Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 881 | 238 | 87 | 46 | 76 | 8 | 19 | 58 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | MKKQF others(876): Show |
chr16 | 24914389 | 25020369 |
| a0002 | 0/0 | 881 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | MKKQF others(876): Show |
chr16 | 24914389 | 25020369 |
| a0003 | 0/0 | 881 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | MKKQF others(876): Show |
chr16 | 24914389 | 25020369 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2643 | 206 | 71 | 39 | 70 | 7 | 17 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | ATGAA others(2638): Show |
chr16 | 24914389 | 25020369 | ||
| a0001c0002 | 0/0 | 2643 | 14 | 0 | 5 | 6 | 1 | 2 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | ATGAA others(2638): Show |
chr16 | 24914389 | 25020369 | ||
| a0001c0003 | 0/0 | 2643 | 8 | 6 | 2 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | ATGAA others(2638): Show |
chr16 | 24914389 | 25020369 | ||
| a0001c0004 | 0/0 | 2643 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | ATGAA others(2638): Show |
chr16 | 24914389 | 25020369 | ||
| a0001c0005 | 0/0 | 2643 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | ATGAA others(2638): Show |
chr16 | 24914389 | 25020369 | ||
| a0002c0007 | 0/0 | 2643 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | ATGAA others(2638): Show |
chr16 | 24914389 | 25020369 | ||
| a0003c0006 | 0/0 | 2643 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | ATGAA others(2638): Show |
chr16 | 24914389 | 25020369 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3495 | 190 | 58 | 38 | 70 | 5 | 17 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3490): Show |
chr16 | 24914389 | 25020369 |
| a0001c0001t0002 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3490): Show |
chr16 | 24914389 | 25020369 |
| a0001c0001t0004 | 0/0 | 3495 | 6 | 5 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3490): Show |
chr16 | 24914389 | 25020369 |
| a0001c0001t0005 | 0/0 | 3494 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3489): Show |
chr16 | 24914389 | 25020369 |
| a0001c0001t0006 | 0/0 | 3495 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3490): Show |
chr16 | 24914389 | 25020369 |
| a0001c0001t0007 | 0/0 | 3495 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3490): Show |
chr16 | 24914389 | 25020369 |
| a0001c0002t0001 | 0/0 | 3495 | 14 | 0 | 5 | 6 | 1 | 2 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3490): Show |
chr16 | 24914389 | 25020369 |
| a0001c0003t0003 | 0/0 | 3495 | 8 | 6 | 2 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3490): Show |
chr16 | 24914389 | 25020369 |
| a0001c0004t0002 | 0/0 | 3495 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3490): Show |
chr16 | 24914389 | 25020369 |
| a0001c0004t0008 | 0/0 | 3494 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3489): Show |
chr16 | 24914389 | 25020369 |
| a0001c0005t0001 | 0/0 | 3495 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3490): Show |
chr16 | 24914389 | 25020369 |
| a0002c0007t0001 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3490): Show |
chr16 | 24914389 | 25020369 |
| a0003c0006t0005 | 0/0 | 3494 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | GAGCC others(3489): Show |
chr16 | 24914389 | 25020369 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0005g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0003t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0003t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0003t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0003t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0003t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0003t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0003t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0003t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0004t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0004t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0004t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0004t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0004t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0004t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0004t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0004t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0001c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0002c0007t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| a0003c0006t0005g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0219 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01243 | hp1 | a0001 | c0003 | t0003 | g0210 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01496 | hp1 | a0001 | c0003 | t0003 | g0213 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | IBS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0072 | EUR | IBS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | IBS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0070 | EUR | IBS | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01884 | hp2 | a0001 | c0003 | t0003 | g0215 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0214 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02257 | hp2 | a0001 | c0004 | t0002 | g0113 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02572 | hp2 | a0001 | c0004 | t0002 | g0115 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0228 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02809 | hp1 | a0001 | c0003 | t0003 | g0209 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0208 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0114 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02922 | hp2 | a0001 | c0004 | t0008 | g0104 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02970 | hp1 | a0001 | c0004 | t0002 | g0111 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02976 | hp2 | a0001 | c0004 | t0002 | g0108 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0216 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0229 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03209 | hp1 | a0001 | c0004 | t0002 | g0110 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0217 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG04115 | hp1 | a0003 | c0006 | t0005 | g0016 | SAS | STU | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | STU | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | YRI | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | LWK | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ASW | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ASW | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02486 | hp1 | a0002 | c0007 | t0001 | g0222 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02486 | hp2 | a0001 | c0004 | t0002 | g0103 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0212 | AFR | MSL | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | USA | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | USA | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA20300 | hp1 | a0001 | c0004 | t0002 | g0112 | AFR | USA | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | USA | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA21309 | hp1 | a0001 | c0005 | t0001 | g0211 | AFR | LWK | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0135 | REF | REF | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0181 | REF | REF | ARHGAP17_chr16_24914389_25020369 | ARHGAP17 | chr16 | 24914389 | 25020369 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:24939403 | G | A | 1 | a0003 | 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 | a0002 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0004 a0003c0006 |
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 | a0001c0003 a0001c0005 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:24919479 | TA | T | 3 | a0001c0001t0005 a0001c0004t0008 a0003c0006t0005 |
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 | a0001c0001t0002 a0001c0004t0002 a0001c0004t0008 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:24920370 | G | A | 10 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0036 others(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 | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): 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 | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): 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 | a0001c0001t0002g0031 a0001c0004t0002g0103 a0001c0004t0002g0108 others(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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0180 a0001c0001t0001g0195 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
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 | 83 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): 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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0065 | 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0001g0173 a0001c0001t0001g0175 |
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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0004g0012 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
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 | a0001c0001t0004g0219 | 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 | 50 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(47): 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 10 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(7): 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 | a0001c0001t0001g0223 | 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 | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(169): Show |
178 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.2516-3468delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | 24923727 | |||||||
| chr16:24923727 | TAA | T | 18 | a0001c0001t0001g0055 a0001c0001t0001g0076 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0026 a0001c0001t0004g0012 a0001c0001t0004g0218 others(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 | 43 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(40): 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 | 13 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(10): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 31 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(28): 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 | 67 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): 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 | 12 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): 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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
124 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(121): 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 | a0001c0001t0001g0186 a0001c0002t0001g0032 a0001c0002t0001g0033 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | 58 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(55): 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 | a0001c0001t0001g0186 a0001c0001t0005g0114 a0001c0002t0001g0032 others(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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0166 |
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 | 67 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): 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 | a0001c0004t0002g0103 a0001c0004t0008g0104 |
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 | a0001c0001t0001g0156 a0001c0001t0001g0197 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0055 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 32 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0148 others(29): 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 | 18 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(15): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0002g0031 a0001c0001t0005g0004 a0001c0001t0005g0228 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(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 | a0001c0001t0004g0012 a0001c0003t0003g0208 a0001c0003t0003g0209 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0004g0012 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 31 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(28): 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 | a0001c0002t0001g0032 | 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 | 68 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): 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 | a0003c0006t0005g0016 | 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 | 10 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(7): 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
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 | 32 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(29): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0001c0001t0001g0014 a0001c0001t0007g0019 a0001c0001t0007g0020 |
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 | a0001c0001t0001g0029 a0001c0001t0005g0004 a0001c0001t0005g0228 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0071 a0001c0001t0001g0077 others(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 | 3 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0160 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0174 a0001c0001t0001g0176 |
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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0213 others(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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0049 | 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0118 a0001c0001t0005g0114 a0001c0002t0001g0032 others(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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0109 a0001c0001t0002g0031 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0003c0006t0005g0016 | 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 | a0001c0004t0002g0110 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 6 | a0001c0001t0001g0003 a0001c0001t0001g0191 a0001c0001t0001g0192 others(3): 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 | a0001c0001t0007g0020 | 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 | 67 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): 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 | 31 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(28): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0003t0003g0208 | 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | 29 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(26): 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 | a0001c0001t0001g0028 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | 31 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(28): 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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0092 a0001c0001t0001g0145 |
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 | a0001c0001t0001g0014 | 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0118 a0001c0001t0005g0114 a0001c0002t0001g0032 others(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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0005g0114 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0004t0002g0110 | 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 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(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 | |||||||
| chr16:24937067 | T | C | 14 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | 32 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(29): 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 | a0001c0004t0002g0110 a0001c0004t0002g0111 a0001c0004t0002g0112 others(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 | 67 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0051 |
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 | a0001c0001t0001g0066 a0001c0001t0001g0148 a0001c0001t0001g0149 others(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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0106 |
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 | a0003c0006t0005g0016 | 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | 20 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(17): 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 | 20 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(17): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0118 a0001c0001t0005g0114 a0001c0002t0001g0032 others(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 | a0003c0006t0005g0016 | 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 | 25 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(22): 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 | a0001c0001t0001g0118 a0001c0001t0005g0114 a0001c0002t0001g0032 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | 22 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(19): 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 | |||||||
| chr16:24938840 | A | AGTTGATC | 2 | a0001c0003t0003g0215 a0001c0003t0003g0217 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1724+523_1724+524i others(9): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | 24938840 | |||||||
| chr16:24938841 | A | C | 2 | a0001c0003t0003g0215 a0001c0003t0003g0217 |
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 | a0001c0003t0003g0215 a0001c0003t0003g0217 |
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 | 22 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(19): 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 | a0001c0002t0001g0032 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0004g0012 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0004g0012 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 67 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0064 | 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 |
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 | a0001c0004t0002g0108 a0001c0004t0002g0115 |
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 | a0001c0001t0005g0229 | 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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0197 |
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 | a0001c0004t0002g0108 a0001c0004t0002g0115 |
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 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0036 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0213 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0003t0003g0216 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(21): 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 | a0001c0001t0001g0023 a0001c0001t0001g0119 a0001c0003t0003g0208 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0127 others(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 | a0003c0006t0005g0016 | 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 | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(21): 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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0098 others(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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): 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 | a0001c0001t0004g0012 a0001c0001t0004g0218 a0001c0001t0004g0219 others(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 | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(32): Show |
35 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(32): 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 | 67 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): 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 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0004g0012 a0001c0001t0004g0218 a0001c0001t0004g0219 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0074 others(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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0069 |
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 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(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 | 28 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(25): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0003c0006t0005g0016 | 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 | 25 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(22): 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 | 83 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): 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 | 67 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): 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 | 66 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0074 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 22 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(19): 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0004g0218 a0001c0001t0004g0220 |
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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(34): Show |
37 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(34): 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 | a0001c0001t0004g0224 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 115 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
118 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(115): 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 | a0003c0006t0005g0016 | 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | 68 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): 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 | 78 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): 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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0055 a0001c0001t0001g0079 others(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 | 25 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(22): 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 | 26 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(23): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
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 | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(34): Show |
37 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(34): 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 | a0001c0001t0001g0118 a0001c0001t0005g0114 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0004g0218 others(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 | a0003c0006t0005g0016 | 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 | a0001c0001t0007g0020 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(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 | a0003c0006t0005g0016 | 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 | 81 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): 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 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0080 others(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 | a0001c0003t0003g0209 a0001c0003t0003g0210 a0001c0003t0003g0213 others(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 | a0001c0004t0002g0103 a0001c0004t0008g0104 |
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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0004g0218 others(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 | a0001c0001t0004g0219 a0001c0001t0004g0224 a0002c0007t0001g0222 |
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 | a0001c0001t0001g0014 a0001c0001t0004g0220 a0001c0004t0002g0111 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0230 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0231 |
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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0204 others(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 | 23 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(20): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0003c0006t0005g0016 | 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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(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 | a0001c0004t0002g0103 a0001c0004t0008g0104 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | 82 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0003t0003g0210 | 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 | a0003c0006t0005g0016 | 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 | 68 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): 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 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
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 | 68 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): 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 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0133 others(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 | 11 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(8): 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 | 34 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(31): 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 | 82 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): 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 | a0001c0001t0005g0004 a0001c0001t0005g0229 a0001c0003t0003g0208 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0106 |
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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0022 a0003c0006t0005g0016 |
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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 |
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 | 82 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): 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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0029 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0003c0006t0005g0016 | 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 | 3 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 |
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 | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(32): Show |
35 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.725-1385C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956115 | |||||||
| chr16:24956218 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(46): Show |
49 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(46): 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 | a0001c0001t0001g0118 a0001c0001t0005g0114 |
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 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0133 |
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 | a0001c0001t0005g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.725-1952C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | 24956682 | |||||||
| chr16:24956893 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(131): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(71): 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 | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(91): 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 | a0001c0001t0001g0065 | 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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0011 |
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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0066 |
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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(131): 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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(133): 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0004g0218 others(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 | a0001c0001t0001g0109 a0001c0001t0002g0031 a0001c0003t0003g0210 |
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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(71): 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(99): 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 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0036 others(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 | a0001c0001t0004g0224 a0001c0001t0004g0225 |
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 | a0001c0002t0001g0035 a0001c0002t0001g0091 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(121): 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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0196 a0001c0001t0001g0197 |
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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0130 |
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 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0036 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(72): 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 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0195 a0001c0001t0004g0218 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(78): 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 | a0001c0001t0001g0127 a0001c0001t0001g0140 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0021 others(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 |
23 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(20): 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 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0001t0001g0231 others(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 | a0001c0004t0002g0110 a0001c0004t0002g0111 |
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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0227 a0001c0004t0002g0103 |
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 | a0001c0001t0005g0114 a0001c0004t0002g0115 a0001c0004t0008g0104 |
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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0107 a0001c0001t0001g0227 others(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 | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0023 others(67): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(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 | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(78): 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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | a0001c0004t0002g0113 | 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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0133 others(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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0003c0006t0005g0016 | 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(164): Show |
173 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(170): 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 | a0001c0001t0001g0011 | 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(72): 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 | 3 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 |
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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0227 | 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 | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(75): 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 | a0001c0002t0001g0032 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 |
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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(100): 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 | |||||||
| chr16:24965312 | TA | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.462-1005delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 6/19 | chr16 | 24965312 | |||||||
| 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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 |
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 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0036 others(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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
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 | a0001c0001t0005g0228 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0146 |
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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(132): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0004g0218 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0197 |
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 | 3 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 |
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 | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(74): 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 | a0001c0003t0003g0215 a0001c0003t0003g0217 |
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 | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(75): 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 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0140 |
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 | a0001c0001t0001g0172 a0001c0001t0001g0177 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0004g0218 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 37 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(34): Show |
39 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.272+452delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4/19 | chr16 | 24970054 | |||||||
| chr16:24970589 | T | C | 3 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 |
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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(93): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0186 | 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 | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(75): 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0227 | 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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0001g0118 a0001c0001t0005g0114 |
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 | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(30): Show |
33 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(30): 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 | a0001c0004t0002g0103 a0001c0004t0002g0110 a0001c0004t0002g0111 others(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 | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(106): 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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0004g0218 others(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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(120): 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 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0036 others(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 | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(75): 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(75): 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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0004g0218 others(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 | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(68): 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
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 | a0001c0001t0001g0227 | 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 | 3 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 |
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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0055 a0001c0001t0001g0079 others(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 | a0001c0003t0003g0210 | 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 |
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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0036 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(168): Show |
177 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.198+403T>C | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 3/19 | chr16 | 24976812 | |||||||
| chr16:24977014 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(132): 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 | a0001c0001t0001g0008 a0001c0004t0002g0103 a0001c0004t0002g0108 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | a0001c0001t0006g0070 a0001c0001t0006g0072 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0146 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0145 |
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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0049 | 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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): 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 | 60 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(57): Show |
62 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.93+99delT | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2/19 | chr16 | 24978866 | |||||||
| chr16:24978866 | TAA | T | 53 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0227 a0001c0001t0005g0004 others(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 | a0003c0006t0005g0016 | 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 | a0003c0006t0005g0016 | 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 | a0003c0006t0005g0016 | 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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0227 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0003c0006t0005g0016 | 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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0145 |
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 | a0001c0001t0001g0077 a0001c0001t0001g0087 |
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 | 6 | a0001c0001t0001g0003 a0001c0001t0001g0191 a0001c0001t0001g0192 others(3): 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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(132): 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 | a0003c0006t0005g0016 | 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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(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 | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(97): 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 | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(33): Show |
36 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.54-3091delA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982095 | |||||||
| chr16:24982115 | T | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 |
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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): 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 | a0001c0001t0001g0028 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0151 others(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 | CATATAT | 2 | a0001c0001t0001g0152 a0001c0001t0001g0159 |
2 | HG00597.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.54-3966_54-3961dup others(6): 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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0011 | 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 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0035 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0015 | 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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0054 others(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 | ATATATT | 2 | a0001c0001t0001g0024 a0001c0001t0002g0031 |
2 | HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.54-3982_54-3981ins others(6): 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 | a0001c0001t0001g0007 | 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 | a0003c0006t0005g0016 | 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 | a0001c0001t0004g0219 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0005g0228 | 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 | a0001c0004t0002g0113 | 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 | a0001c0004t0002g0112 | 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 | a0001c0004t0002g0110 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0064 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0125 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0120 a0001c0001t0001g0158 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0066 a0001c0001t0007g0019 |
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 | 52 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0024 others(49): Show |
52 | HG00597.hp2 HG01243.hp1 HG01496.hp1 others(49): Show |
intron_variant | MODIFIER | c.54-3993A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24982998 | |||||||
| chr16:24982999 | T | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): 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 | a0001c0001t0001g0025 a0001c0001t0001g0078 a0001c0001t0001g0100 others(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 | 39 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0024 others(36): Show |
39 | HG00597.hp2 HG01884.hp2 HG01934.hp1 others(36): 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 | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(80): 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 | a0001c0001t0001g0082 a0001c0001t0001g0096 a0001c0001t0001g0107 |
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 | 31 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0024 others(28): Show |
31 | HG00597.hp2 HG01934.hp1 HG01993.hp1 others(28): Show |
intron_variant | MODIFIER | c.54-3997A>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24983002 | |||||||
| chr16:24983003 | T | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(45): 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 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0099 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0068 |
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 | a0001c0001t0007g0020 | 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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(72): 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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(132): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | 16 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(13): 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0014 | 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0003c0006t0005g0016 | 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(114): 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 | |||||||
| chr16:24985847 | T | TAC | 2 | a0001c0002t0001g0033 a0001c0002t0001g0034 |
2 | NA18946.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.54-6844_54-6843dup others(2): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24985847 | |||||||
| chr16:24985891 | G | A | 1 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(132): 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 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0057 | 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 | 33 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(30): 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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(132): 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0174 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0227 | 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 | 3 | a0001c0001t0001g0126 a0001c0001t0001g0139 a0001c0001t0001g0144 |
3 | HG00642.hp2 HG01123.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.54-8981C>T | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 24987986 | |||||||
| chr16:24988200 | G | T | 8 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0227 a0001c0002t0001g0032 others(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 | a0001c0001t0004g0012 | 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 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(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 | a0001c0002t0001g0036 a0001c0002t0001g0037 a0001c0002t0001g0041 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): 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 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0227 a0001c0002t0001g0032 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(114): 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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(132): 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0227 a0001c0002t0001g0032 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
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 | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(91): 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(114): 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 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(132): 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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(132): 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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0004g0225 | 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 | a0001c0001t0001g0227 | 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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0003c0006t0005g0016 | 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(80): 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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | a0001c0001t0001g0204 | 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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(77): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0003c0006t0005g0016 | 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(127): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0023 others(72): 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0023 others(105): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(115): 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(133): 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 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0004g0225 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0227 a0001c0002t0001g0032 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0227 |
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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0046 others(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 | a0001c0004t0002g0108 a0001c0004t0002g0115 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0002t0001g0035 a0001c0002t0001g0091 |
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 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(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 | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(133): 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | |||||||
| chr16:24998548 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0055 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0027 a0001c0004t0002g0103 a0001c0004t0002g0108 others(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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0149 others(10): 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0004g0224 | 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0227 a0001c0002t0001g0032 others(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 | a0001c0001t0001g0015 a0001c0004t0002g0103 a0001c0004t0002g0108 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | 52 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
54 | HG00642.hp2 HG01123.hp1 HG01168.hp2 others(51): 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 | a0001c0001t0001g0026 a0001c0001t0001g0136 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0227 a0001c0002t0001g0032 others(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 | 16 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(13): 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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0079 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(131): 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 | a0001c0001t0001g0030 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0001g0029 a0001c0001t0005g0004 a0001c0001t0005g0228 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0106 |
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 | 16 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(13): 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 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(135): 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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | 5 | a0001c0001t0001g0003 a0001c0001t0001g0191 a0001c0001t0001g0192 others(2): 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 | 26 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(23): 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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0004g0218 others(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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0140 a0001c0001t0001g0141 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
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 | a0003c0006t0005g0016 | 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(135): 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 | 62 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(59): Show |
62 | HG00323.hp1 HG00438.hp1 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.53+11978dupA | ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | 25003230 | |||||||
| chr16:25003230 | C | CTT | 12 | a0001c0001t0001g0015 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0003t0003g0208 others(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 | a0001c0001t0001g0088 a0001c0002t0001g0034 a0001c0002t0001g0035 others(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 | 27 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(24): 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 |
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 | a0001c0001t0001g0156 a0001c0001t0001g0196 a0001c0001t0001g0197 |
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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0120 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0001c0001t0001g0107 a0001c0004t0002g0103 a0001c0004t0002g0108 others(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 | a0001c0001t0001g0013 a0001c0003t0003g0208 a0001c0003t0003g0209 others(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 | a0001c0001t0004g0224 | 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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0004g0218 others(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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0227 | 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(135): 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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0107 a0001c0004t0002g0108 a0001c0004t0002g0115 |
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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(167): Show |
176 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(173): 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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | 27 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(24): 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0046 a0001c0002t0001g0032 a0001c0002t0001g0033 others(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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(135): 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 | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(172): Show |
181 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(178): 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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0002c0007t0001g0222 |
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 | a0001c0001t0001g0227 | 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 | a0001c0001t0005g0229 | 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(135): 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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0047 others(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 | 41 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(38): 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
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 | a0001c0003t0003g0217 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
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 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
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 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0004g0218 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
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 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
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 | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(167): Show |
176 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(173): 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(135): 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 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0227 a0001c0001t0005g0004 a0001c0001t0005g0228 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
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 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0005g0004 others(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 | 14 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(11): 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0005g0004 a0001c0001t0005g0228 a0001c0001t0005g0229 |
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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(166): Show |
175 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(172): 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 | a0001c0001t0001g0017 | 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 | a0001c0003t0003g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0003c0006t0005g0016 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(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 |