684919
|
G | GA | 3 | a0001c0001t0001g0051a0001c0001t0001g0137a0001c0001t0007g0109 | 3 | HG00642.hp1 NA19089.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.583-6348dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63684919 | ||||||
| chrX:63684919
|
GA | G | 1 | a0001c0001t0002g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.583-6348delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63684919 | ||||||
| chrX:63685361
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.583-6789G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63685361 | ||||||
| chrX:63685379
|
C | T | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-6807G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63685379 | ||||||
| chrX:63685868
|
G | T | 1 | a0001c0001t0001g0105 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.583-7296C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63685868 | ||||||
| chrX:63685917
|
CATAAA | C | 1 | a0001c0001t0010g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.583-7350_583-7346d others(7): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63685917 | ||||||
| chrX:63686202
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.583-7630A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63686202 | ||||||
| chrX:63686283
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.583-7711G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63686283 | ||||||
| chrX:63686301
|
G | A | 22 | a0001c0001t0001g0028a0001c0001t0001g0141a0001c0001t0002g0023others(19): Show | 22 | HG01255.hp1 HG02280.hp1 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.583-7729C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63686301 | ||||||
| chrX:63686355
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.583-7783G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63686355 | ||||||
| chrX:63686553
|
T | C | 1 | a0001c0001t0020g0012 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.583-7981A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63686553 | ||||||
| chrX:63687295
|
G | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0103a0001c0001t0001g0132 | 5 | NA18960.hp1 NA18984.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-8723C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63687295 | ||||||
| chrX:63687312
|
A | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0103a0001c0001t0001g0132 | 5 | NA18960.hp1 NA18984.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-8740T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63687312 | ||||||
| chrX:63687846
|
C | T | 10 | a0001c0001t0003g0043a0001c0001t0003g0072a0001c0001t0003g0073others(7): Show | 10 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.583-9274G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63687846 | ||||||
| chrX:63688211
|
T | C | 2 | a0001c0001t0002g0120a0001c0001t0002g0129 | 2 | HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.582+8914A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63688211 | ||||||
| chrX:63688251
|
A | C | 1 | a0001c0001t0002g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.582+8874T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63688251 | ||||||
| chrX:63688475
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.582+8650T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63688475 | ||||||
| chrX:63689311
|
C | T | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+7814G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63689311 | ||||||
| chrX:63689462
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.582+7663G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63689462 | ||||||
| chrX:63689610
|
G | A | 1 | a0001c0001t0002g0009 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.582+7515C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63689610 | ||||||
| chrX:63689625
|
A | C | 1 | a0001c0001t0002g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.582+7500T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63689625 | ||||||
| chrX:63690529
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0116 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.582+6596C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63690529 | ||||||
| chrX:63690575
|
T | C | 11 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(8): Show | 11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.582+6550A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63690575 | ||||||
| chrX:63690847
|
C | T | 2 | a0001c0001t0002g0037a0001c0001t0019g0034 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.582+6278G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63690847 | ||||||
| chrX:63691248
|
T | TA | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.582+5876dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63691248 | ||||||
| chrX:63691312
|
T | A | 8 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(5): Show | 8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.582+5813A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63691312 | ||||||
| chrX:63691703
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.582+5422T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63691703 | ||||||
| chrX:63692106
|
G | A | 2 | a0001c0001t0008g0004a0001c0001t0008g0005 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.582+5019C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63692106 | ||||||
| chrX:63692141
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.582+4984A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63692141 | ||||||
| chrX:63692243
|
G | A | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+4882C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63692243 | ||||||
| chrX:63693092
|
T | G | 11 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(8): Show | 11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.582+4033A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693092 | ||||||
| chrX:63693611
|
C | CA | 28 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0060others(25): Show | 28 | HG00735.hp1 HG00735.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.582+3513dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693611 | ||||||
| chrX:63693611
|
C | CAA | 5 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(2): Show | 5 | HG01243.hp1 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.582+3512_582+3513d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693611 | ||||||
| chrX:63693611
|
C | CAAA | 1 | a0001c0001t0005g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.582+3511_582+3513d others(5): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693611 | ||||||
| chrX:63693611
|
CA | C | 3 | a0001c0001t0001g0062a0001c0001t0014g0045a0002c0002t0015g0011 | 3 | HG01258.hp1 NA18965.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.582+3513delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693611 | ||||||
| chrX:63693630
|
C | A | 3 | a0001c0001t0006g0019a0001c0001t0006g0020a0001c0001t0006g0021 | 3 | HG00639.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.582+3495G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693630 | ||||||
| chrX:63693643
|
A | G | 5 | a0001c0001t0002g0035a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.582+3482T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693643 | ||||||
| chrX:63693687
|
AAAACT | A | 4 | a0001c0001t0001g0124a0001c0001t0001g0139a0001c0001t0002g0147others(1): Show | 4 | HG02602.hp1 HG02735.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+3433_582+3437d others(7): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693687 | ||||||
| chrX:63693725
|
C | T | 11 | a0001c0001t0001g0055a0001c0001t0005g0015a0001c0001t0005g0016others(8): Show | 11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.582+3400G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693725 | ||||||
| chrX:63693952
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.582+3173C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693952 | ||||||
| chrX:63694183
|
C | CA | 12 | a0001c0001t0001g0047a0001c0001t0001g0071a0001c0001t0001g0093others(9): Show | 12 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.582+2941dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63694183 | ||||||
| chrX:63694575
|
T | C | 1 | a0001c0001t0005g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.582+2550A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63694575 | ||||||
| chrX:63694638
|
C | T | 1 | a0001c0001t0021g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.582+2487G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63694638 | ||||||
| chrX:63694695
|
T | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0160 | 3 | NA18971.hp1 NA19004.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.582+2430A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63694695 | ||||||
| chrX:63694868
|
T | C | 2 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.582+2257A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63694868 | ||||||
| chrX:63695235
|
G | A | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.582+1890C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63695235 | ||||||
| chrX:63695530
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.582+1595A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63695530 | ||||||
| chrX:63695624
|
C | G | 2 | a0001c0001t0001g0010a0002c0002t0015g0011 | 2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.582+1501G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63695624 | ||||||
| chrX:63696298
|
TA | T | 1 | a0001c0001t0001g0077 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.582+826delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63696298 | ||||||
| chrX:63696450
|
C | A | 8 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(5): Show | 8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.582+675G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63696450 | ||||||
| chrX:63697018
|
T | C | 15 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(12): Show | 15 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.582+107A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63697018 | ||||||
| chrX:63697395
|
C | A | 1 | a0001c0001t0002g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.403-91G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63697395 | ||||||
| chrX:63697796
|
T | C | 14 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(11): Show | 14 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.403-492A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63697796 | ||||||
| chrX:63697903
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.403-599T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63697903 | ||||||
| chrX:63698109
|
T | TTA | 1 | a0001c0001t0017g0003 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.403-807_403-806dup others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63698109 | ||||||
| chrX:63698609
|
G | A | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.403-1305C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63698609 | ||||||
| chrX:63699052
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.403-1748A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63699052 | ||||||
| chrX:63699078
|
G | C | 4 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065others(1): Show | 4 | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-1774C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63699078 | ||||||
| chrX:63699521
|
A | G | 16 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.403-2217T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63699521 | ||||||
| chrX:63699804
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.403-2500T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63699804 | ||||||
| chrX:63700045
|
G | C | 1 | a0001c0001t0002g0064 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.403-2741C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63700045 | ||||||
| chrX:63700873
|
C | G | 2 | a0001c0001t0002g0037a0001c0001t0019g0034 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.403-3569G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63700873 | ||||||
| chrX:63701092
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.403-3788G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63701092 | ||||||
| chrX:63701357
|
C | CT | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.403-4054dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63701357 | ||||||
| chrX:63701553
|
T | C | 1 | a0001c0001t0017g0003 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.403-4249A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63701553 | ||||||
| chrX:63701628
|
G | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-4324C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63701628 | ||||||
| chrX:63701719
|
G | A | 1 | a0001c0001t0002g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.403-4415C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63701719 | ||||||
| chrX:63701842
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.402+4416C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63701842 | ||||||
| chrX:63702222
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.402+4036A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63702222 | ||||||
| chrX:63702956
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.402+3302C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63702956 | ||||||
| chrX:63703394
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.402+2864G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63703394 | ||||||
| chrX:63703635
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.402+2623G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63703635 | ||||||
| chrX:63704074
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.402+2184T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704074 | ||||||
| chrX:63704397
|
C | T | 10 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(7): Show | 10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.402+1861G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704397 | ||||||
| chrX:63704463
|
G | GA | 1 | a0001c0001t0001g0094 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.402+1794dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704463 | ||||||
| chrX:63704514
|
G | A | 1 | a0001c0001t0002g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.402+1744C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704514 | ||||||
| chrX:63704525
|
T | A | 5 | a0001c0001t0002g0031a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+1733A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704525 | ||||||
| chrX:63704608
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0161 | 2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.402+1650C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704608 | ||||||
| chrX:63704695
|
T | C | 2 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.402+1563A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704695 | ||||||
| chrX:63704857
|
G | T | 1 | a0001c0001t0002g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.402+1401C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704857 | ||||||
| chrX:63704858
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.402+1400G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704858 | ||||||
| chrX:63705357
|
A | ATG | 3 | a0001c0001t0001g0040a0001c0001t0001g0113a0001c0001t0020g0012 | 3 | HG00673.hp1 HG00738.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.402+899_402+900dup others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | ||||||
| chrX:63705357
|
A | ATGTG | 3 | a0001c0001t0001g0039a0001c0001t0006g0020a0001c0001t0006g0021 | 3 | HG00639.hp2 HG01070.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.402+897_402+900dup others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | ||||||
| chrX:63705357
|
A | ATGTGTG | 1 | a0001c0001t0021g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.402+895_402+900dup others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | ||||||
| chrX:63705357
|
ATG | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(108): Show | 114 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(111): Show |
intron_variant | MODIFIER | c.402+899_402+900del others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | ||||||
| chrX:63705357
|
ATGTG | A | 9 | a0001c0001t0001g0053a0001c0001t0001g0078a0001c0001t0001g0084others(6): Show | 9 | HG00735.hp1 HG01943.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+897_402+900del others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | ||||||
| chrX:63705357
|
ATGTGTG | A | 2 | a0001c0001t0002g0150a0003c0003t0022g0038 | 2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.402+895_402+900del others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | ||||||
| chrX:63705357
|
ATGTGTGT others(1): Show |
A | 1 | a0001c0001t0001g0077 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.402+893_402+900del others(8): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | ||||||
| chrX:63705357
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.402+885_402+900del others(16): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | ||||||
| chrX:63705374
|
T | C | 7 | a0001c0001t0003g0043a0001c0001t0003g0072a0001c0001t0003g0073others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.402+884A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705374 | ||||||
| chrX:63705401
|
GT | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0097 | 2 | HG00639.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.402+856delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705401 | ||||||
| chrX:63705402
|
T | TGTG | 1 | a0001c0001t0006g0019 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.402+855_402+856ins others(3): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705402 | ||||||
| chrX:63705706
|
A | T | 1 | a0001c0001t0013g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.402+552T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705706 | ||||||
| chrX:63705717
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.402+541G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705717 | ||||||
| chrX:63705742
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.402+516A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705742 | ||||||
| chrX:63706668
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.211-219C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63706668 | ||||||
| chrX:63706792
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.211-343G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63706792 | ||||||
| chrX:63707360
|
T | TA | 24 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0044others(21): Show | 24 | HG00609.hp1 HG00673.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.211-912dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63707360 | ||||||
| chrX:63707360
|
T | TAAAA | 1 | a0001c0001t0001g0165 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.211-915_211-912dup others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63707360 | ||||||
| chrX:63707360
|
T | TG | 2 | a0001c0001t0001g0160a0001c0001t0002g0110 | 2 | NA19082.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.211-912_211-911ins others(1): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63707360 | ||||||
| chrX:63707360
|
TA | T | 8 | a0001c0001t0001g0139a0001c0001t0005g0015a0001c0001t0005g0016others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-912delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63707360 | ||||||
| chrX:63707361
|
A | G | 4 | a0001c0001t0001g0081a0001c0001t0001g0112a0001c0001t0001g0121others(1): Show | 4 | NA18971.hp1 NA18986.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-912T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63707361 | ||||||
| chrX:63707475
|
A | AC | 1 | a0001c0001t0005g0022 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.211-1027dupG | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63707475 | ||||||
| chrX:63708133
|
CA | C | 1 | a0001c0001t0002g0076 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.211-1685delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63708133 | ||||||
| chrX:63708178
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.211-1729T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63708178 | ||||||
| chrX:63708266
|
T | C | 11 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(8): Show | 11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.211-1817A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63708266 | ||||||
| chrX:63708745
|
A | C | 1 | a0001c0001t0003g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.211-2296T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63708745 | ||||||
| chrX:63708760
|
T | C | 12 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(9): Show | 12 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.211-2311A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63708760 | ||||||
| chrX:63709057
|
C | T | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.211-2608G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63709057 | ||||||
| chrX:63709193
|
G | T | 4 | a0001c0001t0002g0013a0001c0001t0003g0041a0001c0001t0003g0102others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-2744C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63709193 | ||||||
| chrX:63709195
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.211-2746A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63709195 | ||||||
| chrX:63709474
|
T | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-3025A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63709474 | ||||||
| chrX:63709770
|
G | A | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-3321C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63709770 | ||||||
| chrX:63709944
|
G | A | 13 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(10): Show | 13 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.211-3495C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63709944 | ||||||
| chrX:63710296
|
G | GA | 46 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0028others(43): Show | 48 | HG00609.hp1 HG00735.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.211-3848dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63710296 | ||||||
| chrX:63710296
|
G | GAA | 4 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0100others(1): Show | 4 | HG02896.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-3849_211-3848d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63710296 | ||||||
| chrX:63710296
|
GA | G | 10 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0051others(7): Show | 10 | HG00621.hp1 HG00673.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-3848delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63710296 | ||||||
| chrX:63710499
|
G | A | 5 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-4050C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63710499 | ||||||
| chrX:63710722
|
A | G | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-4273T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63710722 | ||||||
| chrX:63710817
|
C | T | 3 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0022 | 3 | HG01243.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.211-4368G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63710817 | ||||||
| chrX:63710942
|
C | CA | 2 | a0001c0001t0001g0161a0001c0001t0002g0147 | 2 | HG00140.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.211-4494dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63710942 | ||||||
| chrX:63711677
|
T | C | 10 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(7): Show | 10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.211-5228A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63711677 | ||||||
| chrX:63712502
|
G | A | 2 | a0001c0001t0008g0004a0001c0001t0008g0005 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.211-6053C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63712502 | ||||||
| chrX:63712543
|
T | TTTG | 1 | a0001c0001t0001g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.211-6095_211-6094i others(5): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63712543 | ||||||
| chrX:63712789
|
T | C | 11 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(8): Show | 11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.211-6340A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63712789 | ||||||
| chrX:63712992
|
T | A | 1 | a0001c0001t0002g0063 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.211-6543A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63712992 | ||||||
| chrX:63713312
|
C | T | 10 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(7): Show | 10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.211-6863G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713312 | ||||||
| chrX:63713387
|
T | A | 1 | a0001c0001t0008g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.211-6938A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713387 | ||||||
| chrX:63713494
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.211-7045G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713494 | ||||||
| chrX:63713701
|
T | TAC | 2 | a0001c0001t0001g0054a0001c0001t0002g0100 | 2 | HG03579.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.211-7254_211-7253d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | ||||||
| chrX:63713701
|
T | TACAC | 41 | a0001c0001t0001g0028a0001c0001t0001g0089a0001c0001t0001g0137others(38): Show | 41 | HG00642.hp1 HG01167.hp1 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.211-7256_211-7253d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | ||||||
| chrX:63713701
|
T | TACACAC | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.211-7258_211-7253d others(8): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | ||||||
| chrX:63713701
|
T | TACACACA others(1): Show |
7 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.211-7260_211-7253d others(10): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | ||||||
| chrX:63713701
|
T | TACACACA others(3): Show |
3 | a0001c0001t0006g0019a0001c0001t0006g0020a0001c0001t0006g0021 | 3 | HG00639.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.211-7262_211-7253d others(12): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | ||||||
| chrX:63713701
|
T | TACACACA others(5): Show |
2 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.211-7264_211-7253d others(14): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | ||||||
| chrX:63713701
|
T | TACACACA others(7): Show |
1 | a0001c0001t0017g0003 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.211-7266_211-7253d others(16): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | ||||||
| chrX:63713701
|
TAC | T | 6 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 6 | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-7254_211-7253d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | ||||||
| chrX:63713733
|
C | CA | 1 | a0001c0001t0004g0058 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.211-7285_211-7284i others(3): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713733 | ||||||
| chrX:63714700
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.211-8251G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63714700 | ||||||
| chrX:63715341
|
C | T | 6 | a0001c0001t0001g0092a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG02015.hp1 HG02074.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-8892G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715341 | ||||||
| chrX:63715385
|
GCT | G | 3 | a0001c0001t0001g0047a0001c0001t0001g0071a0001c0001t0001g0143 | 3 | NA18953.hp1 NA18955.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.211-8938_211-8937d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715385 | ||||||
| chrX:63715388
|
G | A | 3 | a0001c0001t0001g0047a0001c0001t0001g0071a0001c0001t0001g0143 | 3 | NA18953.hp1 NA18955.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.211-8939C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715388 | ||||||
| chrX:63715445
|
G | GA | 5 | a0001c0001t0001g0060a0001c0001t0001g0130a0001c0001t0006g0019others(2): Show | 5 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-8997dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715445 | ||||||
| chrX:63715445
|
GA | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0126 | 2 | HG01099.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.211-8997delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715445 | ||||||
| chrX:63715621
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.210+8911A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715621 | ||||||
| chrX:63715765
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.210+8767G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715765 | ||||||
| chrX:63715769
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.210+8763T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715769 | ||||||
| chrX:63715776
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.210+8756T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715776 | ||||||
| chrX:63715867
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.210+8665A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715867 | ||||||
| chrX:63716292
|
G | T | 4 | a0001c0001t0002g0013a0001c0001t0003g0041a0001c0001t0003g0102others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+8240C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63716292 | ||||||
| chrX:63716293
|
A | T | 4 | a0001c0001t0002g0013a0001c0001t0003g0041a0001c0001t0003g0102others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+8239T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63716293 | ||||||
| chrX:63716536
|
T | C | 8 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(5): Show | 8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+7996A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63716536 | ||||||
| chrX:63717422
|
T | C | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.210+7110A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63717422 | ||||||
| chrX:63717452
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.210+7080C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63717452 | ||||||
| chrX:63717884
|
A | T | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.210+6648T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63717884 | ||||||
| chrX:63717947
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0155 | 2 | HG01433.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.210+6585C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63717947 | ||||||
| chrX:63718123
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.210+6409G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63718123 | ||||||
| chrX:63718919
|
T | C | 10 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(7): Show | 10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.210+5613A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63718919 | ||||||
| chrX:63718929
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0019g0034 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.210+5603C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63718929 | ||||||
| chrX:63719459
|
G | T | 1 | a0001c0001t0002g0009 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.210+5073C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63719459 | ||||||
| chrX:63719812
|
C | T | 5 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+4720G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63719812 | ||||||
| chrX:63720142
|
A | T | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.210+4390T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63720142 | ||||||
| chrX:63720367
|
A | G | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(3): Show | 6 | HG00735.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+4165T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63720367 | ||||||
| chrX:63720388
|
C | T | 1 | a0001c0001t0020g0012 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.210+4144G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63720388 | ||||||
| chrX:63720919
|
T | C | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.210+3613A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63720919 | ||||||
| chrX:63722410
|
G | GT | 11 | a0001c0001t0001g0010a0001c0001t0001g0053a0001c0001t0001g0068others(8): Show | 11 | HG01074.hp1 HG02074.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+2121dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63722410 | ||||||
| chrX:63722410
|
GT | G | 1 | a0001c0001t0003g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.210+2121delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63722410 | ||||||
| chrX:63722416
|
T | TG | 1 | a0001c0001t0017g0003 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.210+2115_210+2116i others(3): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63722416 | ||||||
| chrX:63722459
|
G | T | 4 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065others(1): Show | 4 | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+2073C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63722459 | ||||||
| chrX:63722772
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.210+1760G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63722772 | ||||||
| chrX:63722884
|
T | G | 32 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(29): Show | 32 | HG00280.hp1 HG01099.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.210+1648A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63722884 | ||||||
| chrX:63722981
|
C | T | 1 | a0001c0001t0021g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.210+1551G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63722981 | ||||||
| chrX:63723144
|
A | G | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0011g0048 | 3 | HG02738.hp1 NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.210+1388T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63723144 | ||||||
| chrX:63723599
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0062 | 2 | HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.210+933C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63723599 | ||||||
| chrX:63724141
|
TA | T | 1 | a0001c0001t0017g0003 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.210+390delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63724141 | ||||||
| chrX:63724159
|
T | C | 4 | a0001c0001t0002g0013a0001c0001t0003g0041a0001c0001t0003g0102others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+373A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63724159 | ||||||
| chrX:63724871
|
G | A | 8 | a0001c0001t0003g0043a0001c0001t0003g0072a0001c0001t0003g0073others(5): Show | 8 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-160C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63724871 | ||||||
| chrX:63725229
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.31-518T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63725229 | ||||||
| chrX:63725329
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(161): Show | 167 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(164): Show |
intron_variant | MODIFIER | c.31-618A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63725329 | ||||||
| chrX:63725425
|
A | G | 1 | a0001c0001t0021g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.31-714T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63725425 | ||||||
| chrX:63726067
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-1356C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726067 | ||||||
| chrX:63726191
|
T | TA | 13 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.31-1481dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726191 | ||||||
| chrX:63726441
|
C | T | 1 | a0001c0001t0007g0138 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.31-1730G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726441 | ||||||
| chrX:63726524
|
A | C | 2 | a0001c0001t0008g0004a0001c0001t0008g0005 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.31-1813T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726524 | ||||||
| chrX:63726704
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.31-1993A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726704 | ||||||
| chrX:63726769
|
G | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-2058C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726769 | ||||||
| chrX:63726975
|
A | G | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-2264T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726975 | ||||||
| chrX:63727602
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.31-2891C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63727602 | ||||||
| chrX:63727906
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.31-3195A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63727906 | ||||||
| chrX:63728452
|
G | A | 7 | a0001c0001t0003g0043a0001c0001t0003g0072a0001c0001t0003g0073others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-3741C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63728452 | ||||||
| chrX:63728481
|
T | A | 1 | a0001c0001t0001g0133 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.31-3770A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63728481 | ||||||
| chrX:63728749
|
A | T | 1 | a0001c0001t0020g0012 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.31-4038T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63728749 | ||||||
| chrX:63729376
|
T | C | 1 | a0001c0001t0002g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.31-4665A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63729376 | ||||||
| chrX:63729673
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.31-4962G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63729673 | ||||||
| chrX:63729911
|
C | A | 1 | a0001c0001t0001g0133 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.31-5200G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63729911 | ||||||
| chrX:63729981
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.31-5270A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63729981 | ||||||
| chrX:63730211
|
G | T | 1 | a0001c0001t0002g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-5500C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63730211 | ||||||
| chrX:63730372
|
G | T | 1 | a0001c0001t0001g0014 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.31-5661C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63730372 | ||||||
| chrX:63731333
|
CTAGATTC others(241): Show |
C | 2 | a0001c0001t0001g0028a0001c0001t0002g0027 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.31-6870_31-6623del | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731333 | ||||||
| chrX:63731552
|
G | GT | 24 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0092others(21): Show | 24 | HG00639.hp2 HG01071.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-6842dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731552 | ||||||
| chrX:63731552
|
G | GTT | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.31-6843_31-6842dup others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731552 | ||||||
| chrX:63731552
|
G | GTTTTT | 1 | a0001c0001t0001g0136 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.31-6846_31-6842dup others(5): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731552 | ||||||
| chrX:63731552
|
GT | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0131a0001c0001t0001g0152others(1): Show | 4 | HG01167.hp1 HG01943.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-6842delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731552 | ||||||
| chrX:63731669
|
C | T | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.31-6958G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731669 | ||||||
| chrX:63731725
|
A | G | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-7014T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731725 | ||||||
| chrX:63731859
|
C | T | 2 | a0001c0001t0001g0010a0002c0002t0015g0011 | 2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.31-7148G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731859 | ||||||
| chrX:63731868
|
GT | G | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-7158delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731868 | ||||||
| chrX:63731898
|
A | C | 1 | a0001c0001t0001g0137 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-7187T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731898 | ||||||
| chrX:63731975
|
G | A | 2 | a0001c0001t0002g0120a0001c0001t0002g0129 | 2 | HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.31-7264C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731975 | ||||||
| chrX:63732006
|
C | T | 1 | a0001c0001t0002g0110 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.31-7295G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63732006 | ||||||
| chrX:63732264
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.31-7553A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63732264 | ||||||
| chrX:63732769
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0160 | 3 | NA18971.hp1 NA19004.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.31-8058C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63732769 | ||||||
| chrX:63732854
|
T | C | 3 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0022 | 3 | HG01243.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.31-8143A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63732854 | ||||||
| chrX:63733087
|
T | C | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.31-8376A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63733087 | ||||||
| chrX:63733216
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.31-8505C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63733216 | ||||||
| chrX:63733583
|
T | C | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-8872A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63733583 | ||||||
| chrX:63734252
|
C | A | 1 | a0001c0001t0002g0147 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.31-9541G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63734252 | ||||||
| chrX:63734447
|
C | T | 1 | a0001c0001t0003g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.31-9736G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63734447 | ||||||
| chrX:63734571
|
T | C | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-9860A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63734571 | ||||||
| chrX:63735460
|
A | G | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-10749T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63735460 | ||||||
| chrX:63735578
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.31-10867C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63735578 | ||||||
| chrX:63736131
|
C | T | 5 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-11420G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63736131 | ||||||
| chrX:63736900
|
T | TA | 2 | a0001c0001t0003g0041a0001c0001t0003g0151 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.31-12190dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63736900 | ||||||
| chrX:63737634
|
C | G | 1 | a0001c0001t0002g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.31-12923G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63737634 | ||||||
| chrX:63737923
|
T | C | 4 | a0001c0001t0002g0013a0001c0001t0003g0041a0001c0001t0003g0102others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-13212A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63737923 | ||||||
| chrX:63737978
|
A | T | 4 | a0001c0001t0002g0013a0001c0001t0003g0041a0001c0001t0003g0102others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-13267T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63737978 | ||||||
| chrX:63738160
|
A | T | 1 | a0001c0001t0002g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.31-13449T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63738160 | ||||||
| chrX:63738563
|
C | T | 10 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(7): Show | 10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-13852G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63738563 | ||||||
| chrX:63738880
|
T | C | 1 | a0001c0001t0002g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.31-14169A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63738880 | ||||||
| chrX:63739094
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.31-14383A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63739094 | ||||||
| chrX:63739174
|
G | T | 2 | a0001c0001t0002g0098a0001c0001t0002g0157 | 2 | HG02257.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.31-14463C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63739174 | ||||||
| chrX:63739368
|
A | T | 57 | a0001c0001t0001g0028a0001c0001t0001g0089a0001c0001t0001g0137others(54): Show | 57 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.31-14657T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63739368 | ||||||
| chrX:63739514
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.31-14803C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63739514 | ||||||
| chrX:63739963
|
C | T | 1 | a0001c0001t0005g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.31-15252G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63739963 | ||||||
| chrX:63739979
|
T | A | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.31-15268A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63739979 | ||||||
| chrX:63740283
|
CTT | C | 1 | a0001c0001t0017g0003 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.31-15574_31-15573d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63740283 | ||||||
| chrX:63740335
|
G | C | 2 | a0001c0001t0008g0004a0001c0001t0008g0005 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.31-15624C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63740335 | ||||||
| chrX:63740696
|
A | C | 13 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.31-15985T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63740696 | ||||||
| chrX:63741088
|
A | G | 13 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.31-16377T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63741088 | ||||||
| chrX:63741668
|
C | T | 5 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-16957G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63741668 | ||||||
| chrX:63742207
|
A | G | 3 | a0001c0001t0006g0019a0001c0001t0006g0020a0001c0001t0006g0021 | 3 | HG00639.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.31-17496T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63742207 | ||||||
| chrX:63742304
|
C | T | 5 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-17593G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63742304 | ||||||
| chrX:63742785
|
A | T | 2 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.31-18074T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63742785 | ||||||
| chrX:63743065
|
G | A | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-18354C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63743065 | ||||||
| chrX:63743209
|
T | TAAAC | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(161): Show | 167 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(164): Show |
intron_variant | MODIFIER | c.31-18502_31-18499d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63743209 | ||||||
| chrX:63743854
|
G | A | 55 | a0001c0001t0001g0028a0001c0001t0001g0089a0001c0001t0001g0137others(52): Show | 55 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.31-19143C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63743854 | ||||||
| chrX:63743872
|
G | A | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-19161C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63743872 | ||||||
| chrX:63743974
|
G | GC | 2 | a0001c0001t0008g0004a0001c0001t0008g0005 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.31-19264dupG | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63743974 | ||||||
| chrX:63744712
|
A | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.31-20001T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63744712 | ||||||
| chrX:63744843
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0164a0001c0001t0001g0165 | 3 | HG00735.hp2 HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.31-20132A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63744843 | ||||||
| chrX:63745710
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.31-20999G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63745710 | ||||||
| chrX:63746145
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0161 | 2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.31-21434G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63746145 | ||||||
| chrX:63746610
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.31-21899G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63746610 | ||||||
| chrX:63746738
|
C | T | 1 | a0001c0001t0005g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.31-22027G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63746738 | ||||||
| chrX:63748168
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.31-23457G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63748168 | ||||||
| chrX:63748329
|
T | C | 1 | a0001c0001t0007g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.31-23618A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63748329 | ||||||
| chrX:63749254
|
C | T | 15 | a0001c0001t0001g0028a0001c0001t0002g0023a0001c0001t0002g0024others(12): Show | 15 | HG01255.hp1 HG02622.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-24543G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63749254 | ||||||
| chrX:63749337
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31-24626G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63749337 | ||||||
| chrX:63749835
|
T | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-25124A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63749835 | ||||||
| chrX:63749864
|
C | T | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.31-25153G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63749864 | ||||||
| chrX:63750129
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0090 | 3 | NA18961.hp1 NA18990.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.31-25418C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63750129 | ||||||
| chrX:63750706
|
C | T | 1 | a0001c0001t0021g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.31-25995G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63750706 | ||||||
| chrX:63750866
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.31-26155C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63750866 | ||||||
| chrX:63750936
|
A | G | 15 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(12): Show | 15 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-26225T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63750936 | ||||||
| chrX:63751007
|
T | G | 1 | a0001c0001t0001g0104 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.31-26296A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63751007 | ||||||
| chrX:63752013
|
G | GA | 1 | a0001c0001t0001g0077 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.31-27303dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63752013 | ||||||
| chrX:63752073
|
C | CA | 2 | a0001c0001t0001g0028a0001c0001t0002g0027 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.31-27363dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63752073 | ||||||
| chrX:63752508
|
G | GA | 1 | a0001c0001t0007g0138 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.31-27798dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63752508 | ||||||
| chrX:63753349
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.31-28638T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63753349 | ||||||
| chrX:63753539
|
TG | T | 1 | a0001c0001t0001g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.31-28829delC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63753539 | ||||||
| chrX:63753543
|
G | GT | 3 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0103 | 3 | HG01192.hp1 NA19000.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.31-28833dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63753543 | ||||||
| chrX:63753543
|
G | GTT | 9 | a0001c0001t0001g0008a0001c0001t0005g0015a0001c0001t0005g0016others(6): Show | 9 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-28834_31-28833d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63753543 | ||||||
| chrX:63753543
|
G | T | 1 | a0001c0001t0020g0012 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.31-28832C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63753543 | ||||||
| chrX:63753543
|
GT | G | 5 | a0001c0001t0001g0124a0001c0001t0001g0139a0001c0001t0002g0098others(2): Show | 5 | HG02257.hp2 HG02602.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-28833delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63753543 | ||||||
| chrX:63754408
|
A | AT | 9 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0134others(6): Show | 9 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-29698dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63754408 | ||||||
| chrX:63754408
|
AT | A | 1 | a0001c0001t0001g0051 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.31-29698delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63754408 | ||||||
| chrX:63755249
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.30+29867G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63755249 | ||||||
| chrX:63755284
|
A | G | 1 | a0001c0001t0002g0076 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.30+29832T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63755284 | ||||||
| chrX:63755862
|
A | T | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(3): Show | 6 | HG02280.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+29254T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63755862 | ||||||
| chrX:63756290
|
T | C | 8 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(5): Show | 8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+28826A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63756290 | ||||||
| chrX:63756421
|
C | CA | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.30+28694dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63756421 | ||||||
| chrX:63756442
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.30+28674T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63756442 | ||||||
| chrX:63756557
|
A | G | 1 | a0001c0001t0016g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.30+28559T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63756557 | ||||||
| chrX:63757515
|
G | A | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0013g0066 | 3 | HG00280.hp1 HG01099.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.30+27601C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63757515 | ||||||
| chrX:63757822
|
A | T | 1 | a0001c0001t0002g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.30+27294T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63757822 | ||||||
| chrX:63758054
|
T | A | 2 | a0001c0001t0008g0004a0001c0001t0008g0005 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.30+27062A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63758054 | ||||||
| chrX:63758127
|
C | CT | 4 | a0001c0001t0001g0044a0001c0001t0001g0104a0001c0001t0001g0162others(1): Show | 4 | HG02738.hp1 NA18945.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+26988dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63758127 | ||||||
| chrX:63758127
|
CT | C | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.30+26988delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63758127 | ||||||
| chrX:63758391
|
C | G | 1 | a0001c0001t0002g0023 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.30+26725G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63758391 | ||||||
| chrX:63758414
|
T | G | 2 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.30+26702A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63758414 | ||||||
| chrX:63758437
|
A | C | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+26679T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63758437 | ||||||
| chrX:63758913
|
G | A | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+26203C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63758913 | ||||||
| chrX:63759218
|
C | A | 4 | a0001c0001t0002g0013a0001c0001t0003g0041a0001c0001t0003g0102others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+25898G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63759218 | ||||||
| chrX:63759275
|
T | A | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+25841A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63759275 | ||||||
| chrX:63759854
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.30+25262T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63759854 | ||||||
| chrX:63760024
|
C | G | 10 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(7): Show | 10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+25092G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760024 | ||||||
| chrX:63760094
|
GA | G | 3 | a0001c0001t0001g0028a0001c0001t0002g0027a0001c0001t0018g0140 | 3 | HG02922.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.30+25021delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760094 | ||||||
| chrX:63760304
|
T | C | 1 | a0001c0001t0002g0009 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.30+24812A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760304 | ||||||
| chrX:63760579
|
A | C | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+24537T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760579 | ||||||
| chrX:63760704
|
G | T | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+24412C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760704 | ||||||
| chrX:63760753
|
G | T | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+24363C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760753 | ||||||
| chrX:63760880
|
C | A | 1 | a0001c0001t0001g0128 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.30+24236G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760880 | ||||||
| chrX:63761439
|
A | G | 1 | a0001c0001t0004g0052 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+23677T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63761439 | ||||||
| chrX:63761565
|
C | G | 1 | a0001c0001t0001g0002 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.30+23551G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63761565 | ||||||
| chrX:63762046
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.30+23070C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63762046 | ||||||
| chrX:63762068
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.30+23048G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63762068 | ||||||
| chrX:63762147
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.30+22969C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63762147 | ||||||
| chrX:63762735
|
T | G | 1 | a0001c0001t0007g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.30+22381A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63762735 | ||||||
| chrX:63762787
|
C | G | 2 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.30+22329G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63762787 | ||||||
| chrX:63764052
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.30+21064A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63764052 | ||||||
| chrX:63764592
|
G | A | 2 | a0001c0001t0003g0041a0001c0001t0003g0151 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.30+20524C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63764592 | ||||||
| chrX:63764621
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0132 | 2 | NA19000.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.30+20495T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63764621 | ||||||
| chrX:63764947
|
C | T | 1 | a0001c0001t0002g0076 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.30+20169G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63764947 | ||||||
| chrX:63764948
|
G | A | 1 | a0001c0001t0021g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.30+20168C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63764948 | ||||||
| chrX:63765363
|
A | G | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG02738.hp1 NA18966.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+19753T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63765363 | ||||||
| chrX:63765699
|
CG | C | 1 | a0001c0001t0002g0009 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.30+19416delC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63765699 | ||||||
| chrX:63765799
|
G | A | 6 | a0001c0001t0001g0092a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG02015.hp1 HG02074.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+19317C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63765799 | ||||||
| chrX:63766058
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.30+19058A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63766058 | ||||||
| chrX:63766061
|
A | C | 12 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(9): Show | 12 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+19055T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63766061 | ||||||
| chrX:63766454
|
T | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+18662A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63766454 | ||||||
| chrX:63766961
|
A | C | 2 | a0001c0001t0006g0019a0001c0001t0006g0020 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.30+18155T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63766961 | ||||||
| chrX:63767412
|
TA | T | 1 | a0001c0001t0002g0009 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.30+17703delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63767412 | ||||||
| chrX:63767545
|
A | C | 15 | a0001c0001t0001g0028a0001c0001t0002g0023a0001c0001t0002g0024others(12): Show | 15 | HG01255.hp1 HG02622.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.30+17571T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63767545 | ||||||
| chrX:63767790
|
C | T | 53 | a0001c0001t0001g0028a0001c0001t0002g0013a0001c0001t0002g0023others(50): Show | 53 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.30+17326G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63767790 | ||||||
| chrX:63767801
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.30+17315C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63767801 | ||||||
| chrX:63767860
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.30+17256A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63767860 | ||||||
| chrX:63768070
|
T | A | 1 | a0001c0001t0001g0002 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.30+17046A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63768070 | ||||||
| chrX:63768205
|
C | T | 1 | a0001c0001t0020g0012 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.30+16911G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63768205 | ||||||
| chrX:63768223
|
C | A | 1 | a0001c0001t0001g0132 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.30+16893G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63768223 | ||||||
| chrX:63768475
|
C | A | 2 | a0001c0001t0005g0017a0001c0001t0005g0018 | 2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.30+16641G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63768475 | ||||||
| chrX:63768759
|
T | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+16357A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63768759 | ||||||
| chrX:63768988
|
T | TA | 1 | a0001c0001t0001g0040 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.30+16127dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63768988 | ||||||
| chrX:63768988
|
TA | T | 1 | a0001c0001t0003g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.30+16127delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63768988 | ||||||
| chrX:63769438
|
G | GA | 2 | a0001c0001t0001g0133a0001c0001t0009g0007 | 2 | HG02922.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.30+15677dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63769438 | ||||||
| chrX:63769890
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.30+15226C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63769890 | ||||||
| chrX:63769998
|
G | A | 5 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+15118C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63769998 | ||||||
| chrX:63770172
|
A | G | 13 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+14944T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63770172 | ||||||
| chrX:63770173
|
T | C | 16 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.30+14943A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63770173 | ||||||
| chrX:63770516
|
C | T | 1 | a0001c0001t0020g0012 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.30+14600G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63770516 | ||||||
| chrX:63770598
|
C | G | 1 | a0001c0001t0002g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.30+14518G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63770598 | ||||||
| chrX:63770958
|
C | T | 1 | a0001c0001t0021g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.30+14158G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63770958 | ||||||
| chrX:63771573
|
C | CT | 9 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(6): Show | 9 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+13542dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63771573 | ||||||
| chrX:63771659
|
T | C | 15 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(12): Show | 15 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.30+13457A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63771659 | ||||||
| chrX:63771719
|
A | T | 1 | a0001c0001t0003g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+13397T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63771719 | ||||||
| chrX:63771748
|
GTAGA | G | 2 | a0001c0001t0003g0072a0001c0001t0003g0073 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.30+13364_30+13367d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63771748 | ||||||
| chrX:63771936
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0148 | 2 | NA18944.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.30+13180A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63771936 | ||||||
| chrX:63772277
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.30+12839C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63772277 | ||||||
| chrX:63772358
|
A | G | 8 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(5): Show | 8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+12758T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63772358 | ||||||
| chrX:63772409
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0135a0001c0001t0001g0155others(3): Show | 6 | HG00735.hp2 HG01109.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+12707A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63772409 | ||||||
| chrX:63772416
|
C | T | 1 | a0001c0001t0003g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.30+12700G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63772416 | ||||||
| chrX:63772906
|
C | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 4 | NA18953.hp1 NA18955.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+12210G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63772906 | ||||||
| chrX:63773116
|
C | T | 1 | a0001c0001t0021g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.30+12000G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63773116 | ||||||
| chrX:63773117
|
A | G | 1 | a0001c0001t0021g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.30+11999T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63773117 | ||||||
| chrX:63773866
|
A | G | 4 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(1): Show | 4 | HG00639.hp1 HG01070.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+11250T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63773866 | ||||||
| chrX:63774045
|
A | ATATC | 1 | a0001c0001t0013g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.30+11067_30+11070d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63774045 | ||||||
| chrX:63774045
|
ATATC | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(78): Show | 83 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.30+11067_30+11070d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63774045 | ||||||
| chrX:63774045
|
ATATCTAT others(1): Show |
A | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0139others(12): Show | 15 | HG00621.hp1 HG00639.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.30+11063_30+11070d others(10): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63774045 | ||||||
| chrX:63774045
|
ATATCTAT others(5): Show |
A | 1 | a0001c0001t0005g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.30+11059_30+11070d others(14): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63774045 | ||||||
| chrX:63774046
|
TATC | T | 1 | a0001c0001t0002g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.30+11067_30+11069d others(5): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63774046 | ||||||
| chrX:63774518
|
C | G | 4 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065others(1): Show | 4 | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+10598G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63774518 | ||||||
| chrX:63774537
|
T | C | 1 | a0001c0001t0002g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.30+10579A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63774537 | ||||||
| chrX:63775059
|
G | C | 12 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(9): Show | 12 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+10057C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775059 | ||||||
| chrX:63775102
|
A | C | 5 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+10014T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775102 | ||||||
| chrX:63775130
|
A | T | 4 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065others(1): Show | 4 | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+9986T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775130 | ||||||
| chrX:63775148
|
T | A | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+9968A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775148 | ||||||
| chrX:63775407
|
C | T | 19 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0049others(16): Show | 19 | HG01258.hp1 HG01261.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+9709G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775407 | ||||||
| chrX:63775504
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.30+9612G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775504 | ||||||
| chrX:63775522
|
G | A | 1 | a0001c0001t0018g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+9594C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775522 | ||||||
| chrX:63775529
|
T | C | 1 | a0001c0001t0005g0022 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.30+9587A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775529 | ||||||
| chrX:63775726
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.30+9390T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775726 | ||||||
| chrX:63775792
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0014g0045 | 2 | NA18945.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.30+9324T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775792 | ||||||
| chrX:63775859
|
C | A | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+9257G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775859 | ||||||
| chrX:63775931
|
G | T | 1 | a0001c0001t0005g0015 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.30+9185C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775931 | ||||||
| chrX:63776005
|
C | T | 5 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+9111G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63776005 | ||||||
| chrX:63776239
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.30+8877G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63776239 | ||||||
| chrX:63776402
|
G | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+8714C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63776402 | ||||||
| chrX:63777212
|
A | G | 1 | a0001c0001t0003g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.30+7904T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777212 | ||||||
| chrX:63777315
|
C | A | 1 | a0001c0001t0001g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.30+7801G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777315 | ||||||
| chrX:63777444
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.30+7672G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777444 | ||||||
| chrX:63777537
|
C | G | 2 | a0001c0001t0003g0041a0001c0001t0003g0151 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.30+7579G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777537 | ||||||
| chrX:63777659
|
T | C | 3 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0022 | 3 | HG01243.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.30+7457A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777659 | ||||||
| chrX:63777685
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.30+7431C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777685 | ||||||
| chrX:63777743
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG00673.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.30+7373G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777743 | ||||||
| chrX:63778171
|
T | G | 1 | a0001c0001t0001g0162 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.30+6945A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63778171 | ||||||
| chrX:63778380
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.30+6736A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63778380 | ||||||
| chrX:63778712
|
TC | T | 1 | a0003c0003t0022g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+6403delG | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63778712 | ||||||
| chrX:63778748
|
A | T | 15 | a0001c0001t0001g0028a0001c0001t0002g0023a0001c0001t0002g0024others(12): Show | 15 | HG01255.hp1 HG02622.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.30+6368T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63778748 | ||||||
| chrX:63778811
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | NA18983.hp1 NA18994.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.30+6305C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63778811 | ||||||
| chrX:63779059
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.30+6057C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63779059 | ||||||
| chrX:63779161
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.30+5955G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63779161 | ||||||
| chrX:63779285
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.30+5831C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63779285 | ||||||
| chrX:63779311
|
A | C | 1 | a0001c0001t0005g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.30+5805T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63779311 | ||||||
| chrX:63779955
|
C | T | 3 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0022 | 3 | HG01243.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.30+5161G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63779955 | ||||||
| chrX:63780224
|
AT | A | 1 | a0001c0001t0002g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.30+4891delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63780224 | ||||||
| chrX:63780342
|
T | C | 2 | a0001c0001t0002g0149a0001c0001t0002g0150 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.30+4774A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63780342 | ||||||
| chrX:63780731
|
C | A | 1 | a0001c0001t0003g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.30+4385G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63780731 | ||||||
| chrX:63780975
|
C | CA | 1 | a0001c0001t0001g0152 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.30+4140dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63780975 | ||||||
| chrX:63781795
|
T | C | 1 | a0001c0001t0005g0022 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.30+3321A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63781795 | ||||||
| chrX:63781827
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.30+3289A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63781827 | ||||||
| chrX:63782119
|
GT | G | 1 | a0001c0001t0001g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.30+2996delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63782119 | ||||||
| chrX:63782264
|
A | G | 8 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0017others(5): Show | 8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+2852T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63782264 | ||||||
| chrX:63782325
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.30+2791G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63782325 | ||||||
| chrX:63782665
|
CG | C | 2 | a0001c0001t0009g0006a0001c0001t0009g0007 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.30+2450delC | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63782665 | ||||||
| chrX:63782844
|
A | G | 1 | a0001c0001t0002g0013 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.30+2272T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63782844 | ||||||
| chrX:63783144
|
T | G | 1 | a0001c0001t0020g0012 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.30+1972A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63783144 | ||||||
| chrX:63783179
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.30+1937A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63783179 | ||||||
| chrX:63783273
|
A | AT | 3 | a0001c0001t0001g0010a0001c0001t0020g0012a0002c0002t0015g0011 | 3 | HG00738.hp1 NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.30+1842dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63783273 | ||||||
| chrX:63783273
|
AT | A | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG00140.hp1 HG01515.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+1842delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63783273 | ||||||
| chrX:63783535
|
C | CT | 1 | a0001c0001t0002g0009 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.30+1580_30+1581ins others(1): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63783535 | ||||||
| chrX:63784030
|
CT | C | 1 | a0001c0001t0001g0008 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.30+1085delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63784030 | ||||||
| chrX:63784036
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.30+1080G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63784036 | ||||||
| chrX:63784418
|
C | T | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0009g0006others(2): Show | 5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+698G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63784418 | ||||||
| chrX:63784423
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.30+693A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63784423 | ||||||
| chrX:63784538
|
G | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.30+578C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63784538 |