Search by Gene
| geneid | 55114 |
|---|---|
| ensemblid | ENSG00000140750.17 |
| hgncid | 18239 |
| symbol | ARHGAP17 |
| name | Rho GTPase activating protein 17 |
| refseq_nuc | NM_001006634.3 |
| refseq_prot | NP_001006635.1 |
| ensembl_nuc | ENST00000289968.11 |
| ensembl_prot | ENSP00000289968.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 24919389 |
| end | 25015369 |
| strand | - |
| ver | v1.2 |
| region | chr16:24919389-25015369 |
| region5000 | chr16:24914389-25020369 |
| regionname0 | ARHGAP17_chr16_24919389_25015369 |
| regionname5000 | ARHGAP17_chr16_24914389_25020369 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 881 | 238 | 87 | 46 | 76 | 8 | 19 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0002 | 0/0 | 881 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0003 | 0/0 | 881 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2646 | 206 | 71 | 39 | 70 | 7 | 17 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| c0002 | 0/0 | 2646 | 14 | 0 | 5 | 6 | 1 | 2 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| c0003 | 0/0 | 2646 | 8 | 6 | 2 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| c0004 | 0/0 | 2646 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| c0005 | 0/0 | 2646 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| c0006 | 0/0 | 2646 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| c0007 | 0/0 | 2646 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 850 | 207 | 61 | 43 | 76 | 6 | 19 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| t0002 | 0/0 | 850 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| t0003 | 0/0 | 850 | 8 | 6 | 2 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| t0004 | 0/0 | 850 | 6 | 5 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| t0005 | 0/0 | 849 | 6 | 5 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| t0006 | 0/0 | 850 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| t0007 | 0/0 | 850 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| t0008 | 0/0 | 849 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 206 | 71 | 39 | 70 | 7 | 17 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 14 | 0 | 5 | 6 | 1 | 2 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0002c0006 | a0002 | c0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0003c0007 | a0003 | c0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 190 | 58 | 38 | 70 | 5 | 17 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 14 | 0 | 5 | 6 | 1 | 2 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0003t0003 | a0001 | c0003 | t0003 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0004t0002 | a0001 | c0004 | t0002 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0004t0008 | a0001 | c0004 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0002c0006t0005 | a0002 | c0006 | t0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| a0003c0007t0001 | a0003 | c0007 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0187 | a0001 | c0001 | t0001 | g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0203 | a0001 | c0001 | t0001 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0225 | a0001 | c0001 | t0001 | g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0228 | a0001 | c0001 | t0001 | g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0229 | a0001 | c0001 | t0001 | g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0234 | a0001 | c0001 | t0001 | g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0001g0235 | a0001 | c0001 | t0001 | g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0002g0031 | a0001 | c0001 | t0002 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0004g0011 | a0001 | c0001 | t0004 | g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0004g0220 | a0001 | c0001 | t0004 | g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0004g0221 | a0001 | c0001 | t0004 | g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0004g0222 | a0001 | c0001 | t0004 | g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0004g0226 | a0001 | c0001 | t0004 | g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0004g0227 | a0001 | c0001 | t0004 | g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0005g0003 | a0001 | c0001 | t0005 | g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0005g0114 | a0001 | c0001 | t0005 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0005g0230 | a0001 | c0001 | t0005 | g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0005g0231 | a0001 | c0001 | t0005 | g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0006g0070 | a0001 | c0001 | t0006 | g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0006g0072 | a0001 | c0001 | t0006 | g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0007g0018 | a0001 | c0001 | t0007 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0001t0007g0019 | a0001 | c0001 | t0007 | g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0032 | a0001 | c0002 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0033 | a0001 | c0002 | t0001 | g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0034 | a0001 | c0002 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0035 | a0001 | c0002 | t0001 | g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0036 | a0001 | c0002 | t0001 | g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0037 | a0001 | c0002 | t0001 | g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0038 | a0001 | c0002 | t0001 | g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0039 | a0001 | c0002 | t0001 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0040 | a0001 | c0002 | t0001 | g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0041 | a0001 | c0002 | t0001 | g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0042 | a0001 | c0002 | t0001 | g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0043 | a0001 | c0002 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0044 | a0001 | c0002 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0002t0001g0091 | a0001 | c0002 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0003t0003g0210 | a0001 | c0003 | t0003 | g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0003t0003g0211 | a0001 | c0003 | t0003 | g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0003t0003g0212 | a0001 | c0003 | t0003 | g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0003t0003g0214 | a0001 | c0003 | t0003 | g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0003t0003g0216 | a0001 | c0003 | t0003 | g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0003t0003g0217 | a0001 | c0003 | t0003 | g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0003t0003g0218 | a0001 | c0003 | t0003 | g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0003t0003g0219 | a0001 | c0003 | t0003 | g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0004t0002g0103 | a0001 | c0004 | t0002 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0004t0002g0108 | a0001 | c0004 | t0002 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0004t0002g0110 | a0001 | c0004 | t0002 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0004t0002g0111 | a0001 | c0004 | t0002 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0004t0002g0112 | a0001 | c0004 | t0002 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0004t0002g0113 | a0001 | c0004 | t0002 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0004t0002g0115 | a0001 | c0004 | t0002 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0004t0008g0104 | a0001 | c0004 | t0008 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0005t0001g0213 | a0001 | c0005 | t0001 | g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0001c0005t0001g0215 | a0001 | c0005 | t0001 | g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0002c0006t0005g0015 | a0002 | c0006 | t0005 | g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| a0003c0007t0001g0224 | a0003 | c0007 | t0001 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0222 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01243 | hp1 | a0001 | c0003 | t0003 | g0212 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01496 | hp1 | a0001 | c0003 | t0003 | g0214 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | IBS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0072 | EUR | IBS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0070 | EUR | IBS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01884 | hp2 | a0001 | c0003 | t0003 | g0217 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0216 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02257 | hp2 | a0001 | c0004 | t0002 | g0110 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02572 | hp2 | a0001 | c0004 | t0002 | g0115 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0226 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0230 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02809 | hp1 | a0001 | c0003 | t0003 | g0211 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0210 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0114 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02922 | hp2 | a0001 | c0004 | t0008 | g0104 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02970 | hp1 | a0001 | c0004 | t0002 | g0113 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02976 | hp2 | a0001 | c0004 | t0002 | g0108 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0218 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0231 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03209 | hp1 | a0001 | c0004 | t0002 | g0112 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0219 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG04115 | hp1 | a0002 | c0006 | t0005 | g0015 | SAS | STU | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | STU | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | YRI | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | YRI | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | LWK | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ASW | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ASW | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02486 | hp1 | a0003 | c0007 | t0001 | g0224 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02486 | hp2 | a0001 | c0004 | t0002 | g0103 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0215 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | USA | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | USA | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA20300 | hp1 | a0001 | c0004 | t0002 | g0111 | AFR | USA | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0221 | AFR | USA | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA21309 | hp1 | a0001 | c0005 | t0001 | g0213 | AFR | LWK | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0135 | REF | REF | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0178 | REF | REF | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:24939403
|
G | A | 1 | a0002 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1685C>T | p.Ala562Val | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/20 | 1793/3495 | 1685/2646 | 562/881 | chr16 | 24939403 | ||
| chr16:24939563
|
G | A | 1 | a0003 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1525C>T | p.Arg509Trp | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/20 | 1633/3495 | 1525/2646 | 509/881 | chr16 | 24939563 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:24931007
|
C | T | 1 | a0001c0003 | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
synonymous_variant | LOW | c.2292G>A | p.Pro764Pro | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/20 | 2400/3495 | 2292/2646 | 764/881 | chr16 | 24931007 | ||
| chr16:24931151
|
C | T | 1 | a0001c0003 | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
synonymous_variant | LOW | c.2148G>A | p.Pro716Pro | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/20 | 2256/3495 | 2148/2646 | 716/881 | chr16 | 24931151 | ||
| chr16:24935486
|
C | T | 2 | a0001c0004a0002c0006 | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
synonymous_variant | LOW | c.1878G>A | p.Pro626Pro | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/20 | 1986/3495 | 1878/2646 | 626/881 | chr16 | 24935486 | ||
| chr16:24943862
|
T | C | 1 | a0001c0002 | 14 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(11): Show |
splice_region_variant&synonymous_variant | LOW | c.1242A>G | p.Gly414Gly | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/20 | 1350/3495 | 1242/2646 | 414/881 | chr16 | 24943862 | ||
| chr16:24968757
|
C | T | 2 | a0001c0003a0001c0005 | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
synonymous_variant | LOW | c.288G>A | p.Thr96Thr | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 5/20 | 396/3495 | 288/2646 | 96/881 | chr16 | 24968757 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:24919479
|
TA | T | 3 | a0001c0001t0005a0001c0004t0008a0002c0006t0005 | 7 | HG01884.hp1 HG02622.hp2 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*650delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 20/20 | 650 | chr16 | 24919479 | |||||
| chr16:24919595
|
T | C | 1 | a0001c0003t0003 | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*535A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 20/20 | 535 | chr16 | 24919595 | |||||
| chr16:24919834
|
C | T | 1 | a0001c0001t0006 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*296G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 20/20 | 296 | chr16 | 24919834 | |||||
| chr16:24919852
|
C | T | 3 | a0001c0001t0002a0001c0004t0002a0001c0004t0008 | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*278G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 20/20 | 278 | chr16 | 24919852 | |||||
| chr16:24919992
|
G | T | 1 | a0001c0001t0004 | 6 | HG01167.hp1 HG02622.hp1 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*138C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 20/20 | 138 | chr16 | 24919992 | |||||
| chr16:24919993
|
C | T | 1 | a0001c0001t0004 | 6 | HG01167.hp1 HG02622.hp1 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*137G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 20/20 | 137 | chr16 | 24919993 | |||||
| chr16:24920110
|
G | A | 1 | a0001c0001t0007 | 2 | HG02109.hp1 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*20C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 20/20 | 20 | chr16 | 24920110 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:24920370
|
G | A | 10 | a0001c0002t0001g0033a0001c0002t0001g0035a0001c0002t0001g0036others(7): Show | 10 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.2516-110C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24920370 | ||||||
| chr16:24920477
|
C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 82 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(79): Show |
intron_variant | MODIFIER | c.2516-217G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24920477 | ||||||
| chr16:24920573
|
A | G | 80 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 82 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(79): Show |
intron_variant | MODIFIER | c.2516-313T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24920573 | ||||||
| chr16:24920605
|
G | T | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2516-345C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24920605 | ||||||
| chr16:24920679
|
T | C | 9 | a0001c0001t0002g0031a0001c0004t0002g0103a0001c0004t0002g0108others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2516-419A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24920679 | ||||||
| chr16:24920797
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2516-537C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24920797 | ||||||
| chr16:24920797
|
G | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0184a0001c0001t0001g0197 | 3 | NA18943.hp2 NA18950.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2516-537C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24920797 | ||||||
| chr16:24920862
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2516-602G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24920862 | ||||||
| chr16:24920890
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2516-630A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24920890 | ||||||
| chr16:24921155
|
C | T | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 25 | HG01074.hp2 HG01099.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.2516-895G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24921155 | ||||||
| chr16:24921229
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2516-969T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24921229 | ||||||
| chr16:24921269
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG01168.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2516-1009C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24921269 | ||||||
| chr16:24921289
|
T | G | 1 | a0001c0001t0001g0140 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2516-1029A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24921289 | ||||||
| chr16:24921524
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2516-1264G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24921524 | ||||||
| chr16:24921599
|
T | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 86 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(83): Show |
intron_variant | MODIFIER | c.2516-1339A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24921599 | ||||||
| chr16:24921640
|
G | T | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2516-1380C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24921640 | ||||||
| chr16:24921957
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2516-1697A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24921957 | ||||||
| chr16:24921984
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01099.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2516-1724G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24921984 | ||||||
| chr16:24921994
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2516-1734G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24921994 | ||||||
| chr16:24922185
|
A | C | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2516-1925T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24922185 | ||||||
| chr16:24922505
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2516-2245A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24922505 | ||||||
| chr16:24922529
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0175 | 2 | HG01074.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2516-2269C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24922529 | ||||||
| chr16:24922655
|
A | C | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2516-2395T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24922655 | ||||||
| chr16:24922735
|
G | A | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2516-2475C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24922735 | ||||||
| chr16:24922808
|
T | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0011others(5): Show | 8 | HG01167.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2516-2548A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24922808 | ||||||
| chr16:24922852
|
T | C | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2516-2592A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24922852 | ||||||
| chr16:24923003
|
C | T | 1 | a0001c0001t0004g0222 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2516-2743G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923003 | ||||||
| chr16:24923143
|
G | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(48): Show | 52 | HG01167.hp1 HG01243.hp1 HG01496.hp1 others(49): Show |
intron_variant | MODIFIER | c.2516-2883C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923143 | ||||||
| chr16:24923209
|
C | T | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2516-2949G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923209 | ||||||
| chr16:24923212
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(12): Show | 15 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2516-2952G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923212 | ||||||
| chr16:24923283
|
C | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(8): Show | 12 | HG02451.hp1 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2516-3023G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923283 | ||||||
| chr16:24923390
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2516-3130C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923390 | ||||||
| chr16:24923479
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2516-3219T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923479 | ||||||
| chr16:24923727
|
TA | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(171): Show | 179 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.2516-3468delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923727 | ||||||
| chr16:24923727
|
TAA | T | 18 | a0001c0001t0001g0055a0001c0001t0001g0076a0001c0001t0001g0082others(15): Show | 18 | HG01074.hp1 HG01168.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.2516-3469_2516-346 others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923727 | ||||||
| chr16:24923728
|
A | T | 6 | a0001c0001t0001g0026a0001c0001t0004g0011a0001c0001t0004g0220others(3): Show | 6 | HG02622.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2516-3468T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923728 | ||||||
| chr16:24923729
|
A | T | 44 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(41): Show | 46 | HG01167.hp1 HG01243.hp1 HG01496.hp1 others(43): Show |
intron_variant | MODIFIER | c.2516-3469T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923729 | ||||||
| chr16:24923730
|
A | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(11): Show | 15 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.2516-3470T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923730 | ||||||
| chr16:24923747
|
A | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2516-3487T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923747 | ||||||
| chr16:24923820
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2516-3560T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923820 | ||||||
| chr16:24923910
|
G | A | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2516-3650C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923910 | ||||||
| chr16:24923983
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2516-3723G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923983 | ||||||
| chr16:24924003
|
A | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(29): Show | 33 | HG01167.hp1 HG01934.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.2516-3743T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924003 | ||||||
| chr16:24924124
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2516-3864G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924124 | ||||||
| chr16:24924245
|
T | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 70 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(67): Show |
intron_variant | MODIFIER | c.2516-3985A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924245 | ||||||
| chr16:24924386
|
A | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 14 | HG00438.hp2 HG02257.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2516-4126T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924386 | ||||||
| chr16:24924418
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2516-4158G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924418 | ||||||
| chr16:24924441
|
T | G | 1 | a0001c0001t0001g0085 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2516-4181A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924441 | ||||||
| chr16:24924442
|
G | GT | 121 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 125 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2516-4183dupA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924442 | ||||||
| chr16:24924456
|
T | C | 1 | a0001c0002t0001g0034 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2516-4196A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924456 | ||||||
| chr16:24924456
|
T | TC | 13 | a0001c0001t0001g0180a0001c0002t0001g0032a0001c0002t0001g0033others(10): Show | 13 | HG01256.hp1 HG01928.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.2516-4197_2516-419 others(5): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924456 | ||||||
| chr16:24924532
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2516-4272T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924532 | ||||||
| chr16:24924629
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2516-4369C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924629 | ||||||
| chr16:24924716
|
A | T | 59 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(56): Show | 61 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.2516-4456T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924716 | ||||||
| chr16:24924868
|
T | TA | 17 | a0001c0001t0001g0180a0001c0001t0005g0114a0001c0002t0001g0032others(14): Show | 17 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.2516-4609dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924868 | ||||||
| chr16:24924895
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2516-4635A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24924895 | ||||||
| chr16:24925056
|
T | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0166 | 2 | NA18943.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.2516-4796A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24925056 | ||||||
| chr16:24925260
|
T | A | 1 | a0001c0001t0001g0046 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2516-5000A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24925260 | ||||||
| chr16:24925265
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2516-5005C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24925265 | ||||||
| chr16:24925306
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 70 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(67): Show |
intron_variant | MODIFIER | c.2516-5046T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24925306 | ||||||
| chr16:24925311
|
A | G | 2 | a0001c0004t0002g0103a0001c0004t0008g0104 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2516-5051T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24925311 | ||||||
| chr16:24925440
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0199 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2516-5180G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24925440 | ||||||
| chr16:24925707
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0079others(2): Show | 8 | NA18983.hp2 NA18986.hp2 NA18994.hp2 others(5): Show |
intron_variant | MODIFIER | c.2515+5077A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24925707 | ||||||
| chr16:24925931
|
A | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG02280.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2515+4853T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24925931 | ||||||
| chr16:24925971
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2515+4813C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24925971 | ||||||
| chr16:24926003
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2515+4781C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926003 | ||||||
| chr16:24926042
|
G | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 25 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.2515+4742C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926042 | ||||||
| chr16:24926044
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2515+4740T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926044 | ||||||
| chr16:24926104
|
C | T | 33 | a0001c0001t0001g0066a0001c0001t0001g0148a0001c0001t0001g0149others(30): Show | 33 | HG00597.hp2 HG01069.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.2515+4680G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926104 | ||||||
| chr16:24926109
|
G | GA | 19 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(16): Show | 20 | HG01167.hp1 HG02109.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.2515+4674dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926109 | ||||||
| chr16:24926109
|
G | GAA | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 24 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.2515+4673_2515+467 others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926109 | ||||||
| chr16:24926109
|
G | GAAA | 4 | a0001c0001t0002g0031a0001c0001t0005g0003a0001c0001t0005g0230others(1): Show | 5 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2515+4672_2515+467 others(7): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926109 | ||||||
| chr16:24926117
|
A | AAAAAAAA others(1): Show |
8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2515+4666_2515+466 others(12): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926117 | ||||||
| chr16:24926118
|
AAAAG | A | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01934.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2515+4662_2515+466 others(8): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926118 | ||||||
| chr16:24926134
|
A | G | 9 | a0001c0001t0004g0011a0001c0003t0003g0210a0001c0003t0003g0211others(6): Show | 9 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2515+4650T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926134 | ||||||
| chr16:24926139
|
G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2515+4645C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926139 | ||||||
| chr16:24926207
|
A | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0011others(5): Show | 8 | HG01167.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2515+4577T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926207 | ||||||
| chr16:24926284
|
A | G | 11 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(8): Show | 12 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2515+4500T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926284 | ||||||
| chr16:24926353
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2515+4431A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926353 | ||||||
| chr16:24926525
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2515+4259C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926525 | ||||||
| chr16:24926537
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2515+4247G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926537 | ||||||
| chr16:24926542
|
G | A | 27 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(24): Show | 28 | HG01074.hp2 HG01099.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.2515+4242C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926542 | ||||||
| chr16:24926819
|
G | C | 1 | a0001c0001t0001g0068 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2515+3965C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926819 | ||||||
| chr16:24926891
|
C | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(29): Show | 33 | HG01167.hp1 HG01934.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.2515+3893G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926891 | ||||||
| chr16:24926897
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2515+3887G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926897 | ||||||
| chr16:24926926
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2515+3858A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24926926 | ||||||
| chr16:24927069
|
G | A | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2515+3715C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24927069 | ||||||
| chr16:24927157
|
G | C | 1 | a0001c0002t0001g0033 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2515+3627C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24927157 | ||||||
| chr16:24927264
|
T | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 71 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(68): Show |
intron_variant | MODIFIER | c.2515+3520A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24927264 | ||||||
| chr16:24927590
|
G | C | 1 | a0001c0001t0001g0148 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2515+3194C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24927590 | ||||||
| chr16:24927889
|
C | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2515+2895G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24927889 | ||||||
| chr16:24928069
|
T | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(8): Show | 12 | HG02451.hp1 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2515+2715A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24928069 | ||||||
| chr16:24928295
|
T | G | 1 | a0001c0001t0001g0228 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2515+2489A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24928295 | ||||||
| chr16:24928410
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18942.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.2515+2374T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24928410 | ||||||
| chr16:24928411
|
C | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(30): Show | 34 | HG01167.hp1 HG01934.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2515+2373G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24928411 | ||||||
| chr16:24928688
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(12): Show | 15 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2515+2096C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24928688 | ||||||
| chr16:24928898
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2515+1886C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24928898 | ||||||
| chr16:24928914
|
T | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2515+1870A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24928914 | ||||||
| chr16:24929121
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0007g0018a0001c0001t0007g0019 | 3 | HG02109.hp1 HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2515+1663G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929121 | ||||||
| chr16:24929154
|
C | CT | 12 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0230others(9): Show | 13 | HG01884.hp1 HG02257.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2515+1629dupA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929154 | ||||||
| chr16:24929154
|
CT | C | 12 | a0001c0001t0001g0053a0001c0001t0001g0071a0001c0001t0001g0077others(9): Show | 12 | HG00323.hp2 HG01069.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.2515+1629delA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929154 | ||||||
| chr16:24929171
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2515+1613A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929171 | ||||||
| chr16:24929172
|
A | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 5 | HG02280.hp2 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2515+1612T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929172 | ||||||
| chr16:24929420
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2515+1364G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929420 | ||||||
| chr16:24929576
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2515+1208G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929576 | ||||||
| chr16:24929612
|
C | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 16 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2515+1172G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929612 | ||||||
| chr16:24929673
|
A | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0074others(1): Show | 4 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2515+1111T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929673 | ||||||
| chr16:24929763
|
C | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 16 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2515+1021G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929763 | ||||||
| chr16:24929862
|
T | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0176 | 2 | NA18747.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2515+922A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929862 | ||||||
| chr16:24929878
|
A | G | 6 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0214others(3): Show | 6 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2515+906T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929878 | ||||||
| chr16:24929885
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2515+899C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929885 | ||||||
| chr16:24929918
|
G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2515+866C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24929918 | ||||||
| chr16:24930315
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2515+469G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24930315 | ||||||
| chr16:24930441
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(12): Show | 15 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2515+343C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24930441 | ||||||
| chr16:24930615
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2515+169A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24930615 | ||||||
| chr16:24930667
|
T | A | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2515+117A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24930667 | ||||||
| chr16:24931722
|
T | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1895-318A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24931722 | ||||||
| chr16:24931749
|
T | TG | 16 | a0001c0001t0001g0118a0001c0001t0005g0114a0001c0002t0001g0032others(13): Show | 16 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.1895-346dupC | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24931749 | ||||||
| chr16:24931788
|
T | C | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1895-384A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24931788 | ||||||
| chr16:24931834
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(3): Show | 6 | HG01099.hp2 HG02723.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1895-430G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24931834 | ||||||
| chr16:24931890
|
C | T | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1895-486G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24931890 | ||||||
| chr16:24931931
|
C | T | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1895-527G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24931931 | ||||||
| chr16:24931945
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1895-541T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24931945 | ||||||
| chr16:24932080
|
C | A | 2 | a0001c0001t0001g0109a0001c0001t0002g0031 | 2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1895-676G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24932080 | ||||||
| chr16:24932108
|
C | CA | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 25 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1895-705dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24932108 | ||||||
| chr16:24932231
|
G | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1895-827C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24932231 | ||||||
| chr16:24932384
|
A | C | 1 | a0001c0004t0002g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1895-980T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24932384 | ||||||
| chr16:24932401
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1895-997G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24932401 | ||||||
| chr16:24932460
|
C | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01074.hp2 HG01099.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.1895-1056G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24932460 | ||||||
| chr16:24932622
|
T | C | 7 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1895-1218A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24932622 | ||||||
| chr16:24932759
|
C | G | 1 | a0001c0001t0007g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1895-1355G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24932759 | ||||||
| chr16:24932825
|
T | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 70 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(67): Show |
intron_variant | MODIFIER | c.1895-1421A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24932825 | ||||||
| chr16:24933254
|
TCTGA | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(29): Show | 33 | HG01167.hp1 HG01934.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1895-1854_1895-185 others(8): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24933254 | ||||||
| chr16:24933425
|
T | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(12): Show | 15 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1895-2021A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24933425 | ||||||
| chr16:24933438
|
C | T | 1 | a0001c0003t0003g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1894+2032G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24933438 | ||||||
| chr16:24933468
|
C | T | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1894+2002G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24933468 | ||||||
| chr16:24933499
|
G | GAA | 30 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(27): Show | 31 | HG01167.hp1 HG01934.hp1 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1894+1969_1894+197 others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24933499 | ||||||
| chr16:24933687
|
G | A | 8 | a0001c0001t0001g0028a0001c0001t0001g0121a0001c0001t0001g0122others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1894+1783C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24933687 | ||||||
| chr16:24933736
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG02280.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1894+1734C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24933736 | ||||||
| chr16:24934073
|
T | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(29): Show | 33 | HG01167.hp1 HG01934.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1894+1397A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934073 | ||||||
| chr16:24934134
|
T | C | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1894+1336A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934134 | ||||||
| chr16:24934348
|
G | C | 1 | a0001c0001t0001g0174 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1894+1122C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934348 | ||||||
| chr16:24934411
|
C | A | 11 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(8): Show | 12 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1894+1059G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934411 | ||||||
| chr16:24934449
|
C | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0092a0001c0001t0001g0145 | 3 | HG04204.hp1 NA18946.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1894+1021G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934449 | ||||||
| chr16:24934460
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1894+1010A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934460 | ||||||
| chr16:24934463
|
T | C | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1894+1007A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934463 | ||||||
| chr16:24934515
|
G | A | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1894+955C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934515 | ||||||
| chr16:24934751
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1894+719G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934751 | ||||||
| chr16:24934847
|
G | A | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1894+623C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934847 | ||||||
| chr16:24934887
|
T | C | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1894+583A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934887 | ||||||
| chr16:24934919
|
A | G | 1 | a0001c0002t0001g0038 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1894+551T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934919 | ||||||
| chr16:24934941
|
G | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 16 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1894+529C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934941 | ||||||
| chr16:24934996
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1894+474G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24934996 | ||||||
| chr16:24935075
|
T | C | 16 | a0001c0001t0001g0118a0001c0001t0005g0114a0001c0002t0001g0032others(13): Show | 16 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.1894+395A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24935075 | ||||||
| chr16:24935136
|
C | A | 9 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1894+334G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24935136 | ||||||
| chr16:24935178
|
TC | T | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1894+291delG | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24935178 | ||||||
| chr16:24935219
|
G | A | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1894+251C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | 24935219 | ||||||
| chr16:24935667
|
G | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1725-28C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24935667 | ||||||
| chr16:24935810
|
T | G | 17 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0005g0114others(14): Show | 17 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.1725-171A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24935810 | ||||||
| chr16:24935844
|
T | G | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 24 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1725-205A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24935844 | ||||||
| chr16:24936018
|
T | C | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1725-379A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24936018 | ||||||
| chr16:24936390
|
T | C | 1 | a0001c0004t0002g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1725-751A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24936390 | ||||||
| chr16:24936705
|
C | CA | 14 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034others(11): Show | 14 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.1725-1067dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24936705 | ||||||
| chr16:24936713
|
A | C | 1 | a0001c0001t0001g0135 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1725-1074T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24936713 | ||||||
| chr16:24937067
|
T | C | 14 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034others(11): Show | 14 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.1725-1428A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937067 | ||||||
| chr16:24937090
|
G | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 16 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1725-1451C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937090 | ||||||
| chr16:24937100
|
G | C | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1725-1461C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937100 | ||||||
| chr16:24937116
|
G | GA | 17 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(14): Show | 18 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1725-1478dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937116 | ||||||
| chr16:24937116
|
G | GAA | 33 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(30): Show | 34 | HG01167.hp1 HG01934.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1725-1479_1725-147 others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937116 | ||||||
| chr16:24937124
|
A | AC | 4 | a0001c0004t0002g0110a0001c0004t0002g0111a0001c0004t0002g0112others(1): Show | 4 | HG02257.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725-1486_1725-148 others(5): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937124 | ||||||
| chr16:24937129
|
C | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 70 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(67): Show |
intron_variant | MODIFIER | c.1725-1490G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937129 | ||||||
| chr16:24937132
|
C | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 16 | HG01074.hp2 HG01099.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1725-1493G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937132 | ||||||
| chr16:24937147
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0051 | 2 | NA18950.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1725-1508C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937147 | ||||||
| chr16:24937160
|
G | A | 8 | a0001c0001t0001g0066a0001c0001t0001g0148a0001c0001t0001g0149others(5): Show | 8 | HG00597.hp2 HG02165.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.1725-1521C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937160 | ||||||
| chr16:24937201
|
C | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1725-1562G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937201 | ||||||
| chr16:24937364
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1725-1725C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937364 | ||||||
| chr16:24937400
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1725-1761G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937400 | ||||||
| chr16:24937433
|
T | A | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725-1794A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937433 | ||||||
| chr16:24937467
|
A | T | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1725-1828T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937467 | ||||||
| chr16:24937530
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0106 | 3 | HG01099.hp1 HG01993.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1724+1834G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937530 | ||||||
| chr16:24937767
|
C | G | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1724+1597G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937767 | ||||||
| chr16:24937800
|
A | T | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1724+1564T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937800 | ||||||
| chr16:24937822
|
G | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(18): Show | 22 | HG01934.hp1 HG02258.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1724+1542C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937822 | ||||||
| chr16:24937861
|
G | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(18): Show | 22 | HG01934.hp1 HG02258.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1724+1503C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937861 | ||||||
| chr16:24937960
|
G | A | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 13 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1724+1404C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24937960 | ||||||
| chr16:24938110
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1724+1254C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938110 | ||||||
| chr16:24938222
|
G | C | 16 | a0001c0001t0001g0118a0001c0001t0005g0114a0001c0002t0001g0032others(13): Show | 16 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.1724+1142C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938222 | ||||||
| chr16:24938439
|
C | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1724+925G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938439 | ||||||
| chr16:24938709
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(23): Show | 27 | HG01934.hp1 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1724+655C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938709 | ||||||
| chr16:24938765
|
C | T | 12 | a0001c0001t0001g0118a0001c0001t0005g0114a0001c0002t0001g0033others(9): Show | 12 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1724+599G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938765 | ||||||
| chr16:24938773
|
GA | G | 21 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0093others(18): Show | 22 | HG01167.hp1 HG01243.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.1724+590delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938773 | ||||||
| chr16:24938773
|
GAA | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 14 | HG01074.hp2 HG01099.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1724+589_1724+590d others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938773 | ||||||
| chr16:24938784
|
A | G | 11 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(8): Show | 12 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1724+580T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938784 | ||||||
| chr16:24938787
|
A | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(20): Show | 24 | HG01934.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1724+577T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938787 | ||||||
| chr16:24938841
|
A | C | 2 | a0001c0003t0003g0217a0001c0003t0003g0219 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1724+523T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938841 | ||||||
| chr16:24938842
|
C | T | 2 | a0001c0003t0003g0217a0001c0003t0003g0219 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1724+522G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938842 | ||||||
| chr16:24938937
|
GAATC | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(20): Show | 24 | HG01934.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1724+423_1724+426d others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938937 | ||||||
| chr16:24938975
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1724+389G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938975 | ||||||
| chr16:24939167
|
T | G | 1 | a0001c0002t0001g0033 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1724+197A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24939167 | ||||||
| chr16:24939179
|
C | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0011others(5): Show | 8 | HG01167.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1724+185G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24939179 | ||||||
| chr16:24939213
|
T | G | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0011others(5): Show | 8 | HG01167.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1724+151A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24939213 | ||||||
| chr16:24939811
|
G | A | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG01069.hp1 HG01257.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1491-214C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24939811 | ||||||
| chr16:24939960
|
G | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(25): Show | 28 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1491-363C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24939960 | ||||||
| chr16:24940086
|
T | TA | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 10 | HG01074.hp2 HG01099.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1491-490dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24940086 | ||||||
| chr16:24940392
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1491-795T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24940392 | ||||||
| chr16:24940571
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1491-974G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24940571 | ||||||
| chr16:24940578
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 70 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(67): Show |
intron_variant | MODIFIER | c.1491-981T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24940578 | ||||||
| chr16:24941019
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1490+968C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24941019 | ||||||
| chr16:24941102
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1490+885A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24941102 | ||||||
| chr16:24941133
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1490+854C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24941133 | ||||||
| chr16:24941389
|
C | T | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1490+598G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24941389 | ||||||
| chr16:24941390
|
C | T | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1490+597G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24941390 | ||||||
| chr16:24941447
|
C | T | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222 | 3 | HG01167.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1490+540G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24941447 | ||||||
| chr16:24941499
|
G | A | 2 | a0001c0004t0002g0108a0001c0004t0002g0115 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1490+488C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24941499 | ||||||
| chr16:24941678
|
C | T | 1 | a0001c0001t0005g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1490+309G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24941678 | ||||||
| chr16:24941685
|
G | A | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1490+302C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24941685 | ||||||
| chr16:24941771
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0199 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1490+216G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24941771 | ||||||
| chr16:24941823
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1490+164C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24941823 | ||||||
| chr16:24941973
|
C | T | 2 | a0001c0004t0002g0108a0001c0004t0002g0115 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1490+14G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 16/19 | chr16 | 24941973 | ||||||
| chr16:24942206
|
G | A | 10 | a0001c0002t0001g0033a0001c0002t0001g0035a0001c0002t0001g0036others(7): Show | 10 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1334-63C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942206 | ||||||
| chr16:24942223
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 13 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1334-80G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942223 | ||||||
| chr16:24942224
|
G | A | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1334-81C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942224 | ||||||
| chr16:24942338
|
CAG | C | 6 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0214others(3): Show | 6 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1334-197_1334-196d others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942338 | ||||||
| chr16:24942365
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1334-222T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942365 | ||||||
| chr16:24942366
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1334-223T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942366 | ||||||
| chr16:24942402
|
A | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1334-259T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942402 | ||||||
| chr16:24942510
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(25): Show | 28 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1334-367G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942510 | ||||||
| chr16:24942643
|
CTG | C | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1334-502_1334-501d others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942643 | ||||||
| chr16:24942683
|
G | A | 1 | a0001c0003t0003g0218 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1334-540C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942683 | ||||||
| chr16:24942724
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1334-581G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942724 | ||||||
| chr16:24942767
|
C | CA | 12 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(9): Show | 12 | HG01099.hp2 HG02055.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1334-625dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942767 | ||||||
| chr16:24942767
|
C | CAA | 25 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(22): Show | 26 | HG01934.hp1 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1334-626_1334-625d others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942767 | ||||||
| chr16:24942767
|
C | CAAA | 10 | a0001c0001t0001g0023a0001c0001t0001g0119a0001c0003t0003g0210others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1334-627_1334-625d others(5): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942767 | ||||||
| chr16:24942767
|
CA | C | 6 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0127others(3): Show | 6 | HG01168.hp2 HG02559.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1334-625delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942767 | ||||||
| chr16:24942783
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1334-640T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942783 | ||||||
| chr16:24942906
|
C | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1334-763G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942906 | ||||||
| chr16:24942907
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1334-764C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942907 | ||||||
| chr16:24942962
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(22): Show | 26 | HG01934.hp1 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1333+809A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942962 | ||||||
| chr16:24942963
|
G | A | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1333+808C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942963 | ||||||
| chr16:24942976
|
T | C | 9 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(6): Show | 9 | HG01934.hp1 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1333+795A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942976 | ||||||
| chr16:24942985
|
A | T | 1 | a0001c0001t0001g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1333+786T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24942985 | ||||||
| chr16:24943032
|
A | G | 8 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(5): Show | 8 | HG01934.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1333+739T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24943032 | ||||||
| chr16:24943038
|
C | G | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1333+733G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24943038 | ||||||
| chr16:24943087
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 82 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(79): Show |
intron_variant | MODIFIER | c.1333+684C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24943087 | ||||||
| chr16:24943129
|
A | T | 6 | a0001c0001t0004g0011a0001c0001t0004g0220a0001c0001t0004g0221others(3): Show | 6 | HG01167.hp1 HG02622.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1333+642T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24943129 | ||||||
| chr16:24943244
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1333+527G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24943244 | ||||||
| chr16:24943402
|
A | G | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(33): Show | 36 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1333+369T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24943402 | ||||||
| chr16:24943419
|
T | C | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1333+352A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24943419 | ||||||
| chr16:24943465
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 70 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(67): Show |
intron_variant | MODIFIER | c.1333+306T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24943465 | ||||||
| chr16:24943562
|
T | C | 14 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034others(11): Show | 14 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.1333+209A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24943562 | ||||||
| chr16:24943718
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1333+53A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24943718 | ||||||
| chr16:24943723
|
C | T | 11 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(8): Show | 12 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1333+48G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24943723 | ||||||
| chr16:24943724
|
GA | G | 6 | a0001c0001t0004g0011a0001c0001t0004g0220a0001c0001t0004g0221others(3): Show | 6 | HG01167.hp1 HG02622.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1333+46delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 15/19 | chr16 | 24943724 | ||||||
| chr16:24943999
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1242-137C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24943999 | ||||||
| chr16:24944048
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1242-186C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944048 | ||||||
| chr16:24944090
|
G | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 13 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1242-228C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944090 | ||||||
| chr16:24944131
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0074others(1): Show | 4 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1242-269G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944131 | ||||||
| chr16:24944149
|
T | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1242-287A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944149 | ||||||
| chr16:24944186
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0069 | 2 | HG04199.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1242-324C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944186 | ||||||
| chr16:24944256
|
C | T | 14 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034others(11): Show | 14 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.1242-394G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944256 | ||||||
| chr16:24944269
|
C | CA | 29 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(26): Show | 30 | HG01358.hp1 HG01934.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1242-408dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944269 | ||||||
| chr16:24944269
|
CA | C | 30 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(27): Show | 31 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1242-408delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944269 | ||||||
| chr16:24944352
|
T | G | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1242-490A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944352 | ||||||
| chr16:24944523
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1242-661G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944523 | ||||||
| chr16:24944525
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1242-663T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944525 | ||||||
| chr16:24944693
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1242-831A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944693 | ||||||
| chr16:24944724
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1242-862G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944724 | ||||||
| chr16:24944773
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1242-911G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944773 | ||||||
| chr16:24944817
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(23): Show | 27 | HG01934.hp1 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1242-955C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944817 | ||||||
| chr16:24944886
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1242-1024C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944886 | ||||||
| chr16:24944998
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1242-1136A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24944998 | ||||||
| chr16:24945135
|
A | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 86 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(83): Show |
intron_variant | MODIFIER | c.1242-1273T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945135 | ||||||
| chr16:24945229
|
T | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 70 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(67): Show |
intron_variant | MODIFIER | c.1242-1367A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945229 | ||||||
| chr16:24945237
|
A | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(64): Show | 69 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.1242-1375T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945237 | ||||||
| chr16:24945237
|
A | T | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1242-1375T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945237 | ||||||
| chr16:24945274
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1242-1412C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945274 | ||||||
| chr16:24945288
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1242-1426T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945288 | ||||||
| chr16:24945306
|
A | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0074others(1): Show | 4 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1242-1444T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945306 | ||||||
| chr16:24945343
|
AAAG | A | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1242-1484_1242-148 others(7): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945343 | ||||||
| chr16:24945364
|
A | G | 6 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1242-1502T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945364 | ||||||
| chr16:24945370
|
AAG | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(20): Show | 24 | HG01934.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1242-1510_1242-150 others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945370 | ||||||
| chr16:24945456
|
C | G | 1 | a0001c0002t0001g0038 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1242-1594G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945456 | ||||||
| chr16:24945611
|
C | T | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1242-1749G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945611 | ||||||
| chr16:24945713
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1241+1769G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945713 | ||||||
| chr16:24945868
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1241+1614C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945868 | ||||||
| chr16:24945930
|
G | A | 2 | a0001c0001t0004g0220a0001c0001t0004g0221 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1241+1552C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24945930 | ||||||
| chr16:24946119
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1241+1363G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24946119 | ||||||
| chr16:24946174
|
C | G | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1241+1308G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24946174 | ||||||
| chr16:24946256
|
G | A | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1241+1226C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24946256 | ||||||
| chr16:24946306
|
C | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(35): Show | 38 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1241+1176G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24946306 | ||||||
| chr16:24946392
|
C | G | 1 | a0001c0002t0001g0040 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1241+1090G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24946392 | ||||||
| chr16:24946408
|
T | C | 1 | a0001c0001t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1241+1074A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24946408 | ||||||
| chr16:24946502
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1241+980C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24946502 | ||||||
| chr16:24946562
|
T | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 13 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1241+920A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24946562 | ||||||
| chr16:24946714
|
G | A | 117 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 119 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.1241+768C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24946714 | ||||||
| chr16:24946870
|
A | G | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1241+612T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24946870 | ||||||
| chr16:24946889
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1241+593C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24946889 | ||||||
| chr16:24947252
|
CA | C | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1241+229delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24947252 | ||||||
| chr16:24947347
|
A | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 71 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(68): Show |
intron_variant | MODIFIER | c.1241+135T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 14/19 | chr16 | 24947347 | ||||||
| chr16:24947664
|
G | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(76): Show | 81 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(78): Show |
intron_variant | MODIFIER | c.1128-69C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24947664 | ||||||
| chr16:24947927
|
A | G | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1128-332T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24947927 | ||||||
| chr16:24948015
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0079others(2): Show | 8 | NA18983.hp2 NA18986.hp2 NA18994.hp2 others(5): Show |
intron_variant | MODIFIER | c.1128-420T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24948015 | ||||||
| chr16:24948336
|
C | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(23): Show | 27 | HG01934.hp1 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1128-741G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24948336 | ||||||
| chr16:24948371
|
T | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(24): Show | 28 | HG01934.hp1 HG02109.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1128-776A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24948371 | ||||||
| chr16:24948444
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1128-849T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24948444 | ||||||
| chr16:24948475
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(26): Show | 29 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1128-880C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24948475 | ||||||
| chr16:24948533
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1127+871C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24948533 | ||||||
| chr16:24948676
|
G | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(35): Show | 38 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1127+728C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24948676 | ||||||
| chr16:24948682
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0005g0114 | 2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1127+722T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24948682 | ||||||
| chr16:24948730
|
C | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(38): Show | 42 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.1127+674G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24948730 | ||||||
| chr16:24948771
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1127+633C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24948771 | ||||||
| chr16:24948863
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 13 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1127+541G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24948863 | ||||||
| chr16:24948937
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1127+467A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24948937 | ||||||
| chr16:24949059
|
A | G | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0220others(4): Show | 7 | HG01167.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1127+345T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24949059 | ||||||
| chr16:24949110
|
C | G | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1127+294G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24949110 | ||||||
| chr16:24949269
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1127+135A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 13/19 | chr16 | 24949269 | ||||||
| chr16:24949918
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1047-434G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24949918 | ||||||
| chr16:24950049
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1047-565G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950049 | ||||||
| chr16:24950122
|
G | A | 1 | a0001c0001t0007g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1047-638C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950122 | ||||||
| chr16:24950248
|
T | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 22 | HG01074.hp2 HG01099.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1047-764A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950248 | ||||||
| chr16:24950381
|
T | C | 5 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-897A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950381 | ||||||
| chr16:24950553
|
G | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1047-1069C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950553 | ||||||
| chr16:24950568
|
T | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 84 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(81): Show |
intron_variant | MODIFIER | c.1047-1084A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950568 | ||||||
| chr16:24950836
|
C | CA | 19 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0080others(16): Show | 19 | HG00597.hp2 HG01256.hp1 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.1047-1353dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
C | CAAAAAAA | 5 | a0001c0003t0003g0211a0001c0003t0003g0212a0001c0003t0003g0214others(2): Show | 5 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047-1359_1047-135 others(11): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
C | CAAAAAAA others(6): Show |
2 | a0001c0004t0002g0103a0001c0004t0008g0104 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1047-1365_1047-135 others(17): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
C | CAAAAAAA others(8): Show |
7 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0004g0220others(4): Show | 7 | HG02257.hp2 HG02258.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1047-1367_1047-135 others(19): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0004g0222a0001c0001t0004g0226a0003c0007t0001g0224 | 3 | HG01167.hp1 HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1047-1368_1047-135 others(20): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
C | CAAAAAAA others(10): Show |
3 | a0001c0001t0001g0013a0001c0001t0004g0221a0001c0004t0002g0113 | 3 | HG02970.hp1 HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1047-1369_1047-135 others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0232 | 2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1047-1370_1047-135 others(22): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
C | CAAAAAAA others(12): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(1): Show | 4 | HG03130.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047-1371_1047-135 others(23): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
C | CAAAAAAA others(13): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0233 | 3 | HG02723.hp1 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1047-1372_1047-135 others(24): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1047-1374_1047-135 others(26): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0001g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1047-1353_1047-135 others(30): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
C | CAAACAAA others(7): Show |
1 | a0001c0004t0002g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1047-1353_1047-135 others(18): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
C | CAAACAAA others(8): Show |
1 | a0001c0004t0002g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1047-1353_1047-135 others(19): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950836
|
CA | C | 5 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0001g0206others(2): Show | 5 | HG01069.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-1353delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950836 | ||||||
| chr16:24950852
|
A | G | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1047-1368T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950852 | ||||||
| chr16:24950855
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(21): Show | 25 | HG01934.hp1 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1047-1371T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950855 | ||||||
| chr16:24950862
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1047-1378T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24950862 | ||||||
| chr16:24951012
|
C | G | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 22 | HG01074.hp2 HG01099.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1046+1277G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24951012 | ||||||
| chr16:24951097
|
C | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1046+1192G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24951097 | ||||||
| chr16:24951356
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1046+933G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24951356 | ||||||
| chr16:24951495
|
C | T | 5 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1046+794G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24951495 | ||||||
| chr16:24951560
|
G | A | 2 | a0001c0004t0002g0103a0001c0004t0008g0104 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1046+729C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24951560 | ||||||
| chr16:24952113
|
AATAATT | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01099.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1046+170_1046+175d others(8): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | 24952113 | ||||||
| chr16:24952716
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.964+215A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 11/19 | chr16 | 24952716 | ||||||
| chr16:24952718
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(80): Show | 85 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(82): Show |
intron_variant | MODIFIER | c.964+213A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 11/19 | chr16 | 24952718 | ||||||
| chr16:24952805
|
G | A | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+126C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 11/19 | chr16 | 24952805 | ||||||
| chr16:24953077
|
A | G | 1 | a0001c0003t0003g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.853-35T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24953077 | ||||||
| chr16:24953090
|
C | G | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.853-48G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24953090 | ||||||
| chr16:24953197
|
T | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 71 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(68): Show |
intron_variant | MODIFIER | c.853-155A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24953197 | ||||||
| chr16:24953248
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.853-206G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24953248 | ||||||
| chr16:24953395
|
G | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 71 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(68): Show |
intron_variant | MODIFIER | c.853-353C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24953395 | ||||||
| chr16:24953482
|
G | A | 4 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0133others(1): Show | 4 | HG01261.hp1 HG01358.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-440C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24953482 | ||||||
| chr16:24953531
|
C | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(9): Show | 13 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.853-489G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24953531 | ||||||
| chr16:24953563
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.853-521A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24953563 | ||||||
| chr16:24953571
|
C | T | 35 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(32): Show | 35 | HG00597.hp2 HG01069.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.853-529G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24953571 | ||||||
| chr16:24953714
|
C | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(80): Show | 85 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(82): Show |
intron_variant | MODIFIER | c.853-672G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24953714 | ||||||
| chr16:24953996
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.852+607A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24953996 | ||||||
| chr16:24954042
|
G | GA | 10 | a0001c0001t0005g0003a0001c0001t0005g0231a0001c0003t0003g0210others(7): Show | 11 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.852+560dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24954042 | ||||||
| chr16:24954188
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0106 | 3 | HG01099.hp1 HG01993.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.852+415T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24954188 | ||||||
| chr16:24954271
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.852+332G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 10/19 | chr16 | 24954271 | ||||||
| chr16:24954990
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.725-260A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24954990 | ||||||
| chr16:24954995
|
C | T | 2 | a0001c0001t0001g0021a0002c0006t0005g0015 | 2 | HG02647.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.725-265G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24954995 | ||||||
| chr16:24955007
|
A | AC | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222 | 3 | HG01167.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.725-278dupG | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24955007 | ||||||
| chr16:24955096
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.725-366C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24955096 | ||||||
| chr16:24955202
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(80): Show | 85 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(82): Show |
intron_variant | MODIFIER | c.725-472A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24955202 | ||||||
| chr16:24955240
|
C | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.725-510G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24955240 | ||||||
| chr16:24955280
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0029others(1): Show | 4 | HG02451.hp2 HG02572.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-550C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24955280 | ||||||
| chr16:24955305
|
G | A | 11 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(8): Show | 12 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.725-575C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24955305 | ||||||
| chr16:24955323
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.725-593C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24955323 | ||||||
| chr16:24955439
|
C | G | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.725-709G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24955439 | ||||||
| chr16:24955453
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.725-723G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24955453 | ||||||
| chr16:24956115
|
G | A | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(33): Show | 36 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.725-1385C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956115 | ||||||
| chr16:24956218
|
C | T | 50 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(47): Show | 50 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.725-1488G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956218 | ||||||
| chr16:24956286
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0005g0114 | 2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.725-1556G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956286 | ||||||
| chr16:24956457
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.725-1727T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956457 | ||||||
| chr16:24956522
|
A | G | 11 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(8): Show | 12 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.725-1792T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956522 | ||||||
| chr16:24956546
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.725-1816C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956546 | ||||||
| chr16:24956620
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0133 | 2 | HG01261.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.725-1890A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956620 | ||||||
| chr16:24956682
|
G | A | 1 | a0001c0001t0005g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.725-1952C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956682 | ||||||
| chr16:24956742
|
G | C | 1 | a0001c0001t0001g0135 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.725-2012C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956742 | ||||||
| chr16:24956893
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(132): Show | 140 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.725-2163C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956893 | ||||||
| chr16:24956935
|
T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(3): Show | 6 | HG01099.hp2 HG02723.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.725-2205A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956935 | ||||||
| chr16:24956940
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(72): Show | 79 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.725-2210G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956940 | ||||||
| chr16:24957064
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(92): Show | 99 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.725-2334C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24957064 | ||||||
| chr16:24957098
|
G | C | 1 | a0001c0001t0001g0063 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.725-2368C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24957098 | ||||||
| chr16:24957118
|
C | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.725-2388G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24957118 | ||||||
| chr16:24957165
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0009 | 2 | HG01099.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.725-2435T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24957165 | ||||||
| chr16:24957621
|
G | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.724+2050C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24957621 | ||||||
| chr16:24957689
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.724+1982C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24957689 | ||||||
| chr16:24957711
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.724+1960C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24957711 | ||||||
| chr16:24957815
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0066 | 2 | NA18963.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.724+1856G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24957815 | ||||||
| chr16:24958091
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.724+1580C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24958091 | ||||||
| chr16:24958119
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(132): Show | 140 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.724+1552A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24958119 | ||||||
| chr16:24958149
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.724+1522C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24958149 | ||||||
| chr16:24958237
|
A | AAAAC | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(134): Show | 142 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.724+1430_724+1433d others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24958237 | ||||||
| chr16:24958276
|
C | T | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.724+1395G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24958276 | ||||||
| chr16:24958396
|
C | A | 1 | a0001c0001t0001g0092 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.724+1275G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24958396 | ||||||
| chr16:24958404
|
T | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0220others(4): Show | 7 | HG01167.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.724+1267A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24958404 | ||||||
| chr16:24958697
|
GAGA | G | 3 | a0001c0001t0001g0109a0001c0001t0002g0031a0001c0003t0003g0212 | 3 | HG01243.hp1 HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.724+971_724+973del others(3): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24958697 | ||||||
| chr16:24958794
|
C | T | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.724+877G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24958794 | ||||||
| chr16:24958864
|
T | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.724+807A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24958864 | ||||||
| chr16:24958943
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(72): Show | 79 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.724+728G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24958943 | ||||||
| chr16:24959010
|
G | GA | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.724+660dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24959010 | ||||||
| chr16:24959372
|
G | A | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.724+299C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24959372 | ||||||
| chr16:24959412
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(100): Show | 108 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.724+259A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24959412 | ||||||
| chr16:24959426
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.724+245C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24959426 | ||||||
| chr16:24959997
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.574-18T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24959997 | ||||||
| chr16:24960266
|
C | T | 10 | a0001c0002t0001g0033a0001c0002t0001g0035a0001c0002t0001g0036others(7): Show | 10 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.574-287G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24960266 | ||||||
| chr16:24960267
|
G | A | 2 | a0001c0001t0004g0226a0001c0001t0004g0227 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.574-288C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24960267 | ||||||
| chr16:24960272
|
C | T | 2 | a0001c0002t0001g0035a0001c0002t0001g0091 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.574-293G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24960272 | ||||||
| chr16:24960437
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.574-458G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24960437 | ||||||
| chr16:24960578
|
C | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(122): Show | 130 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.574-599G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24960578 | ||||||
| chr16:24960593
|
G | A | 9 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(6): Show | 9 | HG01934.hp1 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.574-614C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24960593 | ||||||
| chr16:24960800
|
T | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG01515.hp2 HG01517.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.574-821A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24960800 | ||||||
| chr16:24960811
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0130 | 3 | HG02040.hp1 HG02074.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.574-832C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24960811 | ||||||
| chr16:24960821
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.574-842T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24960821 | ||||||
| chr16:24961213
|
AAAC | A | 10 | a0001c0002t0001g0033a0001c0002t0001g0035a0001c0002t0001g0036others(7): Show | 10 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.574-1237_574-1235d others(5): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961213 | ||||||
| chr16:24961286
|
A | G | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-1307T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961286 | ||||||
| chr16:24961297
|
G | T | 5 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-1318C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961297 | ||||||
| chr16:24961381
|
C | A | 1 | a0001c0002t0001g0034 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.574-1402G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961381 | ||||||
| chr16:24961389
|
G | C | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.574-1410C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961389 | ||||||
| chr16:24961518
|
A | AT | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0016others(73): Show | 80 | HG00323.hp2 HG00609.hp2 HG01069.hp2 others(77): Show |
intron_variant | MODIFIER | c.574-1540dupA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961518 | ||||||
| chr16:24961518
|
A | ATT | 9 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0049others(6): Show | 9 | HG00438.hp1 HG00642.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.574-1541_574-1540d others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961518 | ||||||
| chr16:24961518
|
AT | A | 9 | a0001c0001t0001g0142a0001c0001t0001g0197a0001c0001t0004g0220others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.574-1540delA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961518 | ||||||
| chr16:24961518
|
ATT | A | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.574-1541_574-1540d others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961518 | ||||||
| chr16:24961518
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0063 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.574-1549_574-1540d others(12): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961518 | ||||||
| chr16:24961518
|
ATTTTTTT others(4): Show |
A | 23 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(20): Show | 23 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.574-1550_574-1540d others(13): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961518 | ||||||
| chr16:24961518
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0029a0001c0001t0001g0118 | 2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.574-1551_574-1540d others(14): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961518 | ||||||
| chr16:24961530
|
T | A | 23 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(20): Show | 23 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.574-1551A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961530 | ||||||
| chr16:24961547
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0055others(4): Show | 10 | HG00438.hp1 NA18969.hp2 NA18983.hp2 others(7): Show |
intron_variant | MODIFIER | c.574-1568C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961547 | ||||||
| chr16:24961592
|
G | A | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 22 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.574-1613C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961592 | ||||||
| chr16:24961621
|
C | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(79): Show | 86 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.574-1642G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961621 | ||||||
| chr16:24961622
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.574-1643G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961622 | ||||||
| chr16:24961654
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.574-1675G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961654 | ||||||
| chr16:24961679
|
T | A | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.574-1700A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961679 | ||||||
| chr16:24961911
|
T | TTA | 5 | a0001c0001t0001g0127a0001c0001t0001g0140a0001c0001t0001g0146others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-1934_574-1933d others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTAGGAAT others(8): Show |
48 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(45): Show | 51 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.574-1933_574-1932i others(17): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTAGGAAT others(10): Show |
4 | a0001c0001t0001g0057a0001c0001t0001g0066a0001c0001t0001g0071others(1): Show | 4 | HG01069.hp2 HG03831.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-1933_574-1932i others(19): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTATATAT others(3): Show |
16 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0020others(13): Show | 16 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.574-1942_574-1933d others(12): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTATATAT others(5): Show |
24 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | 25 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.574-1944_574-1933d others(14): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTATATAT others(7): Show |
5 | a0001c0001t0001g0101a0001c0001t0001g0109a0001c0001t0001g0233others(2): Show | 5 | HG01516.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-1946_574-1933d others(16): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTATATAT others(9): Show |
2 | a0001c0004t0002g0112a0001c0004t0002g0113 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.574-1948_574-1933d others(18): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTATATAT others(11): Show |
6 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0002g0031others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-1950_574-1933d others(20): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTATATAT others(17): Show |
2 | a0001c0001t0001g0229a0001c0004t0002g0103 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.574-1933_574-1932i others(26): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTATATAT others(19): Show |
3 | a0001c0001t0005g0114a0001c0004t0002g0115a0001c0004t0008g0104 | 3 | HG02572.hp2 HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.574-1933_574-1932i others(28): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTATATAT others(25): Show |
1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.574-1933_574-1932i others(34): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTATATAT others(29): Show |
1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.574-1933_574-1932i others(38): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTATATAT others(33): Show |
1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.574-1933_574-1932i others(42): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
T | TTATATAT others(35): Show |
1 | a0001c0004t0002g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.574-1933_574-1932i others(44): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961911
|
TTATA | T | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.574-1936_574-1933d others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961911 | ||||||
| chr16:24961968
|
G | GTTT | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 22 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.574-1992_574-1990d others(5): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961968 | ||||||
| chr16:24961968
|
G | GTTTTT | 7 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-1990_574-1989i others(7): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961968 | ||||||
| chr16:24961972
|
G | GTTTT | 24 | a0001c0001t0001g0029a0001c0001t0001g0107a0001c0001t0001g0229others(21): Show | 25 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.574-1997_574-1994d others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961972 | ||||||
| chr16:24961972
|
G | GTTTTT | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(68): Show | 75 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.574-1998_574-1994d others(7): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961972 | ||||||
| chr16:24961972
|
G | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(26): Show | 29 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.574-1993C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24961972 | ||||||
| chr16:24962103
|
GA | G | 9 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(6): Show | 9 | HG01934.hp1 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+2093delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962103 | ||||||
| chr16:24962162
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(79): Show | 86 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.573+2035T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962162 | ||||||
| chr16:24962220
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.573+1977T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962220 | ||||||
| chr16:24962243
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.573+1954C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962243 | ||||||
| chr16:24962345
|
G | A | 1 | a0001c0004t0002g0110 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.573+1852C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962345 | ||||||
| chr16:24962360
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.573+1837G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962360 | ||||||
| chr16:24962431
|
T | C | 21 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(18): Show | 22 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.573+1766A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962431 | ||||||
| chr16:24962496
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.573+1701C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962496 | ||||||
| chr16:24962571
|
G | T | 5 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+1626C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962571 | ||||||
| chr16:24962649
|
A | G | 4 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0133others(1): Show | 4 | HG01261.hp1 HG01358.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+1548T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962649 | ||||||
| chr16:24962676
|
A | G | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+1521T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962676 | ||||||
| chr16:24962808
|
A | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(9): Show | 12 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.573+1389T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962808 | ||||||
| chr16:24962895
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.573+1302A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962895 | ||||||
| chr16:24962954
|
T | G | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.573+1243A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24962954 | ||||||
| chr16:24963049
|
A | G | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.573+1148T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24963049 | ||||||
| chr16:24963105
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(166): Show | 174 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.573+1092C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24963105 | ||||||
| chr16:24963119
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.573+1078G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24963119 | ||||||
| chr16:24963141
|
G | C | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+1056C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24963141 | ||||||
| chr16:24963300
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(73): Show | 80 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.573+897T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24963300 | ||||||
| chr16:24963303
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+894A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24963303 | ||||||
| chr16:24963433
|
AAC | A | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.573+762_573+763del others(2): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24963433 | ||||||
| chr16:24963465
|
C | A | 5 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+732G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24963465 | ||||||
| chr16:24963503
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.573+694C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24963503 | ||||||
| chr16:24963647
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.573+550A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24963647 | ||||||
| chr16:24963902
|
C | A | 1 | a0001c0001t0001g0172 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.573+295G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24963902 | ||||||
| chr16:24963927
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.573+270G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24963927 | ||||||
| chr16:24964098
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.573+99G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24964098 | ||||||
| chr16:24964104
|
G | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(76): Show | 83 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.573+93C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24964104 | ||||||
| chr16:24964176
|
T | C | 1 | a0001c0002t0001g0033 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.573+21A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | 24964176 | ||||||
| chr16:24964381
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.462-73C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24964381 | ||||||
| chr16:24964610
|
CT | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 22 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.462-303delA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24964610 | ||||||
| chr16:24964647
|
G | A | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.462-339C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24964647 | ||||||
| chr16:24964785
|
T | C | 5 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0054others(2): Show | 5 | HG02071.hp1 HG02071.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.462-477A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24964785 | ||||||
| chr16:24964849
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.462-541G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24964849 | ||||||
| chr16:24965053
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.462-745A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965053 | ||||||
| chr16:24965056
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG02615.hp1 HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.462-748T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965056 | ||||||
| chr16:24965085
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-777G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965085 | ||||||
| chr16:24965086
|
T | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-778A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965086 | ||||||
| chr16:24965096
|
T | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-788A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965096 | ||||||
| chr16:24965098
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-790A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965098 | ||||||
| chr16:24965099
|
T | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-791A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965099 | ||||||
| chr16:24965100
|
T | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-792A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965100 | ||||||
| chr16:24965101
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-793C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965101 | ||||||
| chr16:24965108
|
G | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-800C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965108 | ||||||
| chr16:24965109
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-801C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965109 | ||||||
| chr16:24965110
|
T | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-802A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965110 | ||||||
| chr16:24965112
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-804A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965112 | ||||||
| chr16:24965113
|
G | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-805C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965113 | ||||||
| chr16:24965116
|
T | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-808A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965116 | ||||||
| chr16:24965118
|
G | GTCAACTT others(5): Show |
1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-811_462-810ins others(12): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965118 | ||||||
| chr16:24965120
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-812C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965120 | ||||||
| chr16:24965121
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-813A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965121 | ||||||
| chr16:24965125
|
G | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-817C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965125 | ||||||
| chr16:24965127
|
A | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-819T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965127 | ||||||
| chr16:24965128
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-820T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965128 | ||||||
| chr16:24965136
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-828A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965136 | ||||||
| chr16:24965137
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-829G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965137 | ||||||
| chr16:24965142
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-834A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965142 | ||||||
| chr16:24965145
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-837T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965145 | ||||||
| chr16:24965149
|
A | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-841T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965149 | ||||||
| chr16:24965150
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-842T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965150 | ||||||
| chr16:24965151
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-843T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965151 | ||||||
| chr16:24965153
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-845T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965153 | ||||||
| chr16:24965154
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-846A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965154 | ||||||
| chr16:24965155
|
A | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-847T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965155 | ||||||
| chr16:24965156
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-848C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965156 | ||||||
| chr16:24965158
|
T | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-850A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965158 | ||||||
| chr16:24965159
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-851C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965159 | ||||||
| chr16:24965163
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-855A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965163 | ||||||
| chr16:24965171
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-863T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965171 | ||||||
| chr16:24965172
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-864C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965172 | ||||||
| chr16:24965173
|
C | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-865G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965173 | ||||||
| chr16:24965177
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-869T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965177 | ||||||
| chr16:24965183
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-875G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965183 | ||||||
| chr16:24965187
|
T | C | 5 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.462-879A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965187 | ||||||
| chr16:24965188
|
T | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-880A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965188 | ||||||
| chr16:24965192
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.462-884G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965192 | ||||||
| chr16:24965193
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.462-885C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965193 | ||||||
| chr16:24965193
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-885C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965193 | ||||||
| chr16:24965194
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-886C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965194 | ||||||
| chr16:24965196
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-888A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965196 | ||||||
| chr16:24965199
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-891C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965199 | ||||||
| chr16:24965200
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-892A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965200 | ||||||
| chr16:24965209
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-901C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965209 | ||||||
| chr16:24965236
|
C | T | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.462-928G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965236 | ||||||
| chr16:24965263
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-955A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965263 | ||||||
| chr16:24965264
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-956T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965264 | ||||||
| chr16:24965267
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-959C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965267 | ||||||
| chr16:24965274
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.462-966A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965274 | ||||||
| chr16:24965311
|
A | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(101): Show | 108 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.462-1003T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965311 | ||||||
| chr16:24965383
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.462-1075A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965383 | ||||||
| chr16:24965387
|
G | A | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222 | 3 | HG01167.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.462-1079C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965387 | ||||||
| chr16:24965469
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.462-1161A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965469 | ||||||
| chr16:24965597
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.462-1289T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965597 | ||||||
| chr16:24965820
|
G | A | 10 | a0001c0002t0001g0033a0001c0002t0001g0035a0001c0002t0001g0036others(7): Show | 10 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.462-1512C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965820 | ||||||
| chr16:24965841
|
G | A | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.462-1533C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965841 | ||||||
| chr16:24965847
|
C | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.462-1539G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965847 | ||||||
| chr16:24965863
|
T | C | 1 | a0001c0001t0005g0230 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.462-1555A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965863 | ||||||
| chr16:24966188
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0146 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.462-1880G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24966188 | ||||||
| chr16:24966224
|
T | C | 21 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(18): Show | 22 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.462-1916A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24966224 | ||||||
| chr16:24966272
|
C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(49): Show | 55 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.462-1964G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24966272 | ||||||
| chr16:24966409
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 141 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.461+1942T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24966409 | ||||||
| chr16:24966779
|
T | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(9): Show | 12 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.461+1572A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24966779 | ||||||
| chr16:24967281
|
G | T | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.461+1070C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24967281 | ||||||
| chr16:24967292
|
T | C | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.461+1059A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24967292 | ||||||
| chr16:24967374
|
A | G | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.461+977T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24967374 | ||||||
| chr16:24967403
|
G | T | 1 | a0001c0001t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.461+948C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24967403 | ||||||
| chr16:24967530
|
G | C | 21 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(18): Show | 22 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.461+821C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24967530 | ||||||
| chr16:24967778
|
C | CA | 23 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(20): Show | 23 | HG01167.hp1 HG01256.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.461+572dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24967778 | ||||||
| chr16:24967778
|
CA | C | 13 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(10): Show | 13 | HG01074.hp1 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.461+572delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24967778 | ||||||
| chr16:24967911
|
G | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 24 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.461+440C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24967911 | ||||||
| chr16:24967926
|
T | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0220others(4): Show | 7 | HG01167.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.461+425A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24967926 | ||||||
| chr16:24968042
|
T | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0199 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.461+309A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24968042 | ||||||
| chr16:24968174
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+177G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24968174 | ||||||
| chr16:24968189
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(75): Show | 82 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.461+162C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24968189 | ||||||
| chr16:24968500
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.385-73G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 5/19 | chr16 | 24968500 | ||||||
| chr16:24968624
|
C | T | 2 | a0001c0003t0003g0217a0001c0003t0003g0219 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.384+37G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 5/19 | chr16 | 24968624 | ||||||
| chr16:24968868
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(76): Show | 83 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.273-96C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24968868 | ||||||
| chr16:24968888
|
G | A | 1 | a0001c0002t0001g0042 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.273-116C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24968888 | ||||||
| chr16:24968984
|
T | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.273-212A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24968984 | ||||||
| chr16:24969245
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.273-473C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24969245 | ||||||
| chr16:24969297
|
GTC | G | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 22 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.273-527_273-526del others(2): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24969297 | ||||||
| chr16:24969299
|
C | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0140 | 2 | NA18995.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.273-527G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24969299 | ||||||
| chr16:24969403
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0177a0001c0001t0001g0185others(1): Show | 4 | HG00438.hp2 HG00597.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-631C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24969403 | ||||||
| chr16:24969653
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.272+854C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24969653 | ||||||
| chr16:24969722
|
T | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0220others(4): Show | 7 | HG01167.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.272+785A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24969722 | ||||||
| chr16:24970046
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.272+461C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24970046 | ||||||
| chr16:24970054
|
T | TA | 29 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(26): Show | 29 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.272+452dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24970054 | ||||||
| chr16:24970054
|
TA | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 40 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.272+452delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24970054 | ||||||
| chr16:24970589
|
T | C | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222 | 3 | HG01167.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.199-9A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24970589 | ||||||
| chr16:24970722
|
T | A | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.199-142A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24970722 | ||||||
| chr16:24970772
|
T | C | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-192A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24970772 | ||||||
| chr16:24971003
|
G | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(25): Show | 28 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-423C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24971003 | ||||||
| chr16:24971330
|
CT | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(94): Show | 101 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.199-751delA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24971330 | ||||||
| chr16:24971330
|
CTT | C | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 26 | HG01099.hp2 HG01243.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.199-752_199-751del others(2): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24971330 | ||||||
| chr16:24971366
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199-786T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24971366 | ||||||
| chr16:24971656
|
C | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(76): Show | 83 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.199-1076G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24971656 | ||||||
| chr16:24971700
|
G | C | 21 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(18): Show | 22 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.199-1120C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24971700 | ||||||
| chr16:24971826
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.199-1246T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24971826 | ||||||
| chr16:24971962
|
A | G | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.199-1382T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24971962 | ||||||
| chr16:24972232
|
G | C | 4 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG01074.hp2 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-1652C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24972232 | ||||||
| chr16:24972382
|
T | C | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-1802A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24972382 | ||||||
| chr16:24972385
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0005g0114 | 2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.199-1805T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24972385 | ||||||
| chr16:24972425
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.199-1845G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24972425 | ||||||
| chr16:24972831
|
ACT | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(31): Show | 34 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.199-2253_199-2252d others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24972831 | ||||||
| chr16:24972937
|
A | AT | 7 | a0001c0004t0002g0103a0001c0004t0002g0110a0001c0004t0002g0111others(4): Show | 7 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-2358dupA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24972937 | ||||||
| chr16:24972937
|
AT | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(107): Show | 115 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.199-2358delA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24972937 | ||||||
| chr16:24973037
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.199-2457A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24973037 | ||||||
| chr16:24973039
|
T | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0220others(4): Show | 7 | HG01167.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-2459A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24973039 | ||||||
| chr16:24973273
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(121): Show | 129 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-2693T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24973273 | ||||||
| chr16:24973364
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.199-2784G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24973364 | ||||||
| chr16:24973451
|
T | G | 10 | a0001c0002t0001g0033a0001c0002t0001g0035a0001c0002t0001g0036others(7): Show | 10 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-2871A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24973451 | ||||||
| chr16:24973501
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(76): Show | 83 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.199-2921C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24973501 | ||||||
| chr16:24973680
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.199-3100G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24973680 | ||||||
| chr16:24973690
|
C | A | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.199-3110G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24973690 | ||||||
| chr16:24973699
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.199-3119A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24973699 | ||||||
| chr16:24974077
|
A | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(76): Show | 83 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.198+3138T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974077 | ||||||
| chr16:24974172
|
T | A | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0004g0220others(4): Show | 7 | HG01167.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+3043A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974172 | ||||||
| chr16:24974189
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(69): Show | 76 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.198+3026C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974189 | ||||||
| chr16:24974191
|
G | A | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+3024C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974191 | ||||||
| chr16:24974237
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.198+2978G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974237 | ||||||
| chr16:24974237
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.198+2978G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974237 | ||||||
| chr16:24974248
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.198+2967A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974248 | ||||||
| chr16:24974323
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+2892G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974323 | ||||||
| chr16:24974345
|
C | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.198+2870G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974345 | ||||||
| chr16:24974378
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+2837G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974378 | ||||||
| chr16:24974390
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.198+2825G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974390 | ||||||
| chr16:24974393
|
C | T | 21 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(18): Show | 22 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.198+2822G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974393 | ||||||
| chr16:24974428
|
C | G | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+2787G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974428 | ||||||
| chr16:24974458
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0079others(2): Show | 8 | NA18983.hp2 NA18986.hp2 NA18994.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+2757A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974458 | ||||||
| chr16:24974603
|
C | T | 1 | a0001c0003t0003g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.198+2612G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974603 | ||||||
| chr16:24974606
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.198+2609C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974606 | ||||||
| chr16:24974889
|
G | A | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+2326C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974889 | ||||||
| chr16:24974917
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.198+2298G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24974917 | ||||||
| chr16:24975258
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18942.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.198+1957C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24975258 | ||||||
| chr16:24975322
|
C | A | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.198+1893G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24975322 | ||||||
| chr16:24975483
|
C | T | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.198+1732G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24975483 | ||||||
| chr16:24975645
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.198+1570C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24975645 | ||||||
| chr16:24975778
|
T | C | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222 | 3 | HG01167.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.198+1437A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24975778 | ||||||
| chr16:24975880
|
C | A | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+1335G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24975880 | ||||||
| chr16:24975885
|
C | T | 10 | a0001c0002t0001g0033a0001c0002t0001g0035a0001c0002t0001g0036others(7): Show | 10 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+1330G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24975885 | ||||||
| chr16:24976022
|
AC | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 24 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.198+1192delG | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24976022 | ||||||
| chr16:24976142
|
C | T | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.198+1073G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24976142 | ||||||
| chr16:24976505
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.198+710C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24976505 | ||||||
| chr16:24976556
|
A | AGGGAAAG others(12): Show |
1 | a0001c0001t0001g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.198+640_198+658dup others(19): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24976556 | ||||||
| chr16:24976812
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(170): Show | 178 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.198+403T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24976812 | ||||||
| chr16:24977014
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 7 | HG01256.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+201G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24977014 | ||||||
| chr16:24977131
|
A | T | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+84T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24977131 | ||||||
| chr16:24977164
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.198+51T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24977164 | ||||||
| chr16:24977325
|
A | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(9): Show | 12 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.94-6T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24977325 | ||||||
| chr16:24977459
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.94-140G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24977459 | ||||||
| chr16:24977563
|
C | CCA | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 141 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.94-246_94-245dupTG | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24977563 | ||||||
| chr16:24977637
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.94-318G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24977637 | ||||||
| chr16:24977704
|
G | GGT | 9 | a0001c0001t0001g0006a0001c0004t0002g0103a0001c0004t0002g0108others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-387_94-386dupAC | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24977704 | ||||||
| chr16:24977706
|
T | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.94-387A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24977706 | ||||||
| chr16:24977864
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.94-545C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24977864 | ||||||
| chr16:24977999
|
G | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.94-680C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24977999 | ||||||
| chr16:24978028
|
G | A | 4 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG01074.hp2 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-709C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978028 | ||||||
| chr16:24978132
|
G | A | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.94-813C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978132 | ||||||
| chr16:24978273
|
G | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.93+693C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978273 | ||||||
| chr16:24978290
|
A | C | 2 | a0001c0001t0006g0070a0001c0001t0006g0072 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.93+676T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978290 | ||||||
| chr16:24978420
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0146 | 2 | HG02895.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.93+546C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978420 | ||||||
| chr16:24978494
|
C | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0145 | 2 | HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.93+472G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978494 | ||||||
| chr16:24978507
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.93+459C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978507 | ||||||
| chr16:24978519
|
G | A | 7 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(4): Show | 7 | HG01934.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+447C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978519 | ||||||
| chr16:24978580
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.93+386A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978580 | ||||||
| chr16:24978592
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.93+374G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978592 | ||||||
| chr16:24978815
|
G | GA | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(127): Show | 135 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.93+150_93+151insT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978815 | ||||||
| chr16:24978866
|
TA | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 63 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.93+99delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978866 | ||||||
| chr16:24978866
|
TAA | T | 53 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 53 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.93+98_93+99delTT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978866 | ||||||
| chr16:24978866
|
TAAA | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0229a0001c0001t0005g0003others(3): Show | 7 | HG01884.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+97_93+99delTTT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978866 | ||||||
| chr16:24979409
|
A | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-404T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24979409 | ||||||
| chr16:24979411
|
G | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-406C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24979411 | ||||||
| chr16:24979519
|
C | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-514G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24979519 | ||||||
| chr16:24979519
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-514G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24979519 | ||||||
| chr16:24979670
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.54-665C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24979670 | ||||||
| chr16:24979704
|
T | TTTATTAT others(2): Show |
14 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0229others(11): Show | 14 | HG01074.hp2 HG01256.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-708_54-700dupTA others(7): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24979704 | ||||||
| chr16:24979704
|
T | TTTATTAT others(5): Show |
9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(6): Show | 9 | HG01099.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.54-711_54-700dupTA others(10): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24979704 | ||||||
| chr16:24979804
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.54-799C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24979804 | ||||||
| chr16:24980226
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(48): Show | 54 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.54-1221G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24980226 | ||||||
| chr16:24980485
|
C | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.54-1480G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24980485 | ||||||
| chr16:24980496
|
C | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-1491G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24980496 | ||||||
| chr16:24980558
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.54-1553C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24980558 | ||||||
| chr16:24980563
|
G | A | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-1558C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24980563 | ||||||
| chr16:24980996
|
A | G | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-1991T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24980996 | ||||||
| chr16:24981058
|
G | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-2053C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24981058 | ||||||
| chr16:24981130
|
T | C | 5 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-2125A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24981130 | ||||||
| chr16:24981382
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.54-2377T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24981382 | ||||||
| chr16:24981629
|
T | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0145 | 2 | HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.54-2624A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24981629 | ||||||
| chr16:24981640
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0087 | 2 | HG00323.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.54-2635T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24981640 | ||||||
| chr16:24981741
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.54-2736A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24981741 | ||||||
| chr16:24981748
|
C | T | 7 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-2743G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24981748 | ||||||
| chr16:24981750
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 141 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.54-2745G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24981750 | ||||||
| chr16:24981920
|
C | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-2915G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24981920 | ||||||
| chr16:24981971
|
T | C | 5 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-2966A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24981971 | ||||||
| chr16:24982061
|
A | G | 5 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-3056T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982061 | ||||||
| chr16:24982095
|
A | AT | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(98): Show | 106 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.54-3091dupA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982095 | ||||||
| chr16:24982095
|
AT | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(34): Show | 37 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-3091delA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982095 | ||||||
| chr16:24982115
|
T | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(25): Show | 28 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.54-3110A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982115 | ||||||
| chr16:24982122
|
G | C | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222 | 3 | HG01167.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.54-3117C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982122 | ||||||
| chr16:24982166
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(127): Show | 135 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.54-3161T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982166 | ||||||
| chr16:24982183
|
C | G | 6 | a0001c0001t0001g0028a0001c0001t0001g0121a0001c0001t0001g0122others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.54-3178G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982183 | ||||||
| chr16:24982335
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.54-3330G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982335 | ||||||
| chr16:24982503
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.54-3498C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982503 | ||||||
| chr16:24982512
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 64 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.54-3507C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982512 | ||||||
| chr16:24982540
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.54-3535A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982540 | ||||||
| chr16:24982615
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.54-3610G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982615 | ||||||
| chr16:24982615
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.54-3610G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982615 | ||||||
| chr16:24982757
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.54-3752C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982757 | ||||||
| chr16:24982815
|
TTTTTTCT others(23): Show |
T | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-3840_54-3811del others(30): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982815 | ||||||
| chr16:24982965
|
C | CAT | 8 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG02165.hp1 HG02280.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-3962_54-3961dup others(2): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982965 | ||||||
| chr16:24982965
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0068 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.54-3972_54-3961dup others(12): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982965 | ||||||
| chr16:24982980
|
A | ATATATTT others(17): Show |
1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.54-3976_54-3975ins others(24): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982980 | ||||||
| chr16:24982982
|
A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.54-3978_54-3977ins others(10): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982982 | ||||||
| chr16:24982982
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.54-3977T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982982 | ||||||
| chr16:24982982
|
ATATATAT others(12): Show |
A | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG01074.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.54-3996_54-3978del others(19): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982982 | ||||||
| chr16:24982982
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0009 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.54-3997_54-3978del others(20): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982982 | ||||||
| chr16:24982982
|
ATATATAT others(14): Show |
A | 13 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0035others(10): Show | 13 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-3998_54-3978del others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982982 | ||||||
| chr16:24982984
|
ATATATAT others(10): Show |
A | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.54-3996_54-3980del others(17): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982984 | ||||||
| chr16:24982984
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.54-3998_54-3980del others(19): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982984 | ||||||
| chr16:24982984
|
ATATATAT others(15): Show |
A | 1 | a0001c0002t0001g0034 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.54-4001_54-3980del others(22): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982984 | ||||||
| chr16:24982985
|
T | TATACAC | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-3981_54-3980ins others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982985 | ||||||
| chr16:24982986
|
A | ATATATAT others(3): Show |
5 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0097others(2): Show | 5 | HG01934.hp1 HG04204.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-3982_54-3981ins others(10): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982986 | ||||||
| chr16:24982986
|
A | ATATATAT others(1): Show |
8 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0054others(5): Show | 8 | HG02071.hp1 HG02071.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-3982_54-3981ins others(8): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982986 | ||||||
| chr16:24982986
|
A | T | 1 | a0001c0001t0001g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.54-3981T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982986 | ||||||
| chr16:24982986
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.54-4000_54-3982del others(19): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982986 | ||||||
| chr16:24982986
|
ATATATAT others(16): Show |
A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-4004_54-3982del others(23): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982986 | ||||||
| chr16:24982990
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0004g0222 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.54-3995_54-3986del others(10): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982990 | ||||||
| chr16:24982990
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0149 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.54-3997_54-3986del others(12): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982990 | ||||||
| chr16:24982992
|
A | T | 14 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0023others(11): Show | 17 | HG00438.hp1 HG01243.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.54-3987T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982992 | ||||||
| chr16:24982992
|
ATATATTT others(3): Show |
A | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.54-3997_54-3988del others(10): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982992 | ||||||
| chr16:24982994
|
A | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(27): Show | 31 | HG00323.hp2 HG00609.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.54-3989T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982994 | ||||||
| chr16:24982996
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0005g0230 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.54-3992_54-3991ins others(10): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982996 | ||||||
| chr16:24982996
|
A | ATATATAT others(8): Show |
1 | a0001c0004t0002g0110 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.54-3992_54-3991ins others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982996 | ||||||
| chr16:24982996
|
A | ATATATAT others(3): Show |
1 | a0001c0004t0002g0103 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.54-3992_54-3991ins others(10): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982996 | ||||||
| chr16:24982996
|
A | ATATATAT others(5): Show |
1 | a0001c0004t0002g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.54-3992_54-3991ins others(12): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982996 | ||||||
| chr16:24982996
|
A | ATATATTT others(3): Show |
1 | a0001c0004t0002g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54-3992_54-3991ins others(10): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982996 | ||||||
| chr16:24982996
|
A | ATATTTTT others(3): Show |
1 | a0001c0004t0002g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.54-3992_54-3991ins others(10): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982996 | ||||||
| chr16:24982996
|
A | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0061a0001c0001t0001g0069others(2): Show | 5 | HG02109.hp1 HG02809.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-3991T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982996 | ||||||
| chr16:24982996
|
AT | A | 6 | a0001c0001t0001g0106a0001c0001t0001g0125a0001c0001t0001g0143others(3): Show | 6 | HG01099.hp1 HG01123.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-3992delA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982996 | ||||||
| chr16:24982996
|
ATTTTT | A | 5 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0133others(2): Show | 5 | HG00642.hp2 HG01261.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-3996_54-3992del others(5): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982996 | ||||||
| chr16:24982996
|
ATTTTTT | A | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(2): Show | 5 | HG02040.hp1 HG02074.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-3997_54-3992del others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982996 | ||||||
| chr16:24982996
|
ATTTTTTT | A | 14 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0105others(11): Show | 14 | HG00609.hp1 HG01261.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-3998_54-3992del others(7): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982996 | ||||||
| chr16:24982996
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.54-4001_54-3992del others(10): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982996 | ||||||
| chr16:24982997
|
T | TA | 15 | a0001c0001t0001g0166a0001c0001t0001g0170a0001c0001t0001g0171others(12): Show | 15 | HG01074.hp1 HG01257.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.54-3993_54-3992ins others(1): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982997 | ||||||
| chr16:24982997
|
T | TATA | 11 | a0001c0001t0001g0120a0001c0001t0001g0158a0001c0001t0001g0172others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-3993_54-3992ins others(3): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982997 | ||||||
| chr16:24982997
|
T | TATATA | 16 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0055others(13): Show | 19 | HG00323.hp1 HG00438.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.54-3993_54-3992ins others(5): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982997 | ||||||
| chr16:24982997
|
T | TATATATA | 33 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(30): Show | 33 | HG00323.hp2 HG00609.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.54-3993_54-3992ins others(7): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982997 | ||||||
| chr16:24982997
|
T | TATATATA others(2): Show |
10 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0048others(7): Show | 11 | HG01123.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.54-3993_54-3992ins others(9): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982997 | ||||||
| chr16:24982997
|
T | TATATATA others(4): Show |
2 | a0001c0001t0001g0066a0001c0001t0007g0018 | 2 | HG02109.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.54-3993_54-3992ins others(11): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982997 | ||||||
| chr16:24982998
|
T | A | 53 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0030others(50): Show | 53 | HG00597.hp2 HG01243.hp1 HG01496.hp1 others(50): Show |
intron_variant | MODIFIER | c.54-3993A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982998 | ||||||
| chr16:24982999
|
T | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(83): Show | 90 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.54-3994A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982999 | ||||||
| chr16:24982999
|
T | TATATATA others(4): Show |
4 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0001g0100others(1): Show | 4 | HG02258.hp2 HG02451.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-3995_54-3994ins others(11): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982999 | ||||||
| chr16:24983000
|
T | A | 40 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0030others(37): Show | 40 | HG00597.hp2 HG01884.hp2 HG01934.hp1 others(37): Show |
intron_variant | MODIFIER | c.54-3995A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983000 | ||||||
| chr16:24983000
|
T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.54-3996_54-3995ins others(14): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983000 | ||||||
| chr16:24983001
|
T | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(81): Show | 88 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.54-3996A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983001 | ||||||
| chr16:24983001
|
T | TATATATA others(6): Show |
3 | a0001c0001t0001g0082a0001c0001t0001g0096a0001c0001t0001g0107 | 3 | HG02886.hp2 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.54-3997_54-3996ins others(13): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983001 | ||||||
| chr16:24983001
|
T | TATATATA others(32): Show |
1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.54-3997_54-3996ins others(39): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983001 | ||||||
| chr16:24983002
|
T | A | 32 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0030others(29): Show | 32 | HG00597.hp2 HG01934.hp1 HG01993.hp1 others(29): Show |
intron_variant | MODIFIER | c.54-3997A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983002 | ||||||
| chr16:24983003
|
T | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(46): Show | 50 | HG00323.hp1 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.54-3998A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983003 | ||||||
| chr16:24983004
|
T | A | 18 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0030others(15): Show | 18 | HG01934.hp1 HG01993.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.54-3999A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983004 | ||||||
| chr16:24983005
|
T | A | 25 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0025others(22): Show | 25 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.54-4000A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983005 | ||||||
| chr16:24983006
|
T | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0099a0001c0001t0001g0122others(3): Show | 6 | HG02109.hp2 HG02735.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.54-4001A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983006 | ||||||
| chr16:24983007
|
T | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0125others(8): Show | 11 | HG00323.hp1 HG01261.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.54-4002A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983007 | ||||||
| chr16:24983008
|
T | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0068 | 2 | HG02109.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.54-4003A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983008 | ||||||
| chr16:24983009
|
T | A | 1 | a0001c0001t0007g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.54-4004A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983009 | ||||||
| chr16:24983010
|
T | A | 1 | a0001c0001t0001g0068 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.54-4005A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983010 | ||||||
| chr16:24983012
|
T | A | 1 | a0001c0001t0001g0068 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.54-4007A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983012 | ||||||
| chr16:24983028
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-4023T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983028 | ||||||
| chr16:24983030
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-4025C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983030 | ||||||
| chr16:24983037
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-4032A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983037 | ||||||
| chr16:24983044
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-4039T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983044 | ||||||
| chr16:24983254
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.54-4249G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983254 | ||||||
| chr16:24983299
|
G | A | 21 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(18): Show | 22 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.54-4294C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983299 | ||||||
| chr16:24983356
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(73): Show | 80 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.54-4351G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983356 | ||||||
| chr16:24983356
|
CAGTGGCC others(2): Show |
C | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.54-4360_54-4352del others(9): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983356 | ||||||
| chr16:24983398
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 141 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.54-4393A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983398 | ||||||
| chr16:24983440
|
G | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(25): Show | 28 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.54-4435C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983440 | ||||||
| chr16:24983478
|
T | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-4473A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983478 | ||||||
| chr16:24983780
|
C | T | 1 | a0001c0002t0001g0039 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.54-4775G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983780 | ||||||
| chr16:24983981
|
G | A | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.54-4976C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983981 | ||||||
| chr16:24984070
|
A | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(23): Show | 26 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.54-5065T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984070 | ||||||
| chr16:24984100
|
C | A | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(23): Show | 26 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.54-5095G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984100 | ||||||
| chr16:24984206
|
TG | T | 8 | a0001c0001t0001g0105a0001c0001t0001g0116a0001c0001t0001g0117others(5): Show | 8 | HG00609.hp1 HG02040.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-5202delC | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984206 | ||||||
| chr16:24984272
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-5267C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984272 | ||||||
| chr16:24984296
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.54-5291C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984296 | ||||||
| chr16:24984357
|
A | G | 17 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(14): Show | 17 | HG00597.hp2 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.54-5352T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984357 | ||||||
| chr16:24984389
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.54-5384C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984389 | ||||||
| chr16:24984462
|
C | T | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-5457G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984462 | ||||||
| chr16:24984498
|
C | CA | 9 | a0001c0001t0001g0046a0001c0001t0001g0067a0001c0001t0001g0092others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.54-5494dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984498 | ||||||
| chr16:24984504
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.54-5499T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984504 | ||||||
| chr16:24984584
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.54-5579T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984584 | ||||||
| chr16:24984657
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.54-5652C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984657 | ||||||
| chr16:24984686
|
G | A | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-5681C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984686 | ||||||
| chr16:24984887
|
T | G | 1 | a0001c0001t0001g0188 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.54-5882A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984887 | ||||||
| chr16:24984894
|
A | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-5889T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24984894 | ||||||
| chr16:24985069
|
C | G | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-6064G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24985069 | ||||||
| chr16:24985158
|
A | G | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.54-6153T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24985158 | ||||||
| chr16:24985188
|
CCA | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(12): Show | 15 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.54-6185_54-6184del others(2): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24985188 | ||||||
| chr16:24985188
|
CCACA | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(115): Show | 123 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.54-6187_54-6184del others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24985188 | ||||||
| chr16:24985194
|
A | C | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.54-6189T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24985194 | ||||||
| chr16:24985393
|
T | A | 1 | a0001c0001t0001g0050 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.54-6388A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24985393 | ||||||
| chr16:24985710
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54-6705G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24985710 | ||||||
| chr16:24985847
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.54-6842A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24985847 | ||||||
| chr16:24985891
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.54-6886C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24985891 | ||||||
| chr16:24985947
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.54-6942A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24985947 | ||||||
| chr16:24985991
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.54-6986C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24985991 | ||||||
| chr16:24986067
|
G | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 141 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.54-7062C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24986067 | ||||||
| chr16:24986326
|
T | C | 14 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034others(11): Show | 14 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-7321A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24986326 | ||||||
| chr16:24986334
|
T | A | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-7329A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24986334 | ||||||
| chr16:24986348
|
C | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-7343G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24986348 | ||||||
| chr16:24986369
|
TTAGTTTA others(2): Show |
T | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-7373_54-7365del others(9): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24986369 | ||||||
| chr16:24986374
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.54-7369A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24986374 | ||||||
| chr16:24986427
|
G | A | 34 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(31): Show | 34 | HG00597.hp2 HG01069.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.54-7422C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24986427 | ||||||
| chr16:24986459
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 141 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.54-7454T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24986459 | ||||||
| chr16:24986952
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.54-7947C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24986952 | ||||||
| chr16:24987052
|
A | G | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-8047T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24987052 | ||||||
| chr16:24987203
|
C | T | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-8198G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24987203 | ||||||
| chr16:24987353
|
T | C | 21 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(18): Show | 22 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.54-8348A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24987353 | ||||||
| chr16:24987391
|
T | C | 4 | a0001c0001t0001g0165a0001c0001t0001g0174a0001c0001t0001g0176others(1): Show | 4 | HG02074.hp1 HG02145.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-8386A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24987391 | ||||||
| chr16:24987473
|
G | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.54-8468C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24987473 | ||||||
| chr16:24987613
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.54-8608T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24987613 | ||||||
| chr16:24987622
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.54-8617T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24987622 | ||||||
| chr16:24987653
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.54-8648C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24987653 | ||||||
| chr16:24987751
|
G | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(9): Show | 12 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.54-8746C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24987751 | ||||||
| chr16:24987776
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.54-8771G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24987776 | ||||||
| chr16:24987986
|
G | A | 4 | a0001c0001t0001g0126a0001c0001t0001g0135a0001c0001t0001g0139others(1): Show | 4 | HG00642.hp2 HG01123.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-8981C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24987986 | ||||||
| chr16:24988200
|
G | T | 8 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(5): Show | 8 | HG01934.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-9195C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24988200 | ||||||
| chr16:24988697
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.54-9692C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24988697 | ||||||
| chr16:24988959
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.54-9954C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24988959 | ||||||
| chr16:24989217
|
C | T | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-10212G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24989217 | ||||||
| chr16:24989547
|
C | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-10542G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24989547 | ||||||
| chr16:24989671
|
G | A | 16 | a0001c0001t0001g0029a0001c0001t0001g0229a0001c0002t0001g0032others(13): Show | 16 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.54-10666C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24989671 | ||||||
| chr16:24989750
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.54-10745A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24989750 | ||||||
| chr16:24989752
|
T | A | 1 | a0001c0001t0004g0011 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.54-10747A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24989752 | ||||||
| chr16:24989801
|
C | CA | 14 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034others(11): Show | 14 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-10797dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24989801 | ||||||
| chr16:24989963
|
T | C | 5 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-10958A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24989963 | ||||||
| chr16:24990152
|
G | A | 4 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0041others(1): Show | 4 | HG01928.hp1 HG02148.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-11147C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24990152 | ||||||
| chr16:24990203
|
G | T | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-11198C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24990203 | ||||||
| chr16:24990311
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.54-11306G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24990311 | ||||||
| chr16:24990436
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.54-11431G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24990436 | ||||||
| chr16:24990485
|
C | CA | 21 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(18): Show | 22 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.54-11481dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24990485 | ||||||
| chr16:24990771
|
C | CT | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(129): Show | 137 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.54-11767dupA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24990771 | ||||||
| chr16:24990771
|
C | CTT | 13 | a0001c0001t0001g0056a0001c0001t0001g0069a0001c0001t0001g0097others(10): Show | 13 | HG01934.hp1 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.54-11768_54-11767d others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24990771 | ||||||
| chr16:24990968
|
T | C | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.54-11963A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24990968 | ||||||
| chr16:24991029
|
A | T | 16 | a0001c0001t0001g0029a0001c0001t0001g0229a0001c0002t0001g0032others(13): Show | 16 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.54-12024T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991029 | ||||||
| chr16:24991044
|
A | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.54-12039T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991044 | ||||||
| chr16:24991062
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.54-12057G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991062 | ||||||
| chr16:24991099
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(115): Show | 123 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.54-12094A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991099 | ||||||
| chr16:24991143
|
T | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 141 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.54-12138A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991143 | ||||||
| chr16:24991166
|
T | C | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.54-12161A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991166 | ||||||
| chr16:24991234
|
T | A | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-12229A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991234 | ||||||
| chr16:24991279
|
C | T | 16 | a0001c0001t0001g0029a0001c0001t0001g0229a0001c0002t0001g0032others(13): Show | 16 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.54-12274G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991279 | ||||||
| chr16:24991345
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.54-12340C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991345 | ||||||
| chr16:24991386
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(92): Show | 99 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.54-12381A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991386 | ||||||
| chr16:24991419
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(115): Show | 123 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.54-12414A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991419 | ||||||
| chr16:24991498
|
G | C | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.54-12493C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991498 | ||||||
| chr16:24991514
|
C | T | 14 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0057others(11): Show | 14 | HG00323.hp2 HG00609.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.54-12509G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991514 | ||||||
| chr16:24991908
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.54-12903G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991908 | ||||||
| chr16:24991925
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.54-12920T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991925 | ||||||
| chr16:24991983
|
T | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 141 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.54-12978A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991983 | ||||||
| chr16:24991986
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.54-12981G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24991986 | ||||||
| chr16:24992074
|
A | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 141 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.54-13069T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24992074 | ||||||
| chr16:24992418
|
C | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-13413G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24992418 | ||||||
| chr16:24992481
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.54-13476C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24992481 | ||||||
| chr16:24992717
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.54-13712A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24992717 | ||||||
| chr16:24993108
|
A | T | 1 | a0001c0001t0004g0227 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.54-14103T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993108 | ||||||
| chr16:24993171
|
T | A | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.54-14166A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993171 | ||||||
| chr16:24993278
|
G | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-14273C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993278 | ||||||
| chr16:24993323
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.54-14318G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993323 | ||||||
| chr16:24993375
|
C | T | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-14370G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993375 | ||||||
| chr16:24993389
|
C | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-14384G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993389 | ||||||
| chr16:24993457
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.54-14452A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993457 | ||||||
| chr16:24993492
|
G | A | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-14487C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993492 | ||||||
| chr16:24993588
|
CA | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(81): Show | 88 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.54-14584delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993588 | ||||||
| chr16:24993710
|
C | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-14705G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993710 | ||||||
| chr16:24993711
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.54-14706A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993711 | ||||||
| chr16:24993737
|
G | C | 1 | a0001c0002t0001g0037 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.54-14732C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993737 | ||||||
| chr16:24993741
|
C | A | 5 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-14736G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993741 | ||||||
| chr16:24993887
|
A | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(78): Show | 85 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-14882T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24993887 | ||||||
| chr16:24994000
|
A | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.54-14995T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994000 | ||||||
| chr16:24994041
|
C | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-15036G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994041 | ||||||
| chr16:24994057
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.54-15052A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994057 | ||||||
| chr16:24994066
|
G | A | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.54-15061C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994066 | ||||||
| chr16:24994498
|
C | G | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.54-15493G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994498 | ||||||
| chr16:24994653
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(128): Show | 136 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.54-15648G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994653 | ||||||
| chr16:24994664
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(3): Show | 6 | HG01099.hp2 HG02723.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.54-15659C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994664 | ||||||
| chr16:24994684
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(73): Show | 80 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.54-15679G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994684 | ||||||
| chr16:24994695
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(106): Show | 114 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.54-15690C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994695 | ||||||
| chr16:24994731
|
G | A | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.54-15726C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994731 | ||||||
| chr16:24994783
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.54-15778G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994783 | ||||||
| chr16:24994950
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(9): Show | 12 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.54-15945G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994950 | ||||||
| chr16:24994974
|
C | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.54-15969G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994974 | ||||||
| chr16:24994997
|
T | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(116): Show | 124 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.54-15992A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24994997 | ||||||
| chr16:24995015
|
C | T | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-16010G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24995015 | ||||||
| chr16:24995162
|
G | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(134): Show | 142 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.54-16157C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24995162 | ||||||
| chr16:24995176
|
G | A | 8 | a0001c0004t0002g0103a0001c0004t0002g0108a0001c0004t0002g0110others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-16171C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24995176 | ||||||
| chr16:24995451
|
G | A | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-16446C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24995451 | ||||||
| chr16:24995933
|
G | A | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-16928C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24995933 | ||||||
| chr16:24995947
|
C | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG02280.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.54-16942G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24995947 | ||||||
| chr16:24995967
|
A | T | 1 | a0001c0001t0002g0031 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.54-16962T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24995967 | ||||||
| chr16:24995975
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.54-16970C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24995975 | ||||||
| chr16:24995987
|
C | G | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-16982G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24995987 | ||||||
| chr16:24996115
|
G | T | 1 | a0001c0001t0004g0227 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.54-17110C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24996115 | ||||||
| chr16:24996177
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(59): Show | 65 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.54-17172C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24996177 | ||||||
| chr16:24996219
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.54-17214T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24996219 | ||||||
| chr16:24996228
|
G | T | 16 | a0001c0001t0001g0029a0001c0001t0001g0229a0001c0002t0001g0032others(13): Show | 16 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.54-17223C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24996228 | ||||||
| chr16:24996506
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0229 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.54-17501T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24996506 | ||||||
| chr16:24996599
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.54-17594C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24996599 | ||||||
| chr16:24996659
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.54-17654C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24996659 | ||||||
| chr16:24996913
|
C | A | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.54-17908G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24996913 | ||||||
| chr16:24996913
|
C | CA | 72 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0046others(69): Show | 75 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.54-17909dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24996913 | ||||||
| chr16:24996994
|
T | C | 2 | a0001c0004t0002g0108a0001c0004t0002g0115 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.54-17989A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24996994 | ||||||
| chr16:24997196
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG01099.hp2 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.53+18013C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24997196 | ||||||
| chr16:24997363
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.53+17846C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24997363 | ||||||
| chr16:24997464
|
T | C | 7 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0077others(4): Show | 7 | HG00323.hp2 HG01069.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.53+17745A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24997464 | ||||||
| chr16:24997488
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.53+17721C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24997488 | ||||||
| chr16:24997880
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 13 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.53+17329G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24997880 | ||||||
| chr16:24997888
|
T | C | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.53+17321A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24997888 | ||||||
| chr16:24997932
|
G | C | 1 | a0001c0001t0001g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.53+17277C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24997932 | ||||||
| chr16:24998090
|
G | A | 2 | a0001c0002t0001g0035a0001c0002t0001g0091 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.53+17119C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998090 | ||||||
| chr16:24998172
|
C | T | 14 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034others(11): Show | 14 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.53+17037G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998172 | ||||||
| chr16:24998228
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.53+16981C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998228 | ||||||
| chr16:24998383
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.53+16826C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998383 | ||||||
| chr16:24998413
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(134): Show | 142 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.53+16796A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998413 | ||||||
| chr16:24998454
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.53+16755C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998454 | ||||||
| chr16:24998466
|
GC | G | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.53+16742delG | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998466 | ||||||
| chr16:24998506
|
T | C | 1 | a0001c0001t0001g0135 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.53+16703A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998506 | ||||||
| chr16:24998548
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.53+16661C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998548 | ||||||
| chr16:24998610
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(18): Show | 21 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.53+16599G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998610 | ||||||
| chr16:24998698
|
C | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0079others(2): Show | 8 | NA18983.hp2 NA18986.hp2 NA18994.hp2 others(5): Show |
intron_variant | MODIFIER | c.53+16511G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998698 | ||||||
| chr16:24998703
|
C | A | 9 | a0001c0001t0001g0027a0001c0004t0002g0103a0001c0004t0002g0108others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.53+16506G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998703 | ||||||
| chr16:24998890
|
C | T | 14 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(11): Show | 14 | HG00597.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+16319G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24998890 | ||||||
| chr16:24999006
|
CT | C | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+16202delA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999006 | ||||||
| chr16:24999040
|
C | T | 1 | a0001c0001t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.53+16169G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999040 | ||||||
| chr16:24999156
|
G | A | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+16053C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999156 | ||||||
| chr16:24999165
|
A | T | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG01069.hp1 HG01257.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.53+16044T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999165 | ||||||
| chr16:24999168
|
G | A | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+16041C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999168 | ||||||
| chr16:24999191
|
A | G | 16 | a0001c0001t0001g0029a0001c0001t0001g0229a0001c0002t0001g0032others(13): Show | 16 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.53+16018T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999191 | ||||||
| chr16:24999208
|
G | A | 9 | a0001c0001t0001g0014a0001c0004t0002g0103a0001c0004t0002g0108others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+16001C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999208 | ||||||
| chr16:24999344
|
T | C | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+15865A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999344 | ||||||
| chr16:24999399
|
T | TTTTA | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 55 | HG00642.hp2 HG01123.hp1 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.53+15806_53+15809d others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999399 | ||||||
| chr16:24999399
|
T | TTTTATTT others(1): Show |
4 | a0001c0001t0001g0026a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG00323.hp1 HG01934.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+15802_53+15809d others(10): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999399 | ||||||
| chr16:24999525
|
T | G | 16 | a0001c0001t0001g0029a0001c0001t0001g0229a0001c0002t0001g0032others(13): Show | 16 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.53+15684A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999525 | ||||||
| chr16:24999576
|
C | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(14): Show | 18 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.53+15633G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999576 | ||||||
| chr16:24999882
|
C | T | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53+15327G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24999882 | ||||||
| chr16:25000012
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 64 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.53+15197G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000012 | ||||||
| chr16:25000209
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 4 | HG02451.hp2 HG02965.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+15000C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000209 | ||||||
| chr16:25000285
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG01168.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.53+14924C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000285 | ||||||
| chr16:25000298
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(132): Show | 140 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.53+14911G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000298 | ||||||
| chr16:25000354
|
G | A | 13 | a0001c0001t0001g0030a0001c0001t0001g0100a0001c0001t0001g0101others(10): Show | 13 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.53+14855C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000354 | ||||||
| chr16:25000440
|
G | T | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+14769C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000440 | ||||||
| chr16:25000455
|
C | T | 14 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0230others(11): Show | 15 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.53+14754G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000455 | ||||||
| chr16:25000484
|
T | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0106 | 3 | HG01099.hp1 HG01993.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.53+14725A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000484 | ||||||
| chr16:25000525
|
A | G | 17 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(14): Show | 18 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.53+14684T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000525 | ||||||
| chr16:25000621
|
T | C | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53+14588A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000621 | ||||||
| chr16:25000645
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.53+14564T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000645 | ||||||
| chr16:25000678
|
T | G | 13 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034others(10): Show | 13 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.53+14531A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000678 | ||||||
| chr16:25000797
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.53+14412G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25000797 | ||||||
| chr16:25001030
|
A | G | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.53+14179T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25001030 | ||||||
| chr16:25001103
|
T | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 64 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.53+14106A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25001103 | ||||||
| chr16:25001265
|
C | CA | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.53+13943dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25001265 | ||||||
| chr16:25001265
|
CA | C | 14 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034others(11): Show | 14 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.53+13943delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25001265 | ||||||
| chr16:25001525
|
C | T | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+13684G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25001525 | ||||||
| chr16:25001894
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(136): Show | 144 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.53+13315T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25001894 | ||||||
| chr16:25002178
|
C | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 64 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.53+13031G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25002178 | ||||||
| chr16:25002374
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.53+12835C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25002374 | ||||||
| chr16:25002428
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.53+12781A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25002428 | ||||||
| chr16:25002453
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 101 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.53+12756C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25002453 | ||||||
| chr16:25002499
|
G | A | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+12710C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25002499 | ||||||
| chr16:25002620
|
C | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(24): Show | 28 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.53+12589G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25002620 | ||||||
| chr16:25002736
|
T | C | 8 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0004g0220others(5): Show | 8 | HG01167.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.53+12473A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25002736 | ||||||
| chr16:25002741
|
G | A | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222 | 3 | HG01167.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53+12468C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25002741 | ||||||
| chr16:25002807
|
G | A | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53+12402C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25002807 | ||||||
| chr16:25002920
|
T | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.53+12289A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25002920 | ||||||
| chr16:25002978
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.53+12231C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25002978 | ||||||
| chr16:25003000
|
C | T | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+12209G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003000 | ||||||
| chr16:25003038
|
C | CA | 15 | a0001c0001t0001g0028a0001c0001t0001g0140a0001c0001t0001g0141others(12): Show | 15 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+12170dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003038 | ||||||
| chr16:25003038
|
C | CAA | 5 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0053others(2): Show | 5 | HG02735.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+12169_53+12170d others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003038 | ||||||
| chr16:25003038
|
C | CAAA | 49 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0048others(46): Show | 52 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.53+12168_53+12170d others(5): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003038 | ||||||
| chr16:25003038
|
C | CAAAA | 20 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0084others(17): Show | 20 | HG01243.hp2 HG01256.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.53+12167_53+12170d others(6): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003038 | ||||||
| chr16:25003038
|
CAA | C | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.53+12169_53+12170d others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003038 | ||||||
| chr16:25003149
|
A | G | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+12060T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003149 | ||||||
| chr16:25003173
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.53+12036T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003173 | ||||||
| chr16:25003176
|
G | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.53+12033C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003176 | ||||||
| chr16:25003222
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(136): Show | 144 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.53+11987G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003222 | ||||||
| chr16:25003230
|
C | CT | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(60): Show | 63 | HG00323.hp1 HG00438.hp1 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.53+11978dupA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003230 | ||||||
| chr16:25003230
|
C | CTT | 12 | a0001c0001t0001g0014a0001c0001t0001g0124a0001c0001t0001g0125others(9): Show | 12 | HG00642.hp2 HG01243.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.53+11977_53+11978d others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003230 | ||||||
| chr16:25003230
|
C | CTTT | 4 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0003t0003g0210others(1): Show | 5 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.53+11976_53+11978d others(5): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003230 | ||||||
| chr16:25003230
|
CT | C | 13 | a0001c0001t0001g0088a0001c0002t0001g0034a0001c0002t0001g0035others(10): Show | 13 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.53+11978delA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003230 | ||||||
| chr16:25003230
|
CTTTTTTT others(5): Show |
C | 28 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(25): Show | 29 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.53+11967_53+11978d others(14): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003230 | ||||||
| chr16:25003292
|
T | G | 1 | a0001c0001t0001g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.53+11917A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003292 | ||||||
| chr16:25003602
|
T | C | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222 | 3 | HG01167.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53+11607A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003602 | ||||||
| chr16:25003654
|
T | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG01515.hp2 HG01517.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.53+11555A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003654 | ||||||
| chr16:25003684
|
A | G | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.53+11525T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003684 | ||||||
| chr16:25003751
|
G | C | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.53+11458C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003751 | ||||||
| chr16:25003775
|
A | G | 6 | a0001c0001t0001g0028a0001c0001t0001g0120a0001c0001t0001g0121others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.53+11434T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003775 | ||||||
| chr16:25003797
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53+11412A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003797 | ||||||
| chr16:25003822
|
CA | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(72): Show | 78 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.53+11386delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003822 | ||||||
| chr16:25004241
|
T | C | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.53+10968A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25004241 | ||||||
| chr16:25004261
|
G | C | 9 | a0001c0001t0001g0107a0001c0004t0002g0103a0001c0004t0002g0108others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.53+10948C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25004261 | ||||||
| chr16:25004737
|
T | C | 11 | a0001c0001t0001g0012a0001c0003t0003g0210a0001c0003t0003g0211others(8): Show | 11 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.53+10472A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25004737 | ||||||
| chr16:25004785
|
G | T | 1 | a0001c0001t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.53+10424C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25004785 | ||||||
| chr16:25004791
|
G | T | 8 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0004g0220others(5): Show | 8 | HG01167.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.53+10418C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25004791 | ||||||
| chr16:25004819
|
G | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.53+10390C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25004819 | ||||||
| chr16:25005395
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.53+9814A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25005395 | ||||||
| chr16:25005405
|
A | G | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53+9804T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25005405 | ||||||
| chr16:25005426
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.53+9783C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25005426 | ||||||
| chr16:25005710
|
G | GT | 75 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(72): Show | 78 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.53+9498_53+9499ins others(1): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25005710 | ||||||
| chr16:25005719
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.53+9490A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25005719 | ||||||
| chr16:25005841
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.53+9368G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25005841 | ||||||
| chr16:25005874
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.53+9335C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25005874 | ||||||
| chr16:25006073
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(136): Show | 144 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.53+9136A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006073 | ||||||
| chr16:25006099
|
T | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 64 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.53+9110A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006099 | ||||||
| chr16:25006129
|
G | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.53+9080C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006129 | ||||||
| chr16:25006143
|
A | G | 3 | a0001c0001t0001g0107a0001c0004t0002g0108a0001c0004t0002g0115 | 3 | HG02572.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.53+9066T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006143 | ||||||
| chr16:25006190
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.53+9019A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006190 | ||||||
| chr16:25006252
|
C | T | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+8957G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006252 | ||||||
| chr16:25006269
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(169): Show | 177 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.53+8940A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006269 | ||||||
| chr16:25006286
|
A | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.53+8923T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006286 | ||||||
| chr16:25006374
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(25): Show | 29 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.53+8835G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006374 | ||||||
| chr16:25006449
|
C | CA | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(22): Show | 25 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.53+8759dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006449 | ||||||
| chr16:25006449
|
CA | C | 15 | a0001c0001t0001g0046a0001c0002t0001g0032a0001c0002t0001g0033others(12): Show | 15 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.53+8759delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006449 | ||||||
| chr16:25006659
|
T | C | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53+8550A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006659 | ||||||
| chr16:25006718
|
A | C | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.53+8491T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25006718 | ||||||
| chr16:25007080
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(136): Show | 144 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.53+8129A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25007080 | ||||||
| chr16:25007309
|
C | CAATAAAG others(87): Show |
1 | a0001c0002t0001g0044 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.53+7806_53+7899dup others(94): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25007309 | ||||||
| chr16:25007816
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.53+7393G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25007816 | ||||||
| chr16:25007864
|
C | G | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53+7345G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25007864 | ||||||
| chr16:25007964
|
A | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 182 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.53+7245T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25007964 | ||||||
| chr16:25007984
|
C | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 64 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.53+7225G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25007984 | ||||||
| chr16:25008377
|
A | G | 14 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034others(11): Show | 14 | HG01256.hp1 HG01516.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.53+6832T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25008377 | ||||||
| chr16:25008435
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.53+6774T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25008435 | ||||||
| chr16:25008518
|
G | A | 1 | a0001c0001t0005g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53+6691C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25008518 | ||||||
| chr16:25008578
|
A | G | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+6631T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25008578 | ||||||
| chr16:25008640
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0003c0007t0001g0224 | 3 | HG02258.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.53+6569G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25008640 | ||||||
| chr16:25008725
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.53+6484G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25008725 | ||||||
| chr16:25008735
|
C | A | 1 | a0001c0001t0005g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.53+6474G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25008735 | ||||||
| chr16:25008844
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(136): Show | 144 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.53+6365G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25008844 | ||||||
| chr16:25008906
|
T | G | 1 | a0001c0001t0001g0151 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.53+6303A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25008906 | ||||||
| chr16:25008963
|
G | GGAC | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+6243_53+6245dup others(3): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25008963 | ||||||
| chr16:25008985
|
A | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 64 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.53+6224T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25008985 | ||||||
| chr16:25009037
|
T | C | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG01069.hp1 HG01257.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.53+6172A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009037 | ||||||
| chr16:25009235
|
C | T | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+5974G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009235 | ||||||
| chr16:25009345
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.53+5864G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009345 | ||||||
| chr16:25009353
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+5856G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009353 | ||||||
| chr16:25009362
|
G | A | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.53+5847C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009362 | ||||||
| chr16:25009364
|
CA | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(73): Show | 79 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.53+5844delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009364 | ||||||
| chr16:25009364
|
CAA | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(39): Show | 44 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.53+5843_53+5844del others(2): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009364 | ||||||
| chr16:25009364
|
CAAAA | C | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.53+5841_53+5844del others(4): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009364 | ||||||
| chr16:25009383
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.53+5826C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009383 | ||||||
| chr16:25009547
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.53+5662C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009547 | ||||||
| chr16:25009556
|
G | A | 1 | a0001c0003t0003g0219 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.53+5653C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009556 | ||||||
| chr16:25009841
|
G | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 115 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.53+5368C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009841 | ||||||
| chr16:25009866
|
A | T | 1 | a0001c0002t0001g0044 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.53+5343T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009866 | ||||||
| chr16:25009867
|
G | C | 1 | a0001c0002t0001g0044 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.53+5342C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009867 | ||||||
| chr16:25009868
|
T | A | 1 | a0001c0002t0001g0044 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.53+5341A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009868 | ||||||
| chr16:25009870
|
T | A | 1 | a0001c0002t0001g0044 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.53+5339A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009870 | ||||||
| chr16:25009873
|
A | T | 1 | a0001c0002t0001g0044 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.53+5336T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009873 | ||||||
| chr16:25009878
|
ACCAAGCC others(38): Show |
A | 1 | a0001c0002t0001g0044 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.53+5286_53+5330del others(45): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009878 | ||||||
| chr16:25009903
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(71): Show | 77 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.53+5306G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009903 | ||||||
| chr16:25009953
|
AGGCAGCC others(39): Show |
A | 1 | a0001c0002t0001g0044 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.53+5210_53+5255del others(46): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25009953 | ||||||
| chr16:25010082
|
C | CT | 23 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0034others(20): Show | 23 | HG01243.hp1 HG01256.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.53+5126dupA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25010082 | ||||||
| chr16:25010160
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG02040.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.53+5049G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25010160 | ||||||
| chr16:25010220
|
A | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18942.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.53+4989T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25010220 | ||||||
| chr16:25010236
|
C | G | 8 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0004g0220others(5): Show | 8 | HG01167.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.53+4973G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25010236 | ||||||
| chr16:25010308
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(72): Show | 78 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.53+4901T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25010308 | ||||||
| chr16:25010484
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG01168.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.53+4725A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25010484 | ||||||
| chr16:25010533
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.53+4676C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25010533 | ||||||
| chr16:25010844
|
T | C | 8 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(5): Show | 8 | HG01934.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.53+4365A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25010844 | ||||||
| chr16:25010873
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.53+4336C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25010873 | ||||||
| chr16:25010884
|
T | C | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.53+4325A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25010884 | ||||||
| chr16:25010930
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.53+4279T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25010930 | ||||||
| chr16:25010990
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(169): Show | 177 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.53+4219T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25010990 | ||||||
| chr16:25011029
|
T | C | 1 | a0001c0004t0002g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.53+4180A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25011029 | ||||||
| chr16:25011231
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.53+3978A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25011231 | ||||||
| chr16:25011398
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.53+3811C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25011398 | ||||||
| chr16:25011497
|
G | C | 13 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231others(10): Show | 14 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.53+3712C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25011497 | ||||||
| chr16:25011529
|
ACCACATC others(1): Show |
A | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.53+3672_53+3679del others(8): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25011529 | ||||||
| chr16:25011698
|
CA | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 116 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.53+3510delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25011698 | ||||||
| chr16:25011859
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.53+3350A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25011859 | ||||||
| chr16:25012505
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.53+2704C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25012505 | ||||||
| chr16:25012517
|
A | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(136): Show | 144 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.53+2692T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25012517 | ||||||
| chr16:25012755
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.53+2454T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25012755 | ||||||
| chr16:25012818
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.53+2391C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25012818 | ||||||
| chr16:25012864
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(75): Show | 81 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.53+2345G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25012864 | ||||||
| chr16:25012986
|
G | A | 14 | a0001c0001t0001g0229a0001c0001t0005g0003a0001c0001t0005g0230others(11): Show | 15 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.53+2223C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25012986 | ||||||
| chr16:25012998
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.53+2211C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25012998 | ||||||
| chr16:25013148
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.53+2061C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25013148 | ||||||
| chr16:25013420
|
C | T | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222 | 3 | HG01167.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53+1789G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25013420 | ||||||
| chr16:25013525
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.53+1684C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25013525 | ||||||
| chr16:25013548
|
G | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.53+1661C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25013548 | ||||||
| chr16:25013590
|
C | G | 5 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(2): Show | 5 | HG00597.hp2 HG02165.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+1619G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25013590 | ||||||
| chr16:25013817
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.53+1392G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25013817 | ||||||
| chr16:25013845
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.53+1364G>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25013845 | ||||||
| chr16:25014033
|
C | T | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+1176G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25014033 | ||||||
| chr16:25014050
|
G | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.53+1159C>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25014050 | ||||||
| chr16:25014158
|
C | CA | 15 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0005g0003others(12): Show | 16 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.53+1050dupT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25014158 | ||||||
| chr16:25014219
|
A | T | 1 | a0001c0001t0002g0031 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.53+990T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25014219 | ||||||
| chr16:25014338
|
A | G | 15 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0020others(12): Show | 16 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.53+871T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25014338 | ||||||
| chr16:25014493
|
A | C | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.53+716T>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25014493 | ||||||
| chr16:25014726
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.53+483A>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25014726 | ||||||
| chr16:25014908
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.53+301C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25014908 | ||||||
| chr16:25014936
|
T | C | 3 | a0001c0001t0005g0003a0001c0001t0005g0230a0001c0001t0005g0231 | 4 | HG01884.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+273A>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25014936 | ||||||
| chr16:25014996
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(168): Show | 176 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.53+213T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25014996 | ||||||
| chr16:25014996
|
A | T | 1 | a0001c0001t0001g0016 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.53+213T>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25014996 | ||||||
| chr16:25015148
|
C | CCCGCCCT | 10 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+60_53+61insAGGG others(3): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25015148 | ||||||
| chr16:25015149
|
G | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(35): Show | 39 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.53+60C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25015149 | ||||||
| chr16:25015168
|
C | T | 1 | a0002c0006t0005g0015 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.53+41G>A | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25015168 | ||||||
| chr16:25015173
|
C | G | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG01074.hp2 HG01099.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.53+36G>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25015173 | ||||||
| chr16:25015178
|
G | C | 4 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG01074.hp2 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+31C>G | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25015178 |